CAS 88899-55-2 appears in our catalog under these names: Bafilomycin A1, >95% (HPLC), Bafilomycin A1/ 99.14% (existing batch purity), Bafilomycin A1, Bafilomycin A1 , Bafilomycin A1, 0.1 mg/ml in DMSO, sterile-filtered . Offered by: TRC, TargetMol, GLPBio, Thermo Scientific (Alfa Aesar), Biosynth. Available pack sizes: 10mg, 1mg, 5mg, 500µg, 1ml, 2mg, 0.1MG, 100ug.
Bafilomycin A1 is the most used of the bafilomycins, a family of toxic macrolide antibiotics derived from Streptomyces griseus. It has a role as a ferroptosis inhibitor, a fungicide, a toxin, an EC 3.6.3.10 (H(+)/K(+)-exchanging ATPase) inhibitor, an apoptosis inducer, an EC 3.6.3.14 (H(+)-transporting two-sector ATPase) inhibitor, a bacterial metabolite, a potassium ionophore and an autophagy inhibitor. It is a macrolide antibiotic, a member of oxanes and a cyclic hemiketal.
Source: ChEBI
| Molecular formula | C35H58O9 |
|---|---|
| Molecular weight | 622.8 g/mol |
| IUPAC name | (3Z,5E,7R,8S,9S,11E,13E,15S,16R)-16-[(2S,3R,4S)-4-[(2R,4R,5S,6R)-2,4-dihydroxy-5-methyl-6-propan-2-yloxan-2-yl]-3-hydroxypentan-2-yl]-8-hydroxy-3,15-dimethoxy-5,7,9,11-tetramethyl-1-oxacyclohexadeca-3,5,11,13-tetraen-2-one |
| InChIKey | XDHNQDDQEHDUTM-JQWOJBOSSA-N |
| SMILES | C[C@H]1C/C(=C/C=C/[C@@H]([C@H](OC(=O)/C(=C/C(=C/[C@H]([C@H]1O)C)/C)/OC)[C@@H](C)[C@H]([C@H](C)[C@]2(C[C@H]([C@@H]([C@H](O2)C(C)C)C)O)O)O)OC)/C |
Computed by PubChem (NCBI)