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B1508

Sigma-Aldrich

Butyryl coenzyme A lithium salt hydrate

≥90%

Synonym(s):

Butyryl-CoA lithium salt hydrate

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About This Item

Empirical Formula (Hill Notation):
C25H42N7O17P3S · xLi+ · yH2O
Molecular Weight:
837.62 (free acid basis)
MDL number:
MFCD00038616
UNSPSC Code:
41106305
PubChem Substance ID:
329773188

Quality Level

200

assay

≥90%

form

powder

storage temp.

−20°C

SMILES string

[Li+].[Li+].[Li+].[Li+].CCCC(=O)Nc1ncnc2n(cnc12)[C@@H]3O[C@H](COP([O-])(=O)OP([O-])(=O)OCC(C)(C)C(O)C(=O)NCCC(=O)NCCS)[C@@H](OP([O-])([O-])=O)[C@H]3O

InChI

1S/C25H42N7O17P3S.4Li/c1-4-5-16(34)31-21-17-22(29-12-28-21)32(13-30-17)24-18(35)19(48-50(38,39)40)14(47-24)10-45-51(41,42)49-52(43,44)46-11-25(2,3)20(36)23(37)27-7-6-15(33)26-8-9-53;;;;/h12-14,18-20,24,35-36,53H,4-11H2,1-3H3,(H,26,33)(H,27,37)(H,41,42)(H,43,44)(H2,38,39,40)(H,28,29,31,34);;;;/q;4*+1/p-4/t14-,18-,19-,20?,24-;;;;/m1..../s1

InChI key

FKMUWGIOOMBTED-VLFKLNKMSA-J

Related Categories

Application

Butyryl CoA is a substrate for Butyryl CoA Dehydrogenase. Butyryl CoA is involved in both lipid and butanoate metabolism. Butyryl-CoA may be used as a substrate of various lipases and as an alternate substrate for 4-hydroxybutyrate CoA-transferase. Butyryl CoA may be used to study the newly discovered process of post-translational histone modification by butyrylation.

Biochem/physiol Actions

Butyryl CoA is a substrate for Butyryl CoA Dehydrogenase. Butyryl CoA is involved in both lipid and butanoate metabolism.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Sofia Macieira et al.
Archives of microbiology, 194(3), 157-166 (2011-08-13)
Clostridium aminobutyricum ferments 4-aminobutyrate (γ-aminobutyrate, GABA) to ammonia, acetate and butyrate via 4-hydroxybutyrate that is activated to the CoA-thioester catalyzed by 4-hydroxybutyrate CoA-transferase. Then, 4-hydroxybutyryl-CoA is dehydrated to crotonyl-CoA, which disproportionates to butyryl-CoA and acetyl-CoA. Cocrystallization of the CoA-transferase with
Yue Chen et al.
Molecular & cellular proteomics : MCP, 6(5), 812-819 (2007-02-03)
The positively charged lysine residue plays an important role in protein folding and functions. Neutralization of the charge often has a profound impact on the substrate proteins. Accordingly all the known post-translational modifications at lysine have pivotal roles in cell
C Biben et al.
Molecular and cellular biology, 14(5), 3504-3513 (1994-05-01)
A DNase I-hypersensitive site analysis of the 5'-flanking region of the mouse alpha-cardiac actin gene with muscle cell lines derived from C3H mice shows the presence of two such sites, at about -5 and -7 kb. When tested for activity
Li-Chiun Lee et al.
Journal of agricultural and food chemistry, 59(19), 10693-10698 (2011-08-23)
Recombinant Candida rugosa lipase 5 (LIP5) has been functionally expressed along with other isoforms in our laboratory. However, the characterization and codon optimization of LIP5 have not been done. In this work, we characterized, codon-optimized and compared LIP5 with commercial
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The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 26(2), 150-154 (2012-08-30)
To measure the effect labor exerts on fatty acid (FA) oxidation in term human placentas, and to compare enzymes expression and activity between placenta and liver. Placental samples were collected: (a) scheduled non-labored cesarean section and (b) normal vaginal delivery
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