SCHEMBL4396455

SCHEMBL4396455

NC(=O)C(c1ccccc1)(c1ccccc1)[C@H]1CCNC1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 2/20 0.50
MEN1 O00255 1/20 0.50
LMNA P02545 1/20 0.50
CYP2D6 P10635 1/20 0.50
HRH1 P35367 1/20 0.50
SCN1A P35498 1/20 0.50
SCN2A Q99250 1/20 0.50
SCN3A Q9NY46 1/20 0.50
SLC6A4 P31645 2/20 0.40
CHRM2 P08172 2/20 0.40
CHRM1 P11229 2/20 0.40
CHRM3 P20309 2/20 0.40
ADRB2 P07550 1/20 0.40
CHRM4 P08173 1/20 0.40
ADRB1 P08588 1/20 0.40
CHRM5 P08912 1/20 0.40
ADRA2A P08913 1/20 0.40
DRD2 P14416 1/20 0.40
KCNE1 P15382 1/20 0.40
ADRA2B P18089 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
SCHEMBL958241 1.00 KMT2A (0.50) KMT2AMEN1LMNACYP2D6HRH1
SCHEMBL953947 1.00 KMT2A (0.50) KMT2AMEN1LMNACYP2D6HRH1
Hydrochloric Acid SCHEMBL10869034 0.98 KMT2A (0.49) KMT2AMEN1LMNACYP2D6HRH1
Bromide SCHEMBL4505514 0.98 KMT2A (0.49) KMT2AMEN1LMNACYP2D6HRH1
Bromide SCHEMBL4505510 0.98 KMT2A (0.49) KMT2AMEN1LMNACYP2D6HRH1
Maleic Acid SCHEMBL10360499 0.93 HRH1 (0.44) KMT2AMEN1LMNACYP2D6HRH1
Cadaverine Tartrate SCHEMBL5085962 0.92 KMT2A (0.43) KMT2AMEN1LMNACYP2D6HRH1
Cadaverine Tartrate SCHEMBL1975758 0.92 KMT2A (0.43) KMT2AMEN1LMNACYP2D6HRH1
Cadaverine Tartrate SCHEMBL1975759 0.92 KMT2A (0.43) KMT2AMEN1LMNACYP2D6HRH1
SCHEMBL8424910 0.91 KEAP1 (0.43) KMT2AMEN1LMNACYP2D6HRH1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20080312455-A1 Method For Determining Enantiomeric Purity Of Darifenacin And Intermediates MEDICHEM, S.A. (ES) 2008-12-18 US claimed
US-20090306134-A1 Muscarinic receptor antagonists THERAVANCE BIOPHARMA R&D IP, LLC 2009-12-10 US disclosed
WO-2009125430-A2 IMPROVED PROCESS FOR PRODUCING DARIFENACIN MATRIX LABORATOIRES LIMITED (IN) 2009-10-15 WO disclosed
US-20090156831-A1 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE MERLI VALERIANO 2009-06-18 US disclosed
US-20080312455-A1 Method For Determining Enantiomeric Purity Of Darifenacin And Intermediates MEDICHEM, S.A. (ES) 2008-12-18 US disclosed
US-7456203-B2 Muscarinic receptor antagonists THERAVANCE, INC. (US) 2008-11-25 US disclosed
US-20080269505-A1 Processes for preparing darifenacin hydrobromide TEVA PHARMACEUTICALS USA, INC. FOR BARBADOS 2008-10-30 US disclosed
US-20080214835-A1 Processes for preparing darifenacin hydrobromide TEVA PHARMACEUTICALS USA, INC. FOR BARBADOS 2008-09-04 US disclosed
EP-1877393-A2 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE Teva Pharmaceutical Fine Chemicals S.R.L. (IT) 2008-01-16 EP disclosed
US-20070203221-A1 (S)-2-{1-[2-(2,3-dihydrobenzofuran-5-yl)ethyl]-3-pyrrolidinyl}-2,2-diphenylacetamide, selective muscarinic acetylcholine receptor antagonists, used for treating urogenital disorders such as incontinence TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-08-30 US disclosed
US-5233053-A Pyrrolidine derivatives PFIZER INC. (US) 1993-08-03 US disclosed
EP-0505376-A1 MUSCARINIC RECEPTOR ANTAGONISTS. PFIZER LTD (GB) 1992-09-30 EP disclosed
US-5096890-A PYRROLIDINE DERIVATIVES PFIZER INC. (US) 1992-03-17 US disclosed
WO-1991009013-A1 MUSCARINIC RECEPTOR ANTAGONISTS PFIZER LIMITED (GB) 1991-06-27 WO disclosed
EP-0388054-A1 Pyrrolidine derivatives Pfizer Limited (GB) 1990-09-19 EP disclosed
US-4260606-A ANTIDEPRESSANTS A. H. ROBINS COMPANY, INC. (US) 1981-04-07 US disclosed
US-4242261-A REACTING AN A,A-DIPHENYL-A-N-HETEROCYCLIC ACETAMIDE WITH BROMINE AND AN ALKALI METAL ALKOXIDE AND HEATING A. H. ROBINS COMPANY, INC. (US) 1980-12-30 US disclosed
US-4133881-A Azetidinyl acetonitrile and acetamide antiarrhythmia compositions and methods A. H. ROBINS COMPANY, INCORPORATED (US) 1979-01-09 US disclosed
US-4002766-A 1-R-3-PYRROLIDINYL-A,A-DIPHENYLACETAMIDES, -ACETONITRILES, AND -METHANES A. H. ROBINS COMPANY, INCORPORATED (US) 1977-01-11 US disclosed
US-4002766-A 1-R-3-PYRROLIDINYL-A,A-DIPHENYLACETAMIDES, -ACETONITRILES, AND -METHANES A. H. ROBINS COMPANY, INCORPORATED (US) 1977-01-11 US 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 (6 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-20080214835-A1 Processes for preparing darifenacin hydrobromide OPRL1, AVPR2, AVPR1B KMT2A 3578/4885MEN1 2021/4885LMNA 2545/4885
US-20070203221-A1 (S)-2-{1-[2-(2,3-dihydrobenzofuran-5-yl)ethyl]-3-pyrrolidinyl}-2,2-diphenylacetamide, selective muscarinic acetylcholine receptor antagonists, used for treating urogenital disorders such as incontinence CHRNE, CHRM3, CHRM2 KMT2A 1552/4885MEN1 4673/4885LMNA 4555/4885
US-20080312455-A1 Method For Determining Enantiomeric Purity Of Darifenacin And Intermediates OPRL1, ADRB3, ADRB1 KMT2A 3137/4885MEN1 2474/4885LMNA 3411/4885
US-20080269505-A1 Processes for preparing darifenacin hydrobromide OPRL1, AVPR2, AVPR1B KMT2A 3578/4885MEN1 2021/4885LMNA 2545/4885
US-20090306134-A1 Muscarinic receptor antagonists CHRM3, CHRM5, CHRM2 KMT2A 1220/4885MEN1 3774/4885LMNA 4772/4885
US-20090156831-A1 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE OPRL1, AVPR2, AVPR1B KMT2A 3578/4885MEN1 2021/4885LMNA 2545/4885

“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.