Details
Stereochemistry | RACEMIC |
Molecular Formula | C36H41N3O6 |
Molecular Weight | 611.7272 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)C1=C(C)NC(C)=C(C1C2=CC=CC(=C2)[N+]([O-])=O)C(=O)OC(C)(C)CN(C)CCC(C3=CC=CC=C3)C4=CC=CC=C4
InChI
InChIKey=ZDXUKAKRHYTAKV-UHFFFAOYSA-N
InChI=1S/C36H41N3O6/c1-24-31(34(40)44-6)33(28-18-13-19-29(22-28)39(42)43)32(25(2)37-24)35(41)45-36(3,4)23-38(5)21-20-30(26-14-9-7-10-15-26)27-16-11-8-12-17-27/h7-19,22,30,33,37H,20-21,23H2,1-6H3
Molecular Formula | C36H41N3O6 |
Molecular Weight | 611.7272 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 17:54:59 UTC 2023
by
admin
on
Sat Dec 16 17:54:59 UTC 2023
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Record UNII |
V7XTJ4R0BH
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Record Status |
Validated (UNII)
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Record Version |
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-
Download
Name | Type | Language | ||
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Official Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Brand Name | English | ||
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Systematic Name | English |
Classification Tree | Code System | Code | ||
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WHO-ATC |
C09DB08
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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NCI_THESAURUS |
C333
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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WHO-ATC |
C08CA13
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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WHO-ATC |
C09BB02
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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WHO-VATC |
QC09BB02
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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WHO-VATC |
QC08CA13
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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Code System | Code | Type | Description | ||
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C060343
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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PRIMARY | |||
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V7XTJ4R0BH
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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PRIMARY | |||
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LERCANIDIPINE
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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PRIMARY | |||
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DB00528
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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PRIMARY | |||
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4157
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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PRIMARY | |||
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6971
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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PRIMARY | |||
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100000092283
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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PRIMARY | |||
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65866
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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PRIMARY | |||
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C81687
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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PRIMARY | |||
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CHEMBL250270
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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PRIMARY | |||
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100427-26-7
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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PRIMARY | |||
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DTXSID2048327
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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PRIMARY | |||
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m6770
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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PRIMARY | Merck Index | ||
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SUB08437MIG
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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PRIMARY | |||
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135056
Created by
admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
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PRIMARY | RxNorm |
Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE | |||
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SALT/SOLVATE -> PARENT | |||
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TARGET -> INHIBITOR |
Related Record | Type | Details | ||
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ACTIVE MOIETY |