Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL4521162

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

nearest known ligand 0.40

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 9)

geneUniProtsupporting neighboursconfidence
CHRM3 known ✓ P20309 5/20 0.36
CYP2B6 P20813 1/20 0.40
MAPT P10636 1/20 0.39
KMT2A Q03164 1/20 0.39
LMNA P02545 1/20 0.37
GAA P10253 1/20 0.36
KCNN4 O15554 3/20 0.35
RAD52 P43351 1/20 0.34
KIF11 P52732 3/20 0.33

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
SCHEMBL4525774 0.91 CYP2B6 (0.47) CYP2B6MAPTKMT2ALMNACHRM3
SCHEMBL10360491 0.78 MAPT (0.43) MAPTKMT2ALMNACHRM3KCNN4
SCHEMBL9273398 0.76 KMT2A (0.46) MAPTKMT2ACHRM3
SCHEMBL7545842 0.75 KIF11 (0.40) CYP2B6MAPTKMT2ALMNAGAA
SCHEMBL10360494 0.75 MAPT (0.38) CYP2B6MAPTKMT2ALMNACHRM3
SCHEMBL10360472 0.74 MAPT (0.46) MAPTKMT2ALMNACHRM3KCNN4
SCHEMBL6266546 0.70 CYP2B6 (0.56) CYP2B6MAPTKMT2ACHRM3
SCHEMBL7559824 0.69 KCNN4 (0.51) CYP2B6MAPTKMT2ALMNACHRM3
Cadaverine Tartrate SCHEMBL27624850 0.69 KEAP1 (0.58) CHRM3KIF11
Cadaverine Tartrate SCHEMBL28092955 0.68 MAPT (0.45) MAPTKMT2ALMNAKCNN4KIF11

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 14 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-7442806-B2 Processes for preparing darifenacin hydrobromide TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2008-10-28 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
EP-1891034-A2 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE Teva Pharmaceutical Fine Chemicals S.R.L. (IT) 2008-02-27 EP 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-20070197631-A1 Processes for preparing darifenacin hydrobromide TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-08-23 US disclosed
WO-2007076158-A2 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-07-05 WO 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 (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-20080214835-A1 Processes for preparing darifenacin hydrobromide OPRL1, AVPR2, AVPR1B CHRM3 69/4885CYP2B6 667/4885MAPT 2623/4885
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 CHRM3 2/4885CYP2B6 2672/4885MAPT 2830/4885
US-20080221338-A1 Processes for preparing darifenacin hydrobromide OPRL1, AVPR2, AVPR1B CHRM3 69/4885CYP2B6 667/4885MAPT 2623/4885
US-20080269503-A1 Processes for preparing darifenacin hydrobromide OPRL1, AVPR2, AVPR1B CHRM3 69/4885CYP2B6 667/4885MAPT 2623/4885
US-20070197631-A1 Processes for preparing darifenacin hydrobromide OPRL1, AVPR2, AVPR1B CHRM3 69/4885CYP2B6 667/4885MAPT 2623/4885
US-20080269505-A1 Processes for preparing darifenacin hydrobromide OPRL1, AVPR2, AVPR1B CHRM3 69/4885CYP2B6 667/4885MAPT 2623/4885
US-20090156831-A1 PROCESSES FOR PREPARING DARIFENACIN HYDROBROMIDE OPRL1, AVPR2, AVPR1B CHRM3 69/4885CYP2B6 667/4885MAPT 2623/4885

“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.