Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL4493347

CC(C)N(Cc1ccccc1Oc1ccc(F)c(F)c1)[C@H]1CCNC1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.57

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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 7)

geneUniProtsupporting neighboursconfidence
SLC6A2 known ✓ P23975 18/20 0.57
SLC6A3 known ✓ Q01959 7/20 0.57
HTR2A known ✓ P28223 1/20 0.48
SLC6A4 P31645 18/20 0.57
CYP2D6 P10635 4/20 0.52
KCNH2 Q12809 5/20 0.45
MBTPS1 Q14703 1/20 0.44

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 SCHEMBL4493345 1.00 SLC6A4 (0.57) SLC6A4SLC6A2SLC6A3CYP2D6HTR2A
Cadaverine Tartrate SCHEMBL4493702 0.93 SLC6A4 (0.61) SLC6A4SLC6A2SLC6A3CYP2D6KCNH2
SCHEMBL4478195 0.93 SLC6A4 (0.56) SLC6A4SLC6A2SLC6A3CYP2D6HTR2A
SCHEMBL4485599 0.84 SLC6A4 (0.60) SLC6A4SLC6A2SLC6A3CYP2D6HTR2A
Cadaverine Tartrate SCHEMBL4499191 0.80 SLC6A2 (0.58) SLC6A4SLC6A2SLC6A3CYP2D6KCNH2
SCHEMBL5762333 0.79 SLC6A4 (0.54) SLC6A4SLC6A2SLC6A3CYP2D6HTR2A
Cadaverine Tartrate SCHEMBL4485557 0.76 SLC6A4 (0.68) SLC6A4SLC6A2SLC6A3CYP2D6KCNH2
Cadaverine Tartrate SCHEMBL4481330 0.76 SLC6A4 (0.52) SLC6A4SLC6A2SLC6A3CYP2D6KCNH2
Cadaverine Tartrate SCHEMBL4498084 0.76 SLC6A4 (0.68) SLC6A4SLC6A2SLC6A3
Cadaverine Tartrate SCHEMBL4499507 0.76 SLC6A4 (0.68) SLC6A4SLC6A2SLC6A3

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
US-7619096-B2 3-Aminopyrrolidines as inhibitors of monoamine uptake ELI LILLY AND COMPANY (US) 2009-11-17 US disclosed
EP-1638934-B1 3-AMINOPYRROLIDINES AS INHIBITORS OF MONOAMINE UPTAKE LILLY CO ELI (US) 2008-01-09 EP disclosed
US-20060270713-A1 3-Aminopyrrolidines as inhibitors of monoamine uptake ELI LILLY AND COMPANY 2006-11-30 US 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-20060270713-A1 3-Aminopyrrolidines as inhibitors of monoamine uptake SLC6A2, SLC6A3, SLC18A2 SLC6A2 1/4885SLC6A3 2/4885HTR2A 71/4885

“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.