SCHEMBL6184041

SCHEMBL6184041

CN(Cc1ccccc1)C(=O)c1cccc(-c2ccc(CC3SC(=O)NC3=O)cc2)c1

nearest known ligand 0.57

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
FFAR1 O14842 4/20 0.57
KMT2A Q03164 2/20 0.53
MEN1 O00255 1/20 0.53
HSD17B2 P37059 4/20 0.52
HSD17B1 P14061 3/20 0.52
PPARG P37231 6/20 0.51
ERN1 O75460 1/20 0.48
MPC2 O95563 1/20 0.47
CYP2C8 P10632 1/20 0.47
CYP2C9 P11712 1/20 0.47
MAPT P10636 2/20 0.45
ATM Q13315 1/20 0.44
RARG P13631 1/20 0.44
RXRA P19793 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
SCHEMBL6184172 0.94 FFAR1 (0.59) FFAR1KMT2AMEN1HSD17B2HSD17B1
SCHEMBL7090099 0.92 FFAR1 (0.49) FFAR1KMT2AMEN1HSD17B2HSD17B1
SCHEMBL5399098 0.92 FFAR1 (0.59) FFAR1HSD17B2HSD17B1PPARGMPC2
SCHEMBL5403696 0.91 FFAR1 (0.56) FFAR1KMT2AMEN1HSD17B2HSD17B1
SCHEMBL6184175 0.89 HSD17B2 (0.53) FFAR1KMT2AMEN1HSD17B2HSD17B1
SCHEMBL5760451 0.88 FFAR1 (0.55) FFAR1HSD17B2HSD17B1PPARGMPC2
SCHEMBL5389745 0.88 FFAR1 (0.55) FFAR1HSD17B2HSD17B1PPARGMPC2
SCHEMBL6184391 0.88 PPARG (0.59) FFAR1KMT2AMEN1HSD17B2HSD17B1
SCHEMBL5399580 0.88 FFAR1 (0.61) FFAR1PPARGMPC2CYP2C8CYP2C9
SCHEMBL5762215 0.87 FFAR1 (0.54) FFAR1HSD17B2HSD17B1PPARGMPC2

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 8 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 claimed
EP-1309575-B1 BIPHENYL DERIVATIVES AND THEIR USE AS PPAR-GAMMA RECEPTOR ACTIVATORS GALDERMA RES & DEV (FR) 2005-06-08 EP claimed
US-20040039038-A1 Biaromatic compound activators of PPARy-type receptors GALDERMA RESEARCH & DEVELOPMENT S.N.C. (FR) 2004-02-26 US claimed
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-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 FFAR1 6/4885KMT2A 3011/4885MEN1 4750/4885

“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.