SCHEMBL7148510

SCHEMBL7148510

NC[C@H](O)c1ccccc1OC(=O)Cc1ccccc1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPK1 P28482 2/20 0.49
SMN1; SMN2 Q16637 1/20 0.46
TSHR P16473 1/20 0.46
L3MBTL1 Q9Y468 2/20 0.45
ALDH1A1 P00352 1/20 0.45
ATM Q13315 1/20 0.44
TDP1 Q9NUW8 1/20 0.44
PAM P19021 1/20 0.44
CYP19A1 P11511 1/20 0.43
UCHL1 P09936 1/20 0.41
USP5 P45974 1/20 0.41
USP4 Q13107 1/20 0.41
SENP1 Q9P0U3 1/20 0.41
KCNH2 Q12809 1/20 0.40
CES2 O00748 1/20 0.40
CES1 P23141 1/20 0.40
AKR1B1 P15121 1/20 0.40
HPGD P15428 1/20 0.40
KMT2A Q03164 1/20 0.40
ADRB2 P07550 1/20 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
SCHEMBL10573912 0.81 MAPK1 (0.61) MAPK1SMN1; SMN2TSHRL3MBTL1ALDH1A1
SCHEMBL1200603 0.79 MAPK1 (0.47) MAPK1SMN1; SMN2TSHRL3MBTL1ALDH1A1
SCHEMBL7153668 0.76 SGMS2 (0.49) MAPK1L3MBTL1ALDH1A1TDP1
SCHEMBL12322209 0.76 SGMS2 (0.49) MAPK1L3MBTL1ALDH1A1TDP1
SCHEMBL31321692 0.74 L3MBTL1 (0.57) MAPK1SMN1; SMN2TSHRL3MBTL1ALDH1A1
SCHEMBL28754026 0.74 SMN1; SMN2 (0.53) MAPK1SMN1; SMN2TSHRL3MBTL1ALDH1A1
SCHEMBL7146801 0.74 MEN1 (0.44) TSHRL3MBTL1KCNH2CES2CES1
SCHEMBL1171372 0.73 L3MBTL1 (0.60) MAPK1SMN1; SMN2TSHRL3MBTL1ALDH1A1
SCHEMBL1358287 0.73 KDM4E (0.59) MAPK1SMN1; SMN2TSHRL3MBTL1ALDH1A1
SCHEMBL2639771 0.73 L3MBTL1 (0.74) MAPK1SMN1; SMN2TSHRL3MBTL1ALDH1A1

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