Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL1131805

CN(C)CCO.CN(C)CCO.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.57

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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
▸ GBA1 known ✓ P04062 1/20 0.35
▸ CHRM2 known ✓ P08172 1/20 0.32
▸ CHRM4 known ✓ P08173 1/20 0.32
▸ CHRM1 known ✓ P11229 1/20 0.32
▸ CHRM3 known ✓ P20309 1/20 0.32
▸ OPRM1 known ✓ P35372 1/20 0.32
▸ MAPT P10636 1/20 0.57
▸ TSHR P16473 4/20 0.48
▸ CYP2C9 P11712 1/20 0.38
▸ PDE4A P27815 1/20 0.38
▸ OR51E2 Q9H255 1/20 0.35
▸ TP53 P04637 1/20 0.33
▸ GFER P55789 1/20 0.33
▸ NFKB1 P19838 1/20 0.32
▸ CYP2C19 P33261 1/20 0.32
▸ CHRNB2 P17787 2/20 0.32
▸ CHRNA4 P43681 2/20 0.32
▸ CHRM5 P08912 1/20 0.32
▸ CHRNB4 P30926 1/20 0.32
▸ CHRNA3 P32297 1/20 0.32

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 SCHEMBL989096 1.00 MAPT (0.57) MAPTTSHRCYP2C9PDE4AGBA1
Tartaric Acid SCHEMBL30104959 1.00 MAPT (0.57) MAPTTSHRCYP2C9PDE4AGBA1
Lactic Acid SCHEMBL1131790 0.86 MAPT (0.57) MAPTOR51E2TP53CHRNB2CHRNA4
Dimethylaminoethanol SCHEMBL1131465 0.82 MAPT (0.75) MAPTTSHRCHRNB2CHRNA4CHRM2
Dimethylaminoethanol SCHEMBL1131226 0.82 MAPT (0.75) MAPTTSHRCHRNB2CHRNA4CHRM2
Dimethylaminoethanol SCHEMBL13730571 0.80 MAPT (0.50) MAPTOR51E2
Cadaverine Tartrate SCHEMBL8339185 0.80 TSHR (0.53) MAPTTSHRCYP2C9PDE4AGBA1
Cadaverine Tartrate SCHEMBL5874849 0.80 TSHR (0.53) MAPTTSHRCYP2C9PDE4AGBA1
Cadaverine Tartrate SCHEMBL8830362 0.80 TSHR (0.53) MAPTTSHRCYP2C9PDE4AGBA1
Dimethylaminoethanol SCHEMBL358310 0.79 MAPT (0.71) MAPTTSHRCHRNB2CHRNA4CHRM2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070185330-A1 Liquids THE UNIVERSITY OF YORK (GB) 2007-08-09 — — US claimed
US-9328220-B2 Liquids INNOVIA FILMS LIMITED (GB) 2016-05-03 — — US disclosed
US-8992798-B2 Liquids INNOVIA FILMS LIMITED (GB) 2015-03-31 — — US disclosed
US-8784686-B2 Liquids INNOVIA FILMS LIMITED (GB) 2014-07-22 — — US disclosed
US-20140187684-A1 LIQUIDS INNOVIA FILMS LIMITED (GB) 2014-07-03 — — US disclosed
US-20110257433-A1 LIQUIDS THE UNIVERSITY OF YORK (GB) 2011-10-20 — — US disclosed
EP-2322497-A1 Ionic liquids comprising nitrogen containing cations Innovia Films Limited (GB) 2011-05-18 — — EP disclosed
EP-1805131-B1 IONIC LIQUIDS COMPRISING NITROGEN CONTAINING CATIONS INNOVIA FILMS LTD (GB) 2011-02-16 — — EP disclosed
CN-101798237-A The preparation method who is used for flat structures through the rostone of antistatic treatment EVONIK GOLDSCHMIDT GMBH 2010-08-11 — — CN disclosed
CN-101502728-A Defoaming of ionic liquids EVONIK GOLDSCHMIDT GMBH (DE) 2009-08-12 — — CN disclosed
US-20080221361-A1 Ionic Liquids BIONIQS LIMITED (GB) 2008-09-11 — — US disclosed
US-20070185330-A1 Liquids THE UNIVERSITY OF YORK (GB) 2007-08-09 — — US disclosed
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