SCHEMBL6183019

SCHEMBL6183019

Cc1cc(-c2cccc(CN(C)C(=O)O)c2)ccc1CC1SC(=O)NC1=O

nearest known ligand 0.47

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
FFAR1 O14842 5/20 0.47
MAOA P21397 2/20 0.42
CISD1 Q9NZ45 2/20 0.42
MAOB P27338 1/20 0.42
ALDH1A1 P00352 1/20 0.42
NPSR1 Q6W5P4 1/20 0.42
AOC3 Q16853 8/20 0.41
PPARG P37231 2/20 0.41
CA2 P00918 1/20 0.40
PIM3 Q86V86 1/20 0.40
PIM2 Q9P1W9 1/20 0.40

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
SCHEMBL5399580 0.88 FFAR1 (0.61) FFAR1MAOACISD1ALDH1A1NPSR1
SCHEMBL6184677 0.85 FFAR1 (0.41) FFAR1MAOACISD1MAOBALDH1A1
SCHEMBL6184488 0.83 FFAR1 (0.55) FFAR1MAOACISD1MAOBALDH1A1
SCHEMBL5760347 0.83 FFAR1 (0.47) FFAR1MAOACISD1MAOBALDH1A1
SCHEMBL6184000 0.81 FFAR1 (0.49) FFAR1MAOACISD1MAOBALDH1A1
SCHEMBL1751600 0.80 FFAR1 (0.51) FFAR1MAOACISD1AOC3PPARG
SCHEMBL6183022 0.78 FFAR1 (0.52) FFAR1MAOACISD1MAOBALDH1A1
SCHEMBL5399098 0.78 FFAR1 (0.59) FFAR1AOC3PPARG
SCHEMBL6184172 0.78 FFAR1 (0.59) FFAR1AOC3PPARG
SCHEMBL6183905 0.78 FFAR1 (0.59) FFAR1AOC3PPARG

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 FFAR1 6/4885MAOA 719/4885CISD1 2024/4885

“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.