SCHEMBL7652737

SCHEMBL7652737

O=c1c(O)c(-c2ccc(O)c(O)c2)oc2ccc(Cl)cc12

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 7/20 0.68
KMT2A Q03164 7/20 0.68
MAPT P10636 6/20 0.68
KDM4E B2RXH2 6/20 0.68
TP53 P04637 5/20 0.68
CYP3A4 P08684 5/20 0.68
CYP2C9 P11712 5/20 0.68
HSD17B10 Q99714 5/20 0.68
ALOX15 P16050 4/20 0.68
RECQL P46063 4/20 0.68
CDK2 P24941 4/20 0.68
ALOX12 P18054 3/20 0.68
MAPK1 P28482 3/20 0.68
CYP2D6 P10635 2/20 0.68
CYP2C19 P33261 2/20 0.68
ST6GAL1 P15907 1/20 0.68
MKNK2 Q9HBH9 1/20 0.67
CSNK2A2 P19784 4/20 0.64
CSNK2B P67870 4/20 0.64
CSNK2A1 P68400 4/20 0.64

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
SCHEMBL505584 0.86 MEN1 (0.79) MEN1KMT2AMAPTKDM4ETP53
SCHEMBL10037939 0.84 MEN1 (0.76) MEN1KMT2AMAPTKDM4ETP53
SCHEMBL7659883 0.83 MAPT (0.71) MEN1KMT2AMAPTKDM4ETP53
SCHEMBL7656936 0.83 MAPT (0.68) MEN1KMT2AMAPTKDM4ETP53
SCHEMBL8019406 0.83 MAPT (0.85) MEN1KMT2AMAPTKDM4ETP53
SCHEMBL7655634 0.83 MEN1 (0.68) MEN1KMT2AMAPTKDM4ETP53
SCHEMBL7660823 0.83 MEN1 (0.68) MEN1KMT2AMAPTKDM4ETP53
SCHEMBL12941005 0.83 MKNK2 (0.75) MEN1KMT2AMAPTKDM4ETP53
SCHEMBL7658183 0.82 SNCA (0.61) MEN1KMT2AMAPTKDM4ETP53
SCHEMBL25207771 0.81 MAPT (0.68) MEN1KMT2AMAPTKDM4ETP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1109800-A1 NOVEL CDK INHIBITORS HAVING FLAVONE STRUCTURE LG CHEMICAL LIMITED (KR) 2001-06-27 EP claimed
WO-2000012496-A1 NOVEL CDK INHIBITORS HAVING FLAVONE STRUCTURE LG CHEMICAL LTD. (KR) 2000-03-09 WO claimed
US-9301965-B2 Method of treating ovarian cancer using a PKC inhibitor UNIVERSITY OF SOUTH FLORIDA (US) 2016-04-05 US disclosed
US-9301965-B2 Method of treating ovarian cancer using a PKC inhibitor UNIVERSITY OF SOUTH FLORIDA (US) 2016-04-05 US disclosed
US-20150366883-A1 METHOD OF TREATING OVARIAN CANCER USING A PKC INHIBITOR UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INC. (US) 2015-12-24 US disclosed
US-20150366883-A1 METHOD OF TREATING OVARIAN CANCER USING A PKC INHIBITOR UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INC. (US) 2015-12-24 US disclosed
US-6500846-B1 2-(4-CHLOROPHENYL)-7-METHOXYCHROMEN-4-ONE, AS CYCLIN-DEPENDENT KINASE INHIBITORS, USED AS ANTICARCINOGENIC AGENTS OR FOR PROPHYLAXIS OF NEURODEGENERATIVE DISEASE LG CHEMICAL, LTD. (KR) 2002-12-31 US disclosed
EP-1109800-A1 NOVEL CDK INHIBITORS HAVING FLAVONE STRUCTURE LG CHEMICAL LIMITED (KR) 2001-06-27 EP disclosed
WO-2000012496-A1 NOVEL CDK INHIBITORS HAVING FLAVONE STRUCTURE LG CHEMICAL LTD. (KR) 2000-03-09 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-20150366883-A1 METHOD OF TREATING OVARIAN CANCER USING A PKC INHIBITOR PRKD1, PRKCI, ACP3 MEN1 2504/4885KMT2A 1552/4885MAPT 4352/4885

“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.