Rivoglitazone

Rivoglitazone

SCHEMBL1592290

COc1ccc2nc(COc3ccc(CC4SC(=O)NC4=O)cc3)n(C)c2c1.Cl

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PPARG

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

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
PPARG known ✓ P37231 12/20 0.98
ESRRA P11474 1/20 0.72
FFAR1 O14842 11/20 0.62
PPARA Q07869 6/20 0.62
MPC2 O95563 1/20 0.53
CYP2C8 P10632 1/20 0.53
CYP2C9 P11712 1/20 0.53

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
Rivoglitazone SCHEMBL6064788 1.00 PPARG (0.98) PPARGESRRAFFAR1PPARAMPC2
Rivoglitazone SCHEMBL2906120 0.99 PPARG (1.00) PPARGESRRAFFAR1PPARAMPC2
Rivoglitazone SCHEMBL143498 0.99 PPARG (1.00) PPARGESRRAFFAR1PPARAMPC2
Rivoglitazone SCHEMBL5319250 0.99 PPARG (1.00) PPARGESRRAFFAR1PPARAMPC2
Rivoglitazone SCHEMBL4885815 0.95 PPARG (0.91) PPARGESRRAFFAR1PPARAMPC2
Hydrochloric Acid SCHEMBL6544473 0.95 PPARG (0.88) PPARGESRRAFFAR1PPARAMPC2
SCHEMBL6543624 0.94 PPARG (0.90) PPARGESRRAFFAR1PPARAMPC2
SCHEMBL15730390 0.93 PPARG (0.88) PPARGESRRAFFAR1PPARAMPC2
Hydrochloric Acid SCHEMBL6701457 0.92 PPARG (0.83) PPARGESRRAFFAR1PPARA
SCHEMBL6896700 0.92 PPARG (0.86) PPARGESRRAFFAR1PPARAMPC2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110092555-A1 Thiazolidinedione compound DAIICHI SANKYO COMPANY, LIMITED (JP) 2011-04-21 US claimed
US-20090088462-A1 Pharmaceutical Composition for Enhancing Adiponectin Production DAIICHI SANKYO COMPANY, LIMITED (JP) 2009-04-02 US claimed
EP-1990053-A1 PHARMACEUTICAL COMPOSITION FOR ENHANCING ADIPONECTIN PRODUCTION Daiichi Sankyo Company, Limited (JP) 2008-11-12 EP claimed
US-20080262054-A1 incorporating cellulose, a cellulose derivative, a polyvinyl alcohol derivative, a polyvinyl alcohol derivative mixture or a mixture thereof with 5-{4-[(6-methoxy-1-methyl-1H-benzimidazol-2-yl)methoxy]benzyl}thiazolidine-2,4-dione; superior solubility; improving insulin resistance; lowering blood glucose KAWASAKI TAKAO 2008-10-23 US claimed
US-20080103185-A1 Process for Producing Thiazolidinedione Compound and Production Intermediate Thereof DAIICHI SANKYO COMPANY, LIMITED (JP) 2008-05-01 US claimed
EP-1902713-A1 PHARMACEUTICAL COMPOSITION CONTAINING THIAZOLIDINEDIONE COMPOUND Daiichi Sankyo Company, Limited (JP) 2008-03-26 EP claimed
EP-1894929-A1 PROCESS FOR PRODUCING THIAZOLIDINEDIONE COMPOUND AND PRODUCTION INTERMEDIATE THEREOF Daiichi Sankyo Company, Limited (JP) 2008-03-05 EP claimed
US-20070287685-A1 Medicinal composition containing FBPase inhibitor DAIICHI SANKYO COMPANY, LIMITED (JP) 2007-12-13 US claimed
EP-1825854-A1 MEDICINAL COMPOSITION CONTAINING FBPase INHIBITOR Daiichi Sankyo Company, Limited (JP) 2007-08-29 EP claimed
US-20020111373-A1 Hydrochloride salt of a fused heterocyclic compound SANKYO COMPANY, LIMITED (JP) 2002-08-15 US claimed
US-20110092555-A1 Thiazolidinedione compound DAIICHI SANKYO COMPANY, LIMITED (JP) 2011-04-21 US disclosed
US-20110092555-A1 Thiazolidinedione compound DAIICHI SANKYO COMPANY, LIMITED (JP) 2011-04-21 US disclosed
EP-2226321-A2 Process for producing thiazolidinediones and intermediates thereof Daiichi Sankyo Company, Limited (JP) 2010-09-08 EP disclosed
US-20090137626-A1 Pharmaceutical Composition Containing PPARgamma Agonist DAIICHI SANKYO COMPANY, LIMITED (JP) 2009-05-28 US disclosed
US-20090124626-A1 Pharmaceutical agent comprising insulin resistance improving agent DAIICHI SANKYO COMPANY, LIMITED (JP) 2009-05-14 US disclosed
EP-1197211-A1 PREVENTIVE AND THERAPEUTIC AGENTS FOR CANCER Sankyo Company, Limited (JP) 2002-04-17 EP disclosed
EP-1191019-A1 INTERMEDIATES FOR THE SYNTHESIS OF BENZIMIDAZOLE COMPOUNDS AND PROCESS FOR THE PREPARATION THEREOF Sankyo Company, Limited (JP) 2002-03-27 EP disclosed
EP-1180519-A1 HYDROCHLORIDE OF FUSED-HETEROCYCLE COMPOUND Sankyo Company, Limited (JP) 2002-02-20 EP disclosed
EP-1167357-A1 ALPHA-SUBSTITUTED CARBOXYLIC ACID DERIVATIVES Sankyo Company, Limited (JP) 2002-01-02 EP disclosed
JP-2001039976-A HYDROCHLORIDE OF CONDENSED HETEROCYCLIC COMPOUND SANKYO CO LTD 2001-02-13 JP 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 (7 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-20110092555-A1 Thiazolidinedione compound GLP1R, DPP4, KCNK4 PPARG 209/4885ESRRA 1626/4885FFAR1 2235/4885
US-20080262054-A1 incorporating cellulose, a cellulose derivative, a polyvinyl alcohol derivative, a polyvinyl alcohol derivative mixture or a mixture thereof with 5-{4-[(6-methoxy-1-methyl-1H-benzimidazol-2-yl)methoxy]benzyl}thiazolidine-2,4-dione; superior solubility; improving insulin resistance; lowering blood glucose SLC5A2, SLC5A1, INSR PPARG 419/4885ESRRA 3361/4885FFAR1 1293/4885
US-20090124626-A1 Pharmaceutical agent comprising insulin resistance improving agent DPP4, DPP7, IAPP PPARG 135/4885ESRRA 575/4885FFAR1 424/4885
US-20090137626-A1 Pharmaceutical Composition Containing PPARgamma Agonist PPARG, PPARA, PPARD PPARG 1/4885ESRRA 88/4885FFAR1 21/4885
US-20080103185-A1 Process for Producing Thiazolidinedione Compound and Production Intermediate Thereof INSR, GCKR, GPR119 PPARG 28/4885ESRRA 863/4885FFAR1 92/4885
US-20090088462-A1 Pharmaceutical Composition for Enhancing Adiponectin Production ADIPOR1, ADIPOR2, FABP4 PPARG 37/4885ESRRA 453/4885FFAR1 247/4885
US-20020111373-A1 Hydrochloride salt of a fused heterocyclic compound SLC5A1, SLC5A2, SLC2A8 PPARG 1242/4885ESRRA 4462/4885FFAR1 1169/4885

“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.