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bafilomycin D

CAS No.
98813-13-9
Chemical Name:
bafilomycin D
Synonyms
bafilomycin D;TubayMycin, 3D5;Bafilomycin D, from Streptomyces griseus;Oxacyclohexadeca-3,5,11,13-tetraen-2-one, 16-[(1S,2R,3S,5E,7S,8R)-2,8-dihydroxy-1,3,7,9-tetramethyl-4-oxo-5-decen-1-yl]-8-hydroxy-3,15-dimethoxy-5,7,9,11-tetramethyl-, (3Z,5E,7R,8S,9S,11E,13E,15S,16R)-
CBNumber:
CB11315335
Molecular Formula:
C35H56O8
Molecular Weight:
604.81
MDL Number:
MOL File:
98813-13-9.mol
MSDS File:
SDS
Last updated:2023-05-21 10:59:17

bafilomycin D Properties

storage temp. Store at -20°C
solubility Soluble in ethanol;Soluble in methanol;Soluble in DMSO
form powder

bafilomycin D price More Price(7)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 19438 Bafilomycin D ≥99% 98813-13-9 1mg $364 2024-03-01 Buy
Cayman Chemical 19438 Bafilomycin D ≥99% 98813-13-9 5mg $1181 2024-03-01 Buy
TRC B110008 BafilomycinD 98813-13-9 5mg $8350 2021-12-16 Buy
Usbiological B0003-73 Bafilomycin D 98813-13-9 1mg $523 2021-12-16 Buy
Adipogen Life Sciences BVT-0475-M001 BafilomycinD(highpurity) ≥98%(HPLC) 98813-13-9 1mg $180 2021-12-16 Buy
Product number Packaging Price Buy
19438 1mg $364 Buy
19438 5mg $1181 Buy
B110008 5mg $8350 Buy
B0003-73 1mg $523 Buy
BVT-0475-M001 1mg $180 Buy

bafilomycin D Chemical Properties,Uses,Production

Uses

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.

Uses

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.

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.

bafilomycin D Preparation Products And Raw materials

Raw materials

Preparation Products

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98813-13-9(bafilomycin D)Related Search:

bafilomycin D TubayMycin, 3D5 Oxacyclohexadeca-3,5,11,13-tetraen-2-one, 16-[(1S,2R,3S,5E,7S,8R)-2,8-dihydroxy-1,3,7,9-tetramethyl-4-oxo-5-decen-1-yl]-8-hydroxy-3,15-dimethoxy-5,7,9,11-tetramethyl-, (3Z,5E,7R,8S,9S,11E,13E,15S,16R)- Bafilomycin D, from Streptomyces griseus 98813-13-9