SCHEMBL6185300

SCHEMBL6185300

O=Cc1ccc(-c2cccc(NC(=O)O)c2)cc1

nearest known ligand 0.57

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
MGLL Q99685 2/20 0.57
TRIM24 O15164 1/20 0.51
TRIM33 Q9UPN9 1/20 0.51
CNR1 P21554 5/20 0.50
POLB P06746 1/20 0.49
LTB4R Q15722 1/20 0.48
DRD1 P21728 1/20 0.48
HDAC6 Q9UBN7 2/20 0.46
PNPLA2 Q96AD5 1/20 0.46
CYP17A1 P05093 1/20 0.45
CYP11B1 P15538 1/20 0.45
CYP11B2 P19099 1/20 0.45
HDAC1 Q13547 1/20 0.44

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
SCHEMBL26108304 0.89 TRIM24 (0.57) MGLLTRIM24TRIM33CNR1POLB
SCHEMBL6792137 0.86 CYP17A1 (0.60) MGLLCYP17A1CYP11B1CYP11B2
SCHEMBL7511547 0.84 MGLL (0.78) MGLLCNR1POLBHDAC6HDAC1
SCHEMBL30331540 0.84 MGLL (0.78) MGLLCNR1POLBHDAC6HDAC1
SCHEMBL6959297 0.81 UNG (0.53) MGLLTRIM24TRIM33
SCHEMBL4222132 0.78 DRD1 (0.47) MGLLTRIM24TRIM33CNR1DRD1
SCHEMBL27734848 0.77 CFD (0.61) MGLLCNR1POLBHDAC6CYP17A1
SCHEMBL29265483 0.77 MGLL (0.66) MGLLCNR1POLB
SCHEMBL30690003 0.77 CNR1 (0.64) MGLLCNR1POLBHDAC6CYP17A1
SCHEMBL27811104 0.77 CNR1 (0.64) MGLLCNR1POLBHDAC6CYP17A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6927228-B2 Biphenyl compounds usefuf in treatment of human and veterinary medicines such as dermatology, cardivovascular diseases, immune diseases or diseases associated with lipid metabolisms, or in cosmetic formulation GALDERMA RESEARCH & DEVELOPMENT, S.N.C. (FR) 2005-08-09 US disclosed
EP-1309575-B1 BIPHENYL DERIVATIVES AND THEIR USE AS PPAR-GAMMA RECEPTOR ACTIVATORS GALDERMA RES & DEV (FR) 2005-06-08 EP disclosed
US-20040039038-A1 Biaromatic compound activators of PPARy-type receptors GALDERMA RESEARCH & DEVELOPMENT S.N.C. (FR) 2004-02-26 US disclosed
EP-1309575-A1 BIPHENYL DERIVATIVES AND THEIR USE AS PPAR-GAMMA RECEPTOR ACTIVATORS Galderma Research & Development (FR) 2003-05-14 EP disclosed
WO-2002012210-A9 BIPHENYL DERIVATIVES AND THEIR USE AS PPAR-GAMMA RECEPTOR ACTIVATORS GALDERMA RES & DEV (FR) 2002-04-18 WO disclosed
WO-2002012210-A1 BIPHENYL DERIVATIVES AND THEIR USE AS PPAR-GAMMA RECEPTOR ACTIVATORS GALDERMA RESEARCH & DEVELOPMENT (FR) 2002-02-14 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-20040039038-A1 Biaromatic compound activators of PPARy-type receptors PPARG, PPARA, PPARD MGLL 196/4885TRIM24 3617/4885TRIM33 3945/4885

“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.