S5001 |
Tofacitinib (CP-690550) Citrate
|
トファシチニブクエン酸塩 (Tofacitinib citrate (CP-690550、タソシチニブ)) は JAK の新規阻害剤です。IC50は JAK3, JAK2, JAK1 に対してそれぞれ 1 nM, 20 nM, 112 nM です。 トファシチニブクエン酸塩は抗感染作用を持ちます。 |
-
J Exp Clin Cancer Res, 2024, 43(1):64
-
Antimicrob Agents Chemother, 2024, 68(4):e0135023.
-
Front Oncol, 2024, 14:1386190
|
|
S4157 |
Chloroquine diphosphate
|
Chloroquine diphosphate is a 4-aminoquinoline anti-malarial and anti-rheumatoid agent, also acting as an ATM activator. Chloroquine is also an inhibitor of toll-like receptors (TLRs). |
-
Nat Commun, 2024, 15(1):1642
-
Cancer Lett, 2024, 604:217258
-
Phytomedicine, 2024, 135:156053
|
|
S4430 |
Hydroxychloroquine (HCQ) Sulfate
|
Hydroxychloroquine (HCQ) Sulfate is an antimalarial agent used for the treatment of systemic lupus erythematosus, rheumatoid arthritis and other autoimmune, inflammatory and dermatologic conditions. Also acts as an inhibitor of autophagy and toll-like receptor (TLR) 7/9.
|
-
Redox Biol, 2024, 75:103274
-
Phytomedicine, 2024, 10.1016/j.phymed.2023.155152
-
Breast Cancer Res, 2024, 26(1):33
|
|
S8279 |
Shikonin
|
Shikonin, a potent and specific Pyruvate kinase M2 (PKM2) inhibitor, is a major component of zicao (purple gromwell, the dried root of Lithospermum erythrorhizon), a Chinese herbal medicine with various biological activities. It is also an inhibitor of TMEM16A chloride channel activity using cell-based fluorescent-quenching assay. Shikonin exerts an anti-inflammatory effect by inhibiting tumor necrosis factor-α (TNF-α) and prevents activation of nuclear factor-κB (NF-κB) pathway via proteasome inhibition. |
-
Elife, 2024, 12RP91141
-
Elife, 2024, 12RP91141
-
Mol Ther Methods Clin Dev, 2024, 32(3):101307
|
|
S4592 |
SBE-β-CD
|
SBE-β-CDは薬物の溶解性と安定性を最適化するように設計された構造を持つ新規修飾シクロデキストリンです。 Quality confirmed by NMR & HPLC. See customer reviews, validations & product citations. |
-
Nat Commun, 2024, 15(1):5703
-
Cell Death Differ, 2024, 10.1038/s41418-024-01316-3
-
Nat Commun, 2023, 14(1):2806
|
|
S8068 |
Chaetocin
|
Chaetocin, a natural product from Chaetomium species, is a histone methyltransferase inhibitor with IC50 of 0.8 μM, 2.5 μM and 3 μM for dSU(VAR)3-9, mouse G9a and Neurospora crassa DIM5, respectively. Chaetocin is an anticancer agent and inhibitor of thioredoxin reductase (TrxR). |
-
PeerJ, 2024, 12:e17222
-
Asian Pac J Trop Bio, 2023;, 13(6): 268-276
-
Cancer Cell, 2023, 41(6):1118-1133.e12
|
|
S2264 |
Artemether
|
Artemether (SM-224, CGP 56696) is an antimalarial for the treatment of resistant strains of falciparum malaria. |
-
J Pers Med, 2022, 12(2)258
-
Hum Cell, 2022, 10.1007/s13577-022-00671-y
-
Sci Rep, 2021, 11(1):14571
|
|
S2572 |
Streptomycin sulfate
|
Streptomycin sulfate(Phytomycin) is a sulfate salt of streptomycin that is a protein synthesis inhibitor. |
-
Front. Oncol, 2023-, Volume 13
-
Front Oncol, 2023, 13:1118268
-
Transl Oncol, 2022, 26:101502
|
|
S7465 |
FTI 277 HCl
|
FTI 277 HCl is a potent and selective farnesyltransferase (FTase) inhibitor with IC50 of 500 pM, about 100-fold selectivity over the closely related GGTase I. FTI 277 HCl inhibits cell growth and induces apoptosis. FTI 277 HCl is effective in clearing HDV viremia. |
-
Cancer Res, 2023, 83(13):2248-2261
-
PLoS Biol, 2021, 19(4):e3001134
-
Cell Struct Funct, 2021, 46(1):1-9
|
|
S2479 |
Lincomycin HCl
|
Lincomycin hydrochloride (Lincocin, NSC 70731,U10149A) is the monohydrated salt of lincomycin, a substance produced by the growth of a member of the lincolnensis group of Streptomyces lincolnensis. |
-
J Pers Med, 2022, 12(2)258
-
Hum Cell, 2022, 10.1007/s13577-022-00671-y
-
Hum Cell, 2021, 10.1007/s13577-021-00639-4
|
|
S2613 |
Clorsulon
|
Clorsulon (MK-401,L631529) is used in the treatment of Fasciola hepatica infections in calves and sheep. |
-
J Pers Med, 2022, 12(2)258
-
Hum Cell, 2022, 10.1007/s13577-022-00671-y
-
Hum Cell, 2021, 34(6):1911-1918
|
|
S1282 |
Artemisinin
|
Artemisinin is a sesquiterpene endoperoxide which is a potent antimalarial agent. |
-
Virus Res, 2024, 349:199448
-
Drug Des Devel Ther, 2023, 17:1679-1697
-
Cancer Cell, 2022, S1535-6108(22)00312-9
|
|
S4147 |
Azithromycin Dihydrate
|
Azithromycin Dihydrate(CP-62993 dihydrate) is an acid stable orally administered macrolide antimicrobial drug, structurally related to erythromycin. |
-
J Cell Biochem, 2022, 10.1002/jcb.30213
-
Adv Ther (Weinh), 2020, 2000034
-
PLoS Comput Biol, 2020, 16(12):e1008489
|
|
S4420 |
Mefloquine HCl
|
Mefloquine HCl(Mefloquin hydrochloride) is a blood schizonticide by inhibiting hemozoin formation, used as an antimalarial drug.
|
-
Mol Med Rep, 2021, 23(1)40
-
bioRxiv, 2020, 2020/9/20.4.7.30734
-
Int J Parasitol Drugs Drug Resist, 2018, 8(2):331-340
|
|
S3649 |
Ceftazidime
|
Ceftazidime(GR20263) is a third-generation cephalosporin that has activity against Gram-negative bacilli, including Pseudomonas aeruginosa. |
-
Pharmacol Res, 2024, 201:107096
-
ACS Infect Dis, 2023, 10.1021/acsinfecdis.3c00264
-
Molecules, 2023, 28(6)2820
|
|
S7896 |
Sodium Tauroursodeoxycholate (TUDC)
|
Sodium Tauroursodeoxycholate (TUDC) is a water soluble bile salt, used for the treatment of gallstones and liver cirrhosis. |
-
iScience, 2024, 27(8):110598
-
Infect Immun, 2024, 92(8):e0030024
-
Microbiome, 2019, 7(1):145
|
|
S4237 |
Primaquine Diphosphate
|
Primaquine Diphosphate is a transmission-blocking anti-malarial clinically available, displaying a marked activity against gametocytes of all species of human malaria. |
-
J Extracell Vesicles, 2024, 13(7):e12494
-
Front Pharmacol, 2021, 12:695009
-
Cell Syst, 2019, 8(2):97-108
|
|
S3941 |
Pinocembrin
|
Pinocembrin (Dihydrochrysin, Galangin flavanone, 5,7-Dihydroxyflavanone) is a major flavonoid molecule incorporated as multifunctional in the pharmaceutical industry. Its vast range of pharmacological activities has been well researched including antimicrobial, anti-inflammatory, antioxidant, and anticancer activities. |
-
Neurol Res, 2022, 1-10
-
J Neuroinflammation, 2020, 17(1):337
|
|
S5184 |
Dexamethasone palmitate
|
Dexamethasone palmitate (DXP), a lipophilic prodrug of Dexamethasone (DXM), is a glucocorticoid receptor agonist with a 47-fold lower affinity for the glucocorticoid receptor than DXM. Dexamethasone palmitate (DXP) exhibits anti-inflammatory activity. |
-
Dis Model Mech, 2022, dmm.049109
-
Hematology, 2022, 27(1):32-42
|
|
S1553 |
Delafloxacin (ABT-492)
|
Delafloxacin (ABT-492, RX-3341, WQ-3034) is a new fluoroquinolone against 155 aerobic and 171 anaerobic pathogens. |
-
Molecules, 2023, 28(6)2820
-
Molecules, 2023, 28(6), 2820
|
|
S5397 |
Chlorhexidine
|
Chlorhexidine is a disinfectant and topical anti-infective agent that is active against Gram-positive and Gram-negative organisms, facultative anaerobes, aerobes, and yeasts. |
-
J Cell Mol Med, 2021, 10.1111/jcmm.16673
-
BMC Microbiol, 2020, 20(1):275
|
|
S2282 |
Cinchonidine
|
Cinchonidine is an alkaloid used in asymmetric synthesis in organic chemistry. |
-
CNS Neurosci Ther, 2023, 10.1111/cns.14403
-
J Med Virol, 2019, 91(8):1440-1447
|
|
S5967 |
Berberine chloride hydrate
|
Berberine (Natural Yellow 18) chloride hydrate is a quaternary ammonium salt from the group of isoquinoline alkaloids. Berberine activates caspase 3 and caspase 8, cleavage of poly ADP-ribose polymerase (PARP) and the release of cytochrome c. Berberine chloride decreases the expression of c-IAP1, Bcl-2 and Bcl-XL. Berberine chloride induces apoptosis with sustained phosphorylation of JNK and p38 MAPK, as well as generation of the ROS. Berberine chloride is a dual topoisomerase I and II inhibitor. Berberine chloride is also a potential autophagy modulator. |
-
Front Biosci (Landmark Ed), 2022, 27(8):242
-
Front Pharmacol, 2021, 12:632201
|
|
S4192 |
Chlorquinaldol
|
Chlorquinaldol(Chloquinan) is an antimicrobial agent used for local antisepsy. |
-
Biosensors (Basel), 2023, 13(6)571
-
Biosensors (Basel), 2023, 13(6)571
-
ACS Synth Biol, 2022, 11(8):2820-2828
|
|
S5961 |
Prednisolone disodium phosphate
|
Prednisolone disodium phosphate (Hydeltrasol, Prednisolone 21-phosphate disodium) is a synthetic glucocorticoid with anti-inflammatory and immunomodulating properties that exerts late mitogenic and biphasic effects on resistant acute lymphoblastic leukemia cells. |
-
J Immunotoxicol, 2021, 18(1):154-162
-
Eur J Rheumatol, 2021, 10.5152/eurjrheum.2021.20054
|
|
S4759 |
p-Coumaric Acid
|
p-Coumaric acid (4-Hydroxycinnamic acid, P-Hydroxycinnamic acid, 4-Coumaric acid, Trans-p-Coumaric acid, para-Coumaric Acid) is a hydroxy derivative of cinnamic acid found in a variety of edible plants and is reported to have antioxidant, anti-inflammatory, and antimicrobial activity. |
-
Exp Ther Med, 2021, 21(5):503
-
J Nutr Biochem, 2015, 26(11):1379-84
|
|
S7411 |
Ascomycin (FK520)
|
Ascomycin (FK520, FR 900520, Immunomycin), an FK-506 analog, is a neutral macrolide immunosuppressant, which prevents rejection after an organ transplant. Phase 3. |
-
Melanoma Res, 2020, 30(4):325-335
-
Virol Sin, 2019, 34(6):648-661
|
|
S5927 |
Proguanil
|
Proguanil (chlorguanide, chloroguanide) is a prophylactic antimalarial drug. It inhibits the dihydrofolate reductase of plasmodia and thereby blocks the biosynthesis of purines and pyrimidines, which are essential for DNA synthesis and cell multiplication. |
-
Int J Med Sci, 2022, 19(2):233-241
-
Sci Adv, 2021, 7(27)eabh3032
|
|
P1201 |
LL37 (Human cathelicidin)
|
LL37 (Human cathelicidin, Ropocamptide) is a cathelicidin-related antimicrobial peptide with potent chemotactic and immunomodulatory properties. |
-
Biomed Pharmacother, 2023, 157:114091
-
Biomed Pharmacother, 2022, 153:113292
|
|
S3746 |
Lumefantrine
|
Lumefantrine (benflumetol) is an antimalarial agent used to treat acute uncomplicated malaria. |
-
Antimicrob Agents Chemother, 2021, AAC.02137-20
-
ACS Infect Dis, 2020, 10.1021/acsinfecdis.0c00522
|
|
S9131 |
Punicalagin
|
Punicalagin, a major ellagitannin found in pomegranate extracts, has been shown to have antioxidant, anti-inflammatory, and anticancer effects. |
-
SLAS Discov, 2024, S2472-5552(24)00007-8
-
Cell, 2020, 30;181(3):637-652.e15.
-
Cell, 2020, 30;181(3):637-652e15
|
|
S4242 |
Cetrimonium Bromide (CTAB)
|
Cetrimonium Bromide (CTAB) is a known component of the broad-spectrum antiseptic cetrimide, which is a mixture of different quaternary ammonium salts. |
-
Biochem Cell Biol, 2021, 10.1139/bcb-2020-0570
-
Micromachines (Basel), 2018, 9(6)
|
|
S9185 |
Nitidine Chloride
|
Nitidine Chloride, a benzophenanthridine alkaloid found in species of the genus Zanthoxylum, has an anti-malarial activity. |
-
Int Immunopharmacol, 2021, 101(Pt A):108273
-
Front Cell Neurosci, 2020, 14:216
|
|
S3067 |
Chlorhexidine 2HCl
|
Chlorhexidine hydrochloride (NSC-185) is an antiseptic effective against a wide variety of gram-negative and gram-positive organisms. |
-
BMC Microbiol, 2020, 20(1):275
|
|
S2537 |
Secnidazole
|
Secnidazole (Flagentyl, PM 185184, RP 14539) is a nitroimidazole anti-infective. |
-
Microorganisms, 2022, 10(7)1421
|
|
S4195 |
Broxyquinoline
|
Broxyquinoline(Dibromohydroxyquinoline) is an antiprotozoal agent and able to release oxygen free radicals from the water in mucous membranes. |
-
ACS Synth Biol, 2022, 11(8):2820-2828
|
|
S4196 |
Ethacridine lactate monohydrate
|
Ethacridine lactate monohydrate(Acrinol monohydrat) is an aromatic organic compound based on acridine used as an antiseptic agent. |
-
Carcinogenesis, 2014, 35(12):2822-30
|
|
S4726 |
Lauric Acid
|
Lauric Acid (dodecanoic acid, N-Dodecanoic acid, Dodecylic acid) is a saturated medium-chain fatty acid with a 12-carbon backbone. Lauric acid is found naturally in various plant and animal fats and oils, and is a major component of coconut oil and palm kernel oil. |
-
Nat Commun, 2023, 14(1):660
|
|
S6288 |
Chlorhexidine diacetate
|
Chlorhexidine diacetate (Hibitane diacetate) is a disinfectant and topical anti-infective agent used also as mouthwash to prevent oral plaque. |
-
BMC Microbiol, 2020, 20(1):275
|
|
S4041 |
Olsalazine Sodium
|
Olsalazine Sodium is an anti-inflammatory prodrug, which consists of two 5-ASA moieties linked by an azo bond. |
-
Oncotarget, 2017, 8(1):228-237
|
|
S6185 |
Arachidonic acid
|
Arachidonic acid (Arachidonate) is an unsaturated, essential fatty acid found in animal and human fat as well as in the liver, brain, and glandular organs. It is a precursor in the biosynthesis of prostaglandins, thromboxanes, and leukotrienes. |
-
Bone Res, 2022, 10(1):20
|
|
S4172 |
Cetylpyridinium Chloride
|
Cetylpyridinium chloride(CPC) is a cationic quaternary ammonium compound used as oropharyngeal antiseptic. |
-
iScience, 2024, 27(8):110598
-
Int J Mol Sci, 2023, 24(11)9708
|
|
S2395 |
Rheochrysidin
|
Rheochrysidin (Physcione) is an anthraquinone from roots of Rheum officinale Baill. |
-
ACS Chem Biol, 2015, 10.1021/cb5009487
|
|
S4081 |
Sulfacetamide Sodium
|
Sulfacetamide Sodium is an anti-biotic. |
-
G3 (Bethesda), 2020, 4;10(5):1585-1597
|
|
S9387 |
Maackiain
|
Maackiain (Demethylpterocarpin) is a pterocarpan that is widely distributed in leguminous plants. It has anticancer and antimicrobial effects. |
-
Int Immunopharmacol, 2022, 108:108710
|
|
S5096 |
SulfadiMethoxine sodium
|
Sulfadimethoxine (Sulfadimethoxydiazine) is a long-lasting sulfonamide antimicrobial agent used to treat many infections including treatment of respiratory, urinary tract, enteric, and soft tissue infections. |
-
Cell Death Dis, 2018, 9(6):646
|
|
E0206 |
Ginkgetin
|
Ginkgetin is a biflavone from Ginkgo biloba leaves with anti-cancer, anti-inflammatory, anti-microbial, anti-adipogenic, and neuroprotective activities. |
-
Biomed Pharmacother, 2022, 154:113628
|
|
S5214 |
Imidocarb dipropionate
|
Imidocarb is an antiprotozoal agent, used as dipropionate in the treatment of babesiosis and ehrlichiosis. |
-
Nat Commun, 2017, 8(1):823
|
|
S7867 |
Oleuropein
|
Oleuropein is an antioxidant polyphenol isolated from olive leaf. Oleuropein exerts antioxidant, anti-inflammatory and anti-atherogenic effects and suppresses the adipocyte differentiation in vitro. Oleuropein inhibits PPARγ activity. Oleuropein exerts anti-adipogenic effect through direct inhibition of PPARγ transcriptional activity. Oleuropein also inhibits aromatase. Oleuropein induces apoptosis. Phase 2. |
-
Front Endocrinol (Lausanne), 2024, 15:1354435
-
J Med Virol, 2019, 91(8):1440-1447
|
|
S3220 |
Trigonelline
|
Trigonelline (Trigenolline) is a plant alkaloid and a major component of coffee and fenugreek with anti-degranulation, anti-diabetic, antioxidant, anti-inflammatory, and neuroprotective effects. Trigonelline inhibits FcεRI-mediated intracellular signaling pathways, such as phosphorylation of PLCγ1, PI3K, and Akt. Trigonelline (Trigenolline) also inhibits the microtubule formation in RBL-2H3 cells. |
-
Biomed Pharmacother, 2021, 143:112204
|
|
S3279 |
Polyphyllin B (Formosanin C)
|
Polyphyllin B (Formosanin C, FC), a diosgenin saponin isolated from Paris formosana, is an immunomodulator with antitumor activity. Polyphyllin B (Formosanin C, FC) induces apoptosis. |
-
Oncol Lett, 2021, 22(1):550
|
|
S1644 |
Nitrofural
|
Nitrofural (Nitrofurazone) is a topical anti-infective agent with an IC50 of 22.83 ± 1.2 μM. (Rat LD50 = 590 mg/kg) |
|
|
S2469 |
Fleroxacin
|
Fleroxacin (Ro 23-6240,AM-833,Quinodis, Megalocin) is a new broad-spectrum fluoroquinolone. |
|
|
S3116 |
Sulfathiazole
|
Sulfathiazole is an organosulfur compound that has been used as a short-acting sulfa drug. |
|
|
S2511 |
Sulfadoxine
|
Sulfadoxine (Sulphadoxine) is an ultra-long-lasting sulfonamide with an IC50 of 249 μg/ml for P. vivax. |
|
|
S4191 |
Betamipron
|
Betamipron (CS-443,N-Benzoyl-β-alanine) is a chemical compound which is used together with panipenem to inhibit panipenem uptake into the renal tubule and prevent nephrotoxicity. |
|
|
S2612 |
Ribitol
|
Ribitol (Adonitol) is a crystalline pentose alcohol and is formed by the reduction of ribose which is occurs naturally in the plant Adonis vernalis. |
|
|
E0524 |
Spinosad
|
Spinosad, a mixture of spinosyns A and D known as fermentation products of a soil actinomycete, is a biological neurotoxic insecticide with a broader action spectrum, targeting the nicotinic acetylcholine receptor (nAChRs) of the insect nervous system. |
|
|
E0525 |
Colistin
|
Colistin(Polymyxin E), a cyclic polypeptide antibiotic synthesized by Bacillus polymyxa subspecies colistinus Koyama, exerts antimicrobial activity by targeting at the bacterial cell membrane. |
|
|
S3226 |
Dehydroabietic acid
|
Dehydroabietic acid (DAA, DHAA), a naturally occurring diterpene resin acid derived from coniferous plants such as Pinus and Picea, displays anti-inflammatory activity via suppression of Src-, Syk-, and TAK1-mediated pathways. |
|
|
S4945 |
Ethacridine lactate
|
Ethacridine lactate (Acrinol) is an aromatic organic compound based on acridine used as an antiseptic agent. Ethacridine lactate is also a poly(ADP-ribose) glycohydrolase (PARG) inhibitor. |
|
|
S9564 |
p-Hydroxy-cinnamic Acid
|
p-Hydroxy-cinnamic Acid has in vitro antimalarial activity and in vivo anti-osteoporotic properties. |
|
|
E4872New |
Mefloquine
|
Mefloquine(Lariam, WR-142490) is a quinoline antimalarial drug and an antagonist of K+ channel (KvQT1/minK) with an IC50 of ~1 μM. It is widely used in both the treatment and prophylaxis of Plasmodium falciparum malaria, and can prolong cardiac repolarization. |
|
|
S9094 |
Pogostone
|
Pogostone is one of the secondary metabolites from Pogostemon cablin (Blanco) Benth. (Lamiaceae), serving as the effective component of the antimicrobial activity. |
-
J Ethnopharmacol, 2021, 278:114250
|
|
S3269 |
Acetylcorynoline
|
Acetylcorynoline, a major alkaloid component derived from Corydalis bungeana which is a traditional Chinese medical herb, shows anti-inflammatory properties. Acetylcorynoline may decrease egl-1 expression to suppress apoptosis pathways and increase rpn5 expression to enhance the activity of proteasomes. |
|
|
S3270 |
Genipin 1-O-beta-D-gentiobioside
|
Genipin 1-O-beta-D-gentiobioside (GG, Genipin 1-β-D-gentiobioside, Genipin 1-gentiobioside, Genipin 1-β-gentiobioside, Genipin gentiobioside) is a bioactive iridoid glycoside isolated from Gardenia jasminoides Ellis (Zhizi in Chinese) that exhibits hepatoprotective, anti-inflammatory, antioxidant, and antithrombotic activities. |
|
|
S3308 |
Caftaric acid
|
Caftaric acid (CA, Caffeoyl tartaric acid) is a natural product that shows anti-oxidant and anti-inflammatory effects. |
|
|
S4142 |
Clopidol
|
Clopidol (WR 61112) is an antiprotozoal agent. |
|
|
S5700 |
Phthalylsulfathiazole
|
Phthalylsulfathiazole (Sulfathalidine) is a broad-spectrum antimicrobial that can treat different types of infections including intestinal. |
-
Med Oncol, 2024, 41(8):188
|
|
S6136 |
(±)-α-Bisabolol
|
α-bisabolol is a small, plant-derived, oily sesquiterpene alcohol with some anti-inflammatory and even anti-microbial properties. |
|
|
S5757 |
Isoeugenol
|
Isoeugenol (4-Propenylguaiacol), an essential oil constituent of nutmeg, clove, and cinnamon, shows antimicrobial activity. |
|
|
S0320 |
Cycloguanil hydrochloride
|
Cycloguanil hydrochloride, an active metabolite of proguanil, acts on malaria schizonts in erythrocytes and hepatocytes. |
|
|
S4250 |
Sulfamethoxypyridazine
|
Sulfamethoxypyridazine (CL 13494) is a long-acting sulfonamide for treatment of Dermatitis herpetiformis. |
|
|
S6173 |
Amylmetacresol
|
Amylmetacresol is an antiseptic used to treat infections of the mouth and throat. |
|
|
S4946 |
2,3-Dihydroxybenzoic acid
|
2,3-Dihydroxybenzoic acid (Pyrocatechuic acid, 3-Hydroxysalicylic acid, Hypogallic acid) is a natural phenol found in Phyllanthus acidus and in the aquatic fern Salvinia molesta, also a product of human aspirin metabolism. It is a potentially useful iron-chelating drug and has antimicrobial properties. |
|
|
S2271 |
Berberine chloride
|
Berberine chloride is a quaternary ammonium salt from the group of isoquinoline alkaloids. Berberine activates caspase 3 and caspase 8, cleavage of poly ADP-ribose polymerase (PARP) and the release of cytochrome c. Berberine chloride decreases the expression of c-IAP1, Bcl-2 and Bcl-XL. Berberine chloride induces apoptosis with sustained phosphorylation of JNK and p38 MAPK, as well as generation of the ROS. Berberine chloride is a dual topoisomerase I and II inhibitor. Berberine chloride is also a potential autophagy modulator. |
-
Adv Healthc Mater, 2023, e2300591.
-
Transl Oncol, 2023, 35:101712
-
J Biomol Struct Dyn, 2022, 1-11
|
|
S5475 |
Novaluron
|
Novaluron (Rimon) belongs to the class of insecticides called insect growth regulators with pesticide properties. |
|
|
S3218 |
Amiloxate
|
Amiloxate (Amiloxiate, Isoamyl Methoxycinnamate, Isopentyl 4-methoxycinnamate, Isoamyl 4-methoxycinnamate, Isoamyl p-methoxycinnamate, Isopentyl p-methoxycinnamate) is EMA-approved chemical UV-filter used in cosmetics. Amiloxate is a cinnamic acid derivative with anti-inflammatory activity. |
|
|
S5963 |
Sulfathiazole sodium
|
Sulfathiazole sodium, an antimicrobial agent, is an organosulfur compound that has been used as a short-acting sulfa drug. |
|
|
S6243 |
Ethyl pyruvate
|
Ethyl pyruvate (CTI-01) is a simple aliphatic ester of pyruvic acid and has been shown to have robust neuroprotective effects via its anti-inflammatory, anti-oxidative, and anti-apoptotic functions. |
-
BMC Gastroenterol, 2024, 24(1):245
|
|
S3695 |
Cystamine dihydrochloride
|
Cystamine dihydrochloride (Decarboxycystine, 2-Aminoethyl disulfide, 2,2'-Dithiobisethanamine) acts as an anti-infective agent, which is used in the treatment of urinary tract infections and also as a radiation-protective agent that interferes with sulfhydryl enzymes. |
|
|
S4175 |
Sulfaguanidine
|
Sulfaguanidine is a sulfonamide used as an anti-infective agent. |
|
|
S3787 |
Picroside I
|
Picroside I (6'-Cinnamoylcatalpol), an iridoid glycoside, is a hepatoprotective agent which is reported to be antimicrobial and used against hepatitis B. |
|
|
S9016 |
Dipsacoside B
|
Dipsacoside B, extracted from the flowerbuds of Lonicera confusa DC, shows strong antimicrobial activity. |
|
|
S5908 |
Garenoxacin
|
Garenoxacin (T-3811ME, BMS-284756) is a novel des-F(6) quinolone that has been shown to be effective in vitro against a wide range of clinically important pathogens, including gram-positive and gram-negative aerobes and anaerobes. |
|
|
S4062 |
Ronidazole
|
Ronidazole is an antiprotozoal agent. |
|
|
S4971 |
Buparvaquone
|
Buparvaquone (Butalex) is a second-generation hydroxynaphthoquinone related to parvaquone, with novel features that make it a promising compound for the therapy and prophylaxis of all forms of theileriosis. |
|
|
S6761 |
Dalfopristin
|
Dalfopristin (RP54476) is a semi-synthetic analogue of ostreogyrcin A. Quinupristin/dalfopristin (Q/D) is a parental streptogramin with a spectrum of activity that includes Gram-positive pathogens, including those resistant to other classes of antimicrobial compounds. |
|
|
S5292 |
Diazolidinyl urea
|
Diazolidinyl urea (Germall II) is an antimicrobial preservative used in cosmetics. |
|
|
S3210 |
3'-Hydroxy-4'-methoxyacetophenone
|
3'-Hydroxy-4'-methoxyacetophenone (Acetoisovanillone, Isoacetovanillone, Diosmin EP Impurity A) is an active P. spinosa extract with anti-inflammatory potential. |
|
|
E0626 |
AX 20017
|
AX 20017 is a small-molecule protein kinase G (PknG) inhibitor with an IC50 of 0.39 μM. |
|
|
S5887 |
Khellin
|
Khellin (Methafrone, Visammin, Ammivisnagen, Khellinorm, Medekellin, Viscardan, Kalangin), a compound isolated from the seeds of Ammi Visnaga Lam (Umbelliferae), is used to treat a variety of maladies. |
|
|
E0820 |
OX02983
|
OX02983 is a novel anthelmintic agent, actives against both egg and adult stages of Trichuris parasites, immobilising whipworm and reducing the ability of embryonated Trichuris muris eggs to establish infection in the mouse host. |
|
|
S4303 |
9-Aminoacridine
|
9-Aminoacridine (Aminacrine) is a highly fluorescent dye used clinically as a topical antiseptic and experimentally as a mutagen, an intracellular pH indicator and a negative mode small molecule MALDI matrix. |
|
|
S0146 |
Broxaldine
|
Broxaldine (Brobenzoxaldine, AL307) is an antiprotozoal drug and can be used in leprosy. |
|
|
S4417 |
Ceftaroline Fosamil
|
Ceftaroline fosamil (CX-0903, DSP-5990, PPI-0903, TAK-599, Teflaro, Zinforo) is a cephalosporin with activity against Gram-positive pathogens, including methicillin-resistant Staphylococcus aureus (MRSA).
|
|
|
S0846 |
Euquinine
|
Euquinine is generally used as a febrifuge, antimalarial, and tonic. |
|
|
E0749 |
Coumalic acid
|
Coumalic acid is a valuable platform compound which can be prepared from malic acid, can be used in the flavours, fragrances and cosmetics industries, as polymer components, and as pharmaceutical scaffolds displaying anti-bronchial and -malarial activity. |
|
|
S9084 |
Rhoifolin
|
Rhoifolin (Rhoifoloside, Apigenin 7-O-neohesperidoside, Apigenin-7-O-rhamnoglucoside), a natural glycoside of apigenin, has been obtained from the green leaves of Rhus succedanea and possesses a variety of significant biological activities including antioxidant, anti-inflammatory, antimicrobial, hepatoprotective and anticancer effects. |
|
|
E2665 |
Tafenoquine
|
Tafenoquine (WR 238605) is an 8-aminoquinoline, used as an anti-malarial prophylactic agent. |
|
|
S6771 |
MAC-545496
|
MAC-545496 is a nanomolar glycopeptide-resistance-associated protein R(GraR) inhibitor with strong binding affinity to the full-length GraR protein (Kd ≤ 0.1 nM). MAC-545496 can reverse β-lactam resistance in methicillin-resistant strains and synergize with CAMPs. MAC-545496 shows remarkable activity in macrophages and attenuates S. aureus virulence in a G. mellonella larvae infection model. |
|
|
E2812 |
Antimalarial agent 1
|
Antimalarial agent 1 is a potent antimalarial drug. |
|
|
E0938 |
Brincidofovir
|
Brincidofovir (CMX001), the lipid-conjugated prodrug of Cidofovir with long-acting antiviral effect, shows activity against a broad spectrum of DNA viruses including cytomegalovirus (CMV), adenovirus (ADV), varicella zoster virus, herpes simplex virus, polyomaviruses, papillomaviruses, poxviruses, and mixed double-stranded DNA virus infections. |
|
|
S3711 |
Carbasalate Calcium
|
Carbasalate calcium (Iromin, Alcacyl, Omegin, Rheomin, Solupsan) is an analgesic, antipyretic, and anti-inflammatory drug as well as a platelet aggregation inhibitor. |
|
|
S3801 |
Sodium Lauryl Sulfoacetate
|
Sodium Lauryl Sulfoacetate, the active compound of the Houttuynia plant, is mainly used for treating purulent skin infections, respiratory tract infections, including pneumonia in elderly patients, and chronic bronchitis. |
|
|
E1126 |
AFN-1252
|
AFN-1252 (Debio 1452) is a potent inhibitor of enoyl-acyl carrier protein reductase (FabI), inhibits all clinical isolates of Staphylococcus aureus and Staphylococcus epidermidis at concentrations of ≤0.12 μg/ml. |
|
|
E1421 |
A2ti-1
|
A2ti-1 is a selective and high-affinity inhibitor of annexin A2/S100A10 heterotetramer (A2t) with IC50 of 24 μM. A2ti-1 specifically disrupts the protein-protein interaction (PPI) between A2 and S100A10. It also prevents human papillomavirus type 16 (HPV16) infection. |
|
|
S6442 |
Chlorphenesin
|
Chlorphenesin is a synthetic preservative used in skin care as a cosmetic biocide. |
|
|
S9342 |
1,4-Naphthoquinone
|
1,4-Naphthoquinone (α-Naphthoquinone, para-naphthoquinone, P-Naphthoquinone), found in diesel exhaust particles and it is an active metabolite of naphthalene, is a fumigant insecticide. |
|
|
S2564 |
Cloxacillin Sodium
|
Cloxacillin Sodium(Cloxacap,BRL 1621 sodium salt) is a sodium salt of cloxacillin that is a penicillinase-resistant, acid resistant, semi-synthetic penicillin. |
|
|
S9112 |
Kaempferitrin
|
Kaempferitrin (Lespenefril, Lespedin, Lespenephryl, Kaempferol 3,7-dirhamnoside), isolated from the leaves of Hedyotis verticillata and from Onychium japonicum, has antimicrobial, antioxidant, and anti-inflammatory activities. |
|
|
S9113 |
Ononin
|
Ononin (Formononetin glucoside, Formononetin 7-O-glucoside) is an isoflavone glycoside with anti-inflammtory effects. |
|
|
S9341 |
3,4-Dimethoxycinnamic acid
|
3,4-Dimethoxycinnamic acid (Caffeic acid dimethyl ether) is a bioavailable coffee component as a perspective anti-prion compound and bind potently to prion protein with a Kd of 405 nM. |
|
|
S6458 |
Isavuconazonium sulfate
|
Isavuconazonium sulfate (BAL8557-002), the prodrug of the active triazole Isavuconazole, is an orally active antifungal agent, using for invasive aspergillosis and mucormycosis. |
|
|
S6459 |
Nifurtimox
|
Nifurtimox (BAY-2502) is an antiprotozoal agent. |
|
|
S4232 |
Nithiamide
|
Nithiamide (CL 5279) is a non-5-nitroimidazole drugs. |
|
|
S3618 |
Acetylspiramycin (ASPM)
|
Acetylspiramycin (ASPM, Spiramycin II, Foromacidin B) is a macrolide antimicrobial agent.
|
|
|
S4515 |
Ademetionine disulfate tosylate
|
Ademetionine Disulfate Tosylate is the disulfate-tosylate mixed salt of a mixture of diastereoisomers of the ademetionine ions. Ademetionine possesses anti-inflammatory activity and has been used in treatment of chronic liver disease. |
|
|
S4236 |
Proflavine Hemisulfate
|
Proflavine Hemisulfate is a topical antiseptic by interchelating DNA, thereby disrupting DNA synthesis and leading to high levels of mutation in the copied DNA strands. |
|
|
S5212 |
Imidazolidinyl Urea
|
Imidazolidinyl Urea (Imidurea) is an antimicrobial agent used as preservative in cosmetics. |
|
|
S5210 |
Sulfamethazine Sodium Salt
|
Sulfamethazine (Sulfadimethyldiazine) is a sulfanilamide anti-infective agent used in the lifestock industry. |
|
|
S0443 |
Desciclovir
|
Desciclovir (DCV, 6-Deoxyacyclovir, BW A515U) is a prodrug of the antiherpetic agent acyclovir (ACV) that converted into ACV by xanthine oxidase in humans. |
|
|
S4678 |
Povidone iodine
|
Povidone iodine (Betadine, PVP iodine, PVP-I, Isodine) is a stable chemical complex of polyvinylpyrrolidone (povidone, PVP) and elemental iodine. Povidone iodine displays excellent antibacterial activity against MRSA and MSSA strains with MICs of 31.25 mg/L and 7.82 mg/L, respectively. Povidone iodine is used as a topical antiseptic in surgery and for skin and mucous membrane infections, as well as as an aerosol. |
|
|
S0889 |
Dixanthogen
|
Dixanthogen is an ectoparasiticide. |
|
|
S5405 |
Propylparaben
|
Propylparaben (Propyl 4-hydroxybenzoate, Propyl p-hydroxybenzoate, nipasol), a natural substance found in many plants and some insects, is an antimicrobial, preservative and flavouring agent. |
|
|
E4946New |
Tafenoquine Succinate
|
Tafenoquine Succinate(WR 238605 Succinate, Etaquine, Krintafel) is an 8-aminoquinoline (8AQ) anti-malarial drug that kills both the liver and blood stages of the parasite, broadening its applicability for chemoprophylaxis to all species of malaria. It is specifically used for the prevention of Plasmodium vivax relapse. |
|
|
S6802 |
Etosalamide
|
Etosalamide (Ethosalamide) is an anti-inflammatory drug with antipyretic and analgesics properties. |
|
|
S3978 |
5-Phenyl-2,4-pentadienoic acid
|
5-Phenyl-2,4-pentadienoic acid (5-Phenylpenta-2,4-dienoic acid) is used as Synthetic building block, anti-malarial agent. |
|
|
S5390 |
N-(Hytroxymethy)micotinamide
|
N-(Hydroxymethyl)nicotinamide (Nikomethamide, Bilamid, N-hydroxymethylnicotinamide) is an antimicrobial agent. |
|
|
S3261 |
Myrislignan
|
Myrislignan, a lignan isolated from Myristica fragrans Houtt, possesses anti-inflammatory activities. Myrislignan inhibits interleukin-6 (IL-6) and tumour necrosis factor-α (TNF-α). Myrislignan significantly inhibits the expressions of inducible NO synthase (iNOS) and cyclooxygenase-2 (COX-2) dose-dependently in LPS-stimulated macrophage cells. Myrislignan inhibits the NF-κB signalling pathway activation. |
-
Oxid Med Cell Longev, 2023, 2023:7098313
|
|
S5355 |
Piperaquine phosphate
|
Piperaquine phosphate is an orally active bisquinolone antimalarial drug. |
|
|
S9560 |
Anisodamine Hydrobromide
|
Anisodamine (6-Hydroxyhyoscyamine) is a naturally occurring atropine derivative and exhibits anti-inflammatory activity. It also inhibits α1-adrenergic receptors and muscarinic acetylcholine receptors (mAChRs). |
|
|
S5005 |
Cefotiam hydrochloride
|
Cefotiam hydrochloride (Halospor, Pansporin, Pansporine) is the hydrochloride salt form of cefotiam and has a broad spectrum of activity against both gram-positive and gram-negative microorganisms. |
|
|
E0516 |
Nequinate
|
Nequinate, a quinoline compound, is an anticoccidial agent against cecal coccidiosis (Eimeria tenella) infections, also inhibits xanthine oxidoreductase (XOD) activity.This product has poor solubility, animal experiments are available, cell experiments please choose carefully! |
|
|
S1962 |
Sulphadimethoxine
|
Sulphadimethoxine is a non-reducing glucuronide. |
|
|
S4555 |
Carsalam
|
Carsalam (Carbonylsalicylamide) is a nonsteroidal anti-inflammatory drug. |
|
|
E1436 |
A2ti-2
|
A2ti-2 is a selective and low-affinity inhibitor of annexin A2/S100A10 heterotetramer (A2t)with an IC50 of 230 μM. It specifically disrupts the protein-protein interaction (PPI) between A2 and S100A10 and also prevents human papillomavirus type 16 (HPV16) infection. |
|
|
S4521 |
DEET
|
DEET (N,N-Diethyl-meta-toluamide, diethyltoluamide) is a commen active ingredient insect repellent. |
|
|
E2971 |
Influenza Hemagglutinin (HA) Peptide
|
Influenza Hemagglutinin (HA) Peptide is a synthetic peptide with an amino acid sequence of N-Tyr-Pro-Tyr-Asp-Val-Pro-Asp-Tyr-Ala-C. It is extensively used to isolate, purify, detect, and track the protein of interest in cell biology and biochemistry. It is used for competing out the anti-HA antibody binding to HA-tagged fusion proteins in immunoassays. It may also be used to to elute HA-tagged fusion proteins from an affinity column of Monoclonal Anti-HA agarose. |
|
|
S1958 |
Sulbactam
|
Sulbactam(CP45899) is a beta-lactamase inhibitor with an average IC50 of 0.8 μM. |
|
|
S5001 |
Tofacitinib (CP-690550) Citrate
|
トファシチニブクエン酸塩 (Tofacitinib citrate (CP-690550、タソシチニブ)) は JAK の新規阻害剤です。IC50は JAK3, JAK2, JAK1 に対してそれぞれ 1 nM, 20 nM, 112 nM です。 トファシチニブクエン酸塩は抗感染作用を持ちます。 |
- J Exp Clin Cancer Res, 2024, 43(1):64
- Antimicrob Agents Chemother, 2024, 68(4):e0135023.
- Front Oncol, 2024, 14:1386190
|
|
S4157 |
Chloroquine diphosphate
|
Chloroquine diphosphate is a 4-aminoquinoline anti-malarial and anti-rheumatoid agent, also acting as an ATM activator. Chloroquine is also an inhibitor of toll-like receptors (TLRs). |
- Nat Commun, 2024, 15(1):1642
- Cancer Lett, 2024, 604:217258
- Phytomedicine, 2024, 135:156053
|
|
S4430 |
Hydroxychloroquine (HCQ) Sulfate
|
Hydroxychloroquine (HCQ) Sulfate is an antimalarial agent used for the treatment of systemic lupus erythematosus, rheumatoid arthritis and other autoimmune, inflammatory and dermatologic conditions. Also acts as an inhibitor of autophagy and toll-like receptor (TLR) 7/9.
|
- Redox Biol, 2024, 75:103274
- Phytomedicine, 2024, 10.1016/j.phymed.2023.155152
- Breast Cancer Res, 2024, 26(1):33
|
|
S8279 |
Shikonin
|
Shikonin, a potent and specific Pyruvate kinase M2 (PKM2) inhibitor, is a major component of zicao (purple gromwell, the dried root of Lithospermum erythrorhizon), a Chinese herbal medicine with various biological activities. It is also an inhibitor of TMEM16A chloride channel activity using cell-based fluorescent-quenching assay. Shikonin exerts an anti-inflammatory effect by inhibiting tumor necrosis factor-α (TNF-α) and prevents activation of nuclear factor-κB (NF-κB) pathway via proteasome inhibition. |
- Elife, 2024, 12RP91141
- Elife, 2024, 12RP91141
- Mol Ther Methods Clin Dev, 2024, 32(3):101307
|
|
S8068 |
Chaetocin
|
Chaetocin, a natural product from Chaetomium species, is a histone methyltransferase inhibitor with IC50 of 0.8 μM, 2.5 μM and 3 μM for dSU(VAR)3-9, mouse G9a and Neurospora crassa DIM5, respectively. Chaetocin is an anticancer agent and inhibitor of thioredoxin reductase (TrxR). |
- PeerJ, 2024, 12:e17222
- Asian Pac J Trop Bio, 2023;, 13(6): 268-276
- Cancer Cell, 2023, 41(6):1118-1133.e12
|
|
S2572 |
Streptomycin sulfate
|
Streptomycin sulfate(Phytomycin) is a sulfate salt of streptomycin that is a protein synthesis inhibitor. |
- Front. Oncol, 2023-, Volume 13
- Front Oncol, 2023, 13:1118268
- Transl Oncol, 2022, 26:101502
|
|
S7465 |
FTI 277 HCl
|
FTI 277 HCl is a potent and selective farnesyltransferase (FTase) inhibitor with IC50 of 500 pM, about 100-fold selectivity over the closely related GGTase I. FTI 277 HCl inhibits cell growth and induces apoptosis. FTI 277 HCl is effective in clearing HDV viremia. |
- Cancer Res, 2023, 83(13):2248-2261
- PLoS Biol, 2021, 19(4):e3001134
- Cell Struct Funct, 2021, 46(1):1-9
|
|
S5184 |
Dexamethasone palmitate
|
Dexamethasone palmitate (DXP), a lipophilic prodrug of Dexamethasone (DXM), is a glucocorticoid receptor agonist with a 47-fold lower affinity for the glucocorticoid receptor than DXM. Dexamethasone palmitate (DXP) exhibits anti-inflammatory activity. |
- Dis Model Mech, 2022, dmm.049109
- Hematology, 2022, 27(1):32-42
|
|
S1553 |
Delafloxacin (ABT-492)
|
Delafloxacin (ABT-492, RX-3341, WQ-3034) is a new fluoroquinolone against 155 aerobic and 171 anaerobic pathogens. |
- Molecules, 2023, 28(6)2820
- Molecules, 2023, 28(6), 2820
|
|
S5927 |
Proguanil
|
Proguanil (chlorguanide, chloroguanide) is a prophylactic antimalarial drug. It inhibits the dihydrofolate reductase of plasmodia and thereby blocks the biosynthesis of purines and pyrimidines, which are essential for DNA synthesis and cell multiplication. |
- Int J Med Sci, 2022, 19(2):233-241
- Sci Adv, 2021, 7(27)eabh3032
|
|
E0206 |
Ginkgetin
|
Ginkgetin is a biflavone from Ginkgo biloba leaves with anti-cancer, anti-inflammatory, anti-microbial, anti-adipogenic, and neuroprotective activities. |
- Biomed Pharmacother, 2022, 154:113628
|
|
S7867 |
Oleuropein
|
Oleuropein is an antioxidant polyphenol isolated from olive leaf. Oleuropein exerts antioxidant, anti-inflammatory and anti-atherogenic effects and suppresses the adipocyte differentiation in vitro. Oleuropein inhibits PPARγ activity. Oleuropein exerts anti-adipogenic effect through direct inhibition of PPARγ transcriptional activity. Oleuropein also inhibits aromatase. Oleuropein induces apoptosis. Phase 2. |
- Front Endocrinol (Lausanne), 2024, 15:1354435
- J Med Virol, 2019, 91(8):1440-1447
|
|
S3226 |
Dehydroabietic acid
|
Dehydroabietic acid (DAA, DHAA), a naturally occurring diterpene resin acid derived from coniferous plants such as Pinus and Picea, displays anti-inflammatory activity via suppression of Src-, Syk-, and TAK1-mediated pathways. |
|
|
S4945 |
Ethacridine lactate
|
Ethacridine lactate (Acrinol) is an aromatic organic compound based on acridine used as an antiseptic agent. Ethacridine lactate is also a poly(ADP-ribose) glycohydrolase (PARG) inhibitor. |
|
|
S3308 |
Caftaric acid
|
Caftaric acid (CA, Caffeoyl tartaric acid) is a natural product that shows anti-oxidant and anti-inflammatory effects. |
|
|
S4946 |
2,3-Dihydroxybenzoic acid
|
2,3-Dihydroxybenzoic acid (Pyrocatechuic acid, 3-Hydroxysalicylic acid, Hypogallic acid) is a natural phenol found in Phyllanthus acidus and in the aquatic fern Salvinia molesta, also a product of human aspirin metabolism. It is a potentially useful iron-chelating drug and has antimicrobial properties. |
|
|
E0626 |
AX 20017
|
AX 20017 is a small-molecule protein kinase G (PknG) inhibitor with an IC50 of 0.39 μM. |
|
|
S4303 |
9-Aminoacridine
|
9-Aminoacridine (Aminacrine) is a highly fluorescent dye used clinically as a topical antiseptic and experimentally as a mutagen, an intracellular pH indicator and a negative mode small molecule MALDI matrix. |
|
|
S4417 |
Ceftaroline Fosamil
|
Ceftaroline fosamil (CX-0903, DSP-5990, PPI-0903, TAK-599, Teflaro, Zinforo) is a cephalosporin with activity against Gram-positive pathogens, including methicillin-resistant Staphylococcus aureus (MRSA).
|
|
|
S0846 |
Euquinine
|
Euquinine is generally used as a febrifuge, antimalarial, and tonic. |
|
|
S6771 |
MAC-545496
|
MAC-545496 is a nanomolar glycopeptide-resistance-associated protein R(GraR) inhibitor with strong binding affinity to the full-length GraR protein (Kd ≤ 0.1 nM). MAC-545496 can reverse β-lactam resistance in methicillin-resistant strains and synergize with CAMPs. MAC-545496 shows remarkable activity in macrophages and attenuates S. aureus virulence in a G. mellonella larvae infection model. |
|
|
S3711 |
Carbasalate Calcium
|
Carbasalate calcium (Iromin, Alcacyl, Omegin, Rheomin, Solupsan) is an analgesic, antipyretic, and anti-inflammatory drug as well as a platelet aggregation inhibitor. |
|
|
E1126 |
AFN-1252
|
AFN-1252 (Debio 1452) is a potent inhibitor of enoyl-acyl carrier protein reductase (FabI), inhibits all clinical isolates of Staphylococcus aureus and Staphylococcus epidermidis at concentrations of ≤0.12 μg/ml. |
|
|
E1421 |
A2ti-1
|
A2ti-1 is a selective and high-affinity inhibitor of annexin A2/S100A10 heterotetramer (A2t) with IC50 of 24 μM. A2ti-1 specifically disrupts the protein-protein interaction (PPI) between A2 and S100A10. It also prevents human papillomavirus type 16 (HPV16) infection. |
|
|
S9341 |
3,4-Dimethoxycinnamic acid
|
3,4-Dimethoxycinnamic acid (Caffeic acid dimethyl ether) is a bioavailable coffee component as a perspective anti-prion compound and bind potently to prion protein with a Kd of 405 nM. |
|
|
S4515 |
Ademetionine disulfate tosylate
|
Ademetionine Disulfate Tosylate is the disulfate-tosylate mixed salt of a mixture of diastereoisomers of the ademetionine ions. Ademetionine possesses anti-inflammatory activity and has been used in treatment of chronic liver disease. |
|
|
S6802 |
Etosalamide
|
Etosalamide (Ethosalamide) is an anti-inflammatory drug with antipyretic and analgesics properties. |
|
|
S3261 |
Myrislignan
|
Myrislignan, a lignan isolated from Myristica fragrans Houtt, possesses anti-inflammatory activities. Myrislignan inhibits interleukin-6 (IL-6) and tumour necrosis factor-α (TNF-α). Myrislignan significantly inhibits the expressions of inducible NO synthase (iNOS) and cyclooxygenase-2 (COX-2) dose-dependently in LPS-stimulated macrophage cells. Myrislignan inhibits the NF-κB signalling pathway activation. |
- Oxid Med Cell Longev, 2023, 2023:7098313
|
|
E0516 |
Nequinate
|
Nequinate, a quinoline compound, is an anticoccidial agent against cecal coccidiosis (Eimeria tenella) infections, also inhibits xanthine oxidoreductase (XOD) activity.This product has poor solubility, animal experiments are available, cell experiments please choose carefully! |
|
|
E1436 |
A2ti-2
|
A2ti-2 is a selective and low-affinity inhibitor of annexin A2/S100A10 heterotetramer (A2t)with an IC50 of 230 μM. It specifically disrupts the protein-protein interaction (PPI) between A2 and S100A10 and also prevents human papillomavirus type 16 (HPV16) infection. |
|
|
S1958 |
Sulbactam
|
Sulbactam(CP45899) is a beta-lactamase inhibitor with an average IC50 of 0.8 μM. |
|
|