Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL1975758

NC(=O)C(c1ccccc1)(c1ccccc1)C1CCNC1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.43

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3CHRM1CHRM2CHRM3CHRM4ESR1ESR2GABRA1GABRB1GABRG2GBA1HRH1HTR1DHTR2AOPRD1OPRK1OPRM1SLC6A2SLC6A3TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8rplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Cadaverine Tartrate. 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
HRH1 known ✓ P35367 1/20 0.43
CHRM3 known ✓ P20309 2/20 0.36
ADRB2 known ✓ P07550 1/20 0.36
CHRM2 known ✓ P08172 1/20 0.36
CHRM4 known ✓ P08173 1/20 0.36
ADRB1 known ✓ P08588 1/20 0.36
ADRA2A known ✓ P08913 1/20 0.36
CHRM1 known ✓ P11229 1/20 0.36
ADRA2B known ✓ P18089 1/20 0.36
ADRA2C known ✓ P18825 1/20 0.36
HTR2A known ✓ P28223 1/20 0.36
ADRA1A known ✓ P35348 1/20 0.36
OPRM1 known ✓ P35372 1/20 0.36
OPRK1 known ✓ P41145 1/20 0.36
SLC6A2 known ✓ P23975 3/20 0.35
SLC6A3 known ✓ Q01959 1/20 0.34
KMT2A Q03164 2/20 0.43
MEN1 O00255 1/20 0.43
LMNA P02545 1/20 0.43
CYP2D6 P10635 1/20 0.43

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 SCHEMBL1975759 1.00 KMT2A (0.43) KMT2AMEN1LMNACYP2D6HRH1
Cadaverine Tartrate SCHEMBL5085962 1.00 KMT2A (0.43) KMT2AMEN1LMNACYP2D6HRH1
Cadaverine Tartrate SCHEMBL5623544 0.95 KMT2A (0.43) KMT2AMEN1LMNACYP2D6HRH1
Cadaverine Tartrate SCHEMBL5623548 0.95 KMT2A (0.43) KMT2AMEN1LMNACYP2D6HRH1
SCHEMBL953947 0.92 KMT2A (0.50) KMT2AMEN1LMNACYP2D6HRH1
SCHEMBL958241 0.92 KMT2A (0.50) KMT2AMEN1LMNACYP2D6HRH1
SCHEMBL4396455 0.92 KMT2A (0.50) KMT2AMEN1LMNACYP2D6HRH1
Bromide SCHEMBL4505514 0.90 KMT2A (0.49) KMT2AMEN1LMNACYP2D6HRH1
Hydrochloric Acid SCHEMBL10869034 0.90 KMT2A (0.49) KMT2AMEN1LMNACYP2D6HRH1
Bromide SCHEMBL4505510 0.90 KMT2A (0.49) 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 34 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2160372-A1 METHOD FOR DETERMINING ENANTIOMERIC PURITY OF DARIFENACIN AND INTERMEDIATES Medichem, S.A. (ES) 2010-03-10 EP claimed
US-20090156831-A1 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE MERLI VALERIANO 2009-06-18 US claimed
WO-2008152497-A1 METHOD FOR DETERMINING ENANTIOMERIC PURITY OF DARIFENACIN AND INTERMEDIATES MEDICHEM, S.A. (US) 2008-12-18 WO claimed
US-20080312455-A1 Method For Determining Enantiomeric Purity Of Darifenacin And Intermediates MEDICHEM, S.A. (ES) 2008-12-18 US claimed
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 claimed
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 claimed
EP-1877393-A2 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE Teva Pharmaceutical Fine Chemicals S.R.L. (IT) 2008-01-16 EP claimed
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 claimed
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 claimed
WO-2007076158-A2 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-07-05 WO claimed
US-20110144354-A1 Process for Preparation of Darifenacin and Intermediates Used in the Process Watson Pharma Private Limited (IN) 2011-06-16 US disclosed
WO-2010032225-A2 PROCESS FOR PREPARATION OF DARIFENACIN AND INTERMEDIATES USED IN THE PROCESS Watson Pharma Private Limited (IN) 2010-03-25 WO disclosed
EP-2160372-A1 METHOD FOR DETERMINING ENANTIOMERIC PURITY OF DARIFENACIN AND INTERMEDIATES Medichem, S.A. (ES) 2010-03-10 EP disclosed
WO-2009125430-A2 IMPROVED PROCESS FOR PRODUCING DARIFENACIN MATRIX LABORATOIRES LIMITED (IN) 2009-10-15 WO disclosed
WO-2009125426-A2 NOVEL PROCESS FOR THE PREPARATION OF (3SM-[2-(2 J-DIHYDRO-5- BENZOFURANYLϊETHYL]-α.α -DIPHENYL-3-PYRROLIDINEACETAMIDE HYDROBROMIDE NEULAND LABORATORIES LTD (IN) 2009-10-15 WO 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-20070197631-A1 Processes for preparing darifenacin hydrobromide TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-08-23 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
WO-2007076158-A2 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE TEVA PHARMACEUTICAL 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 (7 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-20080269504-A1 Pure darifenacin hydrobromide substantially free of oxidized darifenacin and salts thereof and processes for the preparation thereof OPRL1, OPRK1, OPRD1 HRH1 574/4885CHRM3 87/4885ADRB2 14/4885
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 HRH1 85/4885CHRM3 2/4885ADRB2 4/4885
US-20070197630-A1 Pure darifenacin hydrobromide substantially free of oxidized darifenacin and salts thereof and processes for the preparation thereof OPRL1, OPRK1, OPRD1 HRH1 574/4885CHRM3 87/4885ADRB2 14/4885
US-20110144354-A1 Process for Preparation of Darifenacin and Intermediates Used in the Process OPRL1, OPRD1, OPRK1 HRH1 334/4885CHRM3 19/4885ADRB2 10/4885
US-20070197631-A1 Processes for preparing darifenacin hydrobromide OPRL1, AVPR2, AVPR1B HRH1 214/4885CHRM3 69/4885ADRB2 15/4885
US-20080312455-A1 Method For Determining Enantiomeric Purity Of Darifenacin And Intermediates OPRL1, ADRB3, ADRB1 HRH1 435/4885CHRM3 36/4885ADRB2 4/4885
US-20090156831-A1 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE OPRL1, AVPR2, AVPR1B HRH1 214/4885CHRM3 69/4885ADRB2 15/4885

“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.