SCHEMBL4525774

SCHEMBL4525774

NC(=O)C(c1ccccc1)(c1ccccc1)N1CCCC1

nearest known ligand 0.47

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CYP2B6 P20813 1/20 0.47
MAPT P10636 1/20 0.46
KMT2A Q03164 1/20 0.46
KCNN4 O15554 6/20 0.41
CHRM3 P20309 6/20 0.40
HPGD P15428 1/20 0.39
NPC1 O15118 1/20 0.39
HTT P42858 1/20 0.39
CHRM2 P08172 3/20 0.38
CHRM1 P11229 2/20 0.38
LMNA P02545 1/20 0.38
HTR1A P08908 1/20 0.38
CYP2D6 P10635 1/20 0.38
OPRM1 P35372 1/20 0.38
KCNH2 Q12809 1/20 0.38

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
Cadaverine Tartrate SCHEMBL4521162 0.91 CYP2B6 (0.40) CYP2B6MAPTKMT2AKCNN4CHRM3
SCHEMBL10360491 0.86 MAPT (0.43) MAPTKMT2AKCNN4CHRM3HTT
SCHEMBL9273398 0.84 KMT2A (0.46) MAPTKMT2ACHRM3CHRM2CHRM1
SCHEMBL7545842 0.83 KIF11 (0.40) CYP2B6MAPTKMT2ACHRM3NPC1
SCHEMBL10360494 0.82 MAPT (0.38) CYP2B6MAPTKMT2AKCNN4CHRM3
SCHEMBL10360472 0.81 MAPT (0.46) MAPTKMT2AKCNN4CHRM3HTT
SCHEMBL6266546 0.77 CYP2B6 (0.56) CYP2B6MAPTKMT2ACHRM3
SCHEMBL7559824 0.76 KCNN4 (0.51) CYP2B6MAPTKMT2AKCNN4CHRM3
SCHEMBL4559888 0.74 CYP2B6 (0.47) CYP2B6MAPTKMT2AKCNN4CHRM3
SCHEMBL6903725 0.73 CYP2B6 (0.46) CYP2B6MAPTCHRM3CHRM2CHRM1

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 17 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090156831-A1 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE MERLI VALERIANO 2009-06-18 US disclosed
US-20080269505-A1 Processes for preparing darifenacin hydrobromide TEVA PHARMACEUTICALS USA, INC. FOR BARBADOS 2008-10-30 US disclosed
US-20080269503-A1 Processes for preparing darifenacin hydrobromide TEVA PHARMACEUTICALS USA, INC. FOR BARBADOS 2008-10-30 US disclosed
US-20080269504-A1 Pure darifenacin hydrobromide substantially free of oxidized darifenacin and salts thereof and processes for the preparation thereof TEVA PHARMACEUTICAL FINE CHEMICALS S.R.I. 2008-10-30 US disclosed
US-7442806-B2 Processes for preparing darifenacin hydrobromide TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2008-10-28 US disclosed
WO-2008126106-A2 NOVEL AND IMPROVED PROCESSES FOR THE PREPARATION OF INTERMEDIATES OF DARIFENACIN, DARIFENACIN AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS SATYANARAYANA REDDY MANNE (IN) 2008-10-23 WO disclosed
US-20080216562-A1 Pure darifenacin hydrobromide substantially free of oxidized darifenacin and salts thereof and processes for the preparation thereof TEVA PHARMACEUTICALS USA, INC. FOR BARBADOS 2008-09-11 US disclosed
US-20080221338-A1 Processes for preparing darifenacin hydrobromide TEVA PHARMACEUTICALS U.S.A. INC. FOR BARBADOS 2008-09-11 US disclosed
EP-1966179-A2 DARIFENACIN HYDROBROMIDE COMPOSITION SUBSTANTIALLY FREE OF OXIDIZED DARIFENACIN AND SALTS THEREOF AND PROCESSES FOR THE PREPARATION THEREOF Teva Pharmaceutical Industries Ltd (IL) 2008-09-10 EP disclosed
US-20080214835-A1 Processes for preparing darifenacin hydrobromide TEVA PHARMACEUTICALS USA, INC. FOR BARBADOS 2008-09-04 US disclosed
US-20080214846-A1 Pure darifenacin hydrobromide substantially free of oxidized darifenacin and salts thereof and processes for the preparation thereof TEVA PHARMACEUTICALS USA, INC. FOR BARBADOS 2008-09-04 US disclosed
EP-1891034-A2 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE Teva Pharmaceutical Fine Chemicals S.R.L. (IT) 2008-02-27 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-20070197630-A1 Pure darifenacin hydrobromide substantially free of oxidized darifenacin and salts thereof and processes for the preparation thereof TEVA PHARMACEUTICAL FINE CHEMICALS S.R.L. (IT) 2007-08-23 US disclosed
US-20070197631-A1 Processes for preparing darifenacin hydrobromide TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-08-23 US disclosed
WO-2007076157-A2 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE TEVA PHARMACEUTICALS INDUSTRIES LTD. (IL) 2007-07-05 WO disclosed
WO-2007076159-A2 PURE DARIFENACIN HYDROBROMIDE SUBSTANTIALLY FREE OF OXIDIZED DARIFENACIN AND SALTS THEREOF AND PROCESSES FOR THE PREPARATION THEREOF TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-07-05 WO 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 (10 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 CYP2B6 667/4885MAPT 2623/4885KMT2A 3578/4885
US-20080269504-A1 Pure darifenacin hydrobromide substantially free of oxidized darifenacin and salts thereof and processes for the preparation thereof OPRL1, OPRK1, OPRD1 CYP2B6 318/4885MAPT 2600/4885KMT2A 2973/4885
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 CYP2B6 2672/4885MAPT 2830/4885KMT2A 1552/4885
US-20080221338-A1 Processes for preparing darifenacin hydrobromide OPRL1, AVPR2, AVPR1B CYP2B6 667/4885MAPT 2623/4885KMT2A 3578/4885
US-20070197630-A1 Pure darifenacin hydrobromide substantially free of oxidized darifenacin and salts thereof and processes for the preparation thereof OPRL1, OPRK1, OPRD1 CYP2B6 318/4885MAPT 2600/4885KMT2A 2973/4885
US-20080269503-A1 Processes for preparing darifenacin hydrobromide OPRL1, AVPR2, AVPR1B CYP2B6 667/4885MAPT 2623/4885KMT2A 3578/4885
US-20070197631-A1 Processes for preparing darifenacin hydrobromide OPRL1, AVPR2, AVPR1B CYP2B6 667/4885MAPT 2623/4885KMT2A 3578/4885
US-20080269505-A1 Processes for preparing darifenacin hydrobromide OPRL1, AVPR2, AVPR1B CYP2B6 667/4885MAPT 2623/4885KMT2A 3578/4885
US-20080214846-A1 Pure darifenacin hydrobromide substantially free of oxidized darifenacin and salts thereof and processes for the preparation thereof OPRL1, OPRK1, OPRD1 CYP2B6 318/4885MAPT 2600/4885KMT2A 2973/4885
US-20090156831-A1 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE OPRL1, AVPR2, AVPR1B CYP2B6 667/4885MAPT 2623/4885KMT2A 3578/4885

“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.