Renzapride

Renzapride

SCHEMBL5367707

COc1cc(N)c(Cl)cc1C(=O)NC1CCN2CCCC1C2.Cl

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

HTR3AHTR3BHTR3CHTR3DHTR3EHTR4

The experimentally established mechanism targets of Renzapride. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR3A known ✓ P46098 7/20 0.98
HTR3E known ✓ A5X5Y0 3/20 0.98
HTR3B known ✓ O95264 3/20 0.98
HTR3D known ✓ Q70Z44 3/20 0.98
HTR3C known ✓ Q8WXA8 3/20 0.98
NPSR1 Q6W5P4 1/20 0.98
MAPK1 P28482 1/20 0.76
HTR5A P47898 1/20 0.76
MEN1 O00255 1/20 0.76
CYP2D6 P10635 1/20 0.76
CYP2C9 P11712 1/20 0.76
CYP2C19 P33261 1/20 0.76
KMT2A Q03164 1/20 0.76
ADRA2A P08913 1/20 0.60
ADRA2B P18089 1/20 0.60
ADRA2C P18825 1/20 0.60
HTR2A P28223 1/20 0.60
HTR2C P28335 1/20 0.60
HTR2B P41595 1/20 0.60
DRD2 P14416 1/20 0.59

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
Renzapride SCHEMBL5765864 1.00 HTR3A (0.98) HTR3AHTR3EHTR3BHTR3DHTR3C
Renzapride SCHEMBL5371909 1.00 HTR3A (0.98) HTR3AHTR3EHTR3BHTR3DHTR3C
Renzapride SCHEMBL5767174 0.99 HTR3A (0.96) HTR3AHTR3EHTR3BHTR3DHTR3C
Renzapride SCHEMBL5371617 0.99 HTR3A (0.96) HTR3AHTR3EHTR3BHTR3DHTR3C
Renzapride SCHEMBL17037 0.99 HTR3A (1.00) HTR3AHTR3EHTR3BHTR3DHTR3C
Renzapride SCHEMBL678616 0.99 HTR3A (1.00) HTR3AHTR3EHTR3BHTR3DHTR3C
Renzapride SCHEMBL4534994 0.99 HTR3A (1.00) HTR3AHTR3EHTR3BHTR3DHTR3C
Renzapride SCHEMBL1650356 0.97 HTR3A (0.96) HTR3AHTR3EHTR3BHTR3DHTR3C
SCHEMBL8292934 0.88 HTR3A (0.80) HTR3AHTR3EHTR3BHTR3DHTR3C
Zacopride SCHEMBL667580 0.88 MAPK1 (0.98) HTR3AHTR3EHTR3BHTR3DHTR3C

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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7176198-B2 1H-pyrazole and 1H-pyrrole-azabicyclic compounds for the treatment of disease PFIZER INC. (US) 2007-02-13 US claimed
US-20060116395-A1 1H-pyrazole and 1h-pyrole-azabicyclic compounds for the treatment of disease PFIZER INC 2006-06-01 US claimed
US-20040087616-A1 1H-pyrazole and 1H-pyrrole-azabicyclic compounds for the treatment of disease PIOTROWSKI DAVID W (US) 2004-05-06 US claimed
EP-0239321-B1 CHEMICAL COMPOUND BEECHAM GROUP PLC (GB) 1993-06-16 EP claimed
EP-0239321-A2 Chemical compound BEECHAM GROUP PLC (GB) 1987-09-30 EP claimed
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
US-7176198-B2 1H-pyrazole and 1H-pyrrole-azabicyclic compounds for the treatment of disease PFIZER INC. (US) 2007-02-13 US disclosed
EP-1664048-A2 PROCESS FOR THE PREPARATION OF RENZAPRIDE AND INTERMEDIATES THEREOF Alizyme Therapeutics Limited (GB) 2006-06-07 EP disclosed
US-20060116395-A1 1H-pyrazole and 1h-pyrole-azabicyclic compounds for the treatment of disease PFIZER INC 2006-06-01 US disclosed
US-20050049416-A1 Synthesis ENDOLOGIC LLC 2005-03-03 US disclosed
US-20050049416-A1 Synthesis ENDOLOGIC LLC 2005-03-03 US disclosed
US-20040087616-A1 1H-pyrazole and 1H-pyrrole-azabicyclic compounds for the treatment of disease PIOTROWSKI DAVID W (US) 2004-05-06 US disclosed
EP-0560348-B1 Thieno 3,2-b pyridine derivatives for the treatment of gastrointestinal disorders MITSUBISHI CHEM CORP (JP) 2002-07-10 EP disclosed
US-5352685-A Gastrointestinal disorders MITSUBISHI KASEI CORPORATION (JP) 1994-10-04 US disclosed
EP-0560348-A1 Thieno 3,2-b pyridine derivatives for the treatment of gastrointestinal disorders Mitsubishi Chemical Corporation (JP) 1993-09-15 EP disclosed
US-4800225-A Pharmacologically active hydrated azabicyclo compound BEECHAM GROUP, P.L.C. (GB) 1989-01-24 US disclosed
EP-0239321-A2 Chemical compound BEECHAM GROUP PLC (GB) 1987-09-30 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 (4 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-20050049416-A1 Synthesis ALKBH5, AZI2, ALKBH1 HTR3A 602/4885HTR3E 953/4885HTR3B 795/4885
US-20070135641-A1 Synthesis ALKBH5, AZI2, ALKBH1 HTR3A 602/4885HTR3E 953/4885HTR3B 795/4885
US-20060116395-A1 1H-pyrazole and 1h-pyrole-azabicyclic compounds for the treatment of disease CYP7B1, P2RX7, CYP3A7 HTR3A 791/4885HTR3E 1732/4885HTR3B 537/4885
US-20040087616-A1 1H-pyrazole and 1H-pyrrole-azabicyclic compounds for the treatment of disease CYP1B1, TPMT, CYP7B1 HTR3A 2651/4885HTR3E 3531/4885HTR3B 2381/4885

“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.