SCHEMBL5871923

SCHEMBL5871923

O=C(c1ccccc1)N1CC[C@@H](O)C1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACHE P22303 1/20 0.62
GRM5 P41594 1/20 0.60
EPHX1 P07099 1/20 0.57
L3MBTL3 Q96JM7 1/20 0.57
L3MBTL1 Q9Y468 1/20 0.57
SLC18A3 Q16572 2/20 0.56
HPGD P15428 1/20 0.55
NPC1 O15118 1/20 0.54
RAB9A P51151 1/20 0.54
ATM Q13315 1/20 0.54
PDK2 Q15119 1/20 0.53
KDM4E B2RXH2 1/20 0.52
KMT2A Q03164 1/20 0.52
SMN1; SMN2 Q16637 1/20 0.52
SIGMAR1 Q99720 1/20 0.51
CHRNB2 P17787 1/20 0.51
CHRNB4 P30926 1/20 0.51
CHRNA3 P32297 1/20 0.51
CHRNA7 P36544 1/20 0.51
CHRNA4 P43681 1/20 0.51

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
SCHEMBL2720515 1.00 ACHE (0.62) ACHEGRM5EPHX1L3MBTL3L3MBTL1
SCHEMBL12442621 1.00 ACHE (0.62) ACHEGRM5EPHX1L3MBTL3L3MBTL1
SCHEMBL10098902 0.90 SMN1; SMN2 (0.62) GRM5HPGDKMT2ASMN1; SMN2MGLL
SCHEMBL28200535 0.90 HPGD (0.61) ACHEL3MBTL3L3MBTL1SLC18A3HPGD
SCHEMBL4003986 0.89 GRM5 (0.73) ACHEGRM5EPHX1L3MBTL3L3MBTL1
SCHEMBL6882996 0.87 CHRNB2 (0.51) ACHEGRM5EPHX1L3MBTL3L3MBTL1
SCHEMBL3110491 0.85 CHRNB2 (0.62) ACHEGRM5EPHX1L3MBTL3L3MBTL1
SCHEMBL8919161 0.84 SLC18A3 (0.62) ACHEGRM5EPHX1L3MBTL3L3MBTL1
SCHEMBL2993890 0.83 MGLL (0.55) GRM5L3MBTL3L3MBTL1PDK2MGLL
SCHEMBL4053920 0.83 HDAC4 (0.48) ACHEGRM5L3MBTL3L3MBTL1PDK2

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-3187492-A1 PYRIMIDINONE DERIVATIVE HAVING AUTOTAXIN-INHIBITORY ACTIVITY The University of Tokyo (JP) 2017-07-05 EP disclosed
US-7141412-B2 Process for preparing optically active 3-hydroxypyrrolidine derivatives by enzymatic hydroxylation EIDGENOSSISCHE TECHNISCHE HOCHSCHULE ZURICH (CH) 2006-11-28 US disclosed
EP-1131460-B1 PROCESS FOR PREPARING OPTICALLY ACTIVE 3-HYDROXY-PYRROLIDINE DERIVATIVEES BY ENZYMATIC HYDROXYLATION EIDGENOESS TECH HOCHSCHULE (CH) 2004-10-06 EP disclosed
EP-1131460-A1 PROCESS FOR PREPARING OPTICALLY ACTIVE 3-HYDROXY-PYRROLIDINE DERIVATIVEES BY ENZYMATIC HYDROXYLATION Eidgenössische Technische Hochschule Zürich (CH) 2001-09-12 EP disclosed
WO-2000029606-A1 PROCESS FOR PREPARING OPTICALLY ACTIVE-3-HYDROXY-PYRROLIDINE DERIVATIVES BY ENZYMATIC HYDROXYLATION Eidgenössische Technische Hochschule Zürich (CH) 2000-05-25 WO disclosed