SCHEMBL6183255

SCHEMBL6183255

CC(Cc1ccc(-c2cccc(CN(C)C(=O)c3ccccc3)c2)cc1)C(=O)NO

nearest known ligand 0.54

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
HSD17B2 P37059 6/20 0.54
HSD17B1 P14061 4/20 0.54
HDAC1 Q13547 1/20 0.51
HDAC6 Q9UBN7 1/20 0.51
MEN1 O00255 1/20 0.50
KMT2A Q03164 1/20 0.50
PTGES O14684 1/20 0.48
AOC3 Q16853 5/20 0.48
HDAC8 Q9BY41 1/20 0.47
HPGD P15428 1/20 0.46
ACACB O00763 1/20 0.46
MEP1B Q16820 1/20 0.45

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
SCHEMBL6184866 0.90 HSD17B2 (0.52) HSD17B2HSD17B1MEN1KMT2APTGES
SCHEMBL6184961 0.89 HSD17B2 (0.54) HSD17B2HSD17B1HDAC1HDAC6MEN1
SCHEMBL6184066 0.89 HSD17B2 (0.58) HSD17B2HSD17B1MEN1KMT2APTGES
SCHEMBL6184210 0.87 HSD17B2 (0.56) HSD17B2HSD17B1MEN1KMT2APTGES
SCHEMBL6183482 0.84 HSD17B2 (0.60) HSD17B2HSD17B1HDAC1HDAC6MEN1
SCHEMBL6186838 0.84 HSD17B2 (0.53) HSD17B2HSD17B1MEN1KMT2APTGES
SCHEMBL2847856 0.82 HSD17B2 (0.58) HSD17B2HSD17B1MEN1KMT2AAOC3
SCHEMBL3439044 0.82 HSD17B2 (0.58) HSD17B2HSD17B1MEN1KMT2AAOC3
SCHEMBL2851697 0.82 HSD17B2 (0.58) HSD17B2HSD17B1MEN1KMT2AAOC3
SCHEMBL6473157 0.82 HSD17B2 (0.57) HSD17B2HSD17B1HDAC1HDAC6MEN1

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 8 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1309575-B1 BIPHENYL DERIVATIVES AND THEIR USE AS PPAR-GAMMA RECEPTOR ACTIVATORS GALDERMA RES & DEV (FR) 2005-06-08 EP claimed
US-20040039038-A1 Biaromatic compound activators of PPARy-type receptors GALDERMA RESEARCH & DEVELOPMENT S.N.C. (FR) 2004-02-26 US claimed
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 HSD17B2 368/4885HSD17B1 275/4885HDAC1 502/4885

“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.