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I0383

Isobutyryl coenzyme A lithium salt

≥85%

Synonym(s):

2-Methylpropanoyl-CoA, IB-CoA

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About This Item

Empirical Formula (Hill Notation):
C25H42N7O17P3S · xLi+
CAS Number:
103404-95-1
Molecular Weight:
837.62 (free acid basis)
NACRES:
NA.51
PubChem Substance ID:
24895902
UNSPSC Code:
41106305
MDL number:
MFCD00079368
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Quality Level

200

assay

≥85%

storage temp.

−20°C

SMILES string

[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);;

InChI key

XOJGPZXPXDNYHG-UHFFFAOYSA-N

Related Categories

Biochem/physiol Actions

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).

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0000548174
0000548175
0000548175
0000548174
0000512957

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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
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

Global Trade Item Number

SKUGTIN
I0383-10MG04061833262375
I0383-5MG04061833262382

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