Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C18H28FN5O2.C7H8O3S |
Molecular Weight | 537.647 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=C(C=C1)S(O)(=O)=O.[H][C@@]23CN(C[C@]2([H])C[C@](C)(C3)NCC(=O)N4C[C@@H](F)C[C@H]4C#N)C(=O)N(C)C
InChI
InChIKey=VBMNNLBIPDGFBS-XGXURLCGSA-N
InChI=1S/C18H28FN5O2.C7H8O3S/c1-18(21-8-16(25)24-11-14(19)4-15(24)7-20)5-12-9-23(10-13(12)6-18)17(26)22(2)3;1-6-2-4-7(5-3-6)11(8,9)10/h12-15,21H,4-6,8-11H2,1-3H3;2-5H,1H3,(H,8,9,10)/t12-,13+,14-,15-,18+;/m0./s1
Jiangsu HengRui Medicine Co. is developing SHR-117887, an orally active dipeptidyl peptidase-4 (CD26 antigen) inhibitor for the treatment of type 2 diabetes. SHR-117887 is a potent DPP-4 inhibitor that improves metabolic control and β-cell function in diabetic rodent models. SHR-117887 is in phase II clinical trials for the treatment of type 2 diabetes.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT01984489
Type 2 Diabetes:
Experimental: SHR-117887 (50mg q.d)/Metformin
Patients are administered oral placebo once daily and metformin 500mg TID for 4 weeks at the run-in period. After randomised,patients adminitered SHR117887 50mg QD and metformin 500mg TID for 12 weeks.
Experimental: SHR-117887 (100mg q.d)/Metformin
patients are administered oral placebo once daily and metformin 500mg TID for 4 weeks at the run-in period.After randomised, patients adminitered SHR-117887 100mg QD and metformin 500mg TID for 12 weeks.
Route of Administration:
Oral
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06SMN21EQE
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1177460-72-8
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91667592
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ACTIVE MOIETY
SUBSTANCE RECORD