Mitiglinide

Mitiglinide

SCHEMBL2864873

O=C(O)[C@H](CC(=O)N1CC2CCCCC2C1)Cc1ccccc1

nearest known ligand 0.77

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC8KCNJ11

The experimentally established mechanism targets of Mitiglinide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
CPA1 P15085 7/20 0.53
CPA3 P15088 3/20 0.53
CPB1 P15086 1/20 0.53
CPB2 Q96IY4 1/20 0.53
CYP1A2 P05177 1/20 0.50
MME P08473 1/20 0.47
FOLH1 Q04609 2/20 0.45
BCL2L1 Q07817 1/20 0.44
MCL1 Q07820 1/20 0.44
SLC1A3 P43003 1/20 0.42
SLC1A2 P43004 1/20 0.42
SLC1A1 P43005 1/20 0.42
LTA4H P09960 1/20 0.42

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Mitiglinide SCHEMBL876930 1.00 CPA1 (0.53) CPA1CPA3CPB1CPB2CYP1A2
Mitiglinide SCHEMBL49085 1.00 CPA1 (0.53) CPA1CPA3CPB1CPB2CYP1A2
Mitiglinide SCHEMBL676865 1.00 CPA1 (0.53) CPA1CPA3CPB1CPB2CYP1A2
Mitiglinide SCHEMBL4457950 1.00 CPA1 (0.53) CPA1CPA3CPB1CPB2CYP1A2
Mitiglinide SCHEMBL9049521 1.00 CPA1 (0.53) CPA1CPA3CPB1CPB2CYP1A2
Mitiglinide SCHEMBL4457953 1.00 CPA1 (0.53) CPA1CPA3CPB1CPB2CYP1A2
Mitiglinide SCHEMBL6135224 0.99 CPA1 (0.51) CPA1CPA3CPB1CPB2CYP1A2
Mitiglinide SCHEMBL305840 0.99 CPA1 (0.51) CPA1CPA3CPB1CPB2CYP1A2
Mitiglinide SCHEMBL9047711 0.99 CPA1 (0.51) CPA1CPA3CPB1CPB2CYP1A2
Mitiglinide SCHEMBL9047718 0.99 CPA1 (0.51) CPA1CPA3CPB1CPB2CYP1A2

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 56 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7847107-B2 producing (2S)-2-benzyl-3-(cis-hexahydro-2-isoindolinylcarbonyl)propionic acid by catalytic reduction of 2-benzylidene-3-(cis-hexahydro-2-isoindolinylcarbonyl)propionic acid in the presence of an asymmetric catalyst prepared from a pyrrolidinebisphosphine compound KISSEI PHARMACEUTICAL CO., LTD. (JP) 2010-12-07 US claimed
US-20090043110-A1 Asymmetric Reduction Method KISSEI PHARMACEUTICAL CO., LTD. (JP) 2009-02-12 US claimed
EP-1978016-A1 ASYMMETRIC REDUCTION METHOD Kissei Pharmaceutical Co., Ltd. (JP) 2008-10-08 EP claimed
EP-1178794-B1 USE OF SUCCINIC ACID DERIVATIVES TO OBTAIN A MEDICINE FOR TREATING INFLAMMATION SANOFI AVENTIS (FR) 2005-09-07 EP claimed
EP-1127876-B1 Process for the preparation of isoindoline SERVIER LAB (FR) 2002-11-13 EP claimed
US-20010023294-A1 New process for the preparation of isoindoline KISSEI PHARMACEUTICAL COMPANY LTD (JP) 2001-09-20 US claimed
EP-0507534-B1 Succinic acid compounds KISSEI PHARMACEUTICAL (JP) 1996-02-28 EP claimed
CN-114890933-B Preparation method of racemic mitiglinide 恒升德康(南京)医药科技有限公司 2024-02-06 CN disclosed
CN-114890933-A Preparation method of racemic mitiglinide 恒升德康(南京)医药科技有限公司 2022-08-12 CN disclosed
CN-104311471-B Improved mitiglinide calcium industrialized preparation method 山东省生物医药科学院 2017-05-17 CN disclosed
CN-104311471-A Improved mitiglinide calcium industrialized preparation method SHANDONG ACADEMY OF PHARMACEUTICAL SCIENCES 2015-01-28 CN disclosed
CN-101346352-B Asymmetric reduction method KISSEI PHARMACEUTICAL 2011-04-13 CN disclosed
CN-101346352-B Asymmetric reduction method KISSEI PHARMACEUTICAL 2011-04-13 CN disclosed
WO-2000061127-A2 USE OF INSULIN SENSITISERS FOR IMPROVING KETOSIS TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2000-10-19 WO disclosed
EP-0994854-A1 METHOD FOR PREPARING A SUBSTITUTED PERHYDROISOINDOLE ADIR (FR) 2000-04-26 EP disclosed
EP-0967204-A1 PROCESS FOR PRODUCING BENZYLSUCCINIC ACID DERIVATIVES Kissei Pharmaceutical Co. Ltd. (JP) 1999-12-29 EP disclosed
WO-1999001430-A1 METHOD FOR PREPARING A SUBSTITUTED PERHYDROISOINDOLE ADIR (FR) 1999-01-14 WO disclosed
EP-0507534-B1 Succinic acid compounds KISSEI PHARMACEUTICAL (JP) 1996-02-28 EP disclosed
US-5202335-A Hypoglycemic, antidiabetic agents KISSEI PHARMACEUTICAL CO., LTD. (JP) 1993-04-13 US disclosed
EP-0507534-A1 Succinic acid compounds KISSEI PHARMACEUTICAL CO., LTD. (JP) 1992-10-07 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20090043110-A1 Asymmetric Reduction Method PDXK, BCKDK, AKR1C3 CPA1 515/4885CPA3 659/4885CPB1 906/4885
US-20010023294-A1 New process for the preparation of isoindoline HPD, GABRB2, NISCH CPA1 4815/4885CPA3 4601/4885CPB1 2722/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.