SCHEMBL6962669

SCHEMBL6962669

COc1cc(NC(C)=O)c(Cl)cc1C(=O)Cl

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AGER Q15109 1/20 0.58
HTT P42858 1/20 0.56
HPGD P15428 7/20 0.52
ALDH1A1 P00352 7/20 0.50
SMN1; SMN2 Q16637 3/20 0.50
KDM4E B2RXH2 3/20 0.49
LMNA P02545 3/20 0.49
MAPT P10636 3/20 0.49
RAB9A P51151 2/20 0.49
NPY1R P25929 1/20 0.49
NPY2R P49146 1/20 0.49
POLB P06746 1/20 0.49
HSD17B10 Q99714 1/20 0.48
NPSR1 Q6W5P4 1/20 0.47
DRD2 P14416 2/20 0.46
DRD4 P21917 2/20 0.46
DRD3 P35462 2/20 0.46
MEN1 O00255 2/20 0.46
KMT2A Q03164 2/20 0.46
GLA P06280 1/20 0.45

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
SCHEMBL14490855 0.89 AGER (0.60) AGERHTTHPGDALDH1A1SMN1; SMN2
SCHEMBL133355 0.88 AGER (0.58) AGERHTTHPGDALDH1A1SMN1; SMN2
SCHEMBL130152 0.88 HTT (0.72) AGERHTTHPGDALDH1A1SMN1; SMN2
SCHEMBL10785852 0.86 AGER (0.45) AGERHTTHPGDALDH1A1SMN1; SMN2
SCHEMBL14490806 0.85 HTT (0.60) AGERHTTHPGDALDH1A1SMN1; SMN2
SCHEMBL20920574 0.85 AGER (0.62) AGERHTTHPGDALDH1A1SMN1; SMN2
SCHEMBL9730411 0.83 LMNA (0.61) AGERHTTALDH1A1SMN1; SMN2KDM4E
SCHEMBL11383600 0.83 MEN1 (0.44) AGERHTTALDH1A1LMNAMAPT
SCHEMBL11179877 0.82 HTT (0.51) AGERHTTHPGDALDH1A1SMN1; SMN2
SCHEMBL10827981 0.81 HTT (0.56) AGERHTTHPGDALDH1A1SMN1; SMN2

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 63 patents — showing the first 20. 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
EP-0550550-B1 3,9-DIAZABICYCLO (3.3.1) NONAN-7-YL DERIVATIVES, PROCESS AND INTERMEDIATES FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM BEECHAM GROUP PLC (GB) 2003-07-16 EP disclosed
US-6110934-A Substituted benzamide derivatives and their use as anticonvulsants SMITHKLINE BEECHAM P.L.C. (GB) 2000-08-29 US disclosed
EP-0906283-A1 SUBSTITUTED BENZAMIDE DERIVATIVES AND THEIR USE AS ANTICONVULSANTS SMITHKLINE BEECHAM PLC (GB) 1999-04-07 EP disclosed
WO-1997048683-A1 SUBSTITUTED BENZAMIDE DERIVATIVES AND THEIR USE AS ANTICONVULSANTS SMITHKLINE BEECHAM PLC (GB) 1997-12-24 WO disclosed
EP-0481756-B1 Benzamide derivatives TEIKOKU CHEM IND CO LTD (JP) 1997-07-09 EP disclosed
US-5237066-A Reacting quinuclidone with (R)-alpha-methylbenzylamine; reduction with alkali metal borohydride; hydrogenolysis in acid DELANDE S.A. (FR) 1993-08-17 US disclosed
US-4329344-A 4-(Phenylalkyl)piperazine-1-carboxamides BEECHAM GROUP LIMITED (GB) 1982-05-11 US disclosed
EP-0047620-A1 Aryl diazabicyclyl amides, a process for their preparation and use BEECHAM GROUP PLC (GB) 1982-03-17 EP disclosed
EP-0034015-A2 Pharmaceutically active compounds BEECHAM GROUP PLC (GB) 1981-08-19 EP disclosed
US-4273778-A TREATMENT OF GASTROINTESTINAL DISORDERS, NERVOUS SYSTEM DISORDERS, AND PSYCHOLOGICAL DISORDERS BEECHAM GROUP, LIMITED (GB) 1981-06-16 US disclosed
US-4267175-A FOR USE AS AN ANTIEMETIC, AND TREATMENT FOR GASTROINTESTINAL DISORDERS BEECHAM GROUP LIMITED (GB) 1981-05-12 US disclosed
US-4223034-A TRANQUILIZERS BEECHAM GROUP LIMITED (GB) 1980-09-16 US disclosed
US-4213983-A Treating gastro-intestinal disorders and emesis with n-(heterocyclic substituted) benzamides BEECHAM GROUP LIMITED (GB) 1980-07-22 US disclosed
EP-0013138-A1 Azabicycloalkyl derivatives, a process for their preparation and pharmaceutical compositions containing them BEECHAM GROUP PLC (GB) 1980-07-09 EP disclosed
US-4163789-A Anti-psychotic (cycloalkenylalkylpiperidino) benzamides ANPHAR, S.A. (ES) 1979-08-07 US disclosed
US-4138492-A FOR TREATMENT OF GASTROINTESTINAL DISORDERS ANPHAR, S.A. (ES) 1979-02-06 US 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 AGER 4101/4885HTT 1816/4885HPGD 2216/4885

“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.