SCHEMBL8293162

SCHEMBL8293162

CCOC(=O)C1CN2CCCC(C2)C1=O

nearest known ligand 0.46

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 9/20 0.43
SMN1; SMN2 Q16637 3/20 0.43
MAPT P10636 2/20 0.43
HPGD P15428 3/20 0.41
RAB9A P51151 2/20 0.41
NPC1 O15118 1/20 0.41
TSHR P16473 1/20 0.41
MEN1 O00255 4/20 0.39
KMT2A Q03164 4/20 0.39
POLB P06746 1/20 0.39
TLR4 O00206 1/20 0.39
KDM4E B2RXH2 1/20 0.38
GAA P10253 1/20 0.38
HSD17B10 Q99714 1/20 0.38
CYP2C19 P33261 1/20 0.38

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
Hydrochloric Acid SCHEMBL5419363 0.99 ALDH1A1 (0.42) ALDH1A1SMN1; SMN2MAPTHPGDRAB9A
SCHEMBL8554532 0.91 MAPT (0.44) ALDH1A1SMN1; SMN2MAPTHPGDMEN1
SCHEMBL19360209 0.75 ALDH1A1 (0.53) ALDH1A1SMN1; SMN2MAPTHPGDTSHR
SCHEMBL14810505 0.73 ALDH1A1 (0.43) ALDH1A1SMN1; SMN2MAPTRAB9ATSHR
SCHEMBL20988214 0.72 MEN1 (0.46) ALDH1A1SMN1; SMN2MAPTHPGDRAB9A
SCHEMBL4077853 0.71 TLR4 (0.55) ALDH1A1SMN1; SMN2MAPTHPGDMEN1
SCHEMBL19349886 0.71 ALDH1A1 (0.48) ALDH1A1SMN1; SMN2MAPTHPGDTSHR
SCHEMBL4080364 0.70 ALDH1A1 (0.51) ALDH1A1MAPTHPGDRAB9AMEN1
SCHEMBL16609900 0.70 MEN1 (0.47) ALDH1A1SMN1; SMN2MAPTHPGDMEN1
SCHEMBL23228558 0.69 MEN1 (0.46) ALDH1A1SMN1; SMN2MAPTHPGDRAB9A

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-20070135641-A1 Synthesis PALMER RICHARD M J 2007-06-14 US disclosed
US-20070135641-A1 Synthesis PALMER RICHARD M J 2007-06-14 US disclosed
US-7189852-B2 Preparing renzapride (hydrochloride) on a laboratory or industrial scale by a simplified process of forming the acyl chloride derivative of 2-(methoxy),3-acyamino,5-chlorobenzoic acid by reacting oxalyl or thionyl chloride in a solvent, e.g. dimethylformamide; coupling with 1-diazabicylo(3.3.1)nonane ALIZYME THERAPEUTICS LIMITED (GB) 2007-03-13 US disclosed
US-7189852-B2 Preparing renzapride (hydrochloride) on a laboratory or industrial scale by a simplified process of forming the acyl chloride derivative of 2-(methoxy),3-acyamino,5-chlorobenzoic acid by reacting oxalyl or thionyl chloride in a solvent, e.g. dimethylformamide; coupling with 1-diazabicylo(3.3.1)nonane ALIZYME THERAPEUTICS LIMITED (GB) 2007-03-13 US disclosed
WO-2005023808-A2 PROCESS FOR THE PREPARATION OF RENZAPRIDE AND INTERMEDIATES THEREOF ALIZYME THERAPEUTICS LIMITED (GB) 2005-03-17 WO disclosed
US-4870081-A DEMENTIA BEECHAM GROUP P.L.C. (GB) 1989-09-26 US disclosed
EP-0257741-A2 Azabicyclic compounds, process and intermediates for their preparation and pharmaceutical compositions containing them BEECHAM GROUP PLC (GB) 1988-03-02 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20070135641-A1 Synthesis ALKBH5, AZI2, ALKBH1 ALDH1A1 374/4885SMN1; SMN2 2841/4885MAPT 2366/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.