SCHEMBL7106510

SCHEMBL7106510

O=C(OC(=O)C(Cl)c1ccccc1)C(Cl)c1ccccc1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 2/20 0.47
CYP2D6 P10635 3/20 0.44
SRC P12931 2/20 0.44
TSHR P16473 1/20 0.44
LMNA P02545 4/20 0.43
MAPK1 P28482 1/20 0.43
CYP1A2 P05177 2/20 0.42
PKM P14618 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
NPSR1 Q6W5P4 1/20 0.42
MEN1 O00255 1/20 0.42
CHRM2 P08172 2/20 0.42
CHRM4 P08173 2/20 0.42
CHRM1 P11229 2/20 0.42
CHRM3 P20309 2/20 0.42
CES2 O00748 1/20 0.41
CES1 P23141 1/20 0.41
HPGD P15428 1/20 0.40
TDP1 Q9NUW8 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.40

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
SCHEMBL9051580 0.89 KMT2A (0.45) KMT2ACYP2D6SRCTSHRLMNA
SCHEMBL4642041 0.88 KMT2A (0.41) KMT2ACYP2D6SRCTSHRLMNA
SCHEMBL4642047 0.88 KMT2A (0.46) KMT2ACYP2D6SRCTSHRLMNA
SCHEMBL29819688 0.84 CHRM1 (0.49) KMT2ACYP2D6SRCTSHRLMNA
SCHEMBL4644768 0.83 CYP2D6 (0.39) KMT2ACYP2D6SRCTSHRLMNA
SCHEMBL11600732 0.83 KMT2A (0.44) KMT2ACYP2D6SRCTSHRLMNA
SCHEMBL1526022 0.83 KMT2A (0.64) KMT2ATSHRLMNAMEN1CHRM2
SCHEMBL15514394 0.83 KMT2A (0.44) KMT2ACYP2D6SRCTSHRLMNA
SCHEMBL16904038 0.81 CYP2D6 (0.43) KMT2ACYP2D6SRCTSHRLMNA
SCHEMBL8675334 0.81 L3MBTL1 (0.56) KMT2ACYP2D6SRCTSHRLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0792936-B1 Process for the preparation of optically active 2-halo-1-(substituted phenyl) ethanol MITSUBISHI CHEM CORP (JP) 2003-01-29 EP disclosed
US-5841001-A ALLOWING 2-HALO-1-(SUBSTITUTED PHENYL)ETHANOL TO CONTACT ENZYME STEREOSELECTIVELY CATALYZING ESTER INTERCHANGE IN PRESENCE OF CARBOXYLIC ANHYDRIDE MITSUBISHI CHEMICAL CORPORATION (JP) 1998-11-24 US disclosed
EP-0792936-A2 Process for the preparation of optically active 2-halo-1-(substituted phenyl) ethanol Mitsubishi Chemical Corporation (JP) 1997-09-03 EP disclosed
US-4110465-A ANTIINFLAMMATORY, ANTITHROMBOSIS ELI LILLY AND COMPANY (US) 1978-08-29 US disclosed