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Details

Stereochemistry ABSOLUTE
Molecular Formula C21H23N3O6S
Molecular Weight 445.489
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AZD-6370

SMILES

C[C@@H](CO)OC1=CC(OC2=CC=C(C=C2)S(C)(=O)=O)=CC(=C1)C(=O)NC3=NN(C)C=C3

InChI

InChIKey=RIIDAVMUCMIWKP-AWEZNQCLSA-N
InChI=1S/C21H23N3O6S/c1-14(13-25)29-17-10-15(21(26)22-20-8-9-24(2)23-20)11-18(12-17)30-16-4-6-19(7-5-16)31(3,27)28/h4-12,14,25H,13H2,1-3H3,(H,22,23,26)/t14-/m0/s1

HIDE SMILES / InChI

Molecular Formula C21H23N3O6S
Molecular Weight 445.489
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 12:12:56 UTC 2023
Edited
by admin
on Sat Dec 16 12:12:56 UTC 2023
Record UNII
Z7H4089VLO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AZD-6370
Code English
BENZAMIDE, 3-((1S)-2-HYDROXY-1-METHYLETHOXY)-N-(1-METHYL-1H-PYRAZOL-3-YL)-5-(4-(METHYLSULFONYL)PHENOXY)-
Systematic Name English
3-(((1S)-2-HYDROXY-1-METHYLETHYL)OXY)-N-(1-METHYL-1H-PYRAZOL-3-YL)-5-(4-(METHYLSULFONYL)PHENOXY)BENZAMIDE
Systematic Name English
AZD 6370 [WHO-DD]
Common Name English
Code System Code Type Description
PUBCHEM
11525116
Created by admin on Sat Dec 16 12:12:56 UTC 2023 , Edited by admin on Sat Dec 16 12:12:56 UTC 2023
PRIMARY
CAS
752239-85-3
Created by admin on Sat Dec 16 12:12:56 UTC 2023 , Edited by admin on Sat Dec 16 12:12:56 UTC 2023
PRIMARY
FDA UNII
Z7H4089VLO
Created by admin on Sat Dec 16 12:12:56 UTC 2023 , Edited by admin on Sat Dec 16 12:12:56 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY
Class: Antihyperglycaemic, Pyridine; Mechanism of Action: Glucokinase stimulant; Highest Development Phases: Discontinued for Type 2 diabetes mellitus; Most Recent Events: 27 Jan 2011 Discontinued - Phase-II for Type-2 diabetes mellitus in Sweden (PO), 31 Jul 2008 Phase-II clinical trials in Type-2 diabetes mellitus in Sweden (PO), 31 Jul 2007 Phase-I clinical trials in Type-2 diabetes mellitus in Sweden (PO)
ACTIVE MOIETY
AZD6370 was well tolerated and no safety concerns were raised. AZD6370 was rapidly absorbed and eliminated, and plasma concentration was proportional to dose. Both S-insulin and GIR increased following AZD6370 administration. The observed increase in GIR correlated with increasing AZD6370 area under the plasma concentration vs. time curve, demonstrating a dose-concentration-dependent pharmacodynamic effect. AZD6370 at doses of 50 and 80 mg had similar effects to short-acting insulin 4 U on peripheral S-insulin levels but greater effects on GIR, suggesting an effect beyond the increase of peripheral S-insulin levels at lower doses.