ChemicalBook--->CAS DataBase List--->88979-61-7

88979-61-7

88979-61-7 Structure

88979-61-7 Structure
IdentificationBack Directory
[Name]

BAFILOMYCIN C1
[CAS]

88979-61-7
[Synonyms]

L-681110A1
BAFILOMYCIN C1
Antibiotic L-681110A1
2-Demethyl-2-methoxy-24-methylhygrolidin
2-Butenedioic acid (2E)-, 1-[(2R,4R,5S,6R)-tetrahydro-2-hydroxy-2-[(1S,2R,3S)-2-hydroxy-3-[(2R,3S,4E,6E,9S,10S,11R,12E,14Z)-10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxooxacyclohexadeca-4,6,12,14-tetraen-2-yl]-1-methylbutyl]-5-methyl-6-(1-methylethyl)-2H-pyran-4-yl] ester
[Molecular Formula]

C39H60O12
[MDL Number]

MFCD00904461
[MOL File]

88979-61-7.mol
[Molecular Weight]

720.89
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 5 mg/ml; Methanol: 5 mg/ml
[form ]

White to light-brown solid.
[color ]

Yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS06
[Signal word ]

Danger
Hazard InformationBack Directory
[Uses]

Bafilomycin C1 is a member of a potent family of macrocyclic lactones. Bafilomycin C1 shares a similar mode of action and activity as its more accessible A1 analogue. Bafilomycin C1 is broadly active against bacteria, fungi, insects, nematodes and cestodes. Bafilomycin C1 has attracted interest as a potential agent for treating osteoporosis. The presence of the fumarate group provides an ideal ligand for affinity chromatography of V-ATPase.
[Uses]

Bafilomycin C1 is a selective, reversible inhibitor of vacuolar H+-ATPases (V-ATPases). It blocks these pumps in mammalian, plant, or fungal cells, preventing proton transport and compartment acidification. Bafilomycin C1 has been shown to have angiostatic activity in the chick chorioallantoic membrane assay. It has also been used, when coupled to cellulose, to purify V-ATPases.[Cayman Chemical]
[in vivo]

Bafilomycin C1 (subcutaneous injection; 0.2 mg/kg; 20 days) retards the tumor growth without apparent adverse reactions or side effects in nude mice model[1].

Animal Model:BALB/c nude mice (weighing 18-20 g) subcutaneous injected by SMMC7721 cell suspension (5×106 cells/100 μL)[2]
Dosage:0.2 mg/kg
Administration:Subcutaneous injection; 20 days
Result:Suppressed tumor growth of SMMC7721 tumor xenografts.
[IC 50]

Macrolide
[storage]

Store at -20°C
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