Pruvanserin

Pruvanserin

SCHEMBL678953

Cl.N#Cc1c[nH]c2c(C(=O)N3CCN(CCc4ccc(F)cc4)CC3)cccc12

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

HTR2A

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

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
HTR2A known ✓ P28223 6/20 0.98
HTR2C P28335 4/20 0.98
DRD4 P21917 1/20 0.98
SLC6A2 P23975 1/20 0.98
HTR1D P28221 1/20 0.98
SLC6A4 P31645 1/20 0.98
HTR7 P34969 1/20 0.98
HTR2B P41595 1/20 0.98
TMEM97 Q5BJF2 1/20 0.98
SIGMAR1 Q99720 1/20 0.98
KCNH2 Q12809 1/20 0.76
POLB P06746 1/20 0.44
GAA P10253 1/20 0.44
PRKAA2 P54646 1/20 0.43
HSD11B1 P28845 1/20 0.40

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
Pruvanserin SCHEMBL29489913 1.00 HTR2A (0.98) HTR2AHTR2CDRD4SLC6A2HTR1D
Pruvanserin SCHEMBL678751 0.99 HTR2A (1.00) HTR2AHTR2CDRD4SLC6A2HTR1D
Pruvanserin SCHEMBL9104227 0.99 HTR2A (1.00) HTR2AHTR2CDRD4SLC6A2HTR1D
Pruvanserin SCHEMBL29379046 0.99 HTR2A (1.00) HTR2AHTR2CDRD4SLC6A2HTR1D
Pruvanserin SCHEMBL3902103 0.95 HTR2A (0.93) HTR2AHTR2CDRD4SLC6A2HTR1D
Pruvanserin SCHEMBL3914362 0.95 HTR2A (0.93) HTR2AHTR2CDRD4SLC6A2HTR1D
SCHEMBL6110393 0.90 HTR2A (0.84) HTR2AHTR2CDRD4SLC6A2HTR1D
SCHEMBL5280317 0.90 HTR2A (0.84) HTR2AHTR2CDRD4SLC6A2HTR1D
SCHEMBL6112038 0.90 HTR2A (0.83) HTR2AHTR2CDRD4SLC6A2HTR1D
Hydrochloric Acid SCHEMBL27520162 0.87 HTR2A (0.98) HTR2AHTR2CDRD4SLC6A2HTR1D

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101027284-B Novel crystalline form of (3-cyano-1H-indol-7-yl)-[4-(4-fluorophenethyl)-piperazine-1-yl]-methanone hydrochloride MERCK PATENT GMBH 2010-09-29 CN claimed
CN-101027284-A Novel crystalline form of (3-cyano-1H-indol-7-yl)-[4-(4-fluorophenethyl)-piperazine-1-yl]-methanone hydrochloride MERCK PATENT GMBH (DE) 2007-08-29 CN claimed
EP-2288345-B1 PSYCHO-PHARMACEUTICALS UNIV DUBLIN (IE) 2015-06-10 EP disclosed
US-8507528-B2 2-alkyl-indazole compounds for the treatment of certain cns-related disorders AZIENDE CHIMICHE RIUNITE ANGELINI FRANCESCO A.C.R.A.F. S.P.A. (IT) 2013-08-13 US disclosed
CN-101558057-B 2 -alkyl- indazole compounds for the treatment of certain cns-related disorders ACRAF 2013-05-01 CN disclosed
EP-2099780-B1 2 -ALKYL- INDAZOLE COMPOUNDS FOR THE TREATMENT OF CERTAIN CNS-RELATED DISORDERS ACRAF (IT) 2013-01-09 EP disclosed
US-20110319386-A1 NEUROGENESIS BY MUSCARINIC RECEPTOR MODULATION BRAINCELLS INC. (US) 2011-12-29 US disclosed
US-20110269717-A1 NEUROGENESIS BY MODULATING ANGIOTENSIN BRAINCELLS INC. (US) 2011-11-03 US disclosed
EP-2382975-A2 Neurogenesis by modulating angiotensin Braincells, Inc. (US) 2011-11-02 EP disclosed
EP-2377530-A2 Modulation of neurogenesis by PDE inhibition Braincells, Inc. (US) 2011-10-19 EP disclosed
US-7998971-B2 2-(2-oxopyrrolidin- 1 -yl)-N-(2,3 -dimethyl-5,6,7,8-tetrahydrofuro[2,3-b]quinolin-4-yl)acetoamide (MKC-231) and a second active ingredient for treating central or peripheral nervous system disorders increase neurogenesis; synergistic; drug addiction, psychological disorders, transplant rejection BRAINCELLS INC. (US) 2011-08-16 US disclosed
WO-2007053596-A1 GABA RECEPTOR MEDIATED MODULATION OF NEUROGENESIS BRAINCELLS, INC. (US) 2007-05-10 WO disclosed
US-20070078083-A1 MODULATION OF NEUORGENESIS BY HDac INHIBITION BRAINCELLS, INC. (US) 2007-04-05 US disclosed
WO-2007030697-A2 MODULATION OF NEUROGENESIS BY HDAC INHIBITION BRAINCELLS, INC. (US) 2007-03-15 WO disclosed
US-20070049576-A1 NEUROGENESIS BY MUSCARINIC RECEPTOR MODULATION BRAINCELLS, INC. (US) 2007-03-01 US disclosed
WO-2006034774-A1 NOVEL CRYSTALLINE FORM OF (3-CYANO-1H-INDOL-7-YL)-[4-(4-FLUOROPHENETHYL)-PIPERAZINE-1-YL]-METHANONE HYDROCHLORIDE MERCK PATENT GMBH (DE) 2006-04-06 WO disclosed
CN-1229345-C N-(indolcarbonyl) piperazin derivatives MERCK PATENT GMBH (DE) 2005-11-30 CN disclosed
CN-1213029-C Process for the preparation of (3-cyano-1H-indol-7-yl) (4-(4-fluorophenethyl)piperazin-1-yl)-methanone and salts thereof MERCH PATENT GMBH (DE) 2005-08-03 CN disclosed
CN-1487923-A Process for the preparation of (3-cyano-1H-indol-7-yl) (4- (4-fluorophenethyl) piperazin-1-yl) -methanone and salts thereof Ĭ��ר���ɷ����޹�˾ 2004-04-07 CN disclosed
CN-1364157-A N-(indolcarbonyl) piperazin derivatives MERCK PATENT GMBH (DE) 2002-08-14 CN 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-20110319386-A1 NEUROGENESIS BY MUSCARINIC RECEPTOR MODULATION CHRNB2, CHAT, CHRNB4 HTR2A 406/4885HTR2C 660/4885DRD4 1926/4885
US-20070078083-A1 MODULATION OF NEUORGENESIS BY HDac INHIBITION DCX, BDNF, NTRK2 HTR2A 3184/4885HTR2C 3530/4885DRD4 4415/4885
US-20110269717-A1 NEUROGENESIS BY MODULATING ANGIOTENSIN NGF, DCX, BDNF HTR2A 1201/4885HTR2C 1631/4885DRD4 1701/4885
US-20070049576-A1 NEUROGENESIS BY MUSCARINIC RECEPTOR MODULATION CHRNB2, CHAT, CHRNB4 HTR2A 406/4885HTR2C 660/4885DRD4 1926/4885

“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.