SCHEMBL7143077

SCHEMBL7143077

CCOc1ccc([C@@H](O)CN)cc1OCC

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NFKB1 P19838 3/20 0.57
BLM P54132 5/20 0.55
PMP22 Q01453 3/20 0.55
KDM4E B2RXH2 5/20 0.49
TDP1 Q9NUW8 4/20 0.49
MAPT P10636 4/20 0.49
LMNA P02545 4/20 0.49
APEX1 P27695 3/20 0.49
RECQL P46063 3/20 0.49
TAAR1 Q96RJ0 3/20 0.49
MAPK1 P28482 3/20 0.49
HPGD P15428 2/20 0.49
ADRA2A P08913 2/20 0.49
ADRA1A P35348 2/20 0.49
MEN1 O00255 1/20 0.49
ADRB2 P07550 1/20 0.49
ADRB1 P08588 1/20 0.49
ADORA3 P0DMS8 1/20 0.49
ADRB3 P13945 1/20 0.49
DRD2 P14416 1/20 0.49

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
SCHEMBL6055107 0.87 LMNA (0.48) NFKB1BLMPMP22KDM4EMAPT
SCHEMBL7151218 0.87 NFKB1 (0.71) NFKB1BLMPMP22KDM4ETDP1
SCHEMBL7149100 0.87 BLM (0.59) NFKB1BLMPMP22KDM4ETDP1
SCHEMBL249737 0.87 NFKB1 (0.71) NFKB1BLMPMP22KDM4ETDP1
Hydrochloric Acid SCHEMBL75743 0.85 BLM (0.72) NFKB1BLMPMP22KDM4ETDP1
SCHEMBL11289905 0.84 MAPK1 (0.45) NFKB1BLMPMP22TDP1MAPT
SCHEMBL6055250 0.83 PDE4D (0.49) MAPTLMNAMEN1KMT2ACYP3A4
SCHEMBL6055497 0.81 PDE4D (0.48) LMNAMEN1KMT2ACYP3A4ALDH1A1
SCHEMBL14985291 0.81 ALDH1A1 (0.46) KDM4EMAPTLMNATAAR1MAPK1
SCHEMBL6055134 0.80 ALDH1A1 (0.48) KDM4EMAPTLMNAMAPK1HPGD

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