SCHEMBL7147935

SCHEMBL7147935

CC(=O)Cc1ccc(C(=O)NCc2ccccc2)cc1

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HDAC6 Q9UBN7 6/20 0.66
HDAC2 Q92769 3/20 0.66
HDAC8 Q9BY41 3/20 0.66
HDAC1 Q13547 5/20 0.65
RAB9A P51151 2/20 0.65
LMNA P02545 1/20 0.65
KDM4E B2RXH2 1/20 0.64
POLB P06746 1/20 0.64
TSHR P16473 1/20 0.64
RECQL P46063 1/20 0.64
HPGD P15428 1/20 0.62
HDAC3 O15379 3/20 0.61
HDAC4 P56524 2/20 0.61
HDAC7 Q8WUI4 2/20 0.61
HDAC10 Q969S8 2/20 0.61
HDAC11 Q96DB2 2/20 0.61
HDAC9 Q9UKV0 2/20 0.61
HDAC5 Q9UQL6 2/20 0.61
EPHX2 P34913 2/20 0.60
NR1H4 Q96RI1 2/20 0.60

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
SCHEMBL12368425 0.87 EPHX2 (0.56) HDAC6HDAC8HDAC1RAB9AKDM4E
SCHEMBL26167954 0.87 HDAC6 (0.56) HDAC6HDAC8HDAC1RAB9AKDM4E
SCHEMBL11900090 0.86 HDAC6 (0.85) HDAC6HDAC2HDAC8HDAC1RAB9A
SCHEMBL16589429 0.85 HDAC6 (0.72) HDAC6HDAC2HDAC8HDAC1RAB9A
SCHEMBL10076233 0.83 HDAC6 (0.70) HDAC6HDAC2HDAC8HDAC1RAB9A
SCHEMBL14811272 0.83 HDAC6 (0.78) HDAC6HDAC2HDAC8HDAC1RAB9A
SCHEMBL457082 0.82 HDAC6 (0.79) HDAC6HDAC2HDAC8HDAC1RAB9A
SCHEMBL178366 0.81 MAPK14 (0.75) HDAC6HDAC2HDAC8HDAC1RAB9A
SCHEMBL16058342 0.81 HDAC6 (0.72) HDAC6HDAC2HDAC8HDAC1RAB9A
SCHEMBL14812554 0.81 HDAC6 (0.70) HDAC6HDAC2HDAC8HDAC1RAB9A

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-5811293-A CULTURE PRODUCT AS CHEMICAL INTERMEDIATE FOR ANTI-OBESITY AGENT DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1998-09-22 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