Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL3542905

CN1C2C=C(c3scc4ccccc34)CC1CC2.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.46

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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
SLC6A2 known ✓ P23975 5/20 0.46
SLC6A3 known ✓ Q01959 5/20 0.46
OPRM1 known ✓ P35372 3/20 0.36
OPRD1 known ✓ P41143 3/20 0.36
SLC6A4 P31645 5/20 0.46
NOS3 P29474 1/20 0.36
NOS1 P29475 1/20 0.36
HTR6 P50406 1/20 0.36
KMT2A Q03164 2/20 0.36
MEN1 O00255 1/20 0.36
LMNA P02545 1/20 0.36
POLB P06746 1/20 0.36
CYP3A4 P08684 1/20 0.34
CYP2D6 P10635 1/20 0.34
CYP2C9 P11712 1/20 0.34
CYP2C19 P33261 1/20 0.34
KDM4E B2RXH2 2/20 0.33
GLA P06280 1/20 0.33
ALDH1A1 P00352 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
SCHEMBL3062713 0.90 SLC6A4 (0.52) SLC6A2SLC6A4SLC6A3NOS3NOS1
Hydrochloric Acid SCHEMBL5107087 0.89 SLC6A2 (0.51) SLC6A2SLC6A4SLC6A3NOS3NOS1
SCHEMBL7210033 0.83 SLC6A2 (0.44) SLC6A2SLC6A4SLC6A3NOS3NOS1
Cadaverine Tartrate SCHEMBL3542909 0.77 SLC6A3 (0.48) SLC6A2SLC6A4SLC6A3HTR6OPRM1
SCHEMBL3061086 0.76 SIGMAR1 (0.40) SLC6A2SLC6A4SLC6A3
SCHEMBL3060519 0.71 HTR1A (0.35) SLC6A2SLC6A4SLC6A3OPRM1OPRD1
SCHEMBL6709876 0.69 SLC6A4 (0.58) SLC6A2SLC6A4SLC6A3NOS3NOS1
SCHEMBL6490964 0.69 SLC6A4 (0.58) SLC6A2SLC6A4SLC6A3NOS3NOS1
SCHEMBL6502156 0.67 SLC6A2 (0.50) SLC6A2SLC6A4SLC6A3NOS3NOS1
SCHEMBL6498586 0.66 SLC6A4 (0.53) SLC6A2SLC6A4SLC6A3NOS3NOS1

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 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7781456-B2 Enantiomers of 3-heteroaryl-8H-8-azabicyclo(3.2.1)oct-2-ene and their use as monoamine neurotransmitter re-uptake inhibitors NEUROSEARCH A/S (DK) 2010-08-24 US disclosed
US-20080214820-A1 Enantiomers of 3-Heteroaryl-8H-8-Azabicyclo (3.2.1) Oct-2-Ene and their Use as Monoamine Neurotransmitter Re-Uptake Inhibitors NEUROSEARCH A/S (DK) 2008-09-04 US disclosed
EP-1828173-A1 ENENTIOMERS OF 3-HETEROARYL-8H-8-AZABICYCLO(3.2.1)OCT-2-ENE AND THEIR USE AS MONOAMINE NEUROTRANSMITTER RE-UPTAKE INHIBITORS NEUROSEARCH A/S (DK) 2007-09-05 EP disclosed
WO-2006064031-A1 ENANTIOMERS OF 3-HETEROARYL-8H-8-AZABICYCLO(3.2.1)OCT-2-ENE AND THEIR USE AS MONOAMINE NEUROTRANSMITTER RE-UPTAKE INHIBITORS NEUROSEARCH A/S (DK) 2006-06-22 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20080214820-A1 Enantiomers of 3-Heteroaryl-8H-8-Azabicyclo (3.2.1) Oct-2-Ene and their Use as Monoamine Neurotransmitter Re-Uptake Inhibitors SLC18A2, SLC6A2, SLC18A3 SLC6A2 2/4885SLC6A3 5/4885OPRM1 47/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.