SCHEMBL7684929

SCHEMBL7684929

COCC(=O)N[C@@H](C)c1ccc(Cl)cc1

nearest known ligand 0.55

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
ACACB O00763 3/20 0.55
ACACA Q13085 1/20 0.55
MEN1 O00255 3/20 0.54
KMT2A Q03164 3/20 0.54
ATM Q13315 1/20 0.54
L3MBTL1 Q9Y468 1/20 0.54
ALDH1A1 P00352 5/20 0.54
SMN1; SMN2 Q16637 4/20 0.54
HPGD P15428 3/20 0.54
POLB P06746 1/20 0.52
KDM4E B2RXH2 1/20 0.52
TSHR P16473 1/20 0.51
GPR139 Q6DWJ6 2/20 0.51
LMNA P02545 2/20 0.51
TP53 P04637 1/20 0.51
MAPT P10636 1/20 0.51
MAPK1 P28482 1/20 0.51
GAA P10253 1/20 0.50
HTT P42858 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
SCHEMBL6253330 1.00 ACACB (0.55) ACACBACACAMEN1KMT2AATM
SCHEMBL6254231 0.85 ACACB (0.56) ACACBACACAMEN1KMT2AL3MBTL1
SCHEMBL6252896 0.85 ACACB (0.56) ACACBACACAMEN1KMT2AL3MBTL1
SCHEMBL13683332 0.84 ALDH1A1 (0.63) ACACBACACAMEN1KMT2AL3MBTL1
SCHEMBL7714868 0.84 ALDH1A1 (0.63) ACACBACACAMEN1KMT2AL3MBTL1
SCHEMBL16714724 0.83 TSHR (0.73) MEN1KMT2AL3MBTL1ALDH1A1SMN1; SMN2
SCHEMBL5016632 0.83 TSHR (0.73) MEN1KMT2AL3MBTL1ALDH1A1SMN1; SMN2
SCHEMBL12384758 0.83 ACACB (0.54) ACACBACACAMEN1KMT2AL3MBTL1
SCHEMBL7897298 0.81 SMN1; SMN2 (0.69) MEN1KMT2AATML3MBTL1ALDH1A1
SCHEMBL8445815 0.81 GPR139 (0.55) ACACBACACAMEN1KMT2AATM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6500986-B1 RACEMIZATION OF OPTICALLY ACTIVE AMIDES; CONVERSION TO AMINES BAYER AKTIENGESELLSCHAFT (DE) 2002-12-31 US claimed
EP-0757981-B1 Process for the preparation of racemic amino derivatives BAYER AG (DE) 2000-02-16 EP claimed
EP-0757981-A1 Process for the preparation of racemic amino derivatives BAYER AG (DE) 1997-02-12 EP claimed
US-6500986-B1 RACEMIZATION OF OPTICALLY ACTIVE AMIDES; CONVERSION TO AMINES BAYER AKTIENGESELLSCHAFT (DE) 2002-12-31 US disclosed
EP-0757981-B1 Process for the preparation of racemic amino derivatives BAYER AG (DE) 2000-02-16 EP disclosed
US-5885787-A Process for preparing optically active amines BAYER AKTIEGESELLSCHAFT (DE) 1999-03-23 US disclosed
EP-0757981-A1 Process for the preparation of racemic amino derivatives BAYER AG (DE) 1997-02-12 EP disclosed