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Leukotoxin

HCID 1929
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Basic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
113972-57-9
Standard SMILES
CCCCCC=CCC1OC1CCCCCCCC(=O)O
InChIKey
FBUKMFOXMZRGRB-UHFFFAOYSA-N
Molecular formula
C18H32O3
Average molar mass
296.4 g/mol
Monoisotopic mass
296.23514488

Overview

2E,4E-decadienoic piperideide has been reported in Matricaria discoidea and Matricaria matricarioides with data available.

Names & identifiers

Preferred name
Leukotoxin
IUPAC
8-(3-oct-2-enyloxiran-2-yl)octanoic acid

Names & synonyms

113972-57-9leucotoxinsRefChem:924689Leukotoxin3-(2-Octen-1-yl)-2-oxiraneoctanoic acidCoronarsaeure(?)9(10)-EpOME8-(3-oct-2-enyloxiran-2-yl)octanoic acidCBiol_001808KBioGR_000060KBioSS_000060SCHEMBL2228910
Show more names
KBio2_000060KBio2_002628KBio2_005196KBio3_000119KBio3_000120Bio1_000094Bio1_000583Bio1_001072

Database identifiers

CAS
113972-57-9、65167-83-1
PubChem CID
1929
DTXSID
DTXSID401357890

Properties

Computed structural properties

XLogP
5.6
Topological polar surface area
49.8 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
3
Rotatable bonds
14
Heavy atoms
21
Formal charge
0
Complexity
299

Chemistry & industry

Pharmacology

MeSH Pharmacological Classification · 1 item

Agents that suppress immune function by one of several mechanisms of action. Classical cytotoxic immunosuppressants act by inhibiting DNA synthesis. Others may act through activation of T-CELLS or by inhibiting the activation of HELPER CELLS. While immunosuppression has been brought about in the past primarily to prevent rejection of transplanted organs, new applications involving mediation of the effects of INTERLEUKINS and other CYTOKINES are emerging.

Related reactions

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Compound notes

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