Details
Stereochemistry | ACHIRAL |
Molecular Formula | C14H11Cl2NO2 |
Molecular Weight | 296.149 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=C(Cl)C(NC2=C(C=CC=C2)C(O)=O)=C1Cl
InChI
InChIKey=SBDNJUWAMKYJOX-UHFFFAOYSA-N
InChI=1S/C14H11Cl2NO2/c1-8-6-7-10(15)13(12(8)16)17-11-5-3-2-4-9(11)14(18)19/h2-7,17H,1H3,(H,18,19)
Molecular Formula | C14H11Cl2NO2 |
Molecular Weight | 296.149 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 17:19:21 UTC 2023
by
admin
on
Sat Dec 16 17:19:21 UTC 2023
|
Record UNII |
48I5LU4ZWD
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
LIVERTOX |
588
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
||
|
WHO-ATC |
M01AG04
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
||
|
WHO-VATC |
QM01AG04
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
||
|
NCI_THESAURUS |
C1323
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
||
|
CFR |
21 CFR 520.1330
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
||
|
WHO-VATC |
QM02AA18
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
||
|
WHO-ATC |
M02AA18
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
||
|
CFR |
21 CFR 520.1331
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
48I5LU4ZWD
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
D008469
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
100000081757
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
48I5LU4ZWD
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
m7120
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | Merck Index | ||
|
2165
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
7219
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
DB00939
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
95309
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
588003
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
ALTERNATIVE | |||
|
76230
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
644-62-2
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
4037
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
Meclofenamate
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
C61826
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
SUB08678MIG
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
DTXSID0048559
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
6678
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
211-419-5
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
6710
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
CHEMBL509
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY | |||
|
1650
Created by
admin on Sat Dec 16 17:19:22 UTC 2023 , Edited by admin on Sat Dec 16 17:19:22 UTC 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
METABOLIC ENZYME -> INHIBITOR |
POTENT
|
||
|
SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
---|---|---|---|---|
|
METABOLITE ACTIVE -> PARENT |
Urinary excretion accounts for up to 50-60% of this metabolites. (Active)
MAJOR
URINE
|
||
|
METABOLITE INACTIVE -> PARENT |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |