Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL8448124

C[C@H](ON)c1cccc(C(F)(F)F)c1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.52

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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 17)

geneUniProtsupporting neighboursconfidence
IDO1 P14902 3/20 0.52
TDO2 P48775 3/20 0.52
CES2 O00748 1/20 0.48
PNMT P11086 1/20 0.48
ADAMTS4 O75173 1/20 0.46
MMP13 P45452 1/20 0.46
PPARG P37231 3/20 0.45
FFAR4 Q5NUL3 1/20 0.45
NPSR1 Q6W5P4 2/20 0.45
ACP3 P15309 1/20 0.45
KDM4E B2RXH2 2/20 0.44
LMNA P02545 1/20 0.44
HIF1A Q16665 1/20 0.44
AKR1C3 P42330 2/20 0.44
AKR1C2 P52895 2/20 0.44
SMN1; SMN2 Q16637 1/20 0.43
EPHX1 P07099 1/20 0.43

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
SCHEMBL8464360 0.87 IDO1 (0.61) IDO1TDO2CES2PNMTNPSR1
SCHEMBL8410943 0.87 IDO1 (0.61) IDO1TDO2CES2PNMTNPSR1
SCHEMBL8460159 0.87 IDO1 (0.61) IDO1TDO2CES2PNMTNPSR1
SCHEMBL2166743 0.81 CES2 (0.54) CES2PNMTPPARGNPSR1ACP3
SCHEMBL514285 0.77 EPHX1 (0.49) IDO1TDO2CES2PNMTADAMTS4
SCHEMBL1760202 0.76 AKR1C3 (0.66) CES2PNMTNPSR1ACP3KDM4E
SCHEMBL1993610 0.76 AKR1C3 (0.66) CES2PNMTNPSR1ACP3KDM4E
SCHEMBL3077103 0.76 CES2 (0.50) IDO1TDO2CES2PNMTADAMTS4
SCHEMBL14983791 0.75 CES2 (0.53) IDO1TDO2CES2PNMTADAMTS4
SCHEMBL8410668 0.75 NPSR1 (0.50) IDO1TDO2CES2PNMTADAMTS4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-11322693-A None JP disclosed
JP-H11322693-A PRODUCTION OF OPTICALLY ACTIVE METHOXYIMINOACETAMIDE DERIVATIVE MITSUBISHI CHEMICAL CORP 1999-11-24 JP disclosed