SCHEMBL7589324

SCHEMBL7589324

COCc1cnc2c(O)cccc2c1

nearest known ligand 0.57

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 12/20 0.57
PDE10A Q9Y233 2/20 0.44
PARP1 P09874 1/20 0.43
MMP2 P08253 1/20 0.43
CHRM1 P11229 1/20 0.43
TSHR P16473 1/20 0.43
COMT P21964 1/20 0.43
ADRA1A P35348 1/20 0.43
METAP2 P50579 1/20 0.43
METAP1 P53582 1/20 0.43
HDAC8 Q9BY41 1/20 0.43
MEN1 O00255 1/20 0.42
KMT2A Q03164 1/20 0.42
ALOX12 P18054 2/20 0.40
NPC1 O15118 1/20 0.40
HTT P42858 1/20 0.40
RAB9A P51151 1/20 0.40
NPSR1 Q6W5P4 1/20 0.40
PAX8 Q06710 1/20 0.39

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
SCHEMBL4463430 0.82 KDM4E (0.62) KDM4EPDE10APARP1MMP2CHRM1
SCHEMBL8838482 0.81 PDE10A (0.44) KDM4EPDE10APARP1
SCHEMBL8811070 0.81 HPGDS (0.56) PDE10APARP1MEN1KMT2ANPC1
SCHEMBL8099182 0.81 PDE4A (0.40) KDM4EPARP1HTT
Hydrochloric Acid SCHEMBL9814936 0.81 KDM4E (0.60) KDM4EPDE10APARP1MMP2CHRM1
Hydrochloric Acid SCHEMBL9814926 0.81 KDM4E (0.60) KDM4EPDE10APARP1MMP2CHRM1
SCHEMBL28076889 0.80 PARP1 (0.56) KDM4EPARP1
SCHEMBL21651065 0.78 KDM4E (0.57) KDM4EPARP1MMP2CHRM1TSHR
Bromide SCHEMBL7469974 0.77 KDM4E (0.55) KDM4EPARP1MMP2CHRM1TSHR
SCHEMBL8838403 0.77 PDE10A (0.51) KDM4EPDE10APARP1TSHRMEN1

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 24 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1067380-C Method for conversion of substituted 8-chloroquinolines to substituted 8-hydroxyquinolines AMERICAN CYANAMID CO (US) 2001-06-20 CN claimed
EP-0744399-B1 Conversion of substituted 8-chloroquinolines to substituted 8-hydroxyquinolines AMERICAN CYANAMID CO (US) 2000-10-25 EP claimed
CN-1146989-A Method for conversion of substituted 8-chloroquinolines to substituted 8-hydroxyquinolines AMERICAN CYANAMID CO (US) 1997-04-09 CN claimed
EP-0548520-B1 Process for the manufacture of 2-alkoxymethylacrolein and its use for preparing 3-alkoxymethyl quinolines AMERICAN CYANAMID CO (US) 1997-01-29 EP claimed
US-5597924-A Coversion of substituted 8-chloroquinolines to substituted 8-hydroxyquinolines AMERICAN CYANAMID COMPANY (US) 1997-01-28 US claimed
EP-0744399-A2 Conversion of substituted 8-chloroquinolines to substituted 8-hydroxyquinolines American Cyanamid Company (US) 1996-11-27 EP claimed
US-5281713-A Process for the manufacture of 2-alkoxymethylacrolein AMERICAN CYANAMID COMPANY (US) 1994-01-25 US claimed
EP-0548520-A2 Process for the manufacture of 2-alkoxymethylacrolein and its use for preparing 3-alkoxymethyl quinolines AMERICAN CYANAMID COMPANY (US) 1993-06-30 EP claimed
JP-9003048-A None JP disclosed
CN-1130344-C Substituted quinoline herbicide intermediates and process AMERICAN CYANAMID CO (US) 2003-12-10 CN disclosed
EP-0747362-B1 Substituted quinoline herbicide intermediates and process BASF AG (DE) 2002-10-30 EP disclosed
CN-1067380-C Method for conversion of substituted 8-chloroquinolines to substituted 8-hydroxyquinolines AMERICAN CYANAMID CO (US) 2001-06-20 CN disclosed
EP-0744399-B1 Conversion of substituted 8-chloroquinolines to substituted 8-hydroxyquinolines AMERICAN CYANAMID CO (US) 2000-10-25 EP disclosed
US-5633380-A DEHALOGENATED, DESALTED HERBICIDES AMERICAN CYANAMID COMPANY (US) 1997-05-27 US disclosed
CN-1138034-A Substituted quinoline herbicide intermediates and process AMERICAN CYANAMID CO (US) 1996-12-18 CN disclosed
EP-0747362-A1 Substituted quinoline herbicide intermediates and process American Cyanamid Company (US) 1996-12-11 EP disclosed
EP-0744399-A2 Conversion of substituted 8-chloroquinolines to substituted 8-hydroxyquinolines American Cyanamid Company (US) 1996-11-27 EP disclosed
US-5506360-A Process for the manufacture of 2-alkoxymethylacrolein AMERICAN CYANAMID COMPANY (US) 1996-04-09 US disclosed
US-5281713-A Process for the manufacture of 2-alkoxymethylacrolein AMERICAN CYANAMID COMPANY (US) 1994-01-25 US disclosed
EP-0548520-A2 Process for the manufacture of 2-alkoxymethylacrolein and its use for preparing 3-alkoxymethyl quinolines AMERICAN CYANAMID COMPANY (US) 1993-06-30 EP disclosed