SCHEMBL7149381

SCHEMBL7149381

NC[C@H](O)c1cccc(O)c1Cl

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KIF11 P52732 1/20 0.46
TSHR P16473 2/20 0.45
ADRA2A P08913 4/20 0.43
ADRA2B P18089 4/20 0.43
ADRA2C P18825 4/20 0.43
ADRA1A P35348 3/20 0.43
ADRB2 P07550 3/20 0.43
ADRA1B P35368 2/20 0.43
APEX1 P27695 4/20 0.41
TDP1 Q9NUW8 4/20 0.41
TAAR1 Q96RJ0 3/20 0.41
MAPT P10636 3/20 0.41
RECQL P46063 3/20 0.41
BLM P54132 3/20 0.41
KDM4E B2RXH2 3/20 0.41
CYP3A4 P08684 2/20 0.41
HPGD P15428 2/20 0.41
ADRB1 P08588 2/20 0.41
ADRB3 P13945 2/20 0.41
HSD17B10 Q99714 1/20 0.41

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
SCHEMBL166818 0.82 KCNH2 (0.54) TSHRADRB2TAAR1CYP3A4ADRB1
SCHEMBL7147316 0.82 KCNH2 (0.54) TSHRADRB2TAAR1CYP3A4ADRB1
SCHEMBL4334723 0.79 ADRA2A (0.55) TSHRADRA2AADRA2BADRA2CADRA1A
SCHEMBL11043623 0.79 ADRA2A (0.55) TSHRADRA2AADRA2BADRA2CADRA1A
SCHEMBL9120746 0.79 TSHR (0.50) TSHRADRA2AADRA2BADRA2CADRA1A
SCHEMBL7145871 0.79 TSHR (0.50) TSHRADRA2AADRA2BADRA2CADRA1A
SCHEMBL11214367 0.79 TSHR (0.52) KIF11TSHRADRA2AADRA2BADRA2C
Hydrochloric Acid SCHEMBL7838709 0.77 APEX1 (0.48) TSHRADRA2AADRA2BADRA2CADRA1A
SCHEMBL2250 0.76 ADRA2A (0.61) TSHRADRA2AADRA2BADRA2CADRA1A
SCHEMBL7317693 0.74 ADRB2 (0.65) TSHRADRA2AADRA2BADRA2CADRA1A

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 13 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-5811293-A CULTURE PRODUCT AS CHEMICAL INTERMEDIATE FOR ANTI-OBESITY AGENT DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1998-09-22 US 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