SCHEMBL6183049

SCHEMBL6183049

O=C(Cc1ccccc1)Nc1cccc(-c2ccc(/C=C3/SC(=O)NC3=O)cc2)c1

nearest known ligand 0.54

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
HPGD P15428 7/20 0.54
HDAC4 P56524 3/20 0.54
HDAC8 Q9BY41 2/20 0.54
CFD P00746 1/20 0.54
MAOA P21397 1/20 0.53
MAOB P27338 1/20 0.53
PTPN1 P18031 2/20 0.53
MEN1 O00255 2/20 0.50
KMT2A Q03164 2/20 0.50
ALDH1A1 P00352 1/20 0.50
GAA P10253 1/20 0.50
SMN1; SMN2 Q16637 1/20 0.50
PIM1 P11309 1/20 0.49
PIM3 Q86V86 1/20 0.49
PIM2 Q9P1W9 1/20 0.49

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
SCHEMBL6183051 1.00 HPGD (0.54) HPGDHDAC4HDAC8CFDMAOA
SCHEMBL6203211 0.86 MGLL (0.56) HPGDHDAC4HDAC8MAOAMAOB
SCHEMBL6203208 0.86 MGLL (0.56) HPGDHDAC4HDAC8MAOAMAOB
SCHEMBL6184894 0.86 MEN1 (0.55) HPGDHDAC4HDAC8MAOAMAOB
SCHEMBL6184889 0.86 MEN1 (0.55) HPGDHDAC4HDAC8MAOAMAOB
SCHEMBL6204806 0.82 MAOA (0.55) HPGDHDAC4HDAC8MAOAMAOB
SCHEMBL6204803 0.82 MAOA (0.55) HPGDHDAC4HDAC8MAOAMAOB
Phenylacetic Acid SCHEMBL6477210 0.81 HPGD (0.60) HPGDMAOAMAOBPTPN1MEN1
SCHEMBL6201480 0.79 AOC3 (0.48) HPGDHDAC4HDAC8MAOAMAOB
SCHEMBL6201482 0.79 AOC3 (0.48) HPGDHDAC4HDAC8MAOAMAOB

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 HPGD 492/4885HDAC4 979/4885HDAC8 761/4885

“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.