Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C39H37F3N2O8 |
| Molecular Weight | 718.7149 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(=O)C(COC(=O)CC1=CC(C(=O)N(C)C)=C(NC(=O)C2=CC=CC=C2C3=CC=C(C=C3)C(F)(F)F)C=C1)(C(=O)OCC)C4=CC=CC=C4
InChI
InChIKey=FPUQGCOBYOXAED-UHFFFAOYSA-N
InChI=1S/C39H37F3N2O8/c1-5-50-36(48)38(37(49)51-6-2,27-12-8-7-9-13-27)24-52-33(45)23-25-16-21-32(31(22-25)35(47)44(3)4)43-34(46)30-15-11-10-14-29(30)26-17-19-28(20-18-26)39(40,41)42/h7-22H,5-6,23-24H2,1-4H3,(H,43,46)
| Molecular Formula | C39H37F3N2O8 |
| Molecular Weight | 718.7149 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Granotapide (JTT-130) has been studied for use in treatment of diabetes mellitus type II. This intestine-specific microsomal transfer protein inhibitor has hypoglycemic effects. Granotapide is thought to block fat absorption, which results in enhanced glucose-stimulated insulin secretion and enhanced insulin sensitivity. In an animal study, granotapide improved hyperglycemia and dyslipidemia via a mechanism independent of suppression of food intake. Granotapide enhances glucagon-like peptide-1 secretion and reduces lipotoxicity. A phase 2 study has been conducted to evaluate the effect of JTT-130 on diabetes as well as the safety and tolerability of JTT-130 in obese Type 2 diabetic patients.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:42:51 GMT 2025
by
admin
on
Mon Mar 31 19:42:51 GMT 2025
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| Record UNII |
PSZ2YGB0DK
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| Record Status |
Validated (UNII)
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| Record Version |
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C174852
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9378
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DB12934
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11607299
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300000034209
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594842-13-4
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PSZ2YGB0DK
Created by
admin on Mon Mar 31 19:42:51 GMT 2025 , Edited by admin on Mon Mar 31 19:42:51 GMT 2025
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |