SCHEMBL7148232

SCHEMBL7148232

CNc1c(Cl)cc([C@@H](O)CN)cc1Cl

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.42
ADRB2 P07550 2/20 0.42
ADRB1 P08588 2/20 0.42
ADRA1A P35348 2/20 0.42
TSHR P16473 2/20 0.42
HTR1A P08908 1/20 0.42
SLC6A2 P23975 1/20 0.42
SLC6A4 P31645 1/20 0.42
OPRK1 P41145 1/20 0.42
SLC6A3 Q01959 1/20 0.42
KDM4E B2RXH2 3/20 0.41
CYP3A4 P08684 2/20 0.41
TAAR1 Q96RJ0 3/20 0.39
APEX1 P27695 3/20 0.39
TDP1 Q9NUW8 3/20 0.39
BLM P54132 3/20 0.39
ADRB3 P13945 3/20 0.39
MAPT P10636 2/20 0.39
HPGD P15428 2/20 0.39
RECQL P46063 2/20 0.39

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
SCHEMBL7151236 0.79 LMNA (0.42) LMNAADRB2ADRB1ADRA1ATSHR
SCHEMBL7150188 0.78 HPGD (0.45) LMNAADRB2ADRB1ADRA1ATSHR
SCHEMBL7154509 0.78 BLM (0.39) LMNAADRB2ADRB1ADRA1ATSHR
SCHEMBL7148286 0.78 ADRA2C (0.43) LMNAADRB2ADRB1ADRA1ATSHR
SCHEMBL3983553 0.76 ADRB1 (0.56) LMNAADRB2ADRB1ADRA1ATSHR
SCHEMBL6323504 0.76 ADRB1 (0.56) LMNAADRB2ADRB1ADRA1ATSHR
SCHEMBL10614906 0.76 LMNA (0.69) LMNAADRB2ADRB1ADRA1ATSHR
SCHEMBL7143103 0.74 NLRP3 (0.47) LMNATSHRKDM4EMAPTKMT2A
SCHEMBL8402182 0.71 BLM (0.47) LMNAADRB2ADRB1ADRA1ATSHR
SCHEMBL7151603 0.71 BLM (0.47) LMNAADRB2ADRB1ADRA1ATSHR

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