Details
Stereochemistry | ACHIRAL |
Molecular Formula | C19H20ClN3O |
Molecular Weight | 341.835 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCC(=O)N(C)CC1=C(N=C2C=CC=CN12)C3=CC=C(Cl)C=C3
InChI
InChIKey=LIFDPEORUVTOCP-UHFFFAOYSA-N
InChI=1S/C19H20ClN3O/c1-3-6-18(24)22(2)13-16-19(14-8-10-15(20)11-9-14)21-17-7-4-5-12-23(16)17/h4-5,7-12H,3,6,13H2,1-2H3
Molecular Formula | C19H20ClN3O |
Molecular Weight | 341.835 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Synthélabo developed a saripidem (also known as SL 850274) as a potential anxiolytic agent that modulates the benzodiazepine-binding site on GABAA receptor via primary binding with ω1 subtype. Saripidem was studied in phase II clinical trials for the treatment of patients with anxiety disorders. However, information about the further development of the drug is not available.
Originator
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Behavioural effects of novel benzodiazepine (omega) receptor agonists and partial agonists: increases in punished responding and antagonism of the pentylenetetrazole cue. | 1995 Mar |
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A One Pot Synthesis of Novel Bioactive Tri-Substitute-Condensed-Imidazopyridines that Targets Snake Venom Phospholipase A2. | 2015 |
|
Synthesis of Indolizines via Reaction of 2-Substitued Azaarenes with Enals by an Amine-NHC Relay Catalysis. | 2017 Apr 21 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 16:04:07 GMT 2023
by
admin
on
Sat Dec 16 16:04:07 GMT 2023
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Record UNII |
0J6174G60N
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Record Status |
Validated (UNII)
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Record Version |
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Common Name | English |
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NCI_THESAURUS |
C29756
Created by
admin on Sat Dec 16 16:04:07 GMT 2023 , Edited by admin on Sat Dec 16 16:04:07 GMT 2023
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100000084096
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0J6174G60N
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SARIPIDEM
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C74381
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6932
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DTXSID60146110
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CHEMBL73416
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103844-86-6
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SUB10451MIG
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3058746
Created by
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Related Record | Type | Details | ||
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ACTIVE MOIETY |