SCHEMBL8863508

SCHEMBL8863508

O=C(/C=C/C1CC1)N1C(=O)OCC1c1ccccc1

nearest known ligand 0.41

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.41
GAA P10253 1/20 0.41
HTT P42858 1/20 0.41
NPC1 O15118 1/20 0.41
LMNA P02545 1/20 0.41
TP53 P04637 1/20 0.41
HPGD P15428 1/20 0.41
RAB9A P51151 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
NPSR1 Q6W5P4 1/20 0.41
AVPR1A P37288 1/20 0.37
IDH1 O75874 7/20 0.37
RIPK1 Q13546 1/20 0.35
PADI4 Q9UM07 2/20 0.35
NAAA Q02083 1/20 0.34
GLS O94925 2/20 0.34
HDAC8 Q9BY41 1/20 0.34

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
SCHEMBL8863514 1.00 ALDH1A1 (0.41) ALDH1A1GAAHTTNPC1LMNA
SCHEMBL8863509 1.00 ALDH1A1 (0.41) ALDH1A1GAAHTTNPC1LMNA
SCHEMBL17078163 0.93 RIPK1 (0.39) ALDH1A1GAAHTTNPC1LMNA
SCHEMBL16439471 0.93 RIPK1 (0.39) ALDH1A1GAAHTTNPC1LMNA
SCHEMBL17078162 0.93 RIPK1 (0.39) ALDH1A1GAAHTTNPC1LMNA
SCHEMBL17800375 0.93 RIPK1 (0.39) ALDH1A1GAAHTTNPC1LMNA
SCHEMBL17086509 0.89 SMN1; SMN2 (0.37) ALDH1A1GAAHTTNPC1LMNA
SCHEMBL18603657 0.89 SMN1; SMN2 (0.37) ALDH1A1GAAHTTNPC1LMNA
SCHEMBL18603655 0.89 SMN1; SMN2 (0.37) ALDH1A1GAAHTTNPC1LMNA
SCHEMBL18603429 0.86 ALDH1A1 (0.37) ALDH1A1GAAHTTNPC1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5668164-A Process for synthesis of chiral cis-and trans-3-amino-4 substituted pyrrolidine compounds ABBOTT LABORATORIES (US) 1997-09-16 US disclosed
US-5618949-A Process for synthesis of chiral cis- and trans-3-amino-4-substituted pyrrolidine compounds ABBOTT LABORATORIES (US) 1997-04-08 US disclosed