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

Details

Stereochemistry ACHIRAL
Molecular Formula C14H20N2O3S
Molecular Weight 296.385
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLYCYCLAMIDE

SMILES

CC1=CC=C(C=C1)S(=O)(=O)NC(=O)NC2CCCCC2

InChI

InChIKey=RIGBPMDIGYBTBJ-UHFFFAOYSA-N
InChI=1S/C14H20N2O3S/c1-11-7-9-13(10-8-11)20(18,19)16-14(17)15-12-5-3-2-4-6-12/h7-10,12H,2-6H2,1H3,(H2,15,16,17)

HIDE SMILES / InChI
Glycyclamide (Tolcyclamide) isn a cyclohexyl-containing sulfonylurea compound with antihyperglycemic activity. Tolcyclamide is closely related to tolbutamide, with a cyclohexyl ring in place of the butyl group. It is much less potent than glipizide, being active at a daily dose of 1000 mg.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Diaboral

Approved Use

Treatment of type 2 diabetes mellitus
PubMed

PubMed

TitleDatePubMed
Synthesis, characterization, antioxidant activity, and DNA-binding studies of 1-cyclohexyl-3-tosylurea and its Nd(III), Eu(III) complexes.
2008 Apr
Synthesis of a high-purity chemical library reveals a potent inducer of oxidative stress.
2010 Jun 14
Patents

Sample Use Guides

Name Type Language
GLYCYCLAMIDE
INN   MART.   WHO-DD  
INN  
Official Name English
K-386
Code English
TOLCYCLAMIDE [MI]
Common Name English
Glycyclamide [WHO-DD]
Common Name English
K-38
Code English
1-CYCLOHEXYL-3-P-TOLYLSULFONYLUREA
Common Name English
GLYCYCLAMIDE [MART.]
Common Name English
NSC-142661
Code English
glycyclamide [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C97936
Created by admin on Sat Dec 16 15:54:37 GMT 2023 , Edited by admin on Sat Dec 16 15:54:37 GMT 2023
Code System Code Type Description
INN
1317
Created by admin on Sat Dec 16 15:54:37 GMT 2023 , Edited by admin on Sat Dec 16 15:54:37 GMT 2023
PRIMARY
CAS
664-95-9
Created by admin on Sat Dec 16 15:54:37 GMT 2023 , Edited by admin on Sat Dec 16 15:54:37 GMT 2023
PRIMARY
NCI_THESAURUS
C65809
Created by admin on Sat Dec 16 15:54:37 GMT 2023 , Edited by admin on Sat Dec 16 15:54:37 GMT 2023
PRIMARY
SMS_ID
100000084233
Created by admin on Sat Dec 16 15:54:37 GMT 2023 , Edited by admin on Sat Dec 16 15:54:37 GMT 2023
PRIMARY
MESH
C005008
Created by admin on Sat Dec 16 15:54:37 GMT 2023 , Edited by admin on Sat Dec 16 15:54:37 GMT 2023
PRIMARY
EVMPD
SUB07952MIG
Created by admin on Sat Dec 16 15:54:37 GMT 2023 , Edited by admin on Sat Dec 16 15:54:37 GMT 2023
PRIMARY
FDA UNII
C40N4EJY68
Created by admin on Sat Dec 16 15:54:37 GMT 2023 , Edited by admin on Sat Dec 16 15:54:37 GMT 2023
PRIMARY
ECHA (EC/EINECS)
211-557-6
Created by admin on Sat Dec 16 15:54:37 GMT 2023 , Edited by admin on Sat Dec 16 15:54:37 GMT 2023
PRIMARY
ChEMBL
CHEMBL312394
Created by admin on Sat Dec 16 15:54:37 GMT 2023 , Edited by admin on Sat Dec 16 15:54:37 GMT 2023
PRIMARY
NSC
142661
Created by admin on Sat Dec 16 15:54:37 GMT 2023 , Edited by admin on Sat Dec 16 15:54:37 GMT 2023
PRIMARY
MERCK INDEX
m10941
Created by admin on Sat Dec 16 15:54:37 GMT 2023 , Edited by admin on Sat Dec 16 15:54:37 GMT 2023
PRIMARY Merck Index
DRUG CENTRAL
1324
Created by admin on Sat Dec 16 15:54:37 GMT 2023 , Edited by admin on Sat Dec 16 15:54:37 GMT 2023
PRIMARY
EPA CompTox
DTXSID5046273
Created by admin on Sat Dec 16 15:54:37 GMT 2023 , Edited by admin on Sat Dec 16 15:54:37 GMT 2023
PRIMARY
PUBCHEM
12628
Created by admin on Sat Dec 16 15:54:37 GMT 2023 , Edited by admin on Sat Dec 16 15:54:37 GMT 2023
PRIMARY