SCHEMBL6185038

SCHEMBL6185038

CNC(=O)OCc1cccc(-c2ccc(C=O)cc2)c1

nearest known ligand 0.48

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
MGLL Q99685 4/20 0.48
ENPP2 Q13822 2/20 0.44
MMP1 P03956 2/20 0.44
MMP2 P08253 2/20 0.44
MMP12 P39900 2/20 0.44
DRD1 P21728 1/20 0.44
MMP9 P14780 1/20 0.41
TRIM24 O15164 1/20 0.40
TRIM33 Q9UPN9 1/20 0.40
ERN1 O75460 1/20 0.40
BCL2 P10415 1/20 0.40
FFAR1 O14842 1/20 0.39
NR4A2 P43354 1/20 0.39
AGXT P21549 1/20 0.38

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
SCHEMBL6255495 0.86 MGLL (0.52) MGLLENPP2MMP1MMP2MMP12
SCHEMBL6185514 0.84 FFAR1 (0.42) MGLLENPP2MMP2FFAR1
SCHEMBL6184107 0.84 ERN1 (0.43) MGLLENPP2MMP1MMP2MMP12
SCHEMBL6989558 0.80 PTPN1 (0.53)
SCHEMBL11205908 0.80 MGLL (0.47) MGLL
SCHEMBL27592964 0.77 AOC3 (0.48) DRD1ERN1
SCHEMBL6478104 0.77 TSHR (0.50) DRD1BCL2
SCHEMBL5267820 0.77 DRD1 (0.57) DRD1
SCHEMBL1124854 0.77 ALDH1A1 (0.47) DRD1TRIM24TRIM33ERN1BCL2
SCHEMBL31731111 0.76 DRD1 (0.46) DRD1TRIM24TRIM33BCL2

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 MGLL 196/4885ENPP2 703/4885MMP1 3170/4885

“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.