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Details

Stereochemistry ABSOLUTE
Molecular Formula C25H27ClN2O8.H2O
Molecular Weight 536.959
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLUCAMETACIN MONOHYDRATE

SMILES

O.COC1=CC2=C(C=C1)N(C(=O)C3=CC=C(Cl)C=C3)C(C)=C2CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)[C@H](O)CO

InChI

InChIKey=KXDLNFYVIGTHGT-HQKSCHDUSA-N
InChI=1S/C25H27ClN2O8.H2O/c1-13-17(10-22(32)27-19(11-29)23(33)24(34)21(31)12-30)18-9-16(36-2)7-8-20(18)28(13)25(35)14-3-5-15(26)6-4-14;/h3-9,11,19,21,23-24,30-31,33-34H,10,12H2,1-2H3,(H,27,32);1H2/t19-,21+,23+,24+;/m0./s1

HIDE SMILES / InChI

Molecular Formula C25H27ClN2O8
Molecular Weight 518.943
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Glucametacin is a non-steroidal anti-inflammatory, analgesic, antipyretic agent. Glucametacin was compared with ketoprofen in a double-blind, crossover trial. The drugs were given in total daily doses of 420 mg glucametacin and 300 mg ketoprofen for 20 days to 30 patients with chronic arthropathies of an inflammatory or degenerative nature. Both drugs were well tolerated and resulted in significant improvements in a number of criteria of disease assessment. Although there were no significant differences between results seen with the two drugs, there appeared to be trends in favour of glucametacin in respect to both efficacy and tolerance.

Approval Year

PubMed

PubMed

TitleDatePubMed
Further studies on glucametacin in rheumatoid arthritis and in other chronic types of rheumatism.
1981
Double-blind comparison of glucametacin and ketoprofen in chronic arthropathies.
1983
Patents

Sample Use Guides

Twenty-three patients with rheumatoid arthritis and 9 patients with other forms of rheumatic diseases were treated for 20 days with 420 mg glucametacin per day, given as three 140 mg capsules.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:17:37 GMT 2023
Edited
by admin
on Sat Dec 16 08:17:37 GMT 2023
Record UNII
8923CH1NY1
Record Status Validated (UNII)
Record Version
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Name Type Language
GLUCAMETACIN MONOHYDRATE
MI  
Common Name English
EUMINEX
Brand Name English
2-(1-(4-CHLOROBENZOYL)-5-METHOXY-2-METHYL-1H-INDOL-3-YL)-N-((2R,3R,4S,5R)-3,4,5,6-TETRAHYDROXY-1-OXOHEXAN-2-YL)ACETAMIDE HYDRATE
Systematic Name English
TEOREMA
Brand Name English
TEOREMAC
Brand Name English
GLUCAMETACIN MONOHYDRATE [MI]
Common Name English
Code System Code Type Description
MERCK INDEX
m5753
Created by admin on Sat Dec 16 08:17:37 GMT 2023 , Edited by admin on Sat Dec 16 08:17:37 GMT 2023
PRIMARY Merck Index
FDA UNII
8923CH1NY1
Created by admin on Sat Dec 16 08:17:37 GMT 2023 , Edited by admin on Sat Dec 16 08:17:37 GMT 2023
PRIMARY
PUBCHEM
21150895
Created by admin on Sat Dec 16 08:17:37 GMT 2023 , Edited by admin on Sat Dec 16 08:17:37 GMT 2023
PRIMARY
Related Record Type Details
ANHYDROUS->SOLVATE