SCHEMBL6155794

SCHEMBL6155794

C[C@H](N[C@H](C)c1ccccc1)C(=O)O

nearest known ligand 0.56

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
APAF1 O14727 1/20 0.55
ACP3 P15309 2/20 0.53
HSD17B10 Q99714 2/20 0.51
KDM4E B2RXH2 1/20 0.51
ALDH1A1 P00352 1/20 0.51
LMNA P02545 1/20 0.51
HPGD P15428 1/20 0.51
MMP9 P14780 1/20 0.49
MMP8 P22894 1/20 0.49
MEN1 O00255 1/20 0.49
KMT2A Q03164 1/20 0.49
SIGMAR1 Q99720 1/20 0.48
CYP2D6 P10635 1/20 0.46
SRC P12931 1/20 0.46
MME P08473 2/20 0.46
TDP1 Q9NUW8 1/20 0.46
POLB P06746 1/20 0.46
CTDSP1 Q9GZU7 1/20 0.46

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
SCHEMBL2481352 1.00 APAF1 (0.55) APAF1ACP3HSD17B10KDM4EALDH1A1
SCHEMBL18722284 1.00 APAF1 (0.55) APAF1ACP3HSD17B10KDM4EALDH1A1
SCHEMBL6809827 1.00 APAF1 (0.55) APAF1ACP3HSD17B10KDM4EALDH1A1
SCHEMBL3823989 1.00 APAF1 (0.55) APAF1ACP3HSD17B10KDM4EALDH1A1
SCHEMBL5513822 0.84 ACP3 (0.50) APAF1ACP3HSD17B10KDM4EALDH1A1
SCHEMBL7365794 0.84 ACP3 (0.50) APAF1ACP3HSD17B10KDM4EALDH1A1
SCHEMBL7342569 0.83 APAF1 (0.55) APAF1ACP3HSD17B10KDM4EALDH1A1
SCHEMBL8766752 0.83 LMNA (0.49) APAF1HSD17B10KDM4EALDH1A1LMNA
SCHEMBL7890911 0.83 LMNA (0.49) APAF1HSD17B10KDM4EALDH1A1LMNA
SCHEMBL9574986 0.83 LMNA (0.49) APAF1HSD17B10KDM4EALDH1A1LMNA

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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0857790-B1 PROCESS FOR PRODUCING OPTICALLY ACTIVE AMINO COMPOUNDS KANEKA CORP (JP) 2005-08-17 EP disclosed
US-6344351-B2 USING (R)-FORM-SPECIFIC TRANSAMINASE WITH KETONE AMINO ACCEPTOR AND AMINO DONOR; ANTIDIABETES AND ANTIOBESITY AGENTS KANEKA CORPORATION (JP) 2002-02-05 US disclosed
US-20010031487-A1 Process for producing optically active amino compounds KANEKA CORPORATION 2001-10-18 US disclosed
US-6221638-B1 BY STEREOSELECTIVELY CARRYING OUT AMINO GROUP TRANSFER BY ACTION OF AN (R)-FORM-SPECIFIC TRANSAMINASE IN THE CO-PRESENCE OF A KETONE (AMINO ACCEPTOR) AND AMINO COMPOUND (AMINO DONOR); YIELDS AMINO COMPOUNDS HAIVNG ARYL GROUP AT THE 1-POSITION KANEKA CORPORATION (JP) 2001-04-24 US disclosed
EP-0857790-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE AMINO COMPOUNDS KANEKA CORPORATION (JP) 1998-08-12 EP disclosed