Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL9058804

O=C(O)C(O)C(O)C(=O)O.O=C(O)CC(S)(S)C(=O)O

nearest known ligand 0.46

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 19)

geneUniProtsupporting neighboursconfidence
CHRM1 known ✓ P11229 1/20 0.32
ADRA1A known ✓ P35348 1/20 0.32
TSHR P16473 3/20 0.46
ACLY P53396 3/20 0.43
CPT2 P23786 1/20 0.43
ALDH1A1 P00352 1/20 0.42
CYP2D6 P10635 1/20 0.36
CYP2C19 P33261 1/20 0.36
HIF1A Q16665 1/20 0.36
TDP1 Q9NUW8 1/20 0.33
MIF P14174 1/20 0.32
CYP2C9 P11712 1/20 0.32
PDE4A P27815 1/20 0.32
SMN1; SMN2 Q16637 1/20 0.32
HMGCR P04035 1/20 0.32
TBXA2R P21731 1/20 0.32
HSPD1 P10809 1/20 0.30
BLM P54132 1/20 0.30
HSPE1 P61604 1/20 0.30

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
SCHEMBL14940 0.85 ALDH1A1 (0.55) TSHRACLYCPT2ALDH1A1CYP2D6
SCHEMBL10797042 0.83 ALDH1A1 (0.52) TSHRACLYCPT2ALDH1A1CYP2D6
SCHEMBL8721139 0.83 ALDH1A1 (0.52) TSHRACLYCPT2ALDH1A1CYP2D6
SCHEMBL20973099 0.83 ALDH1A1 (0.52) TSHRACLYCPT2ALDH1A1CYP2D6
SCHEMBL11405967 0.83 ALDH1A1 (0.52) TSHRACLYCPT2ALDH1A1CYP2D6
Succimer SCHEMBL2511150 0.82 TDP1 (0.50) TSHRACLYCPT2ALDH1A1CYP2D6
SCHEMBL330107 0.80 ALDH1A1 (0.50) TSHRACLYCPT2ALDH1A1CYP2D6
SCHEMBL2770806 0.80 ALDH1A1 (0.50) TSHRACLYCPT2ALDH1A1CYP2D6
Citric Acid SCHEMBL1553183 0.79 ALDH1A1 (0.71) TSHRACLYCPT2ALDH1A1CYP2D6
Citric Acid SCHEMBL19205892 0.77 ALDH1A1 (0.68) TSHRACLYCPT2ALDH1A1CYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-1996016327-A1 FLUORESCENT METAL-CHELATING AMPHIPHILE AND SENSOR CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 1996-05-30 WO claimed