Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL9099144

CCC[C@@H](CN1CC(O)C1)N(C)C(=O)c1ccc(Cl)cc1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.42

Full drug profile on Sugi Atlas →

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
▸ OPRK1 known ✓ P41145 3/20 0.38
▸ CHRM2 known ✓ P08172 2/20 0.36
▸ CHRM3 known ✓ P20309 2/20 0.36
▸ OPRM1 known ✓ P35372 2/20 0.35
▸ OPRD1 known ✓ P41143 2/20 0.35
▸ KDM2B Q8NHM5 1/20 0.36
▸ CYP2D6 P10635 1/20 0.36
▸ HRH3 Q9Y5N1 2/20 0.36
▸ P2RX7 Q99572 1/20 0.35
▸ CCR1 P32246 1/20 0.35
▸ AGER Q15109 1/20 0.34

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 SCHEMBL9099141 1.00 OPRK1 (0.38) OPRK1KDM2BCYP2D6CHRM2CHRM3
SCHEMBL9100505 0.94 KDM2B (0.39) OPRK1KDM2BCHRM2CHRM3HRH3
SCHEMBL9100799 0.94 KDM2B (0.39) OPRK1KDM2BCHRM2CHRM3HRH3
SCHEMBL9100511 0.94 KDM2B (0.39) OPRK1KDM2BCHRM2CHRM3HRH3
Hydrochloric Acid SCHEMBL9102959 0.93 KDM2B (0.39) OPRK1KDM2BCHRM2CHRM3HRH3
Hydrochloric Acid SCHEMBL9102951 0.93 KDM2B (0.39) OPRK1KDM2BCHRM2CHRM3HRH3
SCHEMBL9100889 0.88 HRH3 (0.39) OPRK1KDM2BCHRM2CHRM3HRH3
SCHEMBL9100882 0.88 HRH3 (0.39) OPRK1KDM2BCHRM2CHRM3HRH3
SCHEMBL9103163 0.87 HRH3 (0.48) OPRK1KDM2BCYP2D6CHRM2CHRM3
SCHEMBL9103155 0.87 HRH3 (0.48) OPRK1KDM2BCYP2D6CHRM2CHRM3

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 OPRK1 398/4885CHRM2 55/4885CHRM3 63/4885
US-20120142659-A1 COMPOUNDS AND THEIR USE AS IKACH BLOCKERS KCNH2, KCNJ2, KCNH3 OPRK1 398/4885CHRM2 55/4885CHRM3 63/4885

“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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