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Details

Stereochemistry ABSOLUTE
Molecular Formula C10H20BN3O3.C4H6O6
Molecular Weight 391.182
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DUTOGLIPTIN TARTRATE

SMILES

O[C@H]([C@@H](O)C(O)=O)C(O)=O.OB(O)[C@@H]1CCCN1C(=O)CN[C@@H]2CCNC2

InChI

InChIKey=SVWHNLVZPGXBNS-MHDNXTQBSA-N
InChI=1S/C10H20BN3O3.C4H6O6/c15-10(7-13-8-3-4-12-6-8)14-5-1-2-9(14)11(16)17;5-1(3(7)8)2(6)4(9)10/h8-9,12-13,16-17H,1-7H2;1-2,5-6H,(H,7,8)(H,9,10)/t8-,9+;1-,2-/m11/s1

HIDE SMILES / InChI
Dutogliptin (PHX-1149T) is a small-molecule dipeptidyl peptidase-4 (DPP-4) inhibitor for the potential oral treatment of type 2 diabetes mellitus (T2DM). DPP-4 quickly degrades the insulin secretory hormones, glucose-dependent insulinotropic peptide and glucagon-like peptide-1; thus inhibiting the degradation of these hormones is a viable treatment option for patients with T2DM. In preclinical studies, dutogliptin potently inhibited DPP-4 and, in a model of T2DM, treatment with dutogliptin improved glucose homeostasis. Pharmacokinetic analyses in animals, healthy individuals and patients with T2DM demonstrated that drug exposure increased in a dose-dependent manner. Results from phase II clinical trials indicated that once-daily dutogliptin, in combination with other oral diabetes therapies, reduces postprandial blood glucose and HbA1c levels, both indicators of successful diabetes management. The incidence of adverse events was similar in treatment and placebo groups, with slightly more headache, arthralgia, sinusitis, and dizziness occurring in the 400 mg dutogliptin group compared with placebo. Phase II clinical trial for the myocardial infarction treatment is underway.

Approval Year

PubMed

PubMed

TitleDatePubMed
Small molecule dipeptidylpeptidase IV inhibitors under investigation for diabetes mellitus therapy.
2011 Jun

Sample Use Guides

Name Type Language
DUTOGLIPTIN TARTRATE
USAN  
USAN  
Official Name English
DUTOGLIPTIN TARTRATE [USAN]
Common Name English
PHX1149T
Code English
BORONIC ACID, ((2R)-1-(((3R)-3-PYRROLIDINYLAMINO)ACETYL)-2-PYRROLIDINYL)-, (2R,3R)-2,3-DIHYDROXYBUTANEDIOATE (1:1)
Common Name English
[(2R)-1-{N-[(3R)-Pyrrolidin-3-yl]glycyl}pyrrolidin-2-yl]boronic acid (2R,3R)-2,3-dihydroxybutanedioate (1:1)
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C98086
Created by admin on Fri Dec 15 17:13:43 GMT 2023 , Edited by admin on Fri Dec 15 17:13:43 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C87493
Created by admin on Fri Dec 15 17:13:43 GMT 2023 , Edited by admin on Fri Dec 15 17:13:43 GMT 2023
PRIMARY
CAS
890402-81-0
Created by admin on Fri Dec 15 17:13:43 GMT 2023 , Edited by admin on Fri Dec 15 17:13:43 GMT 2023
PRIMARY
FDA UNII
79QH89EV9M
Created by admin on Fri Dec 15 17:13:43 GMT 2023 , Edited by admin on Fri Dec 15 17:13:43 GMT 2023
PRIMARY
EVMPD
SUB32929
Created by admin on Fri Dec 15 17:13:43 GMT 2023 , Edited by admin on Fri Dec 15 17:13:43 GMT 2023
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EPA CompTox
DTXSID301008624
Created by admin on Fri Dec 15 17:13:43 GMT 2023 , Edited by admin on Fri Dec 15 17:13:43 GMT 2023
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DRUG BANK
DBSALT002056
Created by admin on Fri Dec 15 17:13:43 GMT 2023 , Edited by admin on Fri Dec 15 17:13:43 GMT 2023
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PUBCHEM
15949100
Created by admin on Fri Dec 15 17:13:43 GMT 2023 , Edited by admin on Fri Dec 15 17:13:43 GMT 2023
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USAN
TT-19
Created by admin on Fri Dec 15 17:13:43 GMT 2023 , Edited by admin on Fri Dec 15 17:13:43 GMT 2023
PRIMARY
SMS_ID
100000126386
Created by admin on Fri Dec 15 17:13:43 GMT 2023 , Edited by admin on Fri Dec 15 17:13:43 GMT 2023
PRIMARY