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Bafilomycin A1

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Formula: C35H58 O9
CAS: 88899-55-2
search Element: bafilomycin

Identification

Structural Formula
Bafilomycin A1
CAS:
88899-55-2
EINECS:
Molecular Formula:
C35H58 O9
MDL:
MFCD06795130
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
Synonym:
bafilomycin a1, 98+% ; oxacyclohexadeca-3,5,11,13-tetraen-2-one,8-hydroxy-16-[2-hydroxy-1-methyl-3-[tetrahydro-2,4-dihydroxy-5-methyl-6-(1-methylethyl)-2h-pyran-2-yl]butyl]-3,15-dimethoxy-5,7,9,11-tetramethyl-,[7r-[3z,5e,7r*,8s*,9s*,11e,13e,15s*,16r*[1s*,2r*,3s*(2r*,4r*,5s*,6r*)]]]- ; bafilomycin a1 95% ; nsc381866 ; oxacyclohexadecane, hygrolidin deriv. ; bafilomycin a1,95% ; bafilomycina1fromstreptomycesgriseus ; (3z,5e,7r,8s,9s,11e,13e,15s,16r)-8-hydroxy-16-((1s,2r,3s)-2-hydroxy-1-methyl-3-((2r,4r,5s,6r)-tetrahydro-2,4-dihydroxy-5 ; bafilomycin a1 bafilomycin a1 from streptomyces griseus ; oxacyclohexadeca-3,5,11,13-tetraen-2-one,8-hydroxy-16-[(1s,2r,3s)-2-hydroxy-1-methyl-3-[(2r,4r,5s,6r)-tetrahydro-2,4-dihydroxy-5-methyl-6-(1-methylethyl)-2h-pyran-2-yl]butyl]-3,15-dimethoxy-5,7,9,11-tetramethyl-,(3z,5e,7r,8s,9s,11e,13e,15s,16r)- ; 21-o-de(3-carboxy-1-oxo-2-propenyl)-2-demethyl-2-methoxy-24-methyl-hygrolidin ; bafilomycin a1 ; bafilomycin a1, streptomyces griseus ; bafilomycin a1 from streptomycesgriseus, 10 ug ; hygrolidin,21-o-de(3-carboxy-1-oxo-2-propenyl)-2-demethyl-2-methoxy-24-methyl- ; (-)-bafilomycin a1


Description

Bafilomycin A1 is a potent and selective inhibitor of V-ATPase (vacuolar-type H+ ATPase) and belongs to a class of membrane ATPase inhibitors. The compound can inhibit E1E2 ATPases from sarcoplasmic reticulum, Escherichia coli, and ox brain versus F1F0 ATPases found in bacteria and mitochondria. Some of the more bafilomycin A1 affected ATPases include Neurospora and plant vacuoles, as well as chromaffin granules. Additionally, Bafilomycin A1 prevents lysosomal cholesterol trafficking in macrophages and can be used to distinguish different types of ATPases. Research shows that Bafilomycin A1 can inhibit macroautophagy and promote apoptosis in colon cancer cells.


Suppliers

Aea.ltd
A196392
Chemlyte Solutions
CS5041512
Indofine Chemical Co, Inc.
Bio-049
Alpha Biopharmaceuticals Co., Ltd.
AB9522856
Alfa (A Johnson Matthey Company)
A8962688
Iris Biotech GmbH
LS-1081.0000
Xingrui Industry Co., Limited
XIL8123248
BOC Sciences
BS3361008
Leap Chem Co., Ltd
LC5041512
Santa Cruz Biotechnology, Inc.
201550
Dayang Chem (Hangzhou) Co.,Ltd.
DC8683472
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CAS equal suppliers

Bafilomycin A1, 95%
Iris Biotech GmbH
LS-1081
Bafilomycin A1, 0.1mg/mL in DMSO, sterile-filtered
Alfa (A Johnson Matthey Company)
A1120033600

Prices & Availability




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Properties for Bafilomycin A1

Molecular Weight:
622.8296 g·mol−1
Density:
1.12 g/cm3
Boiling point:
770.1 °C at 760 mmHg
Flash point:
232.2 °C
Solubility:
Soluble in methanol, ethanol (0.1 mg/ml), DMSO (0.1 mg/ml), acetone, and chloroform. Insoluble in water.
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Safety & Transport Information

Risk Codes:
R36/37/38 - Irritating to eyes, respiratory system and skin
Safety Codes:
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
S36 - Wear suitable protective clothing
Hazard Classes:
6.1(b)
Hazard Symbols:
Xi
Hazard symbol Xi
Storage temperature :
2-8°C
RID/ADR certification :
3172
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Alternative Distributors of [Bafilomycin A1]

Producers or manufacturers change the product range from time to time. The following companies
have appeared as suppliers in the past / currently not verified

Cfm Oskar Tropitzsch GmbH | BOC Sciences | Jinan Great Chemical Co., Ltd. | Fermentek Ltd.

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MSDS:
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