Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL5328580

O=C(O)C(O)C(O)C(=O)O.O=C1NC(=O)C2(O)CCCCC12

nearest known ligand 0.33

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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 10)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.33
NFKB1 P19838 1/20 0.33
CYP2C19 P33261 1/20 0.33
LMNA P02545 2/20 0.31
HTT P42858 2/20 0.30
MAPT P10636 1/20 0.30
BLM P54132 1/20 0.30
CYP2D6 P10635 1/20 0.30
SMN1; SMN2 Q16637 1/20 0.30
HIF1A Q16665 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
SCHEMBL5031774 0.87 LMNA (0.34) TSHRCYP2C19LMNAHTT
SCHEMBL476025 0.87 LMNA (0.34) TSHRCYP2C19LMNAHTT
Hydrochloric Acid SCHEMBL5234106 0.85 LMNA (0.33) TSHRLMNAHTT
Maleic Acid SCHEMBL5334785 0.84 HTT (0.34) TSHRLMNAHTTMAPTSMN1; SMN2
SCHEMBL6901500 0.63 HSD11B1 (0.31)
Cadaverine Tartrate SCHEMBL4831162 0.60 TSHR (0.53) TSHRNFKB1CYP2C19LMNABLM
Cadaverine Tartrate SCHEMBL28304662 0.60 TSHR (0.53) TSHRNFKB1CYP2C19LMNABLM
Cadaverine Tartrate SCHEMBL21806468 0.59 TSHR (0.41) TSHRNFKB1CYP2C19LMNAHTT
Cadaverine Tartrate SCHEMBL21807026 0.59 TSHR (0.41) TSHRNFKB1CYP2C19LMNAHTT
SCHEMBL22966075 0.59 CYP19A1 (0.44)

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