SCHEMBL6182142

SCHEMBL6182142

CCN(Cc1cccc(-c2ccc(C=C3SC(=O)NC3=O)cc2)c1)C(=O)O

nearest known ligand 0.51

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
PIM1 P11309 3/20 0.51
PIM2 Q9P1W9 3/20 0.51
IGF1R P08069 1/20 0.51
PTPN1 P18031 3/20 0.50
HPGD P15428 9/20 0.49
MEN1 O00255 1/20 0.48
POLB P06746 1/20 0.48
KMT2A Q03164 1/20 0.48
PIM3 Q86V86 1/20 0.46
GSK3B P49841 1/20 0.46
AKR1B1 P15121 1/20 0.46
NAT1 P18440 1/20 0.46

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
SCHEMBL6182139 1.00 PIM1 (0.51) PIM1PIM2IGF1RPTPN1HPGD
SCHEMBL6182708 0.92 PIM1 (0.49) PIM1PIM2IGF1RPTPN1HPGD
SCHEMBL6182707 0.92 PIM1 (0.49) PIM1PIM2IGF1RPTPN1HPGD
SCHEMBL6183613 0.91 PTPN1 (0.50) PIM1PIM2PTPN1HPGDMEN1
SCHEMBL6183616 0.91 PTPN1 (0.50) PIM1PIM2PTPN1HPGDMEN1
SCHEMBL5397253 0.87 MEN1 (0.53) PIM1PIM2IGF1RPTPN1HPGD
SCHEMBL5397249 0.87 MEN1 (0.53) PIM1PIM2IGF1RPTPN1HPGD
SCHEMBL6183241 0.85 PTPN1 (0.48) PIM1PIM2PTPN1HPGDMEN1
SCHEMBL6183238 0.85 PTPN1 (0.48) PIM1PIM2PTPN1HPGDMEN1
SCHEMBL6185163 0.84 HSD17B2 (0.51) PIM1PIM2PTPN1HPGDMEN1

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 PIM1 4083/4885PIM2 4126/4885IGF1R 1106/4885

“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.