Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL8420068

O=C(O)C(O)C(O)C(=O)O.O=S(=O)(O)CCN1CCN(CCO)CC1

nearest known ligand 0.47

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 14)

geneUniProtsupporting neighboursconfidence
CHRM2 known ✓ P08172 1/20 0.35
CHRM1 known ✓ P11229 1/20 0.35
HTT P42858 2/20 0.38
LMNA P02545 1/20 0.38
KMT2A Q03164 1/20 0.38
ALDH1A1 P00352 4/20 0.35
KDM4E B2RXH2 1/20 0.35
TSHR P16473 2/20 0.33
TERT O14746 2/20 0.33
CA12 O43570 1/20 0.33
CA1 P00915 1/20 0.33
CA2 P00918 1/20 0.33
CA9 Q16790 1/20 0.33
HSD11B1 P28845 1/20 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
Lactic Acid SCHEMBL6365192 0.89 CHRM2 (0.40) HTTLMNAKMT2ACHRM2CHRM1
Bicarbonate SCHEMBL5227 0.88 ALDH1A1 (0.41) HTTLMNAKMT2ACHRM2CHRM1
SCHEMBL2417 0.86 ALDH1A1 (0.45) HTTLMNAKMT2ACHRM2CHRM1
SCHEMBL9790 0.86 ALDH1A1 (0.45) HTTLMNAKMT2ACHRM2CHRM1
SCHEMBL2229127 0.86 ALDH1A1 (0.45) HTTLMNAKMT2ACHRM2CHRM1
Acetic Acid SCHEMBL1802264 0.84 TERT (0.41) HTTCHRM2CHRM1ALDH1A1KDM4E
Isopropyl Alcohol SCHEMBL7567318 0.84 KMT2A (0.41) HTTLMNAKMT2ACHRM2CHRM1
SCHEMBL21752879 0.84 ALDH1A1 (0.43) HTTLMNAKMT2ACHRM2CHRM1
SCHEMBL21752846 0.84 ALDH1A1 (0.43) HTTLMNAKMT2ACHRM2CHRM1
Sulfuric Acid SCHEMBL6545396 0.84 ALDH1A1 (0.43) HTTLMNAKMT2ACHRM2CHRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0941065-A1 IONOPHORE-MEDIATED LIPOSOME LOADING OF WEAKLY BASIC DRUG THE UNIVERSITY OF BRITISH COLUMBIA (CA) 1999-09-15 EP disclosed
US-5837282-A DRUG DELIVERY; ENCAPSULATION OF A WEAKLY BASIC DRUG UNIVERSITY OF BRITISH COLUMBIA (CA) 1998-11-17 US disclosed
WO-1998018450-A1 IONOPHORE-MEDIATED LIPOSOME LOADING OF WEAKLY BASIC DRUG THE UNIVERSITY OF BRITISH COLUMBIA (CA) 1998-05-07 WO disclosed