SCHEMBL10128671

SCHEMBL10128671

Cc1ccc(-c2ccc(OCc3ccccc3)cc2)cc1

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.60
CYP1A2 P05177 1/20 0.60
PTGS1 P23219 1/20 0.60
SLC6A2 P23975 1/20 0.60
CYP2C19 P33261 1/20 0.60
PTGS2 P35354 1/20 0.60
SLC6A3 Q01959 1/20 0.60
HIF1A Q16665 1/20 0.60
HDAC6 Q9UBN7 1/20 0.60
ENPP3 O14638 1/20 0.59
ENPP1 P22413 1/20 0.59
GSTP1 P09211 2/20 0.59
MAOB P27338 5/20 0.58
GAA P10253 1/20 0.58
MAPT P10636 1/20 0.58
MAOA P21397 1/20 0.58
RAB9A P51151 1/20 0.58
SMN1; SMN2 Q16637 1/20 0.58
L3MBTL1 Q9Y468 1/20 0.58
AR P10275 1/20 0.57

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
SCHEMBL14864480 0.94 GSTP1 (0.63) LMNACYP1A2PTGS1SLC6A2CYP2C19
SCHEMBL128703 0.94 LMNA (0.67) LMNACYP1A2PTGS1SLC6A2CYP2C19
SCHEMBL1702909 0.90 MAOB (0.62) GSTP1MAOBMAPTRAB9ASMN1; SMN2
SCHEMBL16603392 0.90 MAOB (0.62) GSTP1MAOBMAPTRAB9ASMN1; SMN2
SCHEMBL18635916 0.90 MAOB (0.62) GSTP1MAOBMAPTRAB9ASMN1; SMN2
SCHEMBL12918621 0.90 MAOB (0.62) GSTP1MAOBMAPTRAB9ASMN1; SMN2
SCHEMBL197017 0.90 LMNA (0.72) LMNACYP1A2PTGS1SLC6A2CYP2C19
SCHEMBL17081101 0.89 LMNA (0.57) LMNACYP1A2PTGS1SLC6A2CYP2C19
SCHEMBL8736979 0.89 LMNA (0.60) LMNACYP1A2PTGS1SLC6A2CYP2C19
SCHEMBL23483029 0.88 LMNA (0.69) LMNACYP1A2PTGS1SLC6A2CYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8530689-B2 Processes for the preparation of biphenyl compounds THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2013-09-10 US disclosed
US-8119617-B2 aSMase inhibitors NOVARTIS AG (CH) 2012-02-21 US disclosed
US-8119617-B2 aSMase inhibitors NOVARTIS AG (CH) 2012-02-21 US disclosed
US-20110207957-A1 PROCESSES FOR THE PREPARATION OF BIPHENYL COMPOUNDS THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2011-08-25 US disclosed
US-20100022482-A1 aSMase inhibitors NOVARTIS AG (CH) 2010-01-28 US disclosed
US-20100022482-A1 aSMase inhibitors NOVARTIS AG (CH) 2010-01-28 US disclosed
CN-101306995-A Binaphthalenol derivatives and uses thereof CHITEC TECHNOLOGY CO LTD (CN) 2008-11-19 CN disclosed
US-7416791-B1 Osmium complexes and related organic light-emitting devices UNIVERSITY OF WASHINGTON (US) 2008-08-26 US disclosed
US-7416791-B1 Osmium complexes and related organic light-emitting devices UNIVERSITY OF WASHINGTON (US) 2008-08-26 US disclosed
WO-2008022771-A1 AMIDES AS SPHINGOMYELINE INHIBITORS NOVARTIS AG (CH) 2008-02-28 WO disclosed
CN-1729429-A Color filter black matrix resist composition and carbon black dispersion composition for the same SHOWA DENKO KK (JP) 2006-02-01 CN 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 (2 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-20100022482-A1 aSMase inhibitors SMPD1, SMPD3, SMPD2 LMNA 1589/4885CYP1A2 281/4885PTGS1 1463/4885
US-20110207957-A1 PROCESSES FOR THE PREPARATION OF BIPHENYL COMPOUNDS C1S, BAX, C9 LMNA 1681/4885CYP1A2 295/4885PTGS1 3649/4885

“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.