Details
Stereochemistry | MIXED |
Molecular Formula | C19H40 |
Molecular Weight | 268.5209 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 0 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)CCCC(C)CCCC(C)CCCC(C)C
InChI
InChIKey=XOJVVFBFDXDTEG-UHFFFAOYSA-N
InChI=1S/C19H40/c1-16(2)10-7-12-18(5)14-9-15-19(6)13-8-11-17(3)4/h16-19H,7-15H2,1-6H3
Approval Year
PubMed
Title | Date | PubMed |
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Contribution of mast cell mediators to alterations in macrophage function after malathion administration. | 1996 Sep |
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Differential gene expression in pristane-induced arthritis susceptible DA versus resistant E3 rats. | 2003 |
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Degradation of alkanes and highly chlorinated benzenes, and production of biosurfactants, by a psychrophilic Rhodococcus sp. and genetic characterization of its chlorobenzene dioxygenase. | 2003 Oct |
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Prostaglandin E2 receptors EP2 and EP4 are up-regulated in peritoneal macrophages and joints of pristane-treated mice and modulate TNF-alpha and IL-6 production. | 2004 Jul |
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High prevalence of autoantibodies to RNA helicase A in Mexican patients with systemic lupus erythematosus. | 2010 |
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MicroRNA-26a negatively regulates toll-like receptor 3 expression of rat macrophages and ameliorates pristane induced arthritis in rats. | 2014 Jan 14 |
Patents
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C44351
Created by
admin on Sat Dec 16 20:09:06 GMT 2023 , Edited by admin on Sat Dec 16 20:09:06 GMT 2023
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53181
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C29850
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26HZV48DT1
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8345
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DTXSID70870919
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m9140
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admin on Sat Dec 16 20:09:06 GMT 2023 , Edited by admin on Sat Dec 16 20:09:06 GMT 2023
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1921-70-6
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114852
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217-650-8
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15979
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C009042
Created by
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PRISTANE
Created by
admin on Sat Dec 16 20:09:06 GMT 2023 , Edited by admin on Sat Dec 16 20:09:06 GMT 2023
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SUBSTANCE RECORD