Pruvanserin

Pruvanserin

SCHEMBL678751

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

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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 1.00
HTR2C P28335 4/20 1.00
DRD4 P21917 1/20 1.00
SLC6A2 P23975 1/20 1.00
HTR1D P28221 1/20 1.00
SLC6A4 P31645 1/20 1.00
HTR7 P34969 1/20 1.00
HTR2B P41595 1/20 1.00
TMEM97 Q5BJF2 1/20 1.00
SIGMAR1 Q99720 1/20 1.00
KCNH2 Q12809 1/20 0.77
POLB P06746 1/20 0.44
GAA P10253 1/20 0.44
PRKAA2 P54646 1/20 0.44
HSD11B1 P28845 1/20 0.41

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 SCHEMBL9104227 1.00 HTR2A (1.00) HTR2AHTR2CDRD4SLC6A2HTR1D
Pruvanserin SCHEMBL29379046 1.00 HTR2A (1.00) HTR2AHTR2CDRD4SLC6A2HTR1D
Pruvanserin SCHEMBL678953 0.99 HTR2A (0.98) HTR2AHTR2CDRD4SLC6A2HTR1D
Pruvanserin SCHEMBL29489913 0.99 HTR2A (0.98) HTR2AHTR2CDRD4SLC6A2HTR1D
Pruvanserin SCHEMBL3902103 0.96 HTR2A (0.93) HTR2AHTR2CDRD4SLC6A2HTR1D
Pruvanserin SCHEMBL3914362 0.96 HTR2A (0.93) HTR2AHTR2CDRD4SLC6A2HTR1D
SCHEMBL6110393 0.91 HTR2A (0.84) HTR2AHTR2CDRD4SLC6A2HTR1D
SCHEMBL5280317 0.91 HTR2A (0.84) HTR2AHTR2CDRD4SLC6A2HTR1D
SCHEMBL6112038 0.91 HTR2A (0.83) HTR2AHTR2CDRD4SLC6A2HTR1D
SCHEMBL5925660 0.87 HTR2A (1.00) 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 296 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3630102-B1 FORMULATIONS FOR TREATMENT OF POST-TRAUMATIC STRESS DISORDER GLYTECH LLC (US) 2024-08-14 EP claimed
US-11969431-B2 Formulations for treatment of post-traumatic stress disorder GLYTECH LLC (US) 2024-04-30 US claimed
US-20230201193-A1 COMPOSITION AND METHOD FOR TREATMENT OF DEPRESSION AND PSYCHOSIS IN HUMANS GLYTECH LLC (US) 2023-06-29 US claimed
US-20220252611-A1 METHODS FOR USING MASS SPECTROSCOPY IN MULTIPLEX TARGET EVALUATIONS EUROFINS CEREP (FR) 2022-08-11 US claimed
EP-3973298-A1 METHODS FOR USING MASS SPECTROSCOPY IN MULTIPLEX TARGET EVALUATIONS Eurofins Cerep (FR) 2022-03-30 EP claimed
EP-1794121-B1 NOVEL CRYSTALLINE FORM OF (3-CYANO-1H-INDOL-7-YL)-[4-(4-FLUOROPHENETHYL)-PIPERAZINE-1-YL]-METHANONE HYDROCHLORIDE MERCK PATENT GMBH (DE) 2013-12-25 EP claimed
CN-101437793-B Crystalline (3-cyano-1H-indol-7-yl)-[4-(4-fluorophenethyl)piperazin-1-yl]methanone phosphate MERCK PATENT GMBH 2012-08-22 CN claimed
EP-2016052-B1 CRYSTALLINE (3-CYANO-1H-INDOL-7-YL)-[4-(4-FLUOROPHENETHYL)PIPERAZIN-1-YL]METHANONE PHOSPHATE MERCK PATENT GMBH (DE) 2012-06-06 EP claimed
US-7981897-B2 Crystal form of (3-cyano-1H-Indo1-7-yl)-[4-(4-fluorophenethyl)piperazin-1-yl]methanone, hydrochloride MERCK PATENT GMBH (DE) 2011-07-19 US claimed
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-1589147-A Use of N-(indolecarbonyl-)piperazine derivatives MERCK PATENT GMBH (DE) 2005-03-02 CN claimed
US-20050014766-A1 Use of n-(indolecarbonyl-)piperazine derivatives MERCK PATENT GMBH (DE) 2005-01-20 US claimed
US-6838461-B1 N-(indolcarbonyl-)piperazine derivatives MERCK PATENT GMBH (DE) 2005-01-04 US claimed
EP-1198453-B9 N-(INDOLCARBONYL-)PIPERAZIN DERIVATIVES MERCK PATENT GMBH (DE) 2004-11-10 EP claimed
EP-1353906-B1 PROCESS FOR THE PREPARATION OF (3-CYANO-1H-INDOL-7-YL)(4-(4-FLUOROPHENETHYL)PIPERAZIN-1-YL)-METHANONE AND SALTS THEREOF MERCK PATENT GMBH (DE) 2004-06-23 EP claimed
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 claimed
US-20040063723-A1 Process for the preparation of (3-cyano-1h-indol-7-yl) (4-(4-fluorophenethyl) piperazin-1-yl)- methanone and salts thereof MERCK PATENT GMBH (DE) 2004-04-01 US claimed
EP-1353906-A1 PROCESS FOR THE PREPARATION OF (3-CYANO-1H-INDOL-7-YL)(4-(4-FLUOROPHENETHYL)PIPERAZIN-1-YL)-METHANONE AND SALTS THEREOF MERCK PATENT GmbH (DE) 2003-10-22 EP claimed
EP-1198453-B1 N-(INDOLCARBONYL-)PIPERAZIN DERIVATIVES MERCK PATENT GMBH (DE) 2003-04-09 EP claimed
WO-2002059092-A1 PROCESS FOR THE PREPARATION OF (3-CYANO-1H-INDOL-7-YL)(4-(4-FLUOROPHENETHYL)PIPERAZIN-1-YL)-METHANONE AND SALTS THEREOF MERCK PATENT GMBH (DE) 2002-08-01 WO claimed

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

For each of this compound's patents that has machine-readable text (2 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-20050014766-A1 Use of n-(indolecarbonyl-)piperazine derivatives GPR119, CHRM1, HTR1A HTR2A 11/4885HTR2C 5/4885DRD4 46/4885
US-20040063723-A1 Process for the preparation of (3-cyano-1h-indol-7-yl) (4-(4-fluorophenethyl) piperazin-1-yl)- methanone and salts thereof TPH1, TPH2, IDO1 HTR2A 32/4885HTR2C 15/4885DRD4 274/4885

“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.