SCHEMBL8948396

SCHEMBL8948396

Cc1cc([C@@H]2CCCN2C(=O)OCc2ccccc2)on1

nearest known ligand 0.52

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
AADAT Q8N5Z0 1/20 0.52
GFER P55789 1/20 0.51
EPHX2 P34913 1/20 0.50
MEN1 O00255 1/20 0.49
KMT2A Q03164 1/20 0.49
PREP P48147 2/20 0.48
CHRNB2 P17787 1/20 0.48
CHRNB4 P30926 1/20 0.48
CHRNA3 P32297 1/20 0.48
CHRNA7 P36544 1/20 0.48
CHRNA4 P43681 1/20 0.48
TMEM97 Q5BJF2 3/20 0.48
SIGMAR1 Q99720 3/20 0.48
ALDH1A1 P00352 1/20 0.48
NPSR1 Q6W5P4 1/20 0.48
TP53 P04637 1/20 0.47

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
SCHEMBL953139 0.81 AADAT (0.52) AADATGFERPREPTMEM97SIGMAR1
SCHEMBL952907 0.81 PREP (0.50) AADATGFERPREPTMEM97SIGMAR1
SCHEMBL953138 0.81 AADAT (0.52) AADATGFERPREPTMEM97SIGMAR1
SCHEMBL952909 0.81 PREP (0.50) AADATGFERPREPTMEM97SIGMAR1
SCHEMBL3556069 0.77 AADAT (0.51) AADATGFERMEN1KMT2APREP
SCHEMBL6468480 0.77 AADAT (0.57) AADATGFERPREPTMEM97SIGMAR1
SCHEMBL12234863 0.77 PREP (0.51) AADATGFERPREPTMEM97SIGMAR1
SCHEMBL955550 0.77 AADAT (0.50) AADATGFERMEN1KMT2APREP
SCHEMBL955548 0.77 AADAT (0.50) AADATGFERMEN1KMT2APREP
SCHEMBL8118536 0.76 CHRNB2 (0.62) EPHX2CHRNB2CHRNB4CHRNA3CHRNA7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5559242-A FROM PYROGLUTAMIC ACID, ESTERIFICATION, REACTION WITH DIANION OF ACETONE OXIME, CYCLIZATION, REDUCTION, ALKYLATION ABBOTT LABORATORIES (US) 1996-09-24 US disclosed
EP-0717741-A1 METHOD OF PREPARING ENANTIOMERICALLY-PURE 3-METHYL-5-(1-ALKYL-2(S)-PYRROLIDINYL)ISOXAZOLES ABBOTT LABORATORIES (US) 1996-06-26 EP disclosed
US-5516912-A FROM PROTECTED 2-OXOPYRROLIDINE ABBOTT LABORATORIES (US) 1996-05-14 US disclosed
US-5508418-A FOR MAKING CHOLINERGIC OR ANXIOLYTIC AGENTS ABBOTT LABORATORIES (US) 1996-04-16 US disclosed
US-5424444-A Reacting N-alkyl-L-proline ester with salt of dianion of acetone oxime or acetonitrile or other imine anion compounds; cyclization, dehydration after reaction with Grignard reagent and hydroxylamine ABBOTT LABORATORIES (US) 1995-06-13 US disclosed
WO-1995007277-A1 METHOD OF PREPARING ENANTIOMERICALLY-PURE 3-METHYL-5-(1-ALKYL-2(S)-PYRROLIDINYL)ISOXAZOLES ABBOTT LABORATORIES (US) 1995-03-16 WO disclosed