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Merck

A5837

Arachidonoyl coenzyme A lithium salt

≥85%

Sinónimos:

Arachidonoyl CoA lithium salt, cis,cis,cis,cis-5,8,11,14-Eicosatetraenoyl coenzyme A lithium salt

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About This Item

Fórmula empírica (notación de Hill):
C41H66N7O17P3S · xLi+
Número CAS:
188174-63-2
Peso molecular:
1053.99 (free acid basis)
NACRES:
NA.51
PubChem Substance ID:
24891026
UNSPSC Code:
41106305
MDL number:
MFCD01311885

Nombre del producto

Arachidonoyl coenzyme A lithium salt, ≥85%

InChI

1S/C41H66N7O17P3S.Li/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-32(50)69-25-24-43-31(49)22-23-44-39(53)36(52)41(2,3)27-62-68(59,60)65-67(57,58)61-26-30-35(64-66(54,55)56)34(51)40(63-30)48-29-47-33-37(42)45-28-46-38(33)48;/h8-9,11-12,14-15,17-18,28-30,34-36,40,51-52H,4-7,10,13,16,19-27H2,1-3H3,(H,43,49)(H,44,53)(H,57,58)(H,59,60)(H2,42,45,46)(H2,54,55,56);/q;+1/p-1/b9-8+,12-11+,15-14+,18-17+;/t30-,34-,35-,36+,40-;/m1./s1

SMILES string

[Li+].CCCCC\C=C\C\C=C\C\C=C\C\C=C\CCCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)([O-])=O)n2cnc3c(N)ncnc23

InChI key

PFJKRDANWCBXHE-VKSULDSYSA-M

assay

≥85%

form

powder

storage temp.

−20°C

Quality Level

200

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Application

Arachidonoyl coenzyme (Arachidonoyl CoA) is used as a substrate for the long-chain N-acylation of glycines by enzymes such as glycine N-acyltransferase-like 2 (GLYATL2) and of acytransferases such as lysophosphatidic acid acyltransferase (CGI-58/ABHD5). Arachidonoyl CoA is used as a charged membrane-impermeant analog of arachidonic acid (AA). Arachidonoyl CoA is used in the synthesis of arachidonoyl amino acids by cytochrome c.
Arachidonoyl coenzyme A lithium salt may be used as a substrate for lysophosphatidylcholine acyltransferase 3 (LPCAT3).

Biochem/physiol Actions

Arachidonoyl CoA is used as a charged membrane-impermeable analog of arachidonic acid (AA). It is used as a substrate for the long-chain N-acylation of glycines by enzymes such as glycine N-acyltransferase-like 2 (GLYATL2) in the presence of cytochrome c.

Clase de almacenamiento

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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Certificados de análisis (COA)

Lot/Batch Number
0000521599
0000521599
0000467496
0000467496
0000463818

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Visite la Librería de documentos

Effects of fatty acids on BK channels in GH3cells
Denson D, et al.
American Journal of Physiology. Cell Physiology, 279(4), C1211-C1219 (2000)
The emerging role of acyl-CoA thioesterases and acyltransferases in regulating peroxisomal lipid metabolism
Hunt MC, et al.
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease, 1822(9), 1397-1410 (2012)
Jeffrey M McCue et al.
Prostaglandins & other lipid mediators, 90(1-2), 42-48 (2009-08-18)
Arachidonoyl amino acids are a class of endogenous lipid messengers that are expressed in the mammalian central nervous system and peripherally. While several of their prominent pharmacologic effects have been documented, the mechanism by which arachidonoyl amino acids are biosynthesized
A novel assay for measuring recombinant human lysophosphatidylcholine acyltransferase 3 activity
Du X, et al.
FEBS Open Bio, 9(10), 1734-1743 (2019)
Valerie Yeung-Yam-Wah et al.
Cell calcium, 47(1), 77-83 (2009-12-19)
Arachidonic acid (AA) is generated in the pancreatic islets during glucose stimulation. We investigated whether AA activated extracellular Ca(2+) entry in rat pancreatic beta cells via a pathway that was independent of the activation of voltage-gated Ca(2+) channels. The AA
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