SCHEMBL5147335

SCHEMBL5147335

CCC(Cc1ccc(OC)c(C(=O)NCc2ccc(Oc3ccc(F)cc3)cc2)c1)C(=O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
PPARA Q07869 20/20 1.00
PPARG P37231 11/20 1.00
PPARD Q03181 7/20 1.00
PSEN1 P49768 2/20 0.72
PSEN2 P49810 2/20 0.72
APH1B Q8WW43 2/20 0.72
NCSTN Q92542 2/20 0.72
APH1A Q96BI3 2/20 0.72
PSENEN Q9NZ42 2/20 0.72

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
SCHEMBL2742676 1.00 PPARA (1.00) PPARAPPARGPPARDPSEN1PSEN2
SCHEMBL29557298 1.00 PPARA (1.00) PPARAPPARGPPARDPSEN1PSEN2
SCHEMBL5111743 0.94 PPARA (0.89) PPARAPPARGPPARDPSEN1PSEN2
SCHEMBL5188840 0.93 PPARA (0.86) PPARAPPARGPPARDPSEN1PSEN2
SCHEMBL6376945 0.92 PPARA (0.86) PPARAPPARGPPARDPSEN1PSEN2
SCHEMBL6375543 0.92 PPARA (0.86) PPARAPPARGPPARDPSEN1PSEN2
SCHEMBL6373752 0.92 PPARA (1.00) PPARAPPARGPPARDPSEN1PSEN2
SCHEMBL6373745 0.92 PPARA (1.00) PPARAPPARGPPARDPSEN1PSEN2
SCHEMBL5112917 0.92 PPARA (0.84) PPARAPPARGPPARDPSEN1PSEN2
SCHEMBL5125346 0.92 PPARA (0.84) PPARAPPARGPPARDPSEN1PSEN2

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 12 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1184366-B1 SUBSTITUTED PHENYLPROPIONIC ACID DERIVATIVES AS AGONISTS TO HUMAN PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR ALPHA(PPAR) KYORIN SEIYAKU KK (JP) 2005-02-09 EP claimed
US-6506797-B1 Activate by binding to receptor as ligands of human peroxisome preliferant-activated receptor alpha alpha ), and exhibit potent decreasing action on lipids in blood (cholesterol and triglyceride). KYORIN PHARMACEUTICAL CO., LTD. (JP) 2003-01-14 US claimed
EP-1184366-A1 SUBSTITUTED PHENYLPROPIONIC ACID DERIVATIVES AS AGONISTS TO HUMAN PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR ALPHA(PPAR) KYORIN PHARMACEUTICAL CO., LTD. (JP) 2002-03-06 EP claimed
US-20110112097-A1 Substituted imidazoline-2,4-diones, process for preparation thereof, medicaments comprising these compounds and use thereof SANOFI-AVENTIS (FR) 2011-05-12 US disclosed
US-20110112097-A1 Substituted imidazoline-2,4-diones, process for preparation thereof, medicaments comprising these compounds and use thereof SANOFI-AVENTIS (FR) 2011-05-12 US disclosed
US-20100240580-A1 AZOLOARINE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, PHARMACEUTICALS CONTAINING THESE COMPOUNDS AND THE USE THEREOF SANOFI-AVENTIS (FR) 2010-09-23 US disclosed
US-20100240580-A1 AZOLOARINE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, PHARMACEUTICALS CONTAINING THESE COMPOUNDS AND THE USE THEREOF SANOFI-AVENTIS (FR) 2010-09-23 US disclosed
EP-1614417-A4 SOLID PREPARATION FOR ORAL USE KYORIN SEIYAKU KK (JP) 2007-08-29 EP disclosed
WO-2006093354-A1 PRODUCTION INTERMEDIATE OF (S)-2-[3-(N-{[4-(4-FLUOROPHENOXY)PHENYL]METHYL}CARBAMOYL)-4-METHOXYPHENYLMETHYL]BUTANOIC ACID KYORIN PHARMACEUTICAL CO., LTD. (JP) 2006-09-08 WO disclosed
WO-2006093354-A1 PRODUCTION INTERMEDIATE OF (S)-2-[3-(N-{[4-(4-FLUOROPHENOXY)PHENYL]METHYL}CARBAMOYL)-4-METHOXYPHENYLMETHYL]BUTANOIC ACID KYORIN PHARMACEUTICAL CO., LTD. (JP) 2006-09-08 WO disclosed
WO-2006090756-A1 NOVEL PREVENTIVE OR REMEDY FOR LIPID METABOLISM DISORDER, OBESITY AND DIABETES AND USE THEREFOR KYORIN PHARMACEUTICAL CO., LTD. (JP) 2006-08-31 WO disclosed
WO-2004091600-A1 SOLID PREPARATION FOR ORAL USE KYORIN PHARMACEUTICAL CO., LTD. (JP) 2004-10-28 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 (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-20100240580-A1 AZOLOARINE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, PHARMACEUTICALS CONTAINING THESE COMPOUNDS AND THE USE THEREOF CYP3A43, CYP11B1, CYP11B2 PPARA 1974/4885PPARG 2414/4885PPARD 1607/4885
US-20110112097-A1 Substituted imidazoline-2,4-diones, process for preparation thereof, medicaments comprising these compounds and use thereof GIPR, PGC, DDC PPARA 91/4885PPARG 33/4885PPARD 43/4885

“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.