Darifenacin

Darifenacin

SCHEMBL113331

NC(=O)C(c1ccccc1)(c1ccccc1)C1CCN(CCc2ccc3c(c2)CCO3)C1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CHRM2CHRM3

The experimentally established mechanism targets of Darifenacin. 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
CHRM3 known ✓ P20309 3/20 1.00
CHRM2 known ✓ P08172 2/20 1.00
CHRM5 P08912 5/20 1.00
CHRM1 P11229 5/20 1.00
CHRM4 P08173 3/20 1.00
ADRB2 P07550 1/20 1.00
ADRB1 P08588 1/20 1.00
ADRA2A P08913 1/20 1.00
DRD2 P14416 1/20 1.00
KCNE1 P15382 1/20 1.00
ADRA2B P18089 1/20 1.00
ADRA2C P18825 1/20 1.00
HRH2 P25021 1/20 1.00
HTR2A P28223 1/20 1.00
SLC6A4 P31645 1/20 1.00
ADRA1A P35348 1/20 1.00
OPRM1 P35372 1/20 1.00
OPRK1 P41145 1/20 1.00
HTR2B P41595 1/20 1.00
KCNQ1 P51787 1/20 1.00

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
Darifenacin SCHEMBL31257801 1.00 CHRM5 (1.00) CHRM5CHRM1CHRM4CHRM3CHRM2
Darifenacin SCHEMBL2774455 1.00 CHRM5 (1.00) CHRM5CHRM1CHRM4CHRM3CHRM2
Darifenacin SCHEMBL56574 1.00 CHRM5 (1.00) CHRM5CHRM1CHRM4CHRM3CHRM2
Darifenacin SCHEMBL1023445 0.99 CHRM5 (0.98) CHRM5CHRM1CHRM4CHRM3CHRM2
Darifenacin SCHEMBL3662174 0.99 CHRM5 (0.98) CHRM5CHRM1CHRM4CHRM3CHRM2
Darifenacin SCHEMBL1318587 0.99 CHRM5 (0.98) CHRM5CHRM1CHRM4CHRM3CHRM2
Darifenacin SCHEMBL138745 0.99 CHRM5 (0.98) CHRM5CHRM1CHRM4CHRM3CHRM2
Darifenacin SCHEMBL5085916 0.99 CHRM5 (0.98) CHRM5CHRM1CHRM4CHRM3CHRM2
Darifenacin SCHEMBL453486 0.99 CHRM5 (0.98) CHRM5CHRM1CHRM4CHRM3CHRM2
Darifenacin SCHEMBL1973347 0.99 CHRM5 (0.98) CHRM5CHRM1CHRM4CHRM3CHRM2

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 1034 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2022257986-A1 USE OF CYP450 INHIBITOR IN INHIBITING OR KILLING MITES AND TREATING DRY EYE SYNDROME 广州岐微生物医药科技有限公司 2022-12-15 WO claimed
EP-2336124-B1 Stable hydrate of a muscarinic receptor antagonist NOVARTIS INT PHARM LTD (BM) 2012-08-29 EP claimed
US-8058454-B2 Method for preparing 1,3-disubstituted pyrrolidine compounds MEDICHEM, S.A. (ES) 2011-11-15 US claimed
WO-2011070419-A1 AN IMPROVED PROCESS FOR THE PREPARATION OF DARIFENACIN HYDROBROMIDE AUROBINDO PHARMA LIMITED (IN) 2011-06-16 WO claimed
EP-1490357-B1 Toluene solvate of darifenacin NOVARTIS INT PHARM LTD (BM) 2011-01-12 EP claimed
EP-2236509-A1 Method for obtaining 1,3-difunctionalized pyrrolidine derivatives Ragactives, S.L. (ES) 2010-10-06 EP claimed
US-20100112061-A1 Monophosphates as Mutual Prodrugs of Muscarinic Receptor Antagonists and Beta-Agonists for the Treatment of COPD And Chronic Bronchitis GILEAD SCIENCES, INC. 2010-05-06 US claimed
US-7696357-B2 Stable hydrate of a muscarinic receptor antagonist NOVARTIS INTERNATIONAL PHARMACEUTICAL LTD. (BM) 2010-04-13 US claimed
EP-2160372-A1 METHOD FOR DETERMINING ENANTIOMERIC PURITY OF DARIFENACIN AND INTERMEDIATES Medichem, S.A. (ES) 2010-03-10 EP claimed
US-20090306406-A1 METHOD FOR PREPARING 1,3-DISUBSTITUTED PYRROLIDINE COMPOUNDS MEDICHEM ,S.A. (ES) 2009-12-10 US claimed
US-20050245597-A1 Stable hydrate of a muscarinic receptor antagonist DUNN PETER J 2005-11-03 US claimed
WO-2005092341-A1 COMBINATION THERAPY FOR LOWER URINARY TRACT SYMPTOMS RANBAXY LABORATORIES LIMITED (IN) 2005-10-06 WO claimed
US-6930188-B2 Stable hydrate of a muscarinic receptor antagonist NOVARTIS INTERNATIONAL PHARMACEUTICAL, LTD. (BE) 2005-08-16 US claimed
EP-1490357-A1 STABLE HYDRATE OF A MUSCARINIC RECEPTOR ANTAGONIST Novartis International Pharmaceutical Ltd. (BM) 2004-12-29 EP claimed
US-20030191176-A1 Stable hydrate of a muscarinic receptor antagonist PFIZER INC. 2003-10-09 US claimed
WO-2003080599-A1 STABLE HYDRATE OF A MUSCARINIC RECEPTOR ANTAGONIST NOVARTIS INTERNATIONAL PHARMACEUTICAL LTD. (BM) 2003-10-02 WO claimed
WO-1995019164-A1 USE OF M3 MUSCARINIC ANTAGONISTS FOR THE TREATMENT OF MOTION SICKNESS PFIZER LIMITED (GB) 1995-07-20 WO claimed
EP-0388054-B1 Pyrrolidine derivatives PFIZER LTD (GB) 1993-11-03 EP claimed
US-5096890-A PYRROLIDINE DERIVATIVES PFIZER INC. (US) 1992-03-17 US claimed
EP-0388054-A1 Pyrrolidine derivatives Pfizer Limited (GB) 1990-09-19 EP 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 (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-20030191176-A1 Stable hydrate of a muscarinic receptor antagonist CHRM5, CHRM2, CHRM3 CHRM3 3/4885CHRM2 2/4885CHRM5 1/4885
US-20050245597-A1 Stable hydrate of a muscarinic receptor antagonist CHRM5, CHRM2, CHRM3 CHRM3 3/4885CHRM2 2/4885CHRM5 1/4885
US-20090306406-A1 METHOD FOR PREPARING 1,3-DISUBSTITUTED PYRROLIDINE COMPOUNDS OPRL1, OPRK1, OPRD1 CHRM3 108/4885CHRM2 431/4885CHRM5 423/4885
US-20100112061-A1 Monophosphates as Mutual Prodrugs of Muscarinic Receptor Antagonists and Beta-Agonists for the Treatment of COPD And Chronic Bronchitis ADRB1, ADRB2, CHRM3 CHRM3 3/4885CHRM2 5/4885CHRM5 6/4885

“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.