U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C16H15NO
Molecular Weight 237.2964
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CYHEPTAMIDE

SMILES

NC(=O)C1C2=C(CCC3=C1C=CC=C3)C=CC=C2

InChI

InChIKey=APBVLLORZMAWKI-UHFFFAOYSA-N
InChI=1S/C16H15NO/c17-16(18)15-13-7-3-1-5-11(13)9-10-12-6-2-4-8-14(12)15/h1-8,15H,9-10H2,(H2,17,18)

HIDE SMILES / InChI

Molecular Formula C16H15NO
Molecular Weight 237.2964
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Cyheptamide is anticonvulsant compound, developed by the Canadian company Ayerst Research Laboratories in the 1960s. Oral administration of compound at 14-25 mg/kg protected mice against the tonic phase of pentylenetetrazole convulsion and maximal electroshock seizure. Anticonvulsant activity of cyheptamide was confirmed in initial clinical studies, but the compound was not marketed.

Approval Year

PubMed

PubMed

TitleDatePubMed
Cytenamide-formic acid (1/1).
2008 Jul 5
Cytenamide-1,4-dioxane (2/1).
2008 Jun 28
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:02:01 GMT 2023
Edited
by admin
on Fri Dec 15 15:02:01 GMT 2023
Record UNII
6R22P8K61P
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CYHEPTAMIDE
INN   MI   USAN  
INN   USAN  
Official Name English
AY-8682
Code English
5H-DIBENZO(A,D)CYCLOHEPTENE-5-CARBOXAMIDE, 10,11-DIHYDRO-
Systematic Name English
10,11-Dihydro-5H-dibenzo[a,d]cycloheptene-5-carboxamide
Systematic Name English
CYHEPTAMIDE [MI]
Common Name English
CYHEPTAMIDE [USAN]
Common Name English
cyheptamide [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C264
Created by admin on Fri Dec 15 15:02:01 GMT 2023 , Edited by admin on Fri Dec 15 15:02:01 GMT 2023
Code System Code Type Description
EVMPD
SUB06868MIG
Created by admin on Fri Dec 15 15:02:01 GMT 2023 , Edited by admin on Fri Dec 15 15:02:01 GMT 2023
PRIMARY
FDA UNII
6R22P8K61P
Created by admin on Fri Dec 15 15:02:01 GMT 2023 , Edited by admin on Fri Dec 15 15:02:01 GMT 2023
PRIMARY
ECHA (EC/EINECS)
230-570-8
Created by admin on Fri Dec 15 15:02:01 GMT 2023 , Edited by admin on Fri Dec 15 15:02:01 GMT 2023
PRIMARY
NCI_THESAURUS
C81469
Created by admin on Fri Dec 15 15:02:01 GMT 2023 , Edited by admin on Fri Dec 15 15:02:01 GMT 2023
PRIMARY
CAS
7199-29-3
Created by admin on Fri Dec 15 15:02:01 GMT 2023 , Edited by admin on Fri Dec 15 15:02:01 GMT 2023
PRIMARY
ChEMBL
CHEMBL1868301
Created by admin on Fri Dec 15 15:02:01 GMT 2023 , Edited by admin on Fri Dec 15 15:02:01 GMT 2023
PRIMARY
MERCK INDEX
m1100
Created by admin on Fri Dec 15 15:02:01 GMT 2023 , Edited by admin on Fri Dec 15 15:02:01 GMT 2023
PRIMARY Merck Index
SMS_ID
100000083759
Created by admin on Fri Dec 15 15:02:01 GMT 2023 , Edited by admin on Fri Dec 15 15:02:01 GMT 2023
PRIMARY
PUBCHEM
23603
Created by admin on Fri Dec 15 15:02:01 GMT 2023 , Edited by admin on Fri Dec 15 15:02:01 GMT 2023
PRIMARY
MESH
C002556
Created by admin on Fri Dec 15 15:02:01 GMT 2023 , Edited by admin on Fri Dec 15 15:02:01 GMT 2023
PRIMARY
INN
2191
Created by admin on Fri Dec 15 15:02:01 GMT 2023 , Edited by admin on Fri Dec 15 15:02:01 GMT 2023
PRIMARY
EPA CompTox
DTXSID6046551
Created by admin on Fri Dec 15 15:02:01 GMT 2023 , Edited by admin on Fri Dec 15 15:02:01 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY