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870725P

Avanti

24:1 Coenzyme A

Avanti Research™ - A Croda Brand 870725P, powder

Synonym(s):

(15Z-tetracosenoyl) Coenzyme A (ammonium salt)

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About This Item

Empirical Formula (Hill Notation):
C45H89N10O17P3S
CAS Number:
800376-90-3
Molecular Weight:
1167.23
UNSPSC Code:
12352211
NACRES:
NA.25

form

powder

packaging

pkg of 1 × 5 mg (870725P-5mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 870725P

application(s)

lipidomics

lipid type

coenzymes

shipped in

dry ice

storage temp.

−20°C

SMILES string

O[C@@](C(NCCC(NCCSC(CCCCCCCCCCCCC/C=C\CCCCCCCC)=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/C45H80N7O17P3S.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;;;/h11-12,32-34,38-40,44,55-56H,4-10,13-31H2,1-3H3,(H,47,53)(H,48,57)(H,61,62)(H,63,64)(H2,46,49,50)(H2,58,59,60);3*1H3/b12-11-;;;/t34-,38?,39+,40+,44-;;;/m1.../s1

InChI key

UAIPAWBQHXNXER-PSWOAFEESA-N

General description

24:1 Coenzyme A, also known as (15Z-tetracosenoyl) coenzyme A, is a coenzyme derivative of nervonic acid or cis-15-tetracosenoic acid.

Application

24:1 Coenzyme A has been used as a substrate in ceramide synthase assay.

Packaging

5 mL Amber Glass Screw Cap Vial (870725P-5mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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