Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL9102604

CC(C)C(CN1CCCC1)N(C)C(=O)c1ccc(Br)cc1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.52

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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 11)

geneUniProtsupporting neighboursconfidence
▸ CHRM2 known ✓ P08172 1/20 0.38
▸ ADRA2B known ✓ P18089 1/20 0.38
▸ POLB P06746 1/20 0.40
▸ KDM4E B2RXH2 1/20 0.38
▸ ALDH1A1 P00352 1/20 0.38
▸ ALOX12 P18054 1/20 0.38
▸ NPSR1 Q6W5P4 1/20 0.38
▸ L3MBTL1 Q9Y468 1/20 0.38
▸ DRD3 P35462 1/20 0.38
▸ SIGMAR1 Q99720 1/20 0.38
▸ HRH3 Q9Y5N1 1/20 0.38

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 SCHEMBL9102608 1.00 POLB (0.40) POLBKDM4EALDH1A1ALOX12NPSR1
Cadaverine Tartrate SCHEMBL9103109 0.98 KDM4E (0.38) POLBKDM4EALDH1A1ALOX12NPSR1
Cadaverine Tartrate SCHEMBL9103123 0.98 KDM4E (0.38) POLBKDM4EALDH1A1ALOX12NPSR1
Cadaverine Tartrate SCHEMBL9280582 0.98 KDM4E (0.38) POLBKDM4EALDH1A1ALOX12NPSR1
Cadaverine Tartrate SCHEMBL9281571 0.98 KDM4E (0.38) POLBKDM4EALDH1A1ALOX12NPSR1
Cadaverine Tartrate SCHEMBL9103117 0.98 KDM4E (0.38) POLBKDM4EALDH1A1ALOX12NPSR1
SCHEMBL9100128 0.93 POLB (0.44) POLBKDM4EALDH1A1ALOX12NPSR1
SCHEMBL9108282 0.93 POLB (0.44) POLBKDM4EALDH1A1ALOX12NPSR1
SCHEMBL9100121 0.93 POLB (0.44) POLBKDM4EALDH1A1ALOX12NPSR1
SCHEMBL9103602 0.92 POLB (0.46) POLBALDH1A1CHRM2ADRA2BDRD3

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-20130143858-A1 COMPOUNDS AND THEIR USE AS IKACH BLOCKERS ASTRAZENECA AB (SE) 2013-06-06 — — US disclosed
US-8361998-B2 Compounds and their use as IKACh blockers ASTRAZENECA AB 2013-01-29 — — US disclosed
WO-2012074469-A1 NEW IKACH BLOCKERS ASTRAZENECA AB (SE) 2012-06-07 — — WO disclosed
US-20120142659-A1 COMPOUNDS AND THEIR USE AS IKACH BLOCKERS ASTRAZENECA AB (SE) 2012-06-07 — — 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 (2 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-20130143858-A1 COMPOUNDS AND THEIR USE AS IKACH BLOCKERS KCNH2, KCNJ2, KCNH3 CHRM2 55/4885ADRA2B 165/4885POLB 4552/4885
US-20120142659-A1 COMPOUNDS AND THEIR USE AS IKACH BLOCKERS KCNH2, KCNJ2, KCNH3 CHRM2 55/4885ADRA2B 165/4885POLB 4552/4885

“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.

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