Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

870724P

Avanti

24:0 Coenzyme A

Avanti Research™ - A Croda Brand 870724P, powder

Synonym(s):

lignoceroyl Coenzyme A (ammonium salt)

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C45H91N10O17P3S
CAS Number:
799812-99-0
Molecular Weight:
1169.25
MDL number:
MFCD22416634
UNSPSC Code:
12352211
NACRES:
NA.25

form

powder

packaging

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

manufacturer/tradename

Avanti Research™ - A Croda Brand 870724P

application(s)

lipidomics

lipid type

coenzymes

shipped in

dry ice

storage temp.

−20°C

SMILES string

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

InChI key

BMXJUIXYBGOZPL-SJDXFXGUSA-N

General description

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.

Packaging

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

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Sorry, we don't have COAs for this product available online at this time.

If you need assistance, please contact Customer Support.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service