SCHEMBL6844397

SCHEMBL6844397

O=C(Oc1c(Cl)c(Cl)c(Cl)c(Cl)c1Cl)[C@@H](Cl)c1ccccc1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 3/20 0.44
KMT2A Q03164 2/20 0.40
MEN1 O00255 1/20 0.40
TDP1 Q9NUW8 1/20 0.37
ATM Q13315 1/20 0.37
CYP2D6 P10635 2/20 0.36
SRC P12931 1/20 0.36
LMNA P02545 3/20 0.36
CES2 O00748 2/20 0.36
CES1 P23141 2/20 0.36
CYP1A2 P05177 1/20 0.36
PKM P14618 1/20 0.36
SMN1; SMN2 Q16637 1/20 0.36
NPSR1 Q6W5P4 1/20 0.36
CHRM2 P08172 2/20 0.36
CHRM4 P08173 2/20 0.36
CHRM1 P11229 2/20 0.36
CHRM3 P20309 2/20 0.36
TSHR P16473 1/20 0.35
MAPK1 P28482 1/20 0.35

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
SCHEMBL6839974 1.00 L3MBTL1 (0.44) L3MBTL1KMT2AMEN1TDP1ATM
SCHEMBL11219221 0.84 SRC (0.47) L3MBTL1KMT2ATDP1ATMCYP2D6
SCHEMBL11319434 0.81 SRC (0.53) L3MBTL1KMT2ATDP1ATMCYP2D6
SCHEMBL8675334 0.79 L3MBTL1 (0.56) L3MBTL1KMT2AMEN1TDP1ATM
SCHEMBL11310800 0.78 L3MBTL1 (0.47) L3MBTL1KMT2ATDP1ATMCYP2D6
SCHEMBL10961231 0.77 L3MBTL1 (0.43) L3MBTL1KMT2AMEN1TDP1ATM
SCHEMBL7106510 0.77 KMT2A (0.47) L3MBTL1KMT2AMEN1TDP1CYP2D6
SCHEMBL29819688 0.75 CHRM1 (0.49) KMT2ATDP1CYP2D6SRCLMNA
SCHEMBL9051580 0.75 KMT2A (0.45) L3MBTL1KMT2AMEN1TDP1CYP2D6
SCHEMBL11320690 0.74 MMP8 (0.56) L3MBTL1KMT2AMEN1SMN1; SMN2TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6770775-B2 REACTING ACID HALIDES WITH A CINCHONA ALKALOID CATALYST AND A BASE TO FORM INTERMEDIATE KETENES, WHICH ARE THEN REACTED WITH ELECTROPHILIC HALOGENATING REAGENTS TO PRODUCE ALPHA-HALO-ESTERS WITH HIGH ENANTIOMERIC EXCESS WACK HARALD (DE) 2004-08-03 US disclosed
US-20030050501-A1 Method of synthesizing optically enriched alpha-halo-esters, and product and composition therefrom WACK HARALD (DE) 2003-03-13 US disclosed