Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL1835487

O=C(O)C(O)C(O)C(=O)O.OCCNCCO

nearest known ligand 0.53

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 15)

geneUniProtsupporting neighboursconfidence
GBA1 known ✓ P04062 1/20 0.37
TSHR P16473 2/20 0.53
ALDH1A1 P00352 2/20 0.48
MEN1 O00255 1/20 0.48
USP2 O75604 1/20 0.48
MAPT P10636 1/20 0.48
KMT2A Q03164 1/20 0.48
CYP2C9 P11712 1/20 0.41
PDE4A P27815 1/20 0.41
KDM4E B2RXH2 3/20 0.38
OR51E2 Q9H255 1/20 0.38
SMN1; SMN2 Q16637 3/20 0.33
HTT P42858 1/20 0.33
TOP2B Q02880 1/20 0.32
PGD P52209 1/20 0.31

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 SCHEMBL28438230 1.00 TSHR (0.53) TSHRALDH1A1MEN1USP2MAPT
Cadaverine Tartrate SCHEMBL1839186 1.00 TSHR (0.53) TSHRALDH1A1MEN1USP2MAPT
Mucic Acid SCHEMBL9324765 0.90 PDE4A (0.54) TSHRALDH1A1MEN1USP2MAPT
Mucic Acid SCHEMBL31648927 0.90 PDE4A (0.54) TSHRALDH1A1MEN1USP2MAPT
Diethanolamine SCHEMBL1832717 0.82 TP53 (0.55) TSHRALDH1A1MEN1USP2MAPT
SCHEMBL17307369 0.81 ALDH1A1 (0.38) TSHRALDH1A1MEN1USP2MAPT
Gluconic Acid SCHEMBL18228783 0.81 PDE4A (0.73) TSHRALDH1A1MEN1USP2MAPT
Diethanolamine SCHEMBL2803527 0.80 TP53 (0.52) TSHRALDH1A1MEN1USP2MAPT
Cadaverine Tartrate SCHEMBL1833968 0.80 TSHR (0.48) TSHRALDH1A1MEN1USP2MAPT
Cadaverine Tartrate SCHEMBL1834039 0.80 TSHR (0.48) TSHRALDH1A1MEN1USP2MAPT

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-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
CN-102112102-B Hair conditioner composition SHISEDO CO LTD 2013-09-04 CN disclosed
US-20110257433-A1 LIQUIDS THE UNIVERSITY OF YORK (GB) 2011-10-20 US disclosed
CN-102112102-A Hair conditioner composition SHISEIDO CO LTD 2011-06-29 CN disclosed
EP-2322497-A1 Ionic liquids comprising nitrogen containing cations Innovia Films Limited (GB) 2011-05-18 EP disclosed
CN-101316810-A Ionic liquids BIONIQS LTD (GB) 2008-12-03 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
EP-1805131-A2 IONIC LIQUIDS COMPRISING NITROGEN CONTAINING CATIONS THE UNIVERSITY OF YORK (GB) 2007-07-11 EP disclosed
WO-2005097731-A2 IONIC LIQUIDS COMPRISING NITROGEN CONTAINING CATIONS THE UNIVERSITY OF YORK (GB) 2005-10-20 WO disclosed