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I0383

Sigma-Aldrich

Isobutyryl coenzyme A lithium salt

≥85%

Sinônimo(s):

2-Methylpropanoyl-CoA, IB-CoA

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About This Item

Fórmula empírica (Notação de Hill):
C25H42N7O17P3S · xLi+
Número CAS:
103404-95-1
Peso molecular:
837.62 (free acid basis)
Número MDL:
MFCD00079368
Código UNSPSC:
41106305
ID de substância PubChem:
24895902
NACRES:
NA.51

Nível de qualidade

200

Ensaio

≥85%

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

[Li].CC(C)C(=O)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP(O)(O)=O)n2cnc3c(N)ncnc23

InChI

1S/C25H42N7O17P3S.Li.H/c1-13(2)24(37)53-8-7-27-15(33)5-6-28-22(36)19(35)25(3,4)10-46-52(43,44)49-51(41,42)45-9-14-18(48-50(38,39)40)17(34)23(47-14)32-12-31-16-20(26)29-11-30-21(16)32;;/h11-14,17-19,23,34-35H,5-10H2,1-4H3,(H,27,33)(H,28,36)(H,41,42)(H,43,44)(H2,26,29,30)(H2,38,39,40);;

chave InChI

XOJGPZXPXDNYHG-UHFFFAOYSA-N

Categorias relacionadas

Ações bioquímicas/fisiológicas

Coenzyme A functions as an acyl group carrier, acetyl-CoA. Isobutyryl coenzyme A (IB-CoA), a short-chain branched acyl-CoA, provides the starter unit for biosynthesis of myxalamid B. Isobutyryl coenzyme A is used as a substrate to study the specificity and kinetics of isobutyryl-coenzyme A (CoA) mutase (EC 5.4.99.13).

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

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Certificados de análise (COA)

Lot/Batch Number
SLCH9593
SLCD8424
SLBR6073V
SLBN8535V
SLBG2163V

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Mohini S Ghatge et al.
Applied and environmental microbiology, 75(11), 3469-3476 (2009-03-24)
Phoslactomycins (PLMs) and related leustroducsins (LSNs) have been isolated from a variety of bacteria based on antifungal, anticancer, and other biological assays. Streptomyces sp. strain HK 803 produces five PLM analogs (PLM A and PLMs C to F) in which
A Ratnatilleke et al.
The Journal of biological chemistry, 274(44), 31679-31685 (1999-10-26)
Isobutyryl-CoA mutase (ICM) catalyzes the reversible, coenzyme B(12)-dependent rearrangement of isobutyryl-CoA to n-butyryl-CoA, which is similar to, but distinct from, that catalyzed by methylmalonyl-CoA mutase. ICM has been detected so far in a variety of aerobic and anaerobic bacteria, where
Helge B Bode et al.
Chembiochem : a European journal of chemical biology, 8(17), 2139-2144 (2007-10-24)
Myxalamids are potent inhibitors of the eukaryotic electron transport chain produced by different myxobacteria. Here, we describe the identification of the myxalamid biosynthesis gene cluster from Myxococcus xanthus. Additionally, new myxalamids (5-13) have been obtained by mutasynthesis from bkd mutants
Jinxia Lin et al.
Bioresource technology, 102(2), 1863-1868 (2010-10-29)
Supply of isobutanol to enhance the production of anti-tumor agent ansamitocin P-3 (AP-3) in medium containing agro-industrial residues was investigated with analysis of gene transcription, enzyme activity, and intermediate accumulation. Under the optimal addition of isobutanol, about 4-fold improvement of

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