Gw590735

Gw590735

SCHEMBL3673228

Cc1nc(-c2ccc(C(F)(F)F)cc2)sc1C(=O)NCc1ccc(OC(C)(C)C(=O)O)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PPARA

The experimentally established mechanism targets of Gw590735. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
PPARA known ✓ Q07869 20/20 1.00
PPARD Q03181 9/20 1.00
PPARG P37231 4/20 1.00

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
SCHEMBL6582310 0.92 PPARA (1.00) PPARAPPARDPPARG
SCHEMBL6582529 0.92 PPARA (1.00) PPARAPPARDPPARG
SCHEMBL6582462 0.91 PPARA (1.00) PPARAPPARDPPARG
SCHEMBL18645313 0.91 PPARA (0.83) PPARAPPARDPPARG
SCHEMBL6582584 0.91 PPARA (1.00) PPARAPPARDPPARG
SCHEMBL6582904 0.90 PPARA (1.00) PPARAPPARDPPARG
SCHEMBL6584498 0.90 PPARA (1.00) PPARAPPARDPPARG
SCHEMBL5185069 0.90 PPARA (0.82) PPARAPPARDPPARG
SCHEMBL7465084 0.90 PPARA (0.94) PPARAPPARDPPARG
SCHEMBL6580471 0.89 PPARA (0.87) PPARAPPARDPPARG

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3452041-B1 COMPOSITIONS AND METHODS FOR ADMINISTERING PPAR-GAMMA-AGONISTS, SURFACTANT PEPTIDES AND PHOSPHOLIPIDS LOS ANGELES BIOMEDICAL RES INST HARBOR UCLA MEDICAL CT (US) 2026-01-14 EP claimed
WO-2024251233-A1 USE OF PPAR FULL AGONIST IN COMBINATION WITH THR-β AGONIST IN RESISTING OF METABOLIC-RELATED DISEASES 成都微芯药业有限公司 2024-12-12 WO claimed
US-20240398905-A1 COMPOSITIONS AND METHOD FOR ADMINISTERING PPARgamma AGONISTS, SURFACTANT PEPTIDES AND PHOSOPHOLIPIDS LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER 2024-12-05 US claimed
US-11951158-B2 Compositions and methods for administering PPARγ agonists, surfactant peptides and phospholipids LINDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER (US) 2024-04-09 US claimed
US-20240034761-A1 REGENERATION OF MAMMALIAN TISSUES USING SYNTHETIC IMMODULINS MASCARENHAS DESMOND (US) 2024-02-01 US claimed
CN-116568802-A In vitro method for preparing mature red blood cells 西湖生物医药科技(上海)有限公司 2023-08-08 CN claimed
WO-2023072010-A1 USE OF PPAR AGONIST IN PREPARATION OF DRUG FOR TREATING ACUTE MYELOID LEUKEMIA 厦门大学附属第一医院 2023-05-04 WO claimed
CN-115068618-A Combined pharmaceutical composition for preventing and/or treating acute myeloid leukemia and application thereof 厦门大学附属第一医院 2022-09-20 CN claimed
WO-2022192042-A2 REGENERATION OF MAMMALIAN TISSUES USING SYNTHETIC IMMODULINS MASCARENHAS DESMOND (US) 2022-09-15 WO claimed
CN-114949230-A Combined pharmaceutical composition for preventing and/or treating acute myeloid leukemia and application thereof 厦门大学附属第一医院 2022-08-30 CN claimed
US-20100240627-A1 COMPOSITION AND METHODS RELATING TO GLUCOCORTICOID RECEPTOR-ALPHA AND PEROXISOME PROLIFERATOR-ACTIVATED RECEPTORS UNIVERSITEIT GENT 2010-09-23 US claimed
US-20090111782-A1 COMPOSITION AND METHODS RELATING TO GLUCOCORTICOID RECEPTOR-ALPHA AND PEROXISOME PROLIFERATOR-ACTIVATED RECEPTORS GHENT UNIVERSITY (BE) 2009-04-30 US claimed
US-20070202179-A1 Low Dose Pharmaceutical Products SMITHKLINE BEECHAM CORPORATION 2007-08-30 US claimed
EP-1244642-B1 SUBSTITUTED OXAZOLES AND THIAZOLES DERIVATIVES AS HPPAR ALPHA ACTIVATORS GLAXO GROUP LTD (GB) 2004-04-28 EP claimed
US-6518290-B1 Compounds that activate or otherwise interact with one or more of the PPARs have been implicated in the regulation of triglyceride and cholesterol levels in animal models SMITHKLINE BEECHAM CORPORATION 2003-02-11 US claimed
EP-1244642-A1 SUBSTITUTED OXAZOLES AND THIAZOLES DERIVATIVES AS HPPAR ALPHA ACTIVATORS GLAXO GROUP LIMITED (GB) 2002-10-02 EP claimed
WO-2001040207-A1 SUBSTITUTED OXAZOLES AND THIAZOLES DERIVATIVES AS HPPAR ALPHA ACTIVATORS GLAXO GROUP LIMITED (GB) 2001-06-07 WO claimed
EP-3558298-B1 ANTIDIABETIC SPIROCHROMAN COMPOUNDS MERCK SHARP & DOHME LLC (US) 2026-03-11 EP disclosed
WO-2002046174-A1 1, 2, 4-OXADIAZOLE DERIVATIVES AS HPPAR ALPHA AGONISTS GLAXO GROUP LIMITED (GB) 2002-06-13 WO disclosed
WO-2001040207-A1 SUBSTITUTED OXAZOLES AND THIAZOLES DERIVATIVES AS HPPAR ALPHA ACTIVATORS GLAXO GROUP LIMITED (GB) 2001-06-07 WO 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 (1 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-20070202179-A1 Low Dose Pharmaceutical Products UGT1A7, UGT1A6, CYP3A7 PPARA 1266/4885PPARD 834/4885PPARG 1384/4885

“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.