Details
Stereochemistry | ACHIRAL |
Molecular Formula | C15H14ClN3O3 |
Molecular Weight | 319.743 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(=O)C1=C2CN(C)C(=O)C3=C(Cl)C=CC=C3N2C=N1
InChI
InChIKey=WSDBAFQWNWJTNG-UHFFFAOYSA-N
InChI=1S/C15H14ClN3O3/c1-3-22-15(21)13-11-7-18(2)14(20)12-9(16)5-4-6-10(12)19(11)8-17-13/h4-6,8H,3,7H2,1-2H3
Molecular Formula | C15H14ClN3O3 |
Molecular Weight | 319.743 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Sarmazenil (previously known as RO 153505) was developed as a weak inverse agonist at the omega modulatory sites (benzodiazepine receptors). This compound is used in veterinary medicine in order to rapidly re-awake anesthetized animals. In addition, this compound was studied in the treatment of a moxidectin intoxication in foals. Sarmazenil was also involved in preclinical development for Alzheimer's disease in the USA. However, the information about the further development of the drug is not available.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 17:55:01 GMT 2023
by
admin
on
Sat Dec 16 17:55:01 GMT 2023
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Record UNII |
F84AE7X24P
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Record Status |
Validated (UNII)
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Record Version |
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-
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Official Name | English | ||
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Code | English | ||
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Code | English |
Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C28197
Created by
admin on Sat Dec 16 17:55:01 GMT 2023 , Edited by admin on Sat Dec 16 17:55:01 GMT 2023
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WHO-VATC |
QV03AB91
Created by
admin on Sat Dec 16 17:55:01 GMT 2023 , Edited by admin on Sat Dec 16 17:55:01 GMT 2023
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Code System | Code | Type | Description | ||
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F84AE7X24P
Created by
admin on Sat Dec 16 17:55:01 GMT 2023 , Edited by admin on Sat Dec 16 17:55:01 GMT 2023
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PRIMARY | |||
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78771-13-8
Created by
admin on Sat Dec 16 17:55:01 GMT 2023 , Edited by admin on Sat Dec 16 17:55:01 GMT 2023
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PRIMARY | |||
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SARMAZENIL
Created by
admin on Sat Dec 16 17:55:01 GMT 2023 , Edited by admin on Sat Dec 16 17:55:01 GMT 2023
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PRIMARY | |||
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CHEMBL46547
Created by
admin on Sat Dec 16 17:55:01 GMT 2023 , Edited by admin on Sat Dec 16 17:55:01 GMT 2023
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SUB10452MIG
Created by
admin on Sat Dec 16 17:55:01 GMT 2023 , Edited by admin on Sat Dec 16 17:55:01 GMT 2023
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PRIMARY | |||
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C73206
Created by
admin on Sat Dec 16 17:55:01 GMT 2023 , Edited by admin on Sat Dec 16 17:55:01 GMT 2023
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PRIMARY | |||
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6283
Created by
admin on Sat Dec 16 17:55:01 GMT 2023 , Edited by admin on Sat Dec 16 17:55:01 GMT 2023
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PRIMARY | |||
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100000084077
Created by
admin on Sat Dec 16 17:55:01 GMT 2023 , Edited by admin on Sat Dec 16 17:55:01 GMT 2023
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DTXSID70229281
Created by
admin on Sat Dec 16 17:55:01 GMT 2023 , Edited by admin on Sat Dec 16 17:55:01 GMT 2023
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PRIMARY | |||
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71231
Created by
admin on Sat Dec 16 17:55:01 GMT 2023 , Edited by admin on Sat Dec 16 17:55:01 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ACTIVE MOIETY |