bafilomycin D
- CAS NO.:98813-13-9
- Empirical Formula: C35H56O8
- Molecular Weight: 604.81
- SAFETY DATA SHEET (SDS)
- Update Date: 2023-05-21 10:59:17
![bafilomycin D Structural](https://img.chemicalbook.in/CAS/GIF/98813-13-9.gif)
What is bafilomycin D?
The Uses of bafilomycin D
Bafilomycin D is a member of a potent family of macrocyclic lactones. Bafilomycin D shares the same mode of action as bafilomycin A1 which has been the analogue of choice in cell biology studies of the role of ATPase. Bafilomycin D contains the ring-opened side chain and is a much more stable analogue of bafilomycin A1. Limited availability has restricted a more in depth investigation of this metabolite.
The Uses of bafilomycin D
The bafilomycins are fungal plecomacrolide antibiotics with a 16-membered lactone ring. They inhibit the growth of Gram-positive bacteria and fungi. Bafilomycin D is a potent inhibitor of vacuolar H+ ATPases (V-ATPases) that inhibits the V-ATPase from the fungus N. crassa with an IC50 value of approximately 2 nM. It is about 1,000-fold less effective against the K+-dependent ATPase of E. coli.
Biological Activity
bafilomycin d is a potent inhibitor of vacuolar h+ atpases (v-atpases) with ic50 value of approximately 2 nm for the v-atpase from the fungus n. crassa [1].ion pumps use the energy provided by the hydrolysis of atp to energize ion-transport processes across cell membranes. atpases can be distinguished to p-type, f-type and v-type atpases. p-type atpases have a phosphorylated transitional stage, f-type atpases are primarily used in atp synthesis, and v-type atpases are genetically and functionally related to f-atpases but function only in atp breakdown [1].the bafilomycins are fungal plecomacrolide class macrolide antibiotics isolated from the culture medium of streptomyces sp. and are also high-affinity inhibitors of v-atpases and can be used to study specifically the function of this type of atpase. they inhibited the growth of gram-positive bacteria and fungi. bafilomycin c1 inhibited the enzymatic activity of the na+, k+-atpase with ki value of 11 μmol/l and showed anthelmintic activity against caenorhabditis elegans [1][2].
References
[1]. drse s, altendorf k. bafilomycins and concanamycins as inhibitors of v-atpases and p-atpases. j exp biol. 1997 jan;200(pt 1):1-8.
[2]. bowman ej, siebers a, altendorf k. bafilomycins: a class of inhibitors of membrane atpases from microorganisms, animal cells, and plant cells. proc natl acad sci u s a. 1988 nov;85(21):7972-6.
Properties of bafilomycin D
storage temp. | Store at -20°C |
solubility | Soluble in ethanol;Soluble in methanol;Soluble in DMSO |
form | powder |
Safety information for bafilomycin D
Computed Descriptors for bafilomycin D
New Products
1-Amino-1-cyclohexanecarboxylic acid Cycloleucine 6-Bromo-3-iodo-1-methyl-1H-indazole 3-(2,4-Dimethoxybenzyl)dihydropyrimidine-2,4(1H,3H)-dione 7-Bromo-1H-indazole ELECTROLYTIC IRON POWDER 2-Methyl-2-phenylpropyl acetate 1-Aminocyclobutanecarboxylic acid 1-(2-Ethoxyethyl)-2-(piperidin-4-yl)-1H-benzo[d]imidazole hydrochloride Decanonitrile tert-butyl 4-(1H-benzo[d]iMidazol-2-yl)piperidine-1-carboxylate 4-Ethylbenzylamine Methyl 5-bromo-2-chloro-3-nitrobenzoate N-(5-Amino-2-methylphenyl)acetamide 2-Chloro-3-nitropyridine 5-Bromo-2,3-dimethoxypyridine methyl 6-chloro-2-(chloromethyl)nicotinate 2-methoxy-4-methyl-5-nitro pyridine 2-iodo-5-bromo pyridine 2-amino-4-methyl-5-nitro pyridine 5-Fluoro-2-Oxindole methyl L-alaninate hydrochloride diethyl L-glutamate hydrochloride Ethyl tosylcarbamateRelated products of tetrahydrofuran
You may like
-
Ethoxymethylenemalononitrile 99% HPLCView Details
123-06-8 -
3-hydroxy-2-nitrobenzoic acid 602-00-6 98%View Details
602-00-6 -
Diethyl Disulfide 99% HPLCView Details
110-81-6 -
2-((4-Aminopentyl)(ethyl)amino)ethanol 69559-11-1 98%View Details
69559-11-1 -
6285-05-8. 1-(4-chlorophenyl) propan-1-one 98%View Details
6285-05-8. -
4-chloro-3,5-dinitropyridine 98%View Details
-
401-95-6 99% HPLCView Details
401-95-6 -
171663-13-1 tert-Butyl 3-bromobenzylcarbamate 98%View Details
171663-13-1