Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL5328579

O=C(O)C(O)C(O)C(=O)O.O=C1C2CCCCC2C(=O)N1O

nearest known ligand 0.44

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
TSHR P16473 2/20 0.39
ALDH1A1 P00352 3/20 0.36
CYP2C19 P33261 2/20 0.35
NFKB1 P19838 1/20 0.35
HTT P42858 1/20 0.35
NPC1 O15118 1/20 0.35
RAB9A P51151 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
KMT2A Q03164 2/20 0.34
CYP1A2 P05177 1/20 0.34
CYP2C9 P11712 1/20 0.34
STAT3 P40763 1/20 0.34
KDM4E B2RXH2 3/20 0.33
POLB P06746 2/20 0.33
L3MBTL1 Q9Y468 2/20 0.33
GAA P10253 1/20 0.33
HPGD P15428 1/20 0.33
NTSR1 P30989 1/20 0.33
NPSR1 Q6W5P4 1/20 0.33
BLM P54132 1/20 0.32

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
SCHEMBL44008 0.83 POLB (0.41) TSHRALDH1A1CYP2C19HTTNPC1
SCHEMBL486926 0.83 POLB (0.41) TSHRALDH1A1CYP2C19HTTNPC1
SCHEMBL18072219 0.83 POLB (0.41) TSHRALDH1A1CYP2C19HTTNPC1
Hydrochloric Acid SCHEMBL5234099 0.81 POLB (0.40) TSHRALDH1A1CYP2C19HTTNPC1
Fumaric Acid SCHEMBL5334788 0.78 HTT (0.40) TSHRALDH1A1CYP2C19HTTNPC1
Maleic Acid SCHEMBL5334783 0.78 HTT (0.40) TSHRALDH1A1CYP2C19HTTNPC1
SCHEMBL7802041 0.69 KDM4E (0.45) ALDH1A1HTTNPC1RAB9ASMN1; SMN2
SCHEMBL7796000 0.69 KDM4E (0.45) ALDH1A1HTTNPC1RAB9ASMN1; SMN2
Cadaverine Tartrate SCHEMBL28201992 0.69 TSHR (0.48) TSHRALDH1A1CYP2C19NFKB1
Cadaverine Tartrate SCHEMBL28304662 0.68 TSHR (0.53) TSHRALDH1A1CYP2C19NFKB1SMN1; SMN2

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-2007010504-A2 ACID ADDITION SALTS OF ISOINDOLES ACTING AS ADRENERGIC RECEPTOR ANTAGONISTS RANBAXY LABORATORIES LIMITED (IN) 2007-01-25 WO claimed