ホームページ Epigenetics Sirtuin inhibitor - Src inhibitor - PKC inhibitor - PI3K inhibitor - Apoptosis related activator - Mitophagy activator - Autophagy activator Quercetin For research use only.

Quercetin

別名：Sophoretin, C.I. 75720, NSC 9221

Quercetin, a natural flavonoid present in vegetables, fruit and wine, is a stimulator of recombinant SIRT1 and also a PI3K inhibitor with IC50 of 2.4-5.4 μM. Quercetin induces mitophagy, apoptosis and protective autophagy. Phase 4.

Quercetin化学構造

CAS No. 117-39-5

サイズ 価格(税別) 在庫状況
JPY 22000 国内在庫あり
JPY 59500 国内在庫あり

代表番号: 045-509-1970|電子メール：[email protected]
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文献中Selleckの製品使用例（44）

製品安全説明書

現在のバッチを見る： 純度： 99.01%
99.01

Quercetin関連製品

シグナル伝達経路

Sirtuin Signaling Pathways

Sirtuinシグナル伝達経路

Sirtuin阻害剤の選択性比較

Cell Data

Cell Lines Assay Type Concentration Incubation Time 活性情報 PMID
3T3/A31 Growth inhibition assay 10 to 100 ug/mL 72 hrs Growth inhibition of BALB/c mouse cloned 3T3/A31 cells at 10 to 100 ug/mL after 72 hrs by nigrosin assay 10096863
BGC823 Apoptosis assay 50 uM 48 hrs Induction of apoptotic bodies in human BGC823 cells at 50 uM after 48 hrs 17997321
BGC823 Apoptosis assay 50 uM 48 hrs Induction of apoptosis in human BGC823 cells assessed as increase in DNA fragmentation at 50 uM after 48 hrs 17997321
BGC823 Apoptosis assay 100 uM 48 hrs Induction of apoptosis in human BGC823 cells assessed as increase in DNA fragmentation at 100 uM after 48 hrs 17997321
HL60 Antiproliferative assay 30 uM 48 hrs Antiproliferative activity against human HL60 cells at 30 uM after 48 hrs by MTS assay 18258440
Jurkat Function assay 50 ug/mL 1 hr Inhibition of heat-induced HSP70 expression in human Jurkat cells at 50 ug/mL treated for 1 hr before heat induction by Western blot 19296652
HeLa Function assay 50 ug/mL 1 hr Enhancement of HSP27 Ser78 phosphorylation in human HeLa cells at 50 ug/mL treated for 1 hr 19296652
Jurkat Function assay 50 ug/mL 1 hr Inhibition of HSF1 binding to heat shock element DNA assessed as HSF1/HSE complex formation in human Jurkat cells at 50 ug/mL treated for 1 hr before heat induction 19296652
Jurkat Function assay 50 ug/mL 1 hr Inhibition of of heat-induced increase in nuclear HSF1 protein phosphorylation in human Jurkat cells assessed as decrease in protein mobility at 50 ug/mL treated for 1 hr before heat induction by EMSA 19296652
HeLa Function assay 50 ug/mL 1 hr Inhibition of of heat-induced increase in nuclear HSF1 protein phosphorylation in human HeLa cells assessed as decrease in protein mobility at 50 ug/mL treated for 1 hr before heat induction by EMSA 19296652
MCF7 Function assay 0.5 uM to 10 uM 24 hrs Induction of CYP1A1 expression in human MCF7 cells at 0.5 uM to 10 uM after 24 hrs by RT PCR and DNA electrophoresis 19601638
HCT116 Function assay 5 uM 1 hr Cellular uptake in human HCT116 cells assessed a bright fluorescence light at 5 uM after 1 hr by fluorescence microscopic analysis 21090565
MCF7 Function assay 10 uM 5 hrs Cellular uptake in human MCF7 cells assessed as formation of quercetin glucuronide in cell lysates at 10 uM after 5 hrs by HPLC-mass spectrophotometric analysis 21090565
MCF7 Function assay 10 uM 5 hrs Cellular uptake in human MCF7 cells assessed as formation of quercetin sulphate in cell lysates at 10 uM after 5 hrs by HPLC-mass spectrophotometric analysis 21090565
MCF7 Function assay 10 uM 5 hrs Cellular uptake in human MCF7 cells assessed as formation of oxidised quercetin in cell lysates at 10 uM after 5 hrs by HPLC-mass spectrophotometric analysis 21090565
MCF7 Function assay 10 uM 5 hrs Cellular uptake in human MCF7 cells assessed as formation of methylated quercetin in cell lysates at 10 uM after 5 hrs by HPLC-mass spectrophotometric analysis 21090565
RAW264.7 Antiinflammatory assay 1 to 100 uM 24 hrs Antiinflammatory activity in LPS-stimulated mouse RAW264.7 cells assessed as nitrite level at 1 to 100 uM after 24 hrs by Griess method, Activity=1.38μM 21353543
MDA-MB-231 Function assay 20 uM 30 mins Increase in c-Fos protein expression in human MDA-MB-231 cells at 20 uM within 30 mins by Western blot analysis 21652208
MDA-MB-231 Function assay 20 uM 30 mins Increase in Egr-1 protein expression in human MDA-MB-231 cells at 20 uM within 30 mins by Western blot analysis 21652208
MDA-MB-231 Apoptosis assay 20 uM 12 hrs Induction of apoptosis in human MDA-MB-231 cells assessed as cleaved caspase-7 accumulation at 20 uM after 12 hrs by Western blot analysis 21652208
Jurkat Function assay 145 uM 8 hrs Inhibition of heat shock-induced HSP70 expression in human Jurkat cells at 145 uM treated 2 hrs before beat shock challenge measured after 8 hrs by Western blotting 21798748
HCT116 Function assay 25 uM 10 mins Inhibition of PI3Kalpha in human HCT116 cells using [32P]ATP at 25 uM after 10 mins 22212721
HCT116 Function assay 25 uM 10 mins Inhibition of PI3Kalpha H1047R mutant in human HCT116 cells using [32P]ATP at 25 uM after 10 mins 22212721
HT22 Neuroprotective assay 25 uM 24 hrs Neuroprotective activity against glutamate induced oxidative stress in mouse hippocampal HT22 cells assessed as cell viability at 25 uM after 24 hrs by MTT assay 22624880
RAW264.7 Function assay 50 uM 3 hrs Activation of Nrf2 in mouse RAW264.7 cells assessed as cytosolic accumulation at 50 uM after 3 hrs by Western blotting analysis 23294286
RAW264.7 Function assay 50 uM 3 hrs Activation of Nrf2 in mouse RAW264.7 cells assessed as nuclear accumulation at 50 uM after 3 hrs by Western blotting analysis 23294286
ARPE19 Function assay 20 uM 18 days Inhibition of intracellular A2E photooxidation in human ARPE19 cells at 20 uM after 18 days 23346866
HCT116 Cytotoxicity assay 1 to 100 uM 12 hrs Cytotoxicity against human HCT116 cells at 1 to 100 uM after 12 hrs by MTT assay 23434132
MCF7 Cytotoxicity assay 1 to 100 uM 12 hrs Cytotoxicity against human MCF7 cells at 1 to 100 uM after 12 hrs by MTT assay 23434132
HT22 Neuroprotective assay 40 uM 3 hrs Neuroprotective activity in mouse HT22 cells assessed as t-BOOH-induced toxicity at 40 uM preincubated for 3 hrs followed by t-BOOH induction measured after 9 hrs by MTT assay 24245939
HT22 Neuroprotective assay 40 uM 3 hrs Neuroprotective activity in mouse HT22 cells assessed as reduction of t-BOOH-induced oxidative stress at 40 uM preincubated for 3 hrs followed by t-BOOH induction measured after 20 hrs by MTT assay 24245939
RAW264.7 Antiinflammatory assay 10 uM 18 hrs Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced TNF-alpha secretion at 10 uM after 18 hrs by sandwich ELISA 24679441
HT22 Neuroprotective assay 5 uM 48 hrs Neuroprotection against glutamate challenged mouse HT22 cells assessed as reduction in cell viability at 5 uM after 48 hrs by MTT assay 24819955
HT22 Neuroprotective assay 25 uM 24 hrs Neuroprotective activity against glutamate-induced oxidative stress in mouse HT22 cells assessed as reduction of intracellular ROS formation at 25 uM after 24 hrs by MTT assay 24900407
PC12 Neuroprotective assay 5 uM 24 hrs Neuroprotective activity in rat PC12 cells assessed as inhibition H2O2-induced reduction of cell viability at 5 uM after 24 hrs by MTT assay 24941128
HLF1 Function assay 2 to 5 uM 24 hrs Inhibition of H2O2-induced oxidative stress in human HLF1 cells assessed as increase in cell viability at 2 to 5 uM pretreated for 24 hrs followed by addition of 300 uM H2O2 for 2.5 hrs 24996137
RAW264.7 Antiinflammatory assay 3 uM 24 hrs Antiinflammatory activity in LPS-stimulated mouse RAW264.7 cells assessed as reduction in nitric oxide production at 3 uM after 24 hrs by Griess method based ELISA (Rvb = 52.4 +/- 0.9 uM), Activity=13.5μM 25106885
RAW264.7 Antiinflammatory assay 1.5 uM 24 hrs Antiinflammatory activity in LPS-stimulated mouse RAW264.7 cells assessed as reduction in nitric oxide production at 1.5 uM after 24 hrs by Griess method based ELISA (Rvb = 52.4 +/- 0.9 uM), Activity=20.8μM 25106885
MDA-MB-231 Function assay 5 uM 16 hrs Inhibition of PMA-stimulated NF-kappaB signaling (unknown origin) expressed in MDA-MB-231 cells at 5 uM incubated for 16 hrs by luciferase reporter gene assay 25190466
MDA-MB-231 Apoptosis assay 3.125 to 25 uM 48 hrs Induction apoptosis in PMA-stimulated human MDA-MB-231 cells assessed as mitochondrial disruption 3.125 to 25 uM after 48 hrs by JC1 staining based fluorescence assay 25190466
HCT116 Cytotoxicity assay 1.25 to 20 uM 96 hrs Cytotoxicity against human HCT116 cells at 1.25 to 20 uM after 96 hrs by MTT assay 25397870
HCT116 Apoptosis assay 20 uM 72 hrs Induction of apoptosis in human HCT116 cells assessed as PARP cleavage at 20 uM after 72 hrs by immunoblotting 25397870
HCT116 Antitumor assay 80 uM 4 days Antitumor activity against human HCT116 cells xenografted in 48 hpf zebrafish embryo assessed as inhibition of cancer cell proliferation at 80 uM treated for 4 days 25397870
BL21 Function assay 20 uM 15 mins Inhibition of recombinant human N-terminal His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using all-trans-retinal as substrate at 20 uM incubated for 15 mins by HPLC method 26529431
HT22 Neuroprotective assay 25 uM 24 hrs Neuroprotective activity against glutamate-induced oxycytotic cell death in mouse HT22 cells assessed as cell viability at 25 uM after 24 hrs by MTT assay 26886849
PC12 Function assay 5 uM 2 hrs Protective effect against H2O2-induced cell death in rat PC12 cells at 5 uM preincubated for 2 hrs followed by H2O2 addition for 24 hrs by MTT assay 27343850
PC12 Antioxidant assay 2.5 uM 2 hrs Antioxidant activity in rat PC12 cells assessed as decrease of H2O2-induced ROS production at 2.5 uM preincubated for 2 hrs followed by H2O2 addition for 24 hrs by DCFH-DA /DAPI-based fluorescence assay 27343850
LLC-PK1 Renoprotective assay 10 to 100 uM 2 hrs Renoprotective activity in pig LLC-PK1 cells assessed as inhibition of cisplatin-induced damage by measuring increase in cell viability at 10 to 100 uM preincubated for 2 hrs followed by cisplatin addition after 24 hrs by Ez-Cytox reagent based assay 28487074
PC12 Neuroprotective assay 10 uM 3 hrs Neuroprotective activity in rat PC12 cells assessed as decrease in H2O2 mediated apoptosis at 10 uM preincubated for 3 hrs followed by H2O2 challenge measured after 24 hrs by MTT assay 28803044
SH-SY5Y Neuroprotective assay 100 uM 12 hrs Neuroprotective activity against H2O2-induced cell death in human SH-SY5Y cells assessed as increase in cell viability at 100 uM pretreated for 12 hrs followed by H2O2 challenge measured after 3 hrs by MTT assay 28988761
RAW264.7 Cytoprotective assay 1 pM 2 hrs Cytoprotective activity against H2O2-induced oxidative stress in mouse RAW264.7 cells assessed as increase in cell viability at 1 pM incubated for 2 hrs prior to H2O2 addition measured after 24 hrs by MTT assay 29681148
HCT116 Function assay 2.5 uM 30 mins Inhibition of IP6K2 in human [3H]-inositol-labelled HCT116 cells assessed as reduction in insp7 levels at 2.5 uM after 30 mins by HPLC analysis 30624931
HEK293 Function assay 2.5 uM 3.5 hrs Inhibition of IP6K2 in [3H]-inositol-labelled HEK293 cells assessed as reduction in insp7 levels at 2.5 uM after 3.5 hrs by HPLC analysis relative to control 30624931
3T3-L1 Function assay 2.5 uM 3 hrs Activation of AKT activity in mouse 3T3-L1 cells assessed as increase in AKT phosphorylation at T308 residues at 2.5 uM after 3 hrs by Western blot analysis 30624931
3T3-L1 Function assay 1 uM 3 hrs Inhibition of IP6K2 in mouse 3T3-L1 cells assessed as AKT phosphorylation at T308 at 1 uM after 3 hrs by Western blot analysis 30624931
HCT116 Function assay 2.5 uM 3.5 hrs Inhibition of IP6K2 in human [3H]-inositol-labelled HCT116 cells assessed as reduction in insp7 levels at 2.5 uM after 3.5 hrs by HPLC analysis relative to control 30624931
CGN Neuroprotective assay 5 to 100 uM 24 hrs Neuroprotective activity in Sprague-Dawley rat CGN cells assessed as protection against H2O2-induced cytotoxicity by measuring increase in cell viability at 5 to 100 uM pre-incubated for 24 hrs before H2O2 stimulation for 24 hrs by MTT assay 30935792
PC12 Neuroprotective assay 10 uM 3 hrs Neuroprotective activity in rat PC12 cells assessed as protection against H2O2-induced cytotoxicity at 10 uM pre-incubated for 3 hrs before H2O2 addition and measured after 12 hrs by MTT assay 31128990
SH-SY5Y Neuroprotective assay 100 uM 1 hr Neuroprotective activity against H2O2-induced oxidative stress in human SH-SY5Y cells assessed as reduction in ROS generation at 100 uM preincubated for 1 hr followed by DCFH-DA addition for 30 mins and subsequent co-treatment with compound and H2O2 for 3 31158754
HT22 Neuroprotective assay 25 uM 24 hrs Neuroprotection against glutamate-induced cell death in mouse HT22 cells assessed as increase in cell viability at 25 uM measured after 24 hrs by MTT assay 31609115
HT22 Neuroprotective assay 25 uM 24 hrs Neuroprotective activity at mouse HT22 cells assessed as reduction in glutamate-induced oxidative stress by measuring cell viability at 25 uM incubated for 24 hrs by MTT assay 31609608
BGC823 Function assay 50 uM Effect on cell morphology in human BGC823 cells assessed as chromosomal condensations at 50 uM 17997321
3T3L1 Function assay 10 uM Induction of AMPK phosphorylation in mouse 3T3L1 cells at 10 uM by Western blotting 20822902
3T3L1 Function assay 10 uM Induction of AMPK-mediated ACC phosphorylation in mouse 3T3L1 cells at 10 uM by Western blotting 20822902
HCT116 Function assay 25 uM Inhibition of PI3Kalpha in human HCT116 cells assessed as inhibition of Akt Ser473 phosphorylation at 25 uM by immunoblot analysis 22212721
HCT116 Function assay 25 uM Inhibition of PI3Kalpha H1047R mutant in human HCT116 cells assessed as inhibition of Akt Ser473 phosphorylation at 25 uM by immunoblot analysis 22212721
3T3L1 Antiobesity assay 100 uM Antiobesity activity in mouse 3T3L1 cells assessed as reduction of fat accumulation at 100 uM by oil Red O staining-based ELISA 23642481
HT22 Neuroprotective assay 25 uM Neuroprotective activity in mouse HT22 cells assessed as reduction in glutamate-induced cytotoxicity at 25 uM by MTT assay 25059502
MDA-MB-231 Function assay 25 uM Inhibition of basal NF-kappaB signaling in human MDA-MB-231 cells assessed as reduction in MMP9 mRNA expression at 25 uM by quantitative RT-PCR method relative to untreated control 25190466
MDA-MB-231 Function assay 25 uM Inhibition of NF-kappaB signaling in human MDA-MB-231 cells assessed as reduction in PMA-stimulated MMP9 mRNA expression at 25 uM pre-incubated before PMA stimulation by quantitative RT-PCR method relative to untreated control 25190466
MDA-MB-231 Function assay 25 uM Inhibition of basal NF-kappaB signaling in human MDA-MB-231 cells assessed as reduction in COX2 mRNA expression at 25 uM by quantitative RT-PCR method relative to untreated control 25190466
MDA-MB-231 Function assay 25 uM Inhibition of NF-kappaB signaling in human MDA-MB-231 cells assessed as reduction in PMA-stimulated COX2 mRNA expression at 25 uM pre-incubated before PMA stimulation by quantitative RT-PCR method relative to untreated control 25190466
MDA-MB-231 Function assay 25 uM Inhibition of NF-kappaB signaling in human MDA-MB-231 cells assessed as reduction in PMA-stimulated MMP9 mRNA expression at 25 uM pre-incubated before PMA stimulation by quantitative RT-PCR method 25190466
MDA-MB-231 Function assay 25 uM Inhibition of NF-kappaB signaling in human MDA-MB-231 cells assessed as reduction in PMA-stimulated COX2 mRNA expression at 25 uM pre-incubated before PMA stimulation by quantitative RT-PCR method 25190466
PC12 Function assay 10 uM Inhibition of human amyloid beta (1 to 42) assessed as neuroprotective activity against amyloid beta (1 to 42)-induced toxicity in rat PC12 cells by measuring reduction in cell viability at 10 uM incubated 15 mins prior to amyloid beta (1 to 42) addition 28559058
MDA-MB-468 Function assay 6.6 uM Inhibition of human CYP1B1 expressed in MDA-MB-468 cells assessed as potentiation of cisplatin-induced cytotoxicity by measuring cisplatin EC50 at 6.6 uM (Rvb = 6.70+/- 0.7 uM), EC50=1.1μM 29150398
HEK293 Function assay 20 uM Inhibition of human CYP1A1 transfected in HEK293 cells assessed as protection against CYP1A1 mediated B[a]P toxicity by measuring B[a]P EC50 at 20 uM by MTT assay (Rvb =1.2+/- 0.3 uM), EC50=8.8μM 29150398
L929 Function assay 2 hrs Potentiation of recombinant human TNF-alpha-induced cytotoxicity of mouse L929 cells assessed as survivality treated with drug after 2 hrs of TNFalpha treatment 9287415
L929 Function assay 2 hrs Inhibition of recombinant human TNF-alpha-induced cytotoxicity of mouse L929 cells assessed as survivality treated with drug after 2 hrs of TNFalpha treatment 9287415
L929 Function assay 15 mins Inhibition of recombinant human TNF-alpha-induced cytotoxicity of mouse L929 cells assessed as survivality preincubated for 15 mins before TNFalpha addition measured after 24 hrs by [methyl-3H]thymidine incorporation assay, EC50=26μM 9287415
L929 Function assay 15 mins Inhibition of recombinant human TNF-alpha-induced cytotoxicity of mouse L929 cells assessed as survivality preincubated for 15 mins before TNFalpha addition measured after 24 hrs by crystal violet staining, EC50=20μM 9287415
SKBR3 Antiapoptotic assay 72 hrs Inhibition of HSP70-mediated antiapoptotic activity in human SKBR3 cells assessed as induction of cell growth arrest after 72 hrs by propidium iodide staining-based flow cytometry 17603540
SKBR3 Antiapoptotic assay 24 hrs Inhibition of HSP70-mediated antiapoptotic activity in human SKBR3 cells assessed as increase in caspase-3 activity after 24 hrs by Western blot analysis 17603540
SKBR3 Antiapoptotic assay 24 hrs Inhibition of HSP70-mediated antiapoptotic activity in human SKBR3 cells assessed as induction of caspase-3 cleavage after 24 hrs by Western blot analysis 17603540
SKBR3 Antiapoptotic assay 24 hrs Inhibition of HSP70-mediated antiapoptotic activity in human SKBR3 cells assessed as induction of PARP cleavage after 24 hrs by Western blot analysis 17603540
RAW264.7 Function assay 16 hrs Inhibition of LPS and INF-alpha-induced nitric oxide production in mouse RAW264.7 cells after 16 hrs, IC50=25μM 18027905
RAW264.7 Antiinflammatory assay 24 hrs Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess reagent assay, IC50=9.6μM 19555124
RAW264.7 Antiinflammatory assay 24 hrs Antiinflammatory activity against mouse RAW264.7 cells assessed as inhibition of LPS-induced nitrite accumulation after 24 hrs by Griess reagent method, IC50=11.4μM 19778086
Vero Cytotoxicity assay 3 days Cytotoxicity against african green monkey Vero cells after 3 days by MTT assay, MNCC<20μM 19778089
Vero Cytotoxicity assay 3 days Cytotoxicity against african green monkey Vero cells after 3 days by MTT assay, MNCC<20μM 20092288
RAW264.7 Antiinflammatory assay 24 hrs Antiinflammatory activity against mouse RAW264.7 cells assessed as Inhibition of LPS-induced nitric oxide production after 24 hrs by ELISA, IC50=32.1μM 20121165
B16-4A5 Function assay 72 hrs Inhibition of theophylline-stimulated melanogenesis in mouse B16-4A5 cells after 72 hrs, IC50=15μM 20189399
RAW264.7 Antiinflammatory assay 24 hrs Antiinflammatory activity against LPS-stimulated mouse RAW264.7 cells assessed as inhibition of NO production after 24 hrs, IC50=34.5μM 20825224
HepG2(2.2.15) Cytotoxicity assay 8 days Cytotoxicity against human HepG2(2.2.15) cells after 8 days by MTT assay, CC50=38.1μM 21401115
HepG2 Function assay 24 hrs Inhibition of oleic acid-induced triglyceride over-accumulation in human HepG2 cells incubated for 24 hrs relative to untreated control, IC30=14.9μM 21824690
HepG2 Antioxidant assay 24 hrs Antioxidant activity in human HepG2 cells assessed as reduction of oleic acid-induced ROS generation incubated for 24 hrs by DHCF-DA based fluorimetric assay relative to untreated control, IC30=30.8μM 21824690
MDCK Antiviral assay 4 days Antiviral activity against influenza A virus (A/swine/OH/511445/2007(H1N1)) Oh7 infected in MDCK cells assessed as inhibition of viral replication after 4 days by quantitative RT-PCR, ED50=48.2μM 22115591
HCT116 Growth inhibition assay 48 hrs Growth inhibition of human HCT116 cells overexpressing PI3Kalpha H1047R mutant after 48 hrs by MTT assay, IC50=5.7μM 22212721
HCT116 Growth inhibition assay 48 hrs Growth inhibition of human HCT116 cells after 48 hrs by MTT assay, IC50=6.7μM 22212721
HCT116 Growth inhibition assay 48 hrs Growth inhibition of human HCT116 cells overexpressing PI3Kalpha after 48 hrs by MTT assay, IC50=23μM 22212721
Huh7.5.1 Antiviral assay 72 hrs Antiviral activity against HCV JFH-1 J399EM infected in Human Huh7.5.1 cells assessed as suppression of viral replication after 72 hrs by EGFP assay, EC50=19.8μM 22445328
MV4-11 Cytotoxicity assay 72 hrs Cytotoxicity against human MV4-11 cells harboring FLT3 mutation after 72 hrs by tetrazolium based Ez CyTox cell viability assay, GI50=13.1μM 23411073
RS4:11 Cytotoxicity assay 72 hrs Cytotoxicity against human RS4:11 cells harboring wild type FLT3 after 72 hrs by tetrazolium based Ez CyTox cell viability assay, GI50=21.6μM 23411073
HTLA Function assay 20 mins Inhibition of CX3CL1-stimulated CX3CR1 in human HTLA cells pre-incubated for 20 mins measured on day 4 by beta arrestin-recruitment mediated luciferase reporter gene assay, IC50=4.5μM 23437772
HTLA Function assay 20 mins Inhibition of CX3CL1-stimulated CX3CR1 in human HTLA cells pre-incubated for 20 mins measured on day 4 by beta arrestin-recruitment mediated luciferase reporter gene assay, IC50=5.01187μM 23437772
HTLA Function assay 20 mins Inhibition of vasopressin-stimulated vasopressin V2 receptor in human HTLA cells pre-incubated for 20 mins measured on day 4 by beta arrestin-recruitment mediated luciferase reporter gene assay, IC50=6.30957μM 23437772
HTLA Function assay 20 mins Inhibition of vasopressin-stimulated vasopressin V2 receptor in human HTLA cells pre-incubated for 20 mins measured on day 4 by beta arrestin-recruitment mediated luciferase reporter gene assay, IC50=7μM 23437772
HTLA Function assay 20 mins Inhibition of CCL22-stimulated CCR4 in human HTLA cells pre-incubated for 20 mins measured on day 4 by beta arrestin-recruitment mediated luciferase reporter gene assay, IC50=10μM 23437772
HTLA Function assay 20 mins Inhibition of CCL22-stimulated CCR4 in human HTLA cells pre-incubated for 20 mins measured on day 4 by beta arrestin-recruitment mediated luciferase reporter gene assay, IC50=10.2μM 23437772
HTLA Function assay 20 mins Inhibition of vasopressin-stimulated vasopressin V2 receptor in human HTLA cells pre-incubated for 20 mins with Tween-80-treated compound solution measured on day 4 by beta arrestin-recruitment mediated luciferase reporter gene assay, IC50=15.2μM 23437772
HTLA Function assay 20 mins Inhibition of vasopressin-stimulated vasopressin V2 receptor in human HTLA cells pre-incubated for 20 mins with Tween-80-treated compound solution measured on day 4 by beta arrestin-recruitment mediated luciferase reporter gene assay, IC50=15.8489μM 23437772
HTLA Function assay 20 mins Inhibition of vasopressin-stimulated vasopressin V2 receptor in human HTLA cells pre-incubated for 20 mins with centrifuged compound solution measured on day 4 by beta arrestin-recruitment mediated luciferase reporter gene assay, IC50=37.8μM 23437772
HTLA Function assay 20 mins Inhibition of vasopressin-stimulated vasopressin V2 receptor in human HTLA cells pre-incubated for 20 mins with centrifuged compound solution measured on day 4 by beta arrestin-recruitment mediated luciferase reporter gene assay, IC50=39.8107μM 23437772
RAW264.7 Function assay 24 hrs Inhibition of iNOS-mediated nitric oxide production in LPS-stimulated mouse RAW264.7 cells after 24 hrs by Griess reaction analysis, IC50=16.4μM 23517145
RAW264.7 Function assay 24 hrs Inhibition of LPS-induced NO production in mouse RAW264.7 cells after 24 hrs, IC50=1.3μM 23540981
HepG2 Antioxidant assay 1 hr Antioxidant activity in human HepG2 cells assessed as inhibition of ABAP-induced intracellular peroxyl radical scavenging activity by measuring ROS production measured every 5 mins for 1 hr by absorbance assay, IC50=11μM 24471493
HT22 Neuroprotective assay 24 hrs Neuroprotective activity in mouse HT22 cells assessed as protection against glutamate-induced oxidative damage after 24 hrs by MTT assay, EC50=3.13μM 24602904
HT22 Cytotoxicity assay 24 hrs Cytotoxicity against mouse HT22 cells after 24 hrs by MTT assay, EC50=11.52μM 24602904
U2OS Function assay 5 hrs Agonist activity at GPR35 receptor in human U2OS cells coexpressing Gal4-VP16-TEV assessed as beta arrestin translocation after 5 hrs by beta lactamase reporter gene assay, EC50=5.93μM 24900447
HT-29 Function assay 10 mins Agonist activity at GPR35 receptor in human HT-29 cells after 10 mins by dynamic mass redistribution assay, EC50=8.02μM 24900447
HT-29 Function assay 10 mins Desensitization of GPR35 receptor in human HT-29 cells assessed as inhibition of zaprinast-induced dynamic mass redistribution after 10 mins, IC50=15.4μM 24900447
HT-29 Function assay 10 mins Partial agonist activity at GPR35 receptor in human HT-29 cells after 10 mins by dynamic mass redistribution assay 24900447
HL60 Cytotoxicity assay 72 hrs Cytotoxicity against human HL60 cells after 72 hrs by MTT assay, IC50=47μM 25014747
BV2 Function assay 24 hrs Inhibition of LPS-stimulated NO production in human BV2 cells after 24 hrs by Griess assay, IC50=4.3μM 25127164
RAW264.7 Anti-inflammatory assay 24 hrs Anti-inflammatory activity in mouse RAW264.7 cells assessed as inhibition of lipopolysaccharide-induced nitric oxide production incubated for 24 hrs by Griess reagent based assay, IC50=16.6μM 25245917
C6 Function assay 72 hrs Inhibition of cell proliferation of rat C6 cells assessed as cell viability after 72 hrs by sulforhodamine B assay, IC50=18.38μM 25442304
HCT15 Cytotoxicity assay 72 hrs Cytotoxicity against human HCT15 cells assessed as cell growth inhibition after 72 hrs by MTT assay, IC50=16.35μM 25906385
MCF7 Cytotoxicity assay 72 hrs Cytotoxicity against human MCF7 cells assessed as cell growth inhibition after 72 hrs by MTT assay, IC50=20.9μM 25906385
2008 Cytotoxicity assay 72 hrs Cytotoxicity against human 2008 cells assessed as cell growth inhibition after 72 hrs by MTT assay, IC50=21.18μM 25906385
A431 Cytotoxicity assay 72 hrs Cytotoxicity against human A431 cells assessed as cell growth inhibition after 72 hrs by MTT assay, IC50=23.04μM 25906385
BxPC3 Cytotoxicity assay 72 hrs Cytotoxicity against human BxPC3 cells assessed as cell growth inhibition after 72 hrs by MTT assay, IC50=24.12μM 25906385
A375 Cytotoxicity assay 72 hrs Cytotoxicity against human A375 cells assessed as cell growth inhibition after 72 hrs by MTT assay, IC50=25.13μM 25906385
A431 Cytotoxicity assay 72 hrs Cytotoxicity against cisplatin-resistant human A431 cells assessed as cell growth inhibition after 72 hrs by MTT assay, IC50=34.37μM 25906385
C13 Cytotoxicity assay 72 hrs Cytotoxicity against human C13 cells assessed as cell growth inhibition after 72 hrs by MTT assay, IC50=37.62μM 25906385
B16-4A5 Function assay 72 hrs Inhibition of melanogenesis in theophylline-stimulated mouse B16-4A5 cells after 72 hrs by microplate reader analysis, IC50=15μM 25987378
RAW264.7 Anti-inflammatory assay 24 hrs Anti-inflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production incubated for 24 hrs by Griess reagent based assay, IC50=1.8μM 26143931
BV2 Anti-inflammatory assay 24 hrs Antiinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-stimulated nitric oxide production after 24 hrs by Griess assay, IC50=17.4μM 26327273
LNCAP Cytotoxicity assay 3 days Cytotoxicity against human androgen-dependent LNCAP cells assessed as inhibition of cell viability after 3 days by WST-1 cell proliferation assay, IC50=45.5μM 26341135
BV2 Antineuroinflammatory assay 24 hrs Antineuroinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-stimulated NO production after 24 hrs by Griess assay, EC50=11μM 26473791
BV2 Function assay 24 hrs Inhibition of LPS-induced nitric oxide production in human BV2 cells after 24 hrs by Griess assay, IC50=8.7μM 26696523
HepG2 Antioxidant assay 2.5 hrs Antioxidant activity in human HepG2 cells assessed as decrease in fluorescence level after 2.5 hrs measured every 5 mins for 1 hr by DCFH-DA staining based fluorescence assay, EC50=4.63μM 26974372
RF/6A Antimigratory assay 24 hrs Antimigratory activity in rhesus monkey RF/6A cells measured after 24 hrs by wound assay, IC50=40μM 27015547
RAW264.7 Function assay 24 hrs Inhibition of LPS-induced NO production in mouse RAW264.7 cells after 24 hrs by Griess assay, IC50=15.9μM 27177824
BV2 Antiinflammatory assay 24 hrs Antiinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced NO production incubated for 24 hrs measured after 15 mins by Griess assay, IC50=15.13μM 27335254
LNCAP Antiproliferative assay 3 days Antiproliferative activity against human LNCAP cells after 3 days by WST1 assay, IC50=45.5μM 27476422
BV2 Antineuroinflammatory assay 24 hrs Antineuroinflammatory activity in human BV2 cells assessed as inhibition of LPS-induced NO production after 24 hrs in presence of LPS by Griess reaction, IC50=39.46μM 27623545
N9 Antineuroinflammatory assay 24 hrs Antineuroinflammatory activity in mouse N9 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess assay, IC50=10.22μM 28073678
Escherichia coli competent cells Function assay overnight Inhibition of amyloid beta (1 to 42) aggregation in Escherichia coli competent cells BL21 (DE3) after overnight incubation by Thioflavin-S steady-state fluorescence assay, IC50=15.3μM 28128562
BV2 Antiinflammatory assay 24 hrs Antiinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced nitrite production after 24 hrs by Griess assay, IC50=19.11μM 28165740
RAW264.7 Function assay 1 hr Inhibition of LPS-induced NO production in mouse RAW264.7 cells preincubated for 1 hr followed by LPS stimulation measured after 24 hrs by Griess assay, IC50=4.41μM 28427811
human red blood cells Antiplasmodial assay 48 hrs Antiplasmodial activity against asexual erythrocyte stage of chloroquine-sensitive Plasmodium falciparum 3D7 infected in human red blood cells after 48 hrs by lactate dehydrogenase assay, IC50=17.54μM 28557449
T47D Cytotoxicity assay 48 hrs Cytotoxicity against human T47D cells assessed as decrease in cell viability after 48 hrs by MTT assay, IC50=11μM 28654265
NCI-H460 Cytotoxicity assay 48 hrs Cytotoxicity against human NCI-H460 cells assessed as decrease in cell viability after 48 hrs by MTT assay, IC50=12μM 28654265
SK-MEL-2 Cytotoxicity assay 48 hrs Cytotoxicity against human SK-MEL-2 cells assessed as decrease in cell viability after 48 hrs by MTT assay, IC50=12μM 28654265
LN229 Cytotoxicity assay 48 hrs Cytotoxicity against human LN229 cells assessed as decrease in cell viability after 48 hrs by MTT assay, IC50=12μM 28654265
A549 Cytotoxicity assay 48 hrs Cytotoxicity against human A549 cells assessed as decrease in cell viability after 48 hrs by MTT assay, IC50=13μM 28654265
MML1 Cytotoxicity assay 48 hrs Cytotoxicity against human MML1 cells assessed as decrease in cell viability after 48 hrs by MTT assay, IC50=15μM 28654265
BxPC3 Cytotoxicity assay 48 hrs Cytotoxicity against human BxPC3 cells assessed as decrease in cell viability after 48 hrs by MTT assay, IC50=16μM 28654265
HT-29 Cytotoxicity assay 48 hrs Cytotoxicity against human HT-29 cells assessed as decrease in cell viability after 48 hrs by MTT assay, IC50=18μM 28654265
COLO201 Cytotoxicity assay 48 hrs Cytotoxicity against human COLO201 cells assessed as decrease in cell viability after 48 hrs by MTT assay, IC50=19μM 28654265
MDA-MB-231 Cytotoxicity assay 48 hrs Cytotoxicity against human MDA-MB-231 cells assessed as decrease in cell viability after 48 hrs by MTT assay, IC50=20μM 28654265
U87 Cytotoxicity assay 48 hrs Cytotoxicity against human U87 cells assessed as decrease in cell viability after 48 hrs by MTT assay, IC50=23μM 28654265
LNCAP Antiproliferative assay 3 days Antiproliferative activity against human LNCAP cells after 3 days by WST-1 assay, IC50=45.46μM 28760528
BV2 Antiinflammatory assay 24 hrs Antiinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by griess assay, IC50=7.2μM 29303577
K562 Cytotoxicity assay 5 days Cytotoxicity against human K562 cells assessed as inhibition of cell growth after 5 days by MTT assay, IC50=2.5μM 29553260
HepG2 Antioxidant assay 60 mins Antioxidant activity in human HepG2 cells assessed as inhibition of ABAP-induced peroxyl radical generation incubated for 60 mins measured for 60 mins by DCFH-DA probe based fluorescence assay, IC50=12μM 29553260
BV2 Antiinflammatory assay 24 hrs Antiinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess assay, IC50=4.3μM 30119995
BV2 Function assay 24 hrs Inhibition of LPS-induced nitric oxide production in mouse BV2 cells after 24 hrs by Griess assay, IC50=2.4μM 30132670
MCF10A Cytotoxicity assay 3 days Cytotoxicity against human MCF10A cells assessed as decrease in cell viability after 3 days by WST-1 assay, IC50=11.97μM 30165345
PWR-1E Cytotoxicity assay 3 days Cytotoxicity against human PWR-1E cells assessed as decrease in cell viability after 3 days by WST-1 assay, IC50=15.08μM 30165345
LNCAP Antiproliferative assay 3 days Antiproliferative activity against human LNCAP cells after 3 days by WST-1 assay, IC50=45.5μM 30165345
Jurkat Function assay 24 hrs Inhibition of chymotrypsin-like activity of human 26S proteasome in human Jurkat cells assessed as decrease in AMC hydrolysis using Z-Gly-Gly-Leu-AMC as substrate after 24 hrs by fluorescence based method, IC50=2μM 30776692
Jurkat Function assay 2 hrs Inhibition of chymotrypsin-like activity of purified human 20S proteasome expressed in human Jurkat cells assessed as decrease in AMC hydrolysis using Suc-Leu-Leu-Val-Tyr-AMC as substrate incubated for 2 hrs by fluorescence based method, IC50=3.5μM 30776692
HEK293 Function assay 30 mins Inhibition of human TRPC5 expressed in HEK293 cells assessed as reduction in gadolinium-induced calcium entry after 30 mins by fluo-4 dye based fluorescence assay, IC50=6.5μM 30943030
EPG85-257RDB Function assay 72 hrs Downregulation of ABCB1 gene expression in human EPG85-257RDB cells after 72 hrs by RT-PCR analysis, IC50=12μM 31103904
PANC1 Anti-austerity assay 24 hrs Anti-austerity activity against nutrient-deprived human PANC1 cells assessed as cell death incubated for 24 hrs by WST-8 assay, PC50=21.8μM 31682126
BM Antioxidant assay Antioxidant activity in BALB/c mouse BM cells assessed as inhibition of ROS production, IC25=3.5μM 17166721
Jurkat T Function assay Activity against hydrogen peroxide induced DNA damage in Jurkat T cells, IC50=5μM 16392814
HT22 Function assay Inhibition of glutamate-induced oxytosis of mouse hippocampal HT22 cells, EC50=2.98μM 16392814
RAW264.7 Function assay Inhibition of LPS-induced nitric oxide production in mouse RAW264.7 cells, IC50=26.8μM 16378364
RAW264.7 Function assay Inhibition of LPS and INF-gamma-induced NO production in mouse RAW264.7 cells, IC50=26.8μM 15043424
HeLa Function assay TP_TRANSPORTER: inhibition of LTC4 uptake in membrane vesicle from MRP1-expressing HeLa cells, Ki=8.1μM 11306701
HEK293 Function assay Displacement of [125I]AB-MECA binding to human Adenosine A3 receptor expressed in HEK293 cells, Ki=30μM 8576921
RBL-1 Function assay In vitro inhibition against 5-lipoxygenase in RBL-1 cells was determined, IC50=0.2μM 8254620
WiDr human colon cells Cytotoxicity assay Cytotoxic effect on WiDr human colon cells, IC50=40.2μM 8201603
3T3 Cytotoxicity assay Cytotoxic effect on 3T3 cells, IC50=39.5μM 8201603
ANN-1 Cytotoxicity assay Cytotoxic effect on v-abl transformed murine ANN-1 cells, IC50=32.5μM 8201603
MCF-7 Cytotoxicity assay Cytotoxic effect on MCF-7 human breast carcinoma cells, IC50=24μM 8201603
RBI-1 Function assay In vitro inhibition of 5-lipoxygenase (5-lo) from the 20000 g supernatant of RBI-1 cells, IC50=0.3μM 2066989
Walker 256 Antitumor assay In vivo antitumor activity against rat Walker 256 cells 469554
Sf21 Function assay Inhibition of human recombinant COX2 expressed in insect Sf21 cells by EIA assay, IC50=28.6μM 17378609
LNCaP Function assay Decrease in androgen receptor protein expression in LNCaP cells by Western blotting, EC50=25μM 17383188
RAW264.7 Function assay Inhibition of LPS-induced nitric oxide production in mouse RAW264.7 cells, IC50=26.8μM 18027905
BV2 Function assay Inhibition of LPS-induced NO production in mouse BV2 cells, IC50=29.6μM 18178435
HeLa Function assay Inhibition of MRP1 transfected in human HeLa cells assessed as inhibition of [3H]LTC4 transport by rapid filtration assay, Ki=2.4μM 19725578
MDCK Antiviral assay Antiviral activity against influenza A virus H1N1 A/PR/8/34 infected in MDCK cells assessed as reduction in virus-induced cytopathic effect, EC50=43.1μM 19729316
Sf9 Function assay Inhibition of rat ecto-5'-nucleotidase expressed in Sf9 cells by capillary electrophoresis method, Ki=0.0453μM 20146483
HUVEC Cytoprotective assay Cytoprotective activity against H2O2-induced cell injury in HUVEC cells, EC50=18μM 20621727
HEK293 FS Function assay Inhibition of NOX4 expressed in HEK293 FS cells assessed as H2O2 production by H2O2/Tyr/LPO assay, IC50=0.68μM 20731357
3T3L1 Function assay Inhibition of AMPK-mediated adipocyte differentiation in mouse 3T3L1 cells 20822902
3T3L1 Function assay Inhibition of PPAR-gamma-mediated adipocyte differentiation in mouse 3T3L1 cells 20822902
MDCK Function assay Inhibition of BCRP expressed in MDCK cells using Hoechst 33342 staining, IC50=6.9μM 21354800
MCF-7 MX Function assay Inhibition of BCRP expressed in MCF-7 MX cells using Hoechst 33342 staining, IC50=7.6μM 21354800
HepG2 Cytotoxicity assay Cytotoxicity against human HepG2 cells by MTT assay, IC50=30.9μM 21726077
human mast cells Function assay Inhibition of SYK in human mast cells assessed as reduction in mast cell degranulation, EC50=35μM 22257213
22Rv1 Antiproliferative assay Antiproliferative activity against human 22Rv1 cells incubated up to 144 hrs by Coulter particle count and size analyzer, IC50=15.5μM 22789812
BV2 Antiinflammatory assay Antiinflammatory activity in human BV2 cells assessed as inhibition of LPS-induced nitric oxide production by Griess assay, IC50=10μM 24707938
HeLa Anticancer assay Anticancer activity against human HeLa cells by HTS assay, IC50=3.56μM 25139569
NCI-H1792 Anticancer assay Anticancer activity against human NCI-H1792 cells by HTS assay, IC50=3.85μM 25139569
LOXIMVI Anticancer assay Anticancer activity against human LOXIMVI cells by HTS assay, IC50=4.65μM 25139569
NCI-H522 Anticancer assay Anticancer activity against human NCI-H522 cells by HTS assay, IC50=5.77μM 25139569
NCI-H157 Anticancer assay Anticancer activity against human NCI-H157 cells by HTS assay, IC50=6μM 25139569
A549 Anticancer assay Anticancer activity against human A549 cells by HTS assay, IC50=6.2μM 25139569
HOP62 Anticancer assay Anticancer activity against human HOP62 cells by HTS assay, IC50=7.52μM 25139569
H460 Anticancer assay Anticancer activity against human H460 cells by HTS assay, IC50=9.62μM 25139569
NCI-H1944 Anticancer assay Anticancer activity against human NCI-H1944 cells by HTS assay, IC50=10.18μM 25139569
M14 Anticancer assay Anticancer activity against human M14 cells by HTS assay, IC50=12.77μM 25139569
H1299 Anticancer assay Anticancer activity against human H1299 cells by HTS assay, IC50=13.6μM 25139569
SKBR Anticancer assay Anticancer activity against human SKBR cells by HTS assay, IC50=16.71μM 25139569
H266 Anticancer assay Anticancer activity against human H266 cells by HTS assay, IC50=16.87μM 25139569
M4E Anticancer assay Anticancer activity against human M4E cells by HTS assay, IC50=21.71μM 25139569
Calu1 Anticancer assay Anticancer activity against human Calu1 cells by HTS assay, IC50=23.58μM 25139569
RAW264.7 Anti-inflammatory assay Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced NO production by Griess assay, IC50=15μM 26928174
BV2 Antiinflammatory assay Antiinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-stimulated nitric oxide production by Griess reagent based spectrophotometric analysis, IC50=16.3μM 29122483
HEK293 Function assay Inhibition of human CYP1B1 expressed in HEK293 cells by fluorescence assay, IC50=2.2μM 29150398
MDA-MB-468 Function assay Inhibition of human CYP1B1 expressed in MDA-MB-468 cells assessed as cell toxicity, IC50=2.2μM 29150398
HEK293 Function assay Inhibition of human CYP1A expressed in HEK293 cells by fluorescence assay, IC50=9.9μM 29150398
HEK293 Function assay Inhibition of human CYP1A1 transfected in HEK293 cells assessed as cell toxicity, IC50=9.9μM 29150398
DAOY qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for DAOY cells 29435139
A673 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for A673 cells 29435139
SK-N-MC qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-MC cells 29435139
NB-EBc1 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB-EBc1 cells 29435139
SK-N-SH qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-SH cells 29435139
NB1643 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB1643 cells 29435139
LAN-5 qHTS assay qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for LAN-5 cells 29435139
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生物活性

製品説明 Quercetin, a natural flavonoid present in vegetables, fruit and wine, is a stimulator of recombinant SIRT1 and also a PI3K inhibitor with IC50 of 2.4-5.4 μM. Quercetin induces mitophagy, apoptosis and protective autophagy. Phase 4.
Targets
Sirtuin [4] Src [1] PKC [1] PI3Kγ [1]
(Cell-free assay)		 PI3Kδ [1]
(Cell-free assay)		 もっとクリックする
2.4 μM 3.0 μM
In Vitro
In vitro

Quercetin is a type of plant-based chemical, or phytochemical, known as a flavonol and a plant-derived flavonoid found in fruits, vegetables, leaves and grains. It also may be used as an ingredient in supplements, beverages or foods. In several studies, it may have anti-inflammatory and antioxidant properties, and it is being investigated for a wide range of potential health benefits. Quercetin (Sophoretin) is a PI3K inhibitor with IC50 of 2.4 – 5.4 μM. It strongly abrogated PI3K and Src kinases, mildly inhibited Akt1/2, and slightly affected PKC, p38 and ERK1/2. [1]

Quercetin inhibits TNF-induced LDH% release, EC-dependent neutrophils adhesion to bovine pulmonary artery endothelial cells (BPAEC), and BPAEC DNA synthesis and proliferation. [2]
細胞実験 細胞株 Sertoli cells
濃度 0.1 μM
反応時間 24 h
実験の流れ

Cells were treated with various concentrations of drug for 24 h.
実験結果図 Methods Biomarkers 結果図 PMID
Western blot Her-2 / p-PI3K / p-Akt / Akt p-JAK1 / p-STAT3 / STAT3 / VEGF p-p53 / p53 / p21 Bcl-2 / Bax / Bcl-xl 18655187
Growth inhibition assay Cell viability Cell viability 28280414
In Vivo
In Vivo

Combination of Quercetin (75 mg/kg) and 2-Methoxyestradiol enhances inhibition of human prostate cancer LNCaP and PC-3 cells xenograft tumor growth.[3]

LD50: >3000mg/kg (i.g.) [4]
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT06003270 Recruiting
Chronic Obstructive Pulmonary Disease|Emphysema|Chronic Bronchitis With Airway Obstruction
Temple University|National Center for Complementary and Integrative Health (NCCIH)|Quercegen Pharmaceuticals
 November 1 2023 Phase 2
NCT04907253 Active not recruiting
Coronary Artery Disease
Montreal Heart Institute
 June 4 2021 Phase 2
NCT04474626 Withdrawn
Sickle Cell Disease|Sickle Cell-Beta0-Thalassemia
Jeffrey Zwicker MD|Quercegen Pharmaceuticals|Dana-Farber Cancer Institute
 December 2020 Phase 2
NCT04063124 Completed
Alzheimer Disease
The University of Texas Health Science Center at San Antonio|Mayo Clinic
 February 14 2020 Phase 1|Phase 2
NCT03989271 Recruiting
Chronic Obstructive Pulmonary Disease
Temple University|National Institutes of Health (NIH)|Quercegen Pharmaceuticals|National Center for Complementary and Integrative Health (NCCIH)
 October 1 2019 Phase 1|Phase 2

化学情報

分子量 302.24 化学式

C15H10O7
CAS No. 117-39-5 SDF Download Quercetin SDFをダウンロードする
Smiles C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O
保管

In vitro
Batch:

DMSO : 60 mg/mL ( (198.51 mM)； 吸湿したDMSOは溶解度を減少させます。新しいDMSOをご使用ください。)

Water : Insoluble

Ethanol : Insoluble

モル濃度計算器

in vivo
Batch:

Add solvents to the product individually and in order.

投与溶液組成計算機

実験計算

モル濃度計算器

質量 濃度 体積 分子量

投与溶液組成計算機(クリア溶液)

ステップ１：実験データを入力してください。（実験操作によるロスを考慮し、動物数を1匹分多くして計算・調製することを推奨します）

mg/kg g μL 匹

ステップ２：投与溶媒の組成を入力してください。（ロット毎に適した溶解組成が異なる場合があります。詳細については弊社までお問い合わせください）

% DMSO % % Tween 80 % ddH2O
%DMSO %

計算結果：

投与溶媒濃度： mg/ml;

DMSOストック溶液調製方法： mg 試薬を μL DMSOに溶解する（濃度 mg/mL, 注：濃度が当該ロットのDMSO溶解度を超える場合はご連絡ください。 )

投与溶媒調製方法：Take μL DMSOストック溶液に μL PEG300，を加え、完全溶解後μL Tween 80，を加えて完全溶解させた後 μL ddH2O，を加え完全に溶解させます。

投与溶媒調製方法：μL DMSOストック溶液に μL Corn oil，を加え、完全溶解。

注意：１.ストック溶液に沈殿、混濁などがないことをご確認ください；
２.順番通りに溶剤を加えてください。次のステップに進む前に溶液に沈殿、混濁などがないことを確認してから加えてください。ボルテックス、ソニケーション、水浴加熱など物理的な方法で溶解を早めることは可能です。

技術サポート

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Handling Instructions

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Tags: Quercetinを買う | Quercetin ic50 | Quercetin供給者 | Quercetinを購入する | Quercetin費用 | Quercetin生産者 | オーダーQuercetin | Quercetin化学構造 | Quercetin分子量 | Quercetin代理店