SB-315021

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Category Enzyme inhibitors
Catalog number BBF-03404
CAS
Molecular Weight 554.7
Molecular Formula C28H46N2O9

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Description

SB-315021 is an inhibitor of lipoprotein associated phospholipase A2 produced by Pseudomonas fluorescens DSM 11579.

Specification

Synonyms SB 315021; SB315021
IUPAC Name N-(1,5-dioxo-5a,6,7,8-tetrahydropyrrolo[1,2-c][1,3]oxazepin-3-yl)-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxytetradecanamide
Canonical SMILES CCCCCCCCCCCC(CC(=O)NC1=CC(=O)C2CCCN2C(=O)O1)OC3C(C(C(C(O3)C)O)O)O
InChI InChI=1S/C28H46N2O9/c1-3-4-5-6-7-8-9-10-11-13-19(38-27-26(35)25(34)24(33)18(2)37-27)16-22(32)29-23-17-21(31)20-14-12-15-30(20)28(36)39-23/h17-20,24-27,33-35H,3-16H2,1-2H3,(H,29,32)/t18-,19?,20?,24-,25+,26+,27-/m0/s1
InChI Key WAHMOFCRXZFEQB-KITPZMISSA-N

Properties

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Reference Reading

1. SB-253514 and analogues: novel inhibitors of lipoprotein associated phospholipase A2 produced by Pseudomonas fluorescens DSM 11579. II. Physico-chemical properties and structure elucidation
D J Busby, R C Copley, J A Hueso, S A Readshaw, A Rivera J Antibiot (Tokyo). 2000 Jul;53(7):670-6.
A series of novel inhibitors of lipoprotein associated phospholipase A2 were isolated from the culture broths of Pseudomonas fluorescens strain DSM11579. The inhibitors fall into two structurally isomeric classes each of which comprise compounds incorporating glycosylated hydrocarbon chains. The structure elucidation for the major member of each structural class is reported. The crystal structure of a non-glycosylated analogue of the 5,5-series, produced through biotransformation, is also reported.

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Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2

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Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
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