SCHEMBL6358310

SCHEMBL6358310

OC(CCl)COc1cccc2c(OCC(O)CCl)cccc12

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 5/20 0.57
CYP2C19 P33261 2/20 0.57
KDM4E B2RXH2 1/20 0.57
MEN1 O00255 1/20 0.57
KMT2A Q03164 1/20 0.57
NR2E1 Q9Y466 5/20 0.56
ADRB2 P07550 4/20 0.49
ADRB1 P08588 4/20 0.49
SIGMAR1 Q99720 4/20 0.49
CYP2D6 P10635 3/20 0.49
SLC6A4 P31645 3/20 0.49
HTR2B P41595 3/20 0.49
ALDH1A1 P00352 3/20 0.49
ADRB3 P13945 3/20 0.49
HTR2A P28223 3/20 0.49
HTR2C P28335 3/20 0.49
HTR6 P50406 3/20 0.49
HTR1A P08908 3/20 0.49
SCN1A P35498 2/20 0.49
SLC10A1 Q14973 2/20 0.49

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
SCHEMBL10365539 0.90 CYP1A2 (0.73) CYP1A2CYP2C19KDM4EMEN1KMT2A
SCHEMBL9330063 0.90 CYP1A2 (0.73) CYP1A2CYP2C19KDM4EMEN1KMT2A
SCHEMBL11871935 0.86 CYP1A2 (0.56) CYP1A2CYP2C19KDM4EMEN1KMT2A
SCHEMBL14901592 0.82 ADRB2 (0.49) CYP1A2CYP2C19KDM4EMEN1KMT2A
SCHEMBL14901599 0.81 CYP1A2 (0.51) CYP1A2CYP2C19KDM4EMEN1KMT2A
SCHEMBL12999565 0.81 CYP1A2 (0.57) CYP1A2CYP2C19KDM4EMEN1KMT2A
SCHEMBL10472270 0.81 HTR1A (0.73) CYP1A2KDM4EMEN1KMT2AADRB2
SCHEMBL11867441 0.79 ADRB2 (0.44) CYP1A2KDM4ENR2E1ADRB2ADRB1
SCHEMBL4231217 0.78 TLR4 (0.50) CYP1A2CYP2C19KDM4EMEN1KMT2A
SCHEMBL11468344 0.78 CYP1A2 (0.41) CYP1A2CYP2C19KDM4EMEN1KMT2A

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-20030149219-A1 Process for manufacturing a hydroxyester derivative intermediate and epoxy resins prepared therefrom BORIACK CLINTON J (US) 2003-08-07 US claimed
US-6534621-B2 Epoxidizing an alpha-halohydrin intermediate produced from an in situ halide substitution-deesterification of an alpha-hydroxy ester derivative DOW GLOBAL TECHNOLOGIES INC. 2003-03-18 US claimed
US-20020045707-A1 Process for manufacturing a hydroxyester derivative intermediate and epoxy resins prepared therefrom DOW GLOBAL TECHNOLOGIES INC. 2002-04-18 US claimed
US-20050165201-A1 Epoxidizing an alpha-halohydrin intermediate from a halide substitution-deesterification of an alpha -hydroxy ester derivative obtained by the coupling reaction of a phenol and a glycidyl ester BORIACK CLINTON J (US) 2005-07-28 US disclosed
US-20030149219-A1 Process for manufacturing a hydroxyester derivative intermediate and epoxy resins prepared therefrom BORIACK CLINTON J (US) 2003-08-07 US disclosed
US-6534621-B2 Epoxidizing an alpha-halohydrin intermediate produced from an in situ halide substitution-deesterification of an alpha-hydroxy ester derivative DOW GLOBAL TECHNOLOGIES INC. 2003-03-18 US disclosed
US-20020045707-A1 Process for manufacturing a hydroxyester derivative intermediate and epoxy resins prepared therefrom DOW GLOBAL TECHNOLOGIES INC. 2002-04-18 US disclosed