SCHEMBL6201480

SCHEMBL6201480

CN(Cc1cccc(-c2ccc(/C=C3/SC(=O)NC3=O)cc2)c1)C(=O)Nc1ccccc1

nearest known ligand 0.50

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
AOC3 Q16853 3/20 0.48
PTPN1 P18031 4/20 0.48
MAOA P21397 2/20 0.48
MAOB P27338 2/20 0.48
HDAC4 P56524 1/20 0.48
HDAC8 Q9BY41 1/20 0.48
HPGD P15428 4/20 0.48
CISD1 Q9NZ45 1/20 0.46
MEN1 O00255 2/20 0.45
KMT2A Q03164 2/20 0.45
POLB P06746 1/20 0.45
PIM1 P11309 1/20 0.44
PIM3 Q86V86 1/20 0.44
PIM2 Q9P1W9 1/20 0.44
GSK3B P49841 1/20 0.44
ALDH1A1 P00352 1/20 0.44
GAA P10253 1/20 0.44
SMN1; SMN2 Q16637 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
SCHEMBL6201482 1.00 AOC3 (0.48) AOC3PTPN1MAOAMAOBHDAC4
SCHEMBL5397253 0.87 MEN1 (0.53) PTPN1MAOAMAOBHPGDMEN1
SCHEMBL5397249 0.87 MEN1 (0.53) PTPN1MAOAMAOBHPGDMEN1
SCHEMBL6185163 0.85 HSD17B2 (0.51) PTPN1HPGDMEN1KMT2APOLB
SCHEMBL6185166 0.85 HSD17B2 (0.51) PTPN1HPGDMEN1KMT2APOLB
SCHEMBL6182023 0.84 HPGD (0.54) AOC3PTPN1HPGDKMT2A
SCHEMBL6182018 0.84 HPGD (0.54) AOC3PTPN1HPGDKMT2A
SCHEMBL6204139 0.83 GSK3B (0.52) PTPN1MAOAMAOBHDAC4HDAC8
SCHEMBL6204137 0.83 GSK3B (0.52) PTPN1MAOAMAOBHDAC4HDAC8
SCHEMBL6184071 0.82 MEN1 (0.47) PTPN1HPGDCISD1MEN1KMT2A

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 AOC3 1747/4885PTPN1 1579/4885MAOA 719/4885

“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.