Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL27891978

CCCC(=O)NN.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.71

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 20)

geneUniProtsupporting neighboursconfidence
CTSD P07339 1/20 0.71
KDM4E B2RXH2 1/20 0.46
KDM5C P41229 1/20 0.46
PHF8 Q9UPP1 1/20 0.46
KDM2A Q9Y2K7 1/20 0.46
HDAC3 O15379 2/20 0.43
HDAC1 Q13547 2/20 0.43
HDAC2 Q92769 2/20 0.43
HDAC8 Q9BY41 2/20 0.43
HDAC6 Q9UBN7 1/20 0.43
CYP1A2 P05177 2/20 0.42
CYP3A4 P08684 2/20 0.42
CYP2C19 P33261 2/20 0.42
TSHR P16473 1/20 0.42
FFAR3 O14843 1/20 0.37
ALDH1A1 P00352 1/20 0.37
MAPT P10636 1/20 0.37
HPGD P15428 1/20 0.37
L3MBTL1 Q9Y468 1/20 0.36
HIF1A Q16665 1/20 0.36

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 SCHEMBL27604045 0.88 CTSD (0.54) CTSDKDM4EKDM5CPHF8KDM2A
SCHEMBL924945 0.84
Water SCHEMBL28843605 0.82
Hydrochloric Acid SCHEMBL6177966 0.82
Cadaverine Tartrate SCHEMBL28281422 0.76 TSHR (0.48) CTSDHDAC3HDAC1HDAC2HDAC8
Cadaverine Tartrate SCHEMBL28281421 0.76 TSHR (0.48) CTSDHDAC3HDAC1HDAC2HDAC8
SCHEMBL27312923 0.76 CTSD (0.81) CTSDKDM4EKDM5CPHF8KDM2A
SCHEMBL22719915 0.75 CTSD (0.71) CTSDKDM4EKDM5CPHF8KDM2A
Cadaverine Tartrate SCHEMBL23069531 0.75 FFAR3 (0.68) KDM2AHDAC3HDAC1HDAC2HDAC8
SCHEMBL7866814 0.74 CTSD (0.77) CTSDKDM4EKDM5CPHF8KDM2A

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
CN-102898324-A Method for preparing (S)-2-aminobutanamide hydrochloride FUXIN LONGRUI CHEMICAL CO LTD 2013-01-30 CN claimed
CN-102898324-A Method for preparing (S)-2-aminobutanamide hydrochloride FUXIN LONGRUI CHEMICAL CO LTD 2013-01-30 CN disclosed