Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL5307196

O=C(CN1CCN(c2cc(F)ccc2OC2CCCC2)CC1)CN1C(=O)C2CC=CCC2C1=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
MEN1 O00255 1/20 0.36
KMT2A Q03164 1/20 0.36
RAB9A P51151 2/20 0.36
NPC1 O15118 1/20 0.35
GFER P55789 1/20 0.35
L3MBTL1 Q9Y468 1/20 0.35
LMNA P02545 1/20 0.34
PDE4A P27815 3/20 0.34
PDE4B Q07343 3/20 0.34
PDE4C Q08493 3/20 0.34
PDE4D Q08499 3/20 0.34
CCR3 P51677 3/20 0.34
HTR1A P08908 2/20 0.33
HTR7 P34969 2/20 0.33
TSHR P16473 1/20 0.33
HSD17B10 Q99714 1/20 0.33
ALDH1A1 P00352 1/20 0.33
MAPT P10636 1/20 0.33
FFAR4 Q5NUL3 1/20 0.33

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
SCHEMBL4521906 0.94 MEN1 (0.40) MEN1KMT2ARAB9ANPC1GFER
Hydrochloric Acid SCHEMBL4533811 0.93 MEN1 (0.40) MEN1KMT2ARAB9ANPC1GFER
Cadaverine Tartrate SCHEMBL5328277 0.92 MEN1 (0.36) MEN1KMT2ARAB9APDE4APDE4B
Succinic Acid SCHEMBL5295485 0.92 MEN1 (0.38) MEN1KMT2ARAB9ANPC1GFER
Fumaric Acid SCHEMBL5295663 0.91 MEN1 (0.37) MEN1KMT2ARAB9ANPC1GFER
Maleic Acid SCHEMBL5297128 0.91 MEN1 (0.37) MEN1KMT2ARAB9ANPC1GFER
Phosphoric Acid SCHEMBL5303126 0.91 MEN1 (0.38) MEN1KMT2ARAB9ANPC1GFER
SCHEMBL4535333 0.86 MEN1 (0.40) MEN1KMT2ARAB9APDE4APDE4B
Hydrochloric Acid SCHEMBL4526384 0.85 MEN1 (0.39) MEN1KMT2ARAB9APDE4APDE4B
Succinic Acid SCHEMBL5330872 0.84 MEN1 (0.37) MEN1KMT2ARAB9APDE4APDE4B

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