SCHEMBL7154333

SCHEMBL7154333

COc1ccc(C[C@@H](C)NC[C@H](O)c2ccccc2F)cc1OC

nearest known ligand 0.50

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
ADRB1 P08588 3/20 0.50
ADRB3 P13945 3/20 0.50
ADRB2 P07550 12/20 0.46
SIGMAR1 Q99720 1/20 0.45
KDM1A O60341 1/20 0.45
ALDH1A1 P00352 1/20 0.45
LMNA P02545 1/20 0.45

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
SCHEMBL7154329 1.00 ADRB1 (0.50) ADRB1ADRB3ADRB2SIGMAR1KDM1A
SCHEMBL11088887 0.90 ADRB1 (0.54) ADRB1ADRB3ADRB2SIGMAR1KDM1A
SCHEMBL7152845 0.90 ADRB1 (0.54) ADRB1ADRB3ADRB2SIGMAR1KDM1A
SCHEMBL7152844 0.90 ADRB1 (0.54) ADRB1ADRB3ADRB2SIGMAR1KDM1A
Hydrochloric Acid SCHEMBL11084224 0.89 ADRB1 (0.53) ADRB1ADRB3ADRB2SIGMAR1KDM1A
SCHEMBL7148280 0.87 ADRB1 (0.51) ADRB1ADRB3ADRB2
SCHEMBL7146992 0.87 ADRB1 (0.51) ADRB1ADRB3ADRB2SIGMAR1KDM1A
SCHEMBL7148275 0.87 ADRB1 (0.51) ADRB1ADRB3ADRB2
SCHEMBL11088831 0.87 ADRB1 (0.51) ADRB1ADRB3ADRB2
SCHEMBL7146988 0.87 ADRB1 (0.51) ADRB1ADRB3ADRB2SIGMAR1KDM1A

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 10 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
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
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-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