SCHEMBL7145810

SCHEMBL7145810

CCCC[C@H](Cc1ccccc1)NC[C@H](O)c1ccccc1

nearest known ligand 0.58

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
ADRB3 P13945 7/20 0.58
KDM4E B2RXH2 2/20 0.55
ALDH1A1 P00352 1/20 0.55
SIGMAR1 Q99720 1/20 0.49
ADRB2 P07550 8/20 0.48
ASAH1 Q13510 1/20 0.47
ADRB1 P08588 1/20 0.46
NPC1 O15118 1/20 0.45
LMNA P02545 1/20 0.45
RAB9A P51151 1/20 0.45
SMN1; SMN2 Q16637 1/20 0.45
L3MBTL1 Q9Y468 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
SCHEMBL7145454 1.00 ADRB3 (0.58) ADRB3KDM4EALDH1A1SIGMAR1ADRB2
SCHEMBL7153108 0.91 ADRB2 (0.56) ADRB3KDM4EALDH1A1SIGMAR1ADRB2
SCHEMBL7153113 0.91 ADRB2 (0.56) ADRB3KDM4EALDH1A1SIGMAR1ADRB2
SCHEMBL7152487 0.85 ADRB2 (0.61) ADRB3KDM4EADRB2ADRB1LMNA
SCHEMBL7152484 0.85 ADRB2 (0.61) ADRB3KDM4EADRB2ADRB1LMNA
SCHEMBL25977998 0.82 ADRB2 (0.54) ADRB3SIGMAR1ADRB2ADRB1
Hydrochloric Acid SCHEMBL9489635 0.80 CSNK1E (0.54) ADRB3SIGMAR1
SCHEMBL25469667 0.80 KDM4E (0.55) KDM4EALDH1A1ADRB2ASAH1NPC1
SCHEMBL7153925 0.79 ADRB2 (0.52) ADRB3KDM4ESIGMAR1ADRB2ADRB1
SCHEMBL7153921 0.79 ADRB2 (0.52) ADRB3KDM4ESIGMAR1ADRB2ADRB1

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