SCHEMBL7154320

SCHEMBL7154320

C[C@H](Cc1ccc(O)c(O)c1)NC[C@H](O)c1ccc(O)c(O)c1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ADRB2 P07550 15/20 0.68
MAPK1 P28482 8/20 0.68
MAPT P10636 7/20 0.68
CYP3A4 P08684 7/20 0.68
TSHR P16473 6/20 0.68
HSD17B10 Q99714 6/20 0.68
TDP1 Q9NUW8 6/20 0.68
KDM4E B2RXH2 6/20 0.68
ADRB1 P08588 5/20 0.68
HIF1A Q16665 5/20 0.68
ADRB3 P13945 4/20 0.68
MEN1 O00255 4/20 0.68
KMT2A Q03164 4/20 0.68
CYP1A2 P05177 4/20 0.68
MTOR P42345 3/20 0.68
ADORA3 P0DMS8 3/20 0.68
ADRA1A P35348 3/20 0.68
NFKB1 P19838 3/20 0.68
ALDH1A1 P00352 2/20 0.68
DRD2 P14416 2/20 0.68

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
SCHEMBL7154315 1.00 ADRB2 (0.68) ADRB2MAPK1MAPTCYP3A4TSHR
SCHEMBL29899656 0.92 ADRB2 (0.78) ADRB2MAPK1MAPTCYP3A4TSHR
SCHEMBL2455273 0.92 ADRB2 (0.78) ADRB2MAPK1MAPTCYP3A4TSHR
SCHEMBL8986831 0.89 ADRB2 (0.68) ADRB2MAPK1MAPTCYP3A4TSHR
SCHEMBL7149089 0.89 ADRB2 (0.74) ADRB2MAPK1MAPTCYP3A4TSHR
SCHEMBL11807907 0.89 ADRB2 (0.74) ADRB2MAPK1MAPTCYP3A4TSHR
SCHEMBL7149088 0.89 ADRB2 (0.74) ADRB2MAPK1MAPTCYP3A4TSHR
SCHEMBL18769898 0.88 ADRB2 (0.74) ADRB2MAPK1MAPTCYP3A4TSHR
SCHEMBL11810215 0.87 ADRB2 (0.73) ADRB2MAPK1MAPTCYP3A4TSHR
SCHEMBL11843447 0.86 ADRB2 (0.54) ADRB2MAPK1MAPTCYP3A4TSHR

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 12 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-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