SCHEMBL7148196

SCHEMBL7148196

CC(=O)c1ccc(C[C@@H](C)NC[C@H](O)c2ccccc2)cc1

nearest known ligand 0.79

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ADRB1 P08588 10/20 0.79
ADRB3 P13945 10/20 0.79
ADRB2 P07550 10/20 0.58
CASP3 P42574 1/20 0.57
CASP6 P55212 1/20 0.57
CYP3A4 P08684 2/20 0.52
MAPK1 P28482 2/20 0.52
CYP2D6 P10635 1/20 0.52
TSHR P16473 1/20 0.52
HIF1A Q16665 1/20 0.52
HSD17B10 Q99714 1/20 0.52
ADORA3 P0DMS8 1/20 0.52
PTGS1 P23219 1/20 0.52
SLC6A2 P23975 1/20 0.52
HTR2A P28223 1/20 0.52
SLC6A4 P31645 1/20 0.52
MC4R P32245 1/20 0.52
ADRA1A P35348 1/20 0.52
OPRM1 P35372 1/20 0.52
MC3R P41968 1/20 0.52

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
SCHEMBL11184120 1.00 ADRB1 (0.79) ADRB1ADRB3ADRB2CASP3CASP6
SCHEMBL7148194 1.00 ADRB1 (0.79) ADRB1ADRB3ADRB2CASP3CASP6
SCHEMBL7143114 0.90 ADRB1 (0.95) ADRB1ADRB3ADRB2CASP3CASP6
SCHEMBL7143110 0.90 ADRB1 (0.95) ADRB1ADRB3ADRB2CASP3CASP6
SCHEMBL9006683 0.90 ADRB1 (0.95) ADRB1ADRB3ADRB2CASP3CASP6
SCHEMBL7152836 0.88 ADRB1 (0.77) ADRB1ADRB3ADRB2CASP3CASP6
SCHEMBL11174788 0.88 ADRB3 (0.77) ADRB1ADRB3ADRB2CASP3CASP6
SCHEMBL7152841 0.88 ADRB1 (0.77) ADRB1ADRB3ADRB2CASP3CASP6
SCHEMBL7153666 0.88 ADRB3 (0.77) ADRB1ADRB3ADRB2CASP3CASP6
SCHEMBL9006725 0.88 ADRB3 (0.77) ADRB1ADRB3ADRB2CASP3CASP6

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 11 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