Bafilomycin A1 (Baf-A1)

製品コード：S1413 純度：97%

バフィロマイシン A1 (Bafilomycin A1(Baf-A1)) は液胞 H⁺-ATPase 阻害剤で、IC50 は 0.44 nM です。バフィロマイシン A1 は、オートファジー (autophagy) を阻害する一方で、アポトーシス (apoptosis) を誘導することがわかっています。

CAS No. 88899-55-2

サイズ	価格(税別)	在庫状況
160.6μL(1mM/0.1mg)	JPY 41500	国内在庫なし(納期7~10日)
1mg	JPY 52000	国内在庫あり
1mg*5	JPY 220500	国内在庫なし(納期7~10日)

代表番号: 045-509-1970\|電子メール：[email protected] よく尋ねられる質問

文献中Selleckの製品使用例（479）

質量管理及び製品安全説明書

現在のバッチを見る： 純度：>97%

Bafilomycin A1 (Baf-A1)と併用されることが多い化合物

3-MA (3-Methyladenine)

Bafilomycin A1 and 3-Methyladenine (3-MA) combination plus irradiation leads to more pronounced and prolonged DNA damage in glioma and breast cancer cells.

Tameire F, et al. Semin Cancer Biol. 2015 Aug;33:3-15.

Y-27632 2HCl

Explore the signalling pathways involved in ARV S1133 regulated switch from autophagy to apoptosis.

Lin PY, et al. BMC Vet Res. 2015 May 6;11:103.

Rapamycin

Explore the impact of autophagy on megakaryopoiesis and thrombopoiesis.

Wang Q, et al. Platelets. 2017;28(1):82-89.

Torin 1

Explore TGFBI metabolism and autophagy impairment in TBCD corneal fibroblasts.

Wang L, et al. Autophagy. 2022;18(4):765-782.

Bafilomycin A1 (Baf-A1)関連製品

関連製品	Ilaprazole sodium Ilaprazole Tenatoprazole Revaprazan Hydrochloride	もっと見る
関連化合物ライブラリー	FDA-approved Drug Library Natural Product Library Ion Channel Ligand Library Exosome Secretion Related Compound Library Calcium Channel Blocker Library	もっと見る

シグナル伝達経路

Proton Pumpシグナル伝達経路

Proton Pump阻害剤の選択性比較

Cell Data

Cell Lines	Assay Type	Concentration	Incubation Time	活性情報	PMID
mouse RAW264.7 cells	Apoptosis assay	100 nM	16 h	Induction of apoptosis in mouse RAW264.7 cells assessed as late apoptotic cells at 100 nM after 16 hrs using annexin V-propidium iodide staining by flow cytometry	19307359
human H4 cells	Function assay	0.4 μM	24 h	Induction of light chain 3-GFP level in human H4 cells at 0.4 uM after 24 hrs by high throughput fluorescence microscopy relative to control	18024584
RAW 264.7 cells	Bactericidal activity assay	100 nM	16 h	Bactericidal activity against Salmonella enterica Typhimurium 14028 infected in RAW 264.7 cells assessed as decrease in bacterial growth yield at 100 nM after 16 hrs postinfection by flow cytometry in presence of 10 ug/ml of intracellular replication inhi	19307359
RAW 264.7 cells	Antimicrobial activity assay	100 nM	30 mins	Antimicrobial activity against Salmonella enterica Typhimurium 14028 infected in RAW 264.7 cells assessed as inhibition of bacterial replication at 100 nM treated 30 mins before infection measured after 2 to 16 hrs postinfection by flow cytometry	19307359
human HeLa cells	Function assay	400 nM		Induction of autophagy in human HeLa cells expressing EGFP-LC3 assessed as increase in LC3-2 level at 400 nM	18391949
RAW 264.7 cells	Function assay	100 nM		Antimicrobial activity against Salmonella enterica Typhimurium 14028 infected in RAW 264.7 cells assessed as increased nitric oxide production in infected cells at 100 nM	19307359
RAW 264.7 cells	Antimicrobial activity assay	100 nM		Antimicrobial activity against Salmonella enterica Typhimurium 14028 infected in RAW 264.7 cells assessed as increased nitric oxide production in infected cells at 100 nM	19307359
human MCF7 cells	Function assay		4 h	Inhibition of rapamycin-induced autophagy in human MCF7 cells expressing EGFP-LC3 assessed as decrease in EGFP levels at 100 nM after 4 hrs by Western blotting relative to control	20028134
human Huh7.5.1 cells	Antiviral activity		3 h	Antiviral activity against HCV genotype 2a JFH-1 in human Huh7.5.1 cells assessed as reduction of viral entry up to 3 hrs by luciferase assay	26396683
rat 3Y1 cells	Function assay			Induction of morphological changes in rat 3Y1 cells assessed as elongation of cells	29701963
他の多くの細胞株試験データをご覧になる場合はこちらをクリックして下さい

生物活性

製品説明

Targets

H+-ATPase ^[1]
(Cell-free assay)

0.44 nM

In Vitro
In vitro	Bafilomycin A1 is a toxic macrolide antibiotic derived from Streptomyces griseus. Bafilomycin A1 inhibits the short circuit current induced by the outer mantle epithelium (OME). The IC50 and maximum inhibition dose of Bafilomycin A1 are 0.17 μM and 0.5 μM, respectively. ^[2] In addition, Bilomycin A1 inhibits the acid influx with an IC50 value of 0.4 nM. Bafilomycin A1 inhibits the acidification dose-dependently resulting in a lower quenching, and thus a higher fluorescence. ^[3] Bafilomycin A1 prevents the vacuolization of Hela cells induced by H. pylori, with an inhibitory concentration giving 50% of maximal (ID50) of 4 nM. Bafilomycin A1 is also very efficient in restoring vacuolated cells to a normal appearance. ^[4] Bafilomycin A1 also affects the transport of endocytosed material from early to late endocytic compartments. Bafilomycin not only dissipates the low endosomal pH but also blocks transport from early to late endosomes in HeLa cells. ^[5] Bafilomycin A1 at doses of 0.1-1 μM completely inhibits the acidification of lysosomes revealed by the incubation with acridine orange in BNL CL.2 and A431 cells. ^[6] When Bafilomycin A1 is added to Hanks' balanced salt solution, endogenous protein degradation is strongly inhibited and numerous autophagosomes accumulated in H-4-II-E cells. Bafilomycin A1 also prevents the appearance of endocytosed HRP in autophagic vacuoles. ^[7]
Kinase Assay	ATPase enzyme activity assays
Kinase Assay	The ATPase enzyme assay medium contains 6 mM MgSO₄, 50 mM HEPES (pH 7.4), 200 mM Na₂SO₃ (V-ATPase activator), 0.5 mM sodium ortho-vanadate (P-ATPase inhibitor), 0.5 mM sodium azide (F-ATPase inhibitor) and 3 mM Na₂ATP. This medium (1.0 mL), with or without the addition of the V-type ATPase inhibitor bafilomycin A1, is incubated with the filtered homogenate (0.1 mL) for 60 minutes at 23–25 °C. The reaction is stopped by the addition of 1 mL of TCA 3%. Spectrometric blanks are prepared as for the enzyme assay with the exception that the tissue sample is added after the acid. Phosphate analysis is accomplished by adding 2 mL of 1-butanol and 0.2 mL molybdate solution (5 g ammonium molybdate, 22 mL H₂SO₄ to 100 mL). After vortexing for 15 seconds the solution is neutralised with 0.5 mL citrate solution (100 g/500 mL, pH 7.0) and again vortexed for 15 seconds. The solution is then centrifuged (2000 × g; 3 minutes) to separate the butanol phase and the absorbance of this phase is read at 400 nm. Standards of orthophosphate are prepared (0.1 μM–2.0 μM) and treated in the same way as the enzyme activity assays. Enzyme activity is expressed in μmol of orthophosphate liberated per hour and per milligram of protein. V-ATPase activity is considered to be the difference between the total ATPase activity measured in the presence of Na₂SO₃, sodium orthovanadate and sodium azide and the ATPase activity measured in the presence of these reagents and of the specific V-ATPases inhibitor Bafilomycin A1.
細胞実験	細胞株	HeLa cells
	濃度	~20 nM
	反応時間	20 hours
	実験の流れ	H. pylori bacteria extract is treated with inhibitors, before addition to HeLa cells, as follows: DCCD 10 mM for 1 hour at 30 ºC; NBD-CI 100 μM for 1 hour at 30 ºC and the reaction is blocked with glycine 10 mM final concentration; NEM 275 μM for 1 hour at 30 ºC and the reaction is blocked by addition of β-mercaptoethanol 275 mM; Mg-ATP 14 μM for 1 hour at 0 ºC; 100 μM KNO₃ and 14 μM Mg-ATP for 1 hour at 30 μM; NaCO₃ 100 μM, pH 11 for 1 hour at 0 ºC. The bacterial extract is then added to cell with a 40-fold dilution at a final concentration of 0.65 mg/mL. Controls are HeLa cells incubated with untreated bacterial extracts and cells treated with inhibitor Bafilomycin A1 under the same conditions as bacterial extracts, at the same concentrations or after a 40-fold dilution. The vacuotating activity of the bacterial extracts is assayed.
実験結果図	Methods	Biomarkers	結果図	PMID
	Western blot	Ret / EGFR / p75 NGFR		21559479
	Growth inhibition assay	Cell viability		20534000
	Immunofluorescence	AIF LC3		25512644
	ELISA	TNF-alpha		26240140

In Vivo
In Vivo	Bafilomycin A1 (1 μM and 0.1 μM) completely inhibits the resorptive activity of cultured osteoclasts. ^[8] Bafilomycin A1 dose-dependently inhibits the rate of Na+ uptake in young tilapia with a Ki of 0.16 μM. ^[9]
動物実験	動物モデル	Young (approximately 9 days old) Mozambique tilapia, Oreochromis mossambicus
	投与量	10 μM
	投与経路	--

参考
[1] al-Fifi ZI, et al. Insect BiochemMol Biol, 1998, 28(4), 201-211. [2] Oliveira PF, et al. Comp Biochem Physiol A Mol Integr Physiol, 2004, 139(4), 425-432. [3] S?rensen MG, et al. J Bone Miner Res, 2007, 22(10), 1640-1648. [4] Papini E, et al. Mol Microbiol, 1993, 7(2), 323-327. [5] Bayer N, et al. J Virol, 1998, 72(12), 9645-9655. [6] Yoshimori T, et al. J Biol Chem, 1991, 266(26), 17707-17712. [7] Yamamoto A, et al. Cell Struct Funct, 1998, 23(1), 33-42. [8] Sundquist KT, et al. J Bone Miner Res, 1994, 9(10), 1575-1582. [9] Fenwick JC, et al. J Exp Biol, 1999, 202 Pt 24, 3659-3666. [10] Kanzawa T, et al. Cell Death Differ, 2004, 11(4), 448-457. + 展開

参考

+ 展開

化学情報

分子量	622.83	化学式	C₃₅H₅₈O₉
CAS No.	88899-55-2	SDF	Download Bafilomycin A1 (Baf-A1) SDFをダウンロードする
Smiles	CC1CC(=CC=CC(C(OC(=O)C(=CC(=CC(C1O)C)C)OC)C(C)C(C(C)C2(CC(C(C(O2)C(C)C)C)O)O)O)OC)C
保管	3年-20°C粉	溶液の保管冷凍と解凍の繰り返しを避けるため小分けにしてください	1年-80°Cin solvent
保管	3年-20°C粉	溶液の保管冷凍と解凍の繰り返しを避けるため小分けにしてください	１ケ月-20°Cin solvent

In vitro
Batch:

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
	Clear solution	5%DMSO 1 40%PEG300 2 5%Tween80 3 50%ddH2O	0.3mg/ml (0.48mM)	Taking the 1 mL working solution as an example, add 50 μL 6 mg/ml clarified DMSO stock solution to 400 μL PEG300, mix evenly to clarify it; add 50 μL Tween80 to the above system, mix evenly to clarify it; then continue to add 500 μL ddH2O to adjust the volume to 1 mL. The mixed solution should be used immediately for optimal results.	投与溶液組成計算機
Clear solution	5% DMSO 1 95% Corn oil	1.65mg/ml (2.65mM)	Taking the 1 mL working solution as an example, add 50 μL of 33 mg/ml clear DMSO stock solution to 950 μL of corn oil and mix evenly. The mixed solution should be used immediately for optimal results.
Clear solution	5%DMSO 1 40%PEG300 2 5%Tween80 3 50%ddH2O	5.0mg/ml (8.03mM)	Taking the 1 mL working solution as an example, add 50 μL of 100 mg/ml clarified DMSO stock solution to 400 μL of PEG300, mix evenly to clarify it; add 50 μL of Tween80 to the above system, mix evenly to clarify; then continue to add 500 μL of ddH2O to adjust the volume to 1 mL. The mixed solution should be used immediately for optimal results.

実験計算

モル濃度計算器

質量	濃度	体積	分子量
=	×	×

希釈計算器分子量計算器

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）

投与量 mg/kg 動物平均体重 g 投与体積（動物毎）μL 動物数匹

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

ストックの作り方、阻害剤の保管方法、細胞実験や動物実験の際に注意すべき点など、製品を取扱う時に問い合わせが多かった質問に対しては取扱説明書でお答えしています。

Handling Instructions

他に質問がある場合は、お気軽にお問い合わせください。

* 必須

* 大学・企業名 大学・企業名を記入してください

* 名前 名前を記入してください

* 電子メール 電子メール・アドレスを記入してください 有効なメールアドレスを入力してください

電話番号

* 内容 お問い合わせ内容をご入力ください

よくある質問（FAQ）

質問1:
How to dissolve it？

回答
S1413 Bafilomycin A1(Baf-A1) is soluble in DMSO at 6 mg/ml. Please do not use alcohols as solvent, because this compound will degrade in alcohols.

C1=C0/X	C1:	LOG(C1):
C2=C1/X	C2:	LOG(C2):
C3=C2/X	C3:	LOG(C3):
C4=C3/X	C4:	LOG(C4):
C5=C4/X	C5:	LOG(C5):
C6=C5/X	C6:	LOG(C6):
C7=C6/X	C7:	LOG(C7):
C8=C7/X	C8:	LOG(C8):