Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL5328277

O=C(CN1CCN(c2cc(F)ccc2OC2CCCC2)CC1)CN1C(=O)C2CC(O)C(O)CC2C1=O.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.36

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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 20)

geneUniProtsupporting neighboursconfidence
HRH1 known ✓ P35367 3/20 0.34
HTR2A known ✓ P28223 1/20 0.33
ADRA1D known ✓ P25100 1/20 0.32
ADRA1A known ✓ P35348 1/20 0.32
ADRA1B known ✓ P35368 1/20 0.32
MEN1 O00255 2/20 0.36
KMT2A Q03164 2/20 0.36
RAB9A P51151 1/20 0.36
PDE4A P27815 2/20 0.34
PDE4B Q07343 2/20 0.34
PDE4C Q08493 2/20 0.34
PDE4D Q08499 2/20 0.34
CCR3 P51677 3/20 0.34
HTR1A P08908 4/20 0.33
HTR7 P34969 2/20 0.33
ALDH1A1 P00352 2/20 0.33
MAPT P10636 1/20 0.33
DRD2 P14416 2/20 0.33
HRH3 Q9Y5N1 1/20 0.32
GRIN1 Q05586 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
SCHEMBL4535333 0.95 MEN1 (0.40) MEN1KMT2ARAB9APDE4APDE4B
Hydrochloric Acid SCHEMBL4526384 0.94 MEN1 (0.39) MEN1KMT2ARAB9APDE4APDE4B
Succinic Acid SCHEMBL5330872 0.93 MEN1 (0.37) MEN1KMT2ARAB9APDE4APDE4B
Fumaric Acid SCHEMBL5326133 0.92 MEN1 (0.36) MEN1KMT2ARAB9APDE4APDE4B
Maleic Acid SCHEMBL5326128 0.92 MEN1 (0.36) MEN1KMT2ARAB9APDE4APDE4B
Cadaverine Tartrate SCHEMBL5307196 0.92 MEN1 (0.36) MEN1KMT2ARAB9APDE4APDE4B
Phosphoric Acid SCHEMBL5329669 0.92 MEN1 (0.38) MEN1KMT2ARAB9APDE4APDE4B
Cadaverine Tartrate SCHEMBL5326825 0.90 RAB9A (0.46) MEN1KMT2ARAB9AHTR1AHTR7
Cadaverine Tartrate SCHEMBL5329934 0.89 HTR1A (0.43) MEN1KMT2AHTR1AHTR7DRD2
Cadaverine Tartrate SCHEMBL5332008 0.89 HTR1A (0.38) MEN1KMT2APDE4DHRH1CCR3

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 disclosed