SCHEMBL6183546

SCHEMBL6183546

CCCNCc1cccc(Br)c1

nearest known ligand 0.76

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 3/20 0.76
CYP2D6 P10635 3/20 0.76
CYP2C19 P33261 3/20 0.76
TAAR1 Q96RJ0 3/20 0.53
L3MBTL1 Q9Y468 1/20 0.47
LMNA P02545 1/20 0.45
CARM1 Q86X55 1/20 0.44
PRMT6 Q96LA8 1/20 0.44
SIGMAR1 Q99720 1/20 0.44
KDM4E B2RXH2 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
SCHEMBL19633152 0.89 CYP1A2 (0.88) CYP1A2CYP2D6CYP2C19TAAR1LMNA
SCHEMBL29672948 0.85 CYP1A2 (0.65) CYP1A2CYP2D6CYP2C19TAAR1LMNA
SCHEMBL8583518 0.85 CYP1A2 (0.65) CYP1A2CYP2D6CYP2C19TAAR1LMNA
SCHEMBL1420648 0.84 CYP1A2 (0.62) CYP1A2CYP2D6CYP2C19TAAR1KDM4E
SCHEMBL552961 0.84 TAAR1 (0.66) CYP1A2CYP2D6CYP2C19TAAR1L3MBTL1
SCHEMBL6364808 0.82 CYP1A2 (0.61) CYP1A2CYP2D6CYP2C19TAAR1LMNA
SCHEMBL5275606 0.81 CYP1A2 (0.66) CYP1A2CYP2D6CYP2C19TAAR1SIGMAR1
SCHEMBL16619429 0.81 CYP1A2 (0.61) CYP1A2CYP2D6CYP2C19TAAR1KDM4E
SCHEMBL16269355 0.81 TAAR1 (0.62) CYP1A2CYP2D6CYP2C19TAAR1CARM1
SCHEMBL3622330 0.81 CYP1A2 (0.60) CYP1A2CYP2D6CYP2C19TAAR1L3MBTL1

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 7 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
CN-1468226-A Biphenyl derivatives and their use as ppar-gamma receptor activators �������о�����չ˽�����޹�˾ 2004-01-14 CN 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 CYP1A2 93/4885CYP2D6 294/4885CYP2C19 174/4885

“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.