Details
Stereochemistry | ACHIRAL |
Molecular Formula | C18H35NO2 |
Molecular Weight | 297.476 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCN(CC)CCOC(=O)C1(CCC(C)C)CCCCC1
InChI
InChIKey=BHSHHNNBVMXJNZ-UHFFFAOYSA-N
InChI=1S/C18H35NO2/c1-5-19(6-2)14-15-21-17(20)18(13-10-16(3)4)11-8-7-9-12-18/h16H,5-15H2,1-4H3
Molecular Formula | C18H35NO2 |
Molecular Weight | 297.476 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
PubMed
Title | Date | PubMed |
---|---|---|
Plan and pack an a-plus lunch. | 2002 Fall |
|
Design features of the Avasimibe and Progression of coronary Lesions assessed by intravascular UltraSound (A-PLUS) clinical trial. | 2002 Oct |
|
The clopidogrel after surgery for coronary artery disease (CASCADE) randomized controlled trial: clopidogrel and aspirin versus aspirin alone after coronary bypass surgery [NCT00228423]. | 2005 Oct 11 |
|
Improved and simplified recombineering approach for influenza virus reverse genetics. | 2009 Dec 1 |
|
Impact of medical therapy on atheroma volume measured by different cardiovascular imaging modalities. | 2010 |
|
Community perceptions of malaria and malaria treatment behaviour in a rural district of Ghana: implications for artemisinin combination therapy. | 2010 Jul 12 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:15:36 GMT 2023
by
admin
on
Fri Dec 15 16:15:36 GMT 2023
|
Record UNII |
8E2I9ESU8N
|
Record Status |
Validated (UNII)
|
Record Version |
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-
Download
Name | Type | Language | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Common Name | English |
Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29696
Created by
admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
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Code System | Code | Type | Description | ||
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28221
Created by
admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
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PRIMARY | |||
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C83843
Created by
admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
|
PRIMARY | |||
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DTXSID80183007
Created by
admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
|
PRIMARY | |||
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8E2I9ESU8N
Created by
admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
|
PRIMARY | |||
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28815-27-2
Created by
admin on Fri Dec 15 16:15:36 GMT 2023 , Edited by admin on Fri Dec 15 16:15:36 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
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ACTIVE MOIETY |