SCHEMBL7147289

SCHEMBL7147289

CCOc1ccc(O)c([C@@H](O)CN)c1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ADRA2A P08913 3/20 0.50
ADRA1A P35348 3/20 0.50
NFKB1 P19838 1/20 0.45
TDP1 Q9NUW8 4/20 0.44
MAPT P10636 3/20 0.44
BLM P54132 3/20 0.44
MEN1 O00255 3/20 0.44
KMT2A Q03164 3/20 0.44
ADRB2 P07550 3/20 0.44
HPGD P15428 2/20 0.44
APEX1 P27695 2/20 0.44
RECQL P46063 2/20 0.44
ADRA2B P18089 2/20 0.44
ADRA2C P18825 2/20 0.44
ADRA1B P35368 2/20 0.44
CYP3A4 P08684 2/20 0.44
LMNA P02545 1/20 0.44
ADRB1 P08588 1/20 0.44
ADORA3 P0DMS8 1/20 0.44
ADRB3 P13945 1/20 0.44

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
SCHEMBL7148830 0.86 ADRA2A (0.46) ADRA2AADRA1ANFKB1TDP1MAPT
SCHEMBL7149085 0.84 ADRA1A (0.70) ADRA2AADRA1ANFKB1TDP1MAPT
SCHEMBL7152597 0.83 ADRA1A (0.63) ADRA2AADRA1ATDP1MEN1KMT2A
SCHEMBL9201107 0.81 TDP1 (0.48) TDP1MAPTMEN1KMT2ACYP3A4
SCHEMBL9461113 0.79 ALDH1A1 (0.44) TDP1MAPTMEN1KMT2ACYP3A4
SCHEMBL7144089 0.79 ADRA2A (0.50) ADRA2AADRA1ATDP1MAPTMEN1
SCHEMBL25244231 0.79 RORC (0.54) TDP1MAPTMEN1KMT2AADRB2
SCHEMBL5710919 0.77 ALDH1A1 (0.45) TDP1MAPTMEN1KMT2AHPGD
SCHEMBL7148796 0.77 NQO1 (0.54) ADRA2AADRA1ANFKB1TDP1MAPT
SCHEMBL1051397 0.75 LTA4H (0.57) TDP1MAPTMEN1KMT2AADRB2

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-0924194-A2 Processes for producing optically active 2-amino-1-phenylethanol derivatives DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1999-06-23 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
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