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870724P

Avanti

24:0 Coenzyme A

Avanti Research™ - A Croda Brand 870724P, powder

Synonyme(s) :

lignoceroyl Coenzyme A (ammonium salt)

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About This Item

Formule empirique (notation de Hill):
C45H91N10O17P3S
Numéro CAS:
799812-99-0
Poids moléculaire :
1169.25
Code UNSPSC :
12352211
Nomenclature NACRES :
NA.25

Forme

powder

Conditionnement

pkg of 1 × 25 mg (870724P-25mg)
pkg of 1 × 5 mg (870724P-5mg)

Fabricant/nom de marque

Avanti Research™ - A Croda Brand 870724P

Application(s)

lipidomics

Type de lipide

coenzymes

Conditions d'expédition

dry ice

Température de stockage

−20°C

Chaîne SMILES 

O[C@@](C(NCCC(NCCSC(CCCCCCCCCCCCCCCCCCCCCCC)=O)=O)=O)(C(C)(COP([O-])(OP([O-])(OC[C@H]([C@H]1OP([O-])(O)=O)O[C@H]([C@@H]1O)N2C3=C(C(N)=NC=N3)N=C2)=O)=O)C)[H].[NH4+].[NH4+].[NH4+]

InChI

1S/C45H82N7O17P3S.3H3N/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-36(54)73-29-28-47-35(53)26-27-48-43(57)40(56)45(2,3)31-66-72(63,64)69-71(61,62)65-30-34-39(68-70(58,59)60)38(55)44(67-34)52-33-51-37-41(46)49-32-50-42(37)52;;;/h32-34,38-40,44,55-56H,4-31H2,1-3H3,(H,47,53)(H,48,57)(H,61,62)(H,63,64)(H2,46,49,50)(H2,58,59,60);3*1H3/t34-,38?,39+,40+,44-;;;/m1.../s1

Clé InChI

BMXJUIXYBGOZPL-SJDXFXGUSA-N

Description générale

24:0 Coenzyme A, also referred as lignoceroyl coenzyme A, is a long chain fatty acyl CoA and derivative of lignoceric acid. It is a metabolic intermediate of hydroxyceramide synthesis.

Application

24:0 Coenzyme A has been used as a substrate in fatty acyl-CoA reductase (AmFAR1) enzyme assay and ceramide synthase assay.

Conditionnement

5 mL Amber Glass Screw Cap Vial (870724P-25mg)
5 mL Amber Glass Screw Cap Vial (870724P-5mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Code de la classe de stockage

11 - Combustible Solids

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Consulter la Bibliothèque de documents

H Shigematsu et al.
The International journal of biochemistry, 22(12), 1427-1432 (1990-01-01)
1. The enzymatic mechanism of the alpha-hydroxylation of lignoceroyl-CoA, an intermediate in the synthesis of hydroxyceramide, was studied. In the presence of NADPH, sphingosine and microsomes from 20-day-old rat brain, 14C from [1-14C]lignoceroyl-CoA was incorporated into hydroxyceramide. 2. The alpha-hydroxylation
Prapapan Teerawanichpan et al.
Insect biochemistry and molecular biology, 40(9), 641-649 (2010-06-15)
Honey bees (Apis mellifera) are social insects which have remarkable complexity in communication pheromones. These chemical signals comprise a mixture of hydrocarbons, wax esters, fatty acids, aldehydes and alcohols. In this study, we detected several long chain aliphatic alcohols ranging
Evgeny V Berdyshev et al.
The Journal of biological chemistry, 284(9), 5467-5477 (2009-01-03)
Novel immunomodulatory molecule FTY720 is a synthetic analog of myriocin, but unlike myriocin FTY720 does not inhibit serine palmitoyltransferase. Although many of the effects of FTY720 are ascribed to its phosphorylation and subsequent sphingosine 1-phosphate (S1P)-like action through S1P(1,3-5) receptors

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