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Details

Stereochemistry ACHIRAL
Molecular Formula C21H29N5O6S
Molecular Weight 479.55
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ADP-597

SMILES

COC1=C(OC2CCN(CC2)C(=O)OC(C)C)N=CN=C1NC3=C(C)N=C(C=C3)S(C)(=O)=O

InChI

InChIKey=WPDCHTSXOPUOII-UHFFFAOYSA-N
InChI=1S/C21H29N5O6S/c1-13(2)31-21(27)26-10-8-15(9-11-26)32-20-18(30-4)19(22-12-23-20)25-16-6-7-17(24-14(16)3)33(5,28)29/h6-7,12-13,15H,8-11H2,1-5H3,(H,22,23,25)

HIDE SMILES / InChI
Arena Pharmaceuticals was developing APD-597 (JNJ-38431055), a small molecule, an orally active agonist of the G-protein coupled receptor 119 (GPR119), for the treatment of Type 2 diabetes mellitus. JNJ-38431055 was selected for preclinical development based on a good balance between agonist potency, intrinsic activity and in particular on its good solubility and reduced drug-drug interaction potential. In addition, extensive in vivo studies showed a more favorable metabolic profile that may avoid the generation of long-lasting metabolites with the potential to accumulate in clinical studies. In humans, single-dose oral JNJ-38431055 increased postmeal plasma glucagon-like peptide 1 (GLP-1), glucose-dependent insulinotropic peptide (GIP), and peptide YY (PYY) concentrations but did not significantly decrease glucose excursion or increase insulin secretion. However, in a graded glucose infusion study, JNJ-38431055 was shown to induce a higher insulin secretion rate (ISR) relative to placebo at elevated plasma glucose levels. These studies provide evidence for the potential efficacy of JNJ-38431055 as an antidiabetes agent in humans.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q8TDV5
Gene ID: 139760.0
Gene Symbol: GPR119
Target Organism: Homo sapiens (Human)
46.0 nM [EC50]
46.0 nM [EC50]
13000.0 nM [IC50]
PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

Type 2 diabetes mellitus: APD-597 (100 and 500 mg) or sitagliptin (100 mg) as a single-dose or APD-597 (500 mg) once daily for 14 consecutive days were tested.
Route of Administration: Oral
APD-597 agonist potency for human GPR119 receptor - EC50 46 nM. APD-597 showed no significant activity in a standard CEREP receptor selectivity panel when tested at 1 uM. In addition, no significant inhibition of hERG channel binding (IC50 >10 uM) was observed and in a patch clamp study APD-597 showed an IC50 of 13 ± 0.2 uM.
Name Type Language
ADP-597
Common Name English
4-((6-((6-METHYLSULFONYL-2-METHYLPYRIDIN-3-YL)AMINO)-5-METHOXYPYRIMIDIN-4-YL)OXY)PIPERIDINE-1-CARBOXYLIC ACID ISOPROPYL ESTER
Systematic Name English
JNJ-38431055
Code English
Code System Code Type Description
FDA UNII
345354O7AT
Created by admin on Sat Dec 16 05:31:53 GMT 2023 , Edited by admin on Sat Dec 16 05:31:53 GMT 2023
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CAS
897732-93-3
Created by admin on Sat Dec 16 05:31:53 GMT 2023 , Edited by admin on Sat Dec 16 05:31:53 GMT 2023
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EPA CompTox
DTXSID10237885
Created by admin on Sat Dec 16 05:31:53 GMT 2023 , Edited by admin on Sat Dec 16 05:31:53 GMT 2023
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PUBCHEM
11691484
Created by admin on Sat Dec 16 05:31:53 GMT 2023 , Edited by admin on Sat Dec 16 05:31:53 GMT 2023
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DRUG BANK
DB12084
Created by admin on Sat Dec 16 05:31:53 GMT 2023 , Edited by admin on Sat Dec 16 05:31:53 GMT 2023
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