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

Details

Stereochemistry ABSOLUTE
Molecular Formula C21H24N4O6S
Molecular Weight 460.503
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MK-0941 FREE BASE

SMILES

CCS(=O)(=O)C1=CC=C(OC2=CC(=CC(O[C@@H](C)CO)=C2)C(=O)NC3=NN(C)C=C3)C=N1

InChI

InChIKey=KJSGTWFWVTYPFZ-AWEZNQCLSA-N
InChI=1S/C21H24N4O6S/c1-4-32(28,29)20-6-5-16(12-22-20)31-18-10-15(9-17(11-18)30-14(2)13-26)21(27)23-19-7-8-25(3)24-19/h5-12,14,26H,4,13H2,1-3H3,(H,23,24,27)/t14-/m0/s1

HIDE SMILES / InChI

Molecular Formula C21H24N4O6S
Molecular Weight 460.503
Charge 0
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Description

MK-0941 is selective, allosteric glucokinase activator (GKA) that activates glucokinase (hexokinase subtype IV) with greater selectivity than over different hexokinase isoforms. In chronic oral toxicity studies in animals with MK-0941, cataracts were observed in rats and dogs at drug exposures of 3 and 1.5 times, respectively, the maximum predicted human exposure based on doses planned for further clinical development. No cataracts were observed in either species at drug exposures equal to the maximum predicted human exposure. In patients receiving stable-dose insulin glargine, the glucokinase activator MK-0941 led to improvements in glycemic control that were not sustained. MK-0941 was associated with an increased incidence of hypoglycemia and elevations in triglycerides and blood pressure.

Originator

Approval Year

Targets

Primary TargetPharmacologyConditionPotency
240.0 nM [EC50]
65.0 nM [EC50]

PubMed

Patents

Sample Use Guides

In Vivo Use Guide
10, 20, 30, or 40 mg/day for 40-weeks
Route of Administration: Oral
Substance Class Chemical
Record UNII
YZ1L3KR377
Record Status Validated (UNII)
Record Version