SCHEMBL7144095

SCHEMBL7144095

NC[C@H](O)c1cccc(CO)c1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PNMT P11086 1/20 0.54
BLM P54132 5/20 0.48
TDP1 Q9NUW8 4/20 0.48
KDM4E B2RXH2 4/20 0.48
APEX1 P27695 3/20 0.48
MAPT P10636 3/20 0.48
RECQL P46063 3/20 0.48
TAAR1 Q96RJ0 3/20 0.48
HPGD P15428 2/20 0.48
LMNA P02545 2/20 0.48
MAPK1 P28482 2/20 0.48
MEN1 O00255 1/20 0.48
ADRB2 P07550 1/20 0.48
ADRB1 P08588 1/20 0.48
ADRA2A P08913 1/20 0.48
ADORA3 P0DMS8 1/20 0.48
ADRB3 P13945 1/20 0.48
DRD2 P14416 1/20 0.48
ADRA2B P18089 1/20 0.48
ADRA2C P18825 1/20 0.48

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
SCHEMBL27317287 0.86 PNMT (0.56) PNMTBLMTDP1KDM4EAPEX1
SCHEMBL13959620 0.85 PRSS1 (0.41) PNMTADRB2PRSS1PRSS2PRSS3
SCHEMBL10891671 0.83 PNMT (0.53) PNMTBLMTDP1KDM4EAPEX1
SCHEMBL7153571 0.83 PNMT (0.53) PNMTBLMTDP1KDM4EAPEX1
SCHEMBL7149096 0.83 PNMT (0.53) PNMTBLMTDP1KDM4EAPEX1
SCHEMBL24015105 0.81 LMNA (0.55) BLMKDM4ELMNAADRB2ADRB1
SCHEMBL7147971 0.80 PNMT (0.50) PNMTBLMTDP1KDM4EAPEX1
SCHEMBL7145461 0.80 PNMT (0.50) PNMTBLMTDP1KDM4EAPEX1
SCHEMBL10606510 0.79 ENPP2 (0.47) TSHRPRSS1PRSS2PRSS3PRKCI
SCHEMBL14943966 0.79 TAAR1 (0.59) TAAR1TSHRPRSS1PRSS2PRSS3

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