Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL7413552

COc1ccc([C@H]2Sc3c(ccc4ccccc34)N(CCN(C)C)C(=O)[C@H]2O)cc1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.50

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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
▸ ADRA1A known ✓ P35348 1/20 0.50
▸ CACNA1S Q13698 14/20 0.50
▸ CYP3A4 P08684 3/20 0.50
▸ TSHR P16473 2/20 0.50
▸ ABCB11 O95342 2/20 0.50
▸ LMNA P02545 2/20 0.50
▸ KCNH2 Q12809 2/20 0.50
▸ SLC22A1 O15245 1/20 0.50
▸ CACNA1F O60840 1/20 0.50
▸ ABCB1 P08183 1/20 0.50
▸ HRH2 P25021 1/20 0.50
▸ SCN1A P35498 1/20 0.50
▸ SCN4A P35499 1/20 0.50
▸ HTT P42858 1/20 0.50
▸ SCN7A Q01118 1/20 0.50
▸ CACNA1D Q01668 1/20 0.50
▸ PLAUR Q03405 1/20 0.50
▸ CACNA1C Q13936 1/20 0.50
▸ SCN5A Q14524 1/20 0.50
▸ SCN9A Q15858 1/20 0.50

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
SCHEMBL7408217 0.94 CACNA1S (0.55) CACNA1SCYP3A4TSHRABCB11LMNA
SCHEMBL7341326 0.94 CACNA1S (0.55) CACNA1SCYP3A4TSHRABCB11LMNA
SCHEMBL7341332 0.94 CACNA1S (0.55) CACNA1SCYP3A4TSHRABCB11LMNA
Hydrochloric Acid SCHEMBL7407218 0.93 CACNA1S (0.55) CACNA1SCYP3A4TSHRABCB11LMNA
Hydrochloric Acid SCHEMBL7410583 0.93 CACNA1S (0.55) CACNA1SCYP3A4TSHRABCB11LMNA
SCHEMBL7412147 0.89 CACNA1S (0.49) CACNA1SCYP3A4TSHRABCB11LMNA
Hydrochloric Acid SCHEMBL7404446 0.88 CACNA1S (0.49) CACNA1SCYP3A4TSHRABCB11LMNA
SCHEMBL7412063 0.86 CACNA1S (0.45) CACNA1SCYP3A4TSHRABCB11LMNA
SCHEMBL7408989 0.85 CACNA1S (0.45) CACNA1SCYP3A4TSHRABCB11LMNA
SCHEMBL10721502 0.85 CACNA1S (0.45) CACNA1SCYP3A4TSHRABCB11LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0234561-A2 2,3-Dihydro-2-phenyl-5-aminoalkyl-naphtho [1,2-b]-1,4-thiazepin-4(5H)-one derivatives F. HOFFMANN-LA ROCHE AG (CH) 1987-09-02 — — EP disclosed
US-4652561-A HYPOTENSIVE AGENTS, ANTIISCHEMIC AGENTS HOFFMANN-LA ROCHE INC. (US) 1987-03-24 — — US disclosed
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