SCHEMBL7150334

SCHEMBL7150334

CCc1ccc([C@@H](O)CN)cc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 4/20 0.59
TSHR P16473 3/20 0.59
NFKB1 P19838 3/20 0.59
HIF1A Q16665 2/20 0.59
HTR3A P46098 1/20 0.59
TDP1 Q9NUW8 5/20 0.57
KDM4E B2RXH2 4/20 0.57
APEX1 P27695 3/20 0.57
ALOX15 P16050 1/20 0.57
BLM P54132 5/20 0.48
MAPT P10636 3/20 0.48
RECQL P46063 3/20 0.48
MAPK1 P28482 3/20 0.48
LMNA P02545 3/20 0.48
HPGD P15428 2/20 0.48
ADRB3 P13945 2/20 0.48
MEN1 O00255 1/20 0.48
ADRB2 P07550 1/20 0.48
ADRB1 P08588 1/20 0.48
ADRA2A P08913 1/20 0.48

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
SCHEMBL9639314 1.00 TAAR1 (0.59) TAAR1TSHRNFKB1HIF1AHTR3A
SCHEMBL4074768 0.83 TAAR1 (0.80) TAAR1TSHRNFKB1HIF1AHTR3A
SCHEMBL7148521 0.83 TAAR1 (0.55) TAAR1TSHRNFKB1HIF1AHTR3A
SCHEMBL4284221 0.82 TAAR1 (0.64) TAAR1TSHRNFKB1HIF1AHTR3A
SCHEMBL31435839 0.82 TSHR (0.50) TAAR1TSHRNFKB1TDP1BLM
SCHEMBL3917903 0.82 LMNA (0.60) TAAR1TSHRTDP1ALOX15MAPT
SCHEMBL3917902 0.82 LMNA (0.60) TAAR1TSHRTDP1ALOX15MAPT
SCHEMBL14544262 0.80 TSHR (0.48) TAAR1TSHRTDP1MAPK1LMNA
Hydrochloric Acid SCHEMBL3669220 0.80 APEX1 (0.65) TAAR1TSHRNFKB1HIF1AHTR3A
SCHEMBL15865826 0.80 TSHR (0.48) TAAR1TSHRTDP1MAPK1LMNA

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