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

Details

Stereochemistry ABSOLUTE
Molecular Formula C18H26N2O4S
Molecular Weight 366.475
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLIBORNURIDE

SMILES

CC1=CC=C(C=C1)S(=O)(=O)NC(=O)N[C@@H]2[C@H](O)[C@]3(C)CC[C@H]2C3(C)C

InChI

InChIKey=RMTYNAPTNBJHQI-LLDVTBCESA-N
InChI=1S/C18H26N2O4S/c1-11-5-7-12(8-6-11)25(23,24)20-16(22)19-14-13-9-10-18(4,15(14)21)17(13,2)3/h5-8,13-15,21H,9-10H2,1-4H3,(H2,19,20,22)/t13-,14+,15+,18+/m1/s1

HIDE SMILES / InChI

Molecular Formula C18H26N2O4S
Molecular Weight 366.475
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Glibornuride is sulphonylurea derivative used as an oral hypoglycemic drug in patients with diabetes. The drug was marketed under the name Glutril, however, it is no longer available.

Originator

Curator's Comment: # Hoffmann La Roche

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
GLUTRIL

Approved Use

Glutril is used for the treatment of diabetes.
PubMed

PubMed

TitleDatePubMed
Screening, library-assisted identification and validated quantification of oral antidiabetics of the sulfonylurea-type in plasma by atmospheric pressure chemical ionization liquid chromatography-mass spectrometry.
2002 Jun 15
The morphological and biochemical effects of glibornuride on rat liver in experimental diabetes.
2004 May
Identification and quantification of 8 sulfonylureas with clinical toxicology interest by liquid chromatography-ion-trap tandem mass spectrometry and library searching.
2005 Sep
Effects of glibornuride versus metformin on eye lenses and skin in experimental diabetes.
2006
Effects of parsley (Petroselinum crispum) extract versus glibornuride on the liver of streptozotocin-induced diabetic rats.
2006 Mar 8
Metformin, sulfonylureas, or other antidiabetes drugs and the risk of lactic acidosis or hypoglycemia: a nested case-control analysis.
2008 Nov
Patents

Patents

Sample Use Guides

The recommended dose is 0.5 tablet (1 tablet contains 25 mg of glibornuride) per day, given at breakfast time. Do not take more than 3 tablets per day.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:17:30 GMT 2023
Edited
by admin
on Fri Dec 15 15:17:30 GMT 2023
Record UNII
VP83E7434R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GLIBORNURIDE
INN   MART.   MI   USAN   WHO-DD  
INN   USAN  
Official Name English
GLIBORNURIDE [MART.]
Common Name English
RO 6-4563
Code English
GLIBORNURIDE [USAN]
Common Name English
RO-6-4563
Code English
BENZENESULFONAMIDE, N-(((3-HYDROXY-4,7,7-TRIMETHYLBICYCLO(2.2.1)HEPT-2-YL)AMINO)CARBONYL)-4-METHYL-, (1S-(ENDO, ENDO))-
Common Name English
Glibornuride [WHO-DD]
Common Name English
GLUTRIL
Brand Name English
ENDO, ENDO-1-((1R)-(2-HYDROXY-3-BORNYL))-3-(P-TOLYLSULFONYL)UREA
Common Name English
glibornuride [INN]
Common Name English
GLIBORNURIDE [MI]
Common Name English
RO-64563
Code English
Classification Tree Code System Code
WHO-VATC QA10BB04
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
WHO-ATC A10BB04
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
NCI_THESAURUS C97936
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
Code System Code Type Description
FDA UNII
VP83E7434R
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
PRIMARY
NCI_THESAURUS
C123430
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
PRIMARY
CAS
26944-48-9
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID001016937
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
PRIMARY
DRUG CENTRAL
1298
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
PRIMARY
INN
2751
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
PRIMARY
SMS_ID
100000080423
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
PRIMARY
MESH
C073323
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
PRIMARY
DRUG BANK
DB08962
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
PRIMARY
RXCUI
102846
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
PRIMARY RxNorm
WIKIPEDIA
GLIBORNURIDE
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
PRIMARY
ECHA (EC/EINECS)
248-124-6
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
PRIMARY
PUBCHEM
12818200
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
PRIMARY
ChEMBL
CHEMBL529888
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
PRIMARY
EVMPD
SUB07917MIG
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
PRIMARY
MERCK INDEX
m5743
Created by admin on Fri Dec 15 15:17:30 GMT 2023 , Edited by admin on Fri Dec 15 15:17:30 GMT 2023
PRIMARY Merck Index
Related Record Type Details
ACTIVE MOIETY