Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL9518010

CNC(CCCc1cccc2ccccc12)c1ccccc1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.45

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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 14)

geneUniProtsupporting neighboursconfidence
OPRD1 known ✓ P41143 1/20 0.40
OPRK1 known ✓ P41145 1/20 0.40
MTNR1A P48039 2/20 0.45
KMT2A Q03164 1/20 0.43
SIGMAR1 Q99720 1/20 0.42
METAP2 P50579 1/20 0.42
LMNA P02545 1/20 0.41
MCL1 Q07820 2/20 0.40
TDP1 Q9NUW8 1/20 0.40
CMA1 P23946 1/20 0.40
ABCB1 P08183 2/20 0.39
MMP9 P14780 1/20 0.39
MMP8 P22894 1/20 0.39
MMP14 P50281 1/20 0.39

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
Cadaverine Tartrate SCHEMBL9518009 1.00 MTNR1A (0.45) MTNR1AKMT2ASIGMAR1METAP2LMNA
Oxalic Acid SCHEMBL9517878 0.91 KMT2A (0.51) MTNR1AKMT2ASIGMAR1LMNAMCL1
Oxalic Acid SCHEMBL9517875 0.91 KMT2A (0.51) MTNR1AKMT2ASIGMAR1LMNAMCL1
SCHEMBL10484309 0.90 SIGMAR1 (0.49) MTNR1AKMT2ASIGMAR1
Cadaverine Tartrate SCHEMBL9518089 0.81 METAP2 (0.47) MTNR1AKMT2ASIGMAR1METAP2LMNA
Cadaverine Tartrate SCHEMBL9518091 0.81 METAP2 (0.47) MTNR1AKMT2ASIGMAR1METAP2LMNA
Phosphoric Acid SCHEMBL9519025 0.80 ACP3 (0.47) MTNR1AKMT2ASIGMAR1LMNATDP1
Phosphoric Acid SCHEMBL9519019 0.80 ACP3 (0.47) MTNR1AKMT2ASIGMAR1LMNATDP1
Hydrochloric Acid SCHEMBL9520766 0.79 MC4R (0.47) MTNR1ASIGMAR1
Cadaverine Tartrate SCHEMBL9517398 0.78 METAP2 (0.46) MTNR1AKMT2ASIGMAR1METAP2LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0318234-B1 IMPROVEMENTS IN OR RELATING TO SELECTIVE SEROTONIN UPTAKE INHIBITORS ELI LILLY AND COMPANY (US) 1993-03-17 EP disclosed
US-4876282-A ANTIDEPRESSANT, DIETETICS, ANTIALCOHOLISM AGENT ELI LILLY AND COMPANY (US) 1989-10-24 US disclosed
EP-0318234-A2 Improvements in or relating to selective serotonin uptake inhibitors ELI LILLY AND COMPANY (US) 1989-05-31 EP disclosed