SCHEMBL7148362

SCHEMBL7148362

CC(Cc1ccccc1Cl)NC[C@H](O)c1ccccc1Cl

nearest known ligand 0.68

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
ADRB2 P07550 12/20 0.68
ADRB1 P08588 7/20 0.68
CYP2D6 P10635 1/20 0.54
NFKB1 P19838 1/20 0.54
HIF1A Q16665 1/20 0.54
BLM P54132 1/20 0.52
LMNA P02545 1/20 0.49
AOC3 Q16853 1/20 0.44
ADRB3 P13945 5/20 0.43

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
SCHEMBL7148365 1.00 ADRB2 (0.68) ADRB2ADRB1CYP2D6NFKB1HIF1A
SCHEMBL7148201 0.90 ADRB2 (0.62) ADRB2ADRB1CYP2D6NFKB1HIF1A
SCHEMBL7148204 0.90 ADRB2 (0.62) ADRB2ADRB1CYP2D6NFKB1HIF1A
SCHEMBL7146552 0.90 ADRB2 (0.55) ADRB2ADRB1CYP2D6NFKB1HIF1A
SCHEMBL7148245 0.90 ADRB2 (0.55) ADRB2ADRB1CYP2D6NFKB1HIF1A
SCHEMBL7146550 0.90 ADRB2 (0.55) ADRB2ADRB1CYP2D6NFKB1HIF1A
SCHEMBL7148247 0.90 ADRB2 (0.55) ADRB2ADRB1CYP2D6NFKB1HIF1A
SCHEMBL7153435 0.89 ADRB2 (0.54) ADRB2ADRB1CYP2D6NFKB1HIF1A
SCHEMBL7153434 0.89 ADRB2 (0.54) ADRB2ADRB1CYP2D6NFKB1HIF1A
SCHEMBL7149318 0.88 ADRB2 (0.52) ADRB2ADRB1CYP2D6NFKB1HIF1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20030143701-A1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEMICAL INDUSTRIES, LTD. 2003-07-31 US disclosed
EP-0924194-B1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEM (JP) 2003-05-14 EP disclosed
US-6528686-B1 Reacting primary amine and ketone functionalized derivatives; catalytically reducing DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2003-03-04 US disclosed
EP-0924193-B1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEM (JP) 2003-02-19 EP disclosed
EP-0939134-B1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEM (JP) 2002-09-11 EP disclosed
US-6114582-A DECYCLIZATION TO FORM A CHEMICAL INTERMEDIATE FOR PRODUCING AN ANTI-OBESITY AGENT AND ANTIDIABETIC AGENT DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2000-09-05 US disclosed
EP-0654534-B1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEM (JP) 2000-03-01 EP disclosed
EP-0939134-A1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1999-09-01 EP disclosed
EP-0924193-A1 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1999-06-23 EP disclosed
EP-0924194-A2 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1999-06-23 EP disclosed
US-5629200-A MICROORGANISM DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1997-05-13 US disclosed
EP-0654534-A2 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1995-05-24 EP disclosed