Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H18NO |
| Molecular Weight | 156.2453 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1(C)CCCC(C)(C)N1[O]
InChI
InChIKey=VUZNLSBZRVZGIK-UHFFFAOYSA-N
InChI=1S/C9H19NO/c1-8(2)6-5-7-9(3,4)10(8)11/h11H,5-7H2,1-4H3
| Molecular Formula | C9H18NO |
| Molecular Weight | 156.2453 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Reactive oxygen species regulate macrophage scavenger receptor type I, but not type II, in the human monocytic cell line THP-1. | 1998 Jun |
|
| Hydrogen peroxide mediates FK506-induced cytotoxicity in renal cells. | 2004 Jan |
|
| Molecular investigation of the effects of lindane in rat hepatocytes: microarray and mechanistic studies. | 2011 Dec |
|
| The inhibitory effect of raloxifene on lipopolysaccharide-induced nitric oxide production in RAW264.7 cells is mediated through a ROS/p38 MAPK/CREB pathway to the up-regulation of heme oxygenase-1 independent of estrogen receptor. | 2011 Feb |
|
| Reactive oxygen species and c-Jun N-terminal kinases contribute to TEMPO-induced apoptosis in L5178Y cells. | 2015 Jun 25 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:17:30 GMT 2023
by
admin
on
Fri Dec 15 18:17:30 GMT 2023
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| Record UNII |
VQN7359ICQ
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| Record Status |
Validated (UNII)
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| Record Version |
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32849
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2564-83-2
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VQN7359ICQ
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2724126
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219-888-8
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DTXSID2073300
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m10553
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C003959
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TEMPO
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admin on Fri Dec 15 18:17:30 GMT 2023 , Edited by admin on Fri Dec 15 18:17:30 GMT 2023
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| Related Record | Type | Details | ||
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PARENT -> IMPURITY |
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