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Compound Detail

CHEMBL471498

MITIGLINIDE
🧪 Phase III
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🧪 Phase III
O=C(O)[C@H](CC(=O)N1C[C@H]2CCCC[C@H]2C1)Cc1ccccc1

Basic Information

ChEMBL ID CHEMBL471498
Name MITIGLINIDE
Phase Phase III
Structure Type MOL
InChI Key WPGGHFDDFPHPOB-BBWFWOEESA-N

Known Names

Mitiglinida Mitiglinide
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
20
Publications
2
Known Names
2
Indications
1
Mechanisms

Molecular Properties

315.4
MW (Da)
2.97
ALogP
2
HBA
1
HBD
57.6
PSA (Ų)
0.91
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Chirality Single Enantiomer

Flags

Natural Product
USAN Stem -glinide

Extended Properties

Molecular Formula C19H25NO3
MW 315.41
Aromatic Rings 1
Heavy Atoms 23
NP-Likeness -0.16

Mechanism of Action

Mechanism Action Type Target Direct Efficacy
Sulfonylurea receptor 1, Kir6.2 blocker BLOCKER Sulfonylurea receptor 1, Kir6.2

Indications

Diabetes Mellitus Diabetes Mellitus, Type 2

ATC Classification

A10BX08
mitiglinide
Level 1: ALIMENTARY TRACT AND METABOLISM
Level 2: DRUGS USED IN DIABETES

Activity Summary

EC50 1 meas. best 6.15

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
EC50 6.15 6.15 708.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked EC50 = 708.0 nM 6.15 Increase in insulin releasing activity in Syrian golden hamster HIT-T15 cells af... 18191001

Literature References

PubMed DOI Target Context # Activities
18191001 10.1016/j.ejmech.2007.11.018 Rattus norvegicus 5
18191001 10.1016/j.ejmech.2007.11.018 Unchecked 4
20014752 10.1021/tx900326k Hepatotoxicity 3
37468498 10.1038/s41467-023-40064-9 Muscarinic acetylcholine receptor M2 2
37468498 10.1038/s41467-023-40064-9 5-hydroxytryptamine receptor 1A 2
37468498 10.1038/s41467-023-40064-9 Alpha-2A adrenergic receptor 2
37468498 10.1038/s41467-023-40064-9 5-hydroxytryptamine receptor 2B 2
37468498 10.1038/s41467-023-40064-9 Gamma-aminobutyric acid receptor subunit alpha-1 2
37468498 10.1038/s41467-023-40064-9 Progesterone receptor 2
37468498 10.1038/s41467-023-40064-9 5-hydroxytryptamine receptor 2A 2
- 10.6019/CHEMBL4808148 Histone deacetylase 6 2
33369426 10.1021/acs.jmedchem.0c01762 2-amino-3-carboxymuconate-6-semialdehyde decarboxylase 2
37468498 10.1038/s41467-023-40064-9 Glutamate receptor ionotropic, NMDA 1 1
37468498 10.1038/s41467-023-40064-9 Beta-2 adrenergic receptor 1
37468498 10.1038/s41467-023-40064-9 Sodium-dependent dopamine transporter 1
37468498 10.1038/s41467-023-40064-9 Neuronal acetylcholine receptor subunit alpha-4 1
37468498 10.1038/s41467-023-40064-9 Voltage-dependent L-type calcium channel subunit alpha-1C 1
37468498 10.1038/s41467-023-40064-9 Kappa-type opioid receptor 1
37468498 10.1038/s41467-023-40064-9 Adenosine receptor A3 1
37468498 10.1038/s41467-023-40064-9 Muscarinic acetylcholine receptor M1 1

Data from ChEMBL 36 via Core Engine