SCHEMBL6183033

SCHEMBL6183033

CNCc1ccc(OCc2ccccc2)c(Br)c1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.51
RAB9A P51151 2/20 0.51
SMN1; SMN2 Q16637 2/20 0.51
KDM4E B2RXH2 3/20 0.50
HPGD P15428 1/20 0.50
TLR9 Q9NR96 1/20 0.50
CCR5 P51681 2/20 0.49
ALDH1A1 P00352 2/20 0.48
PKM P14618 1/20 0.48
HTR7 P34969 1/20 0.47
KMT2A Q03164 2/20 0.46
MEN1 O00255 1/20 0.46
ATM Q13315 1/20 0.46
MRGPRX4 Q96LA9 1/20 0.46
SLC2A1 P11166 1/20 0.46
CYP3A4 P08684 1/20 0.46
BCHE P06276 2/20 0.45
LMNA P02545 1/20 0.45
NPY1R P25929 1/20 0.45
HTT P42858 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
SCHEMBL990347 0.85 MAPT (0.47) MAPTRAB9ASMN1; SMN2KDM4ECCR5
SCHEMBL12772163 0.84 RAB9A (0.56) MAPTRAB9ASMN1; SMN2KDM4EHPGD
SCHEMBL3986458 0.83 RAB9A (0.55) MAPTRAB9ASMN1; SMN2KDM4EHPGD
SCHEMBL5525095 0.82 BCHE (0.64) MAPTRAB9ASMN1; SMN2KDM4EALDH1A1
SCHEMBL1995693 0.81 RAB9A (0.56) MAPTRAB9ASMN1; SMN2KDM4EHPGD
SCHEMBL3237202 0.81 RAB9A (0.56) MAPTRAB9ASMN1; SMN2KDM4EHPGD
SCHEMBL1989845 0.81 SMN1; SMN2 (0.60) MAPTRAB9ASMN1; SMN2KDM4EHPGD
SCHEMBL2860906 0.81 RAB9A (0.50) MAPTRAB9ASMN1; SMN2KDM4EHPGD
Hydrochloric Acid SCHEMBL9454575 0.80 ALDH1A1 (0.52) MAPTSMN1; SMN2KDM4EALDH1A1PKM
SCHEMBL12563216 0.80 RAB9A (0.52) MAPTRAB9ASMN1; SMN2KDM4EHPGD

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 7 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
CN-1468226-A Biphenyl derivatives and their use as ppar-gamma receptor activators �������о�����չ˽�����޹�˾ 2004-01-14 CN 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 MAPT 4411/4885RAB9A 2019/4885SMN1; SMN2 4783/4885

“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.