Imiglitazar

Imiglitazar

SCHEMBL440905

Cc1oc(-c2ccccc2)nc1COc1ccc(CON=C(CCC(=O)O)c2ccccc2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PPARAPPARG

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

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
PPARG known ✓ P37231 16/20 1.00
PPARA known ✓ Q07869 14/20 1.00
FFAR1 O14842 1/20 0.69
PPARD Q03181 1/20 0.52
KDR P35968 1/20 0.50
MAPT P10636 1/20 0.50

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
Imiglitazar SCHEMBL297183 1.00 PPARG (1.00) PPARGPPARAFFAR1PPARDKDR
Imiglitazar SCHEMBL4057640 1.00 PPARG (1.00) PPARGPPARAFFAR1PPARDKDR
SCHEMBL6159699 0.95 PPARG (0.90) PPARGPPARAFFAR1PPARD
SCHEMBL7823357 0.95 PPARG (0.90) PPARGPPARAFFAR1PPARD
SCHEMBL6160402 0.95 PPARG (0.90) PPARGPPARAFFAR1PPARDKDR
SCHEMBL6159690 0.95 PPARG (0.90) PPARGPPARAFFAR1PPARD
SCHEMBL6160399 0.95 PPARG (0.90) PPARGPPARAFFAR1PPARDKDR
SCHEMBL6158370 0.95 PPARG (0.90) PPARGPPARAFFAR1PPARDKDR
SCHEMBL6159745 0.95 PPARG (0.90) PPARGPPARAFFAR1PPARDKDR
SCHEMBL6159738 0.95 PPARG (0.90) PPARGPPARAFFAR1PPARDKDR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20080070958-A1 Therapeutic Agent for Keratoconjunctival Disorder SANTEN PHARMACEUTICAL CO., LTD. (JP) 2008-03-20 US claimed
EP-1790338-A1 THERAPEUTIC AGENT FOR KERATOCONJUNCTIVA DISORDER SANTEN PHARMACEUTICAL CO., LTD. (JP) 2007-05-30 EP claimed
US-20060177444-A1 Concomitant drug as therapeutic agent for inflammatory bowel disease EISAI R&D MANAGEMENT CO., LTD. (JP) 2006-08-10 US claimed
EP-1607103-A1 CONCOMITANT DRUG AS THERAPEUTIC AGENT FOR INFLAMMATORY BOWEL DISEASE Eisai Co., Ltd. (JP) 2005-12-21 EP claimed
US-6777435-B1 RETINOID-RELATED RECEPTOR FUNCTION REGULATING AGENT TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2004-08-17 US claimed
EP-1077957-B1 OXYIMINOALKANOIC ACID DERIVATIVES WITH HYPOGLYCEMIC AND HYPOLIPIDEMIC ACTIVITY TAKEDA CHEMICAL INDUSTRIES LTD (JP) 2004-08-04 EP claimed
EP-1428531-A1 Oxyiminoalkanoic acid derivatives with hypoglycemic and hypolipidemic activity TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2004-06-16 EP claimed
US-20040077689-A1 Abc expression promoters TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2004-04-22 US claimed
EP-1382336-A1 ABC EXPRESSION PROMOTERS Takeda Chemical Industries, Ltd. (JP) 2004-01-21 EP claimed
US-6677363-B1 ADMINISTERING PIOGLITAZONE OR SALT, OXIME INSULIN SENSITIZER, FK-614, KRP-297, AND 5-((6-(2-FLUOROBENZYLOXY)-2-NAPHTHYL)METHYL)-2,4-THIAZOLIDINEDIONE TO TREAT DIABETES TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2004-01-13 US claimed
EP-1224178-B1 CRYSTALS OF AN OXYIMINOALKANOIC ACID DERIVATIVE AND THEIR USE AS ANTIDIABETICS TAKEDA CHEMICAL INDUSTRIES LTD (JP) 2003-06-25 EP claimed
EP-1304121-A1 BODY WEIGHT GAIN INHIBITORS Takeda Chemical Industries, Ltd. (JP) 2003-04-23 EP claimed
US-6518435-B1 Production method, a method of producing a compound represented by the formula (III) production method of oxyimino- alkanoic acid derivatives having an anti-diabetic activity. TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2003-02-11 US claimed
EP-1277730-A1 NEOVASCULARIZATION INHIBITORS Takeda Chemical Industries, Ltd. (JP) 2003-01-22 EP claimed
EP-1227081-A1 PROCESS FOR THE PREPARATION OF OXYIMINOALKANOIC ACID DERIVATIVES Takeda Chemical Industries, Ltd. (JP) 2002-07-31 EP claimed
EP-1224178-A1 CRYSTALS OF AN OXYIMINOALKANOIC ACID DERIVATIVE AND THEIR USE AS ANTIDIABETICS Takeda Chemical Industries, Ltd. (JP) 2002-07-24 EP claimed
US-6251926-B1 OXYIMINOALKANOIC ACID DERIVATIVES HAVING HYPOGLYCEMIC EFFECT AND HYPOLIPIDEMIC EFFECT, IS USEFUL FOR TREATMENT OF DIABETES MELLITUS, HYPERLIPEMIA, IMPAIRED GLUCOSE TOLERANCE INFLAMMATORY DISEASE AND ARTERIOSCLEROSIS TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2001-06-26 US claimed
WO-2001032637-A1 CRYSTALS OF AN OXYIMINOALKANOIC ACID DERIVATIVE AND THEIR USE AS ANTIDIABETICS TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2001-05-10 WO claimed
EP-1077957-A1 OXYIMINOALKANOIC ACID DERIVATIVES WITH HYPOGLYCEMIC AND HYPOLIPIDEMIC ACTIVITY Takeda Chemical Industries, Ltd. (JP) 2001-02-28 EP claimed
WO-1999058510-A1 OXYIMINOALKANOIC ACID DERIVATIVES WITH HYPOGLYCEMIC AND HYPOLIPIDEMIC ACTIVITY TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1999-11-18 WO claimed

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-20040077689-A1 Abc expression promoters SREBF1, SREBF2, ABCB4 PPARG 189/4885PPARA 355/4885FFAR1 1498/4885
US-20060177444-A1 Concomitant drug as therapeutic agent for inflammatory bowel disease PPARG, PPARA, NR3C1 PPARG 1/4885PPARA 2/4885FFAR1 250/4885

“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.