Pipenzolate

Pipenzolate

SCHEMBL249587

CC[N+]1(C)CCCC(OC(=O)C(O)(c2ccccc2)c2ccccc2)C1.[Br-]

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1

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

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
CHRM2 known ✓ P08172 10/20 0.98
CHRM3 known ✓ P20309 9/20 0.98
CHRM1 known ✓ P11229 4/20 0.98
CHRM4 known ✓ P08173 2/20 0.54
CHRM5 known ✓ P08912 2/20 0.54
RAB9A P51151 1/20 1.00
KCNH2 Q12809 5/20 0.98
CYP2D6 P10635 3/20 0.98
HRH1 P35367 3/20 0.98
LMNA P02545 2/20 0.98
SLC22A1 O15245 1/20 0.78
SLC6A4 P31645 2/20 0.76
CYP2C19 P33261 1/20 0.76
HTR2B P41595 1/20 0.54

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
Pipenzolate SCHEMBL31682328 0.99 CHRM2 (1.00) RAB9ACHRM2CHRM3KCNH2CHRM1
Pipenzolate SCHEMBL25957021 0.99 CHRM2 (1.00) RAB9ACHRM2CHRM3KCNH2CHRM1
Bromide SCHEMBL21530608 0.88 RAB9A (0.79) RAB9ACHRM2CHRM3KCNH2CHRM1
Mepenzolate SCHEMBL17008166 0.88 CHRM3 (1.00) RAB9ACHRM2CHRM3KCNH2CHRM1
Mepenzolate SCHEMBL99030 0.88 CHRM3 (1.00) RAB9ACHRM2CHRM3KCNH2CHRM1
Mepenzolate SCHEMBL15575981 0.88 CHRM3 (1.00) RAB9ACHRM2CHRM3KCNH2CHRM1
Mepenzolate SCHEMBL147471 0.88 CHRM3 (1.00) RAB9ACHRM2CHRM3KCNH2CHRM1
Mepenzolate SCHEMBL15575855 0.88 CHRM3 (1.00) RAB9ACHRM2CHRM3KCNH2CHRM1
Mepenzolate SCHEMBL19411950 0.86 CHRM3 (0.97) RAB9ACHRM2CHRM3KCNH2CHRM1
Mepenzolate SCHEMBL15865414 0.86 CHRM3 (0.97) RAB9ACHRM2CHRM3KCNH2CHRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230248734-A1 ANTIVIRAL COMPOSITION OBTAINED THROUGH DRUG REPOSITIONING KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2023-08-10 US claimed
US-20230003721-A1 MITOTHERAPEUTICS FOR THE TREATMENT OF BRAIN DISORDERS THE UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INC. 2023-01-05 US claimed
WO-2017147104-A1 MUSCARINIC M2-ANTAGONIST COMBINATIONS CHASE PHARMACEUTICALS CORPORATION (US) 2017-08-31 WO claimed
US-20160257952-A1 IDENTIFICATION OF STRUCTURALLY SIMILAR SMALL MOLECULES THAT ENHANCE THERAPEUTIC EXON SKIPPING NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2016-09-08 US claimed
US-20140171645-A1 ELECTROPHILIC ALKYLATING REAGENTS, THEIR PREPARATION AND USE HOVIONE INTER LTD. (CH) 2014-06-19 US claimed
EP-2691367-A1 ELECTROPHILIC ALKYLATING REAGENTS, THEIR PREPARATION AND USE Hovione Inter Ltd. (CH) 2014-02-05 EP claimed
CN-103502211-A Electrophilic alkylating reagents, preparation and use thereof HOVIONE FARMACIENCIA S A 2014-01-08 CN claimed
EP-2665739-A1 METHODS AND COMPOSITIONS RELATED TO SYNERGISTIC RESPONSES TO ONCOGENIC MUTATIONS THE UNIVERSITY OF ROCHESTER (US) 2013-11-27 EP claimed
WO-2012131286-A1 ELECTROPHILIC ALKYLATING REAGENTS, THEIR PREPARATION AND USE HOVIONE INTER. LTD (CH) 2012-10-04 WO claimed
WO-2012100248-A1 METHODS AND COMPOSITIONS RELATED TO SYNERGISTIC RESPONSES TO ONCOGENIC MUTATIONS THE UNIVERSITY OF ROCHESTER (US) 2012-07-26 WO claimed
EP-2188630-A2 METHODS AND COMPOSITIONS RELATED TO SYNERGISTIC RESPONSES TO ONCOGENIC MUTATIONS THE UNIVERSITY OF ROCHESTER (US) 2010-05-26 EP claimed
WO-2009045443-A2 METHODS AND COMPOSITIONS RELATED TO SYNERGISTIC RESPONSES TO ONCOGENIC MUTATIONS THE UNIVERSITY OF ROCHESTER (US) 2009-04-09 WO claimed
EP-1273301-B1 Pharmaceutical preparations based on active ingredients susceptible to illicit administration ALTERGON SA (CH) 2006-09-06 EP claimed
EP-1273301-A2 Pharmaceutical preparations based on active ingredients susceptible to illicit administration ALTERGON S.A. (CH) 2003-01-08 EP claimed
EP-1073470-A1 PHARMACEUTICAL COMPOSITIONS CONTAINING COMPOUNDS WITH ACTIVITY FOR THE ENHANCEMENT OF ABSORPTION OF ACTIVE INGREDIENTS INPHARMA S.A. (CH) 2001-02-07 EP claimed
WO-2000048636-A1 PHARMACEUTICAL COMPOSITIONS CONTAINING COMPOUNDS WITH ACTIVITY FOR THE ENHANCEMENT OF ABSORPTION OF ACTIVE INGREDIENTS INPHARMA S.A. (CH) 2000-08-24 WO claimed
US-5316772-A Bilayered oral pharmaceutical composition with pH dependent release SOLVAY & CIE, S.A. (SOCIETE ANONYME) (BE) 1994-05-31 US claimed
WO-1992011001-A1 ORAL PHARMACEUTICAL COMPOSITION SOLVAY (SOCIETE ANONYME) (BE) 1992-07-09 WO claimed
US-5008111-A Pretreating skin with anticholinergic quaternary ammonium salt to suppress perspiration SCHERING CORPORATION (US) 1991-04-16 US claimed
US-4824676-A ANTICHOLINERGIC AGENT TO SUPPRESS PERSPIRATION SCHERING CORPORATION (US) 1989-04-25 US 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-20230248734-A1 ANTIVIRAL COMPOSITION OBTAINED THROUGH DRUG REPOSITIONING SARS1, EIF2AK2, ACE2 CHRM2 4822/4885CHRM3 4594/4885CHRM1 4876/4885
US-20140171645-A1 ELECTROPHILIC ALKYLATING REAGENTS, THEIR PREPARATION AND USE MGMT, MCL1, TOP2B CHRM2 2607/4885CHRM3 3125/4885CHRM1 3157/4885

“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.