Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL3828146

Fc1ccc(-c2nc(C3CCN(C4CC4)CC3)no2)cc1F.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.45

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 20)

geneUniProtsupporting neighboursconfidence
ACKR3 P25106 2/20 0.45
USP7 Q93009 2/20 0.44
USP30 Q70CQ3 4/20 0.42
HTT P42858 1/20 0.41
LMNA P02545 1/20 0.41
KMT2A Q03164 1/20 0.41
NPC1 O15118 2/20 0.40
RAB9A P51151 2/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
S1PR4 O95977 1/20 0.39
S1PR1 P21453 1/20 0.39
S1PR3 Q99500 1/20 0.39
S1PR5 Q9H228 1/20 0.39
PLAT P00750 1/20 0.39
POLB P06746 1/20 0.39
CASP3 P42574 1/20 0.39
SENP7 Q9BQF6 1/20 0.39
SENP6 Q9GZR1 1/20 0.39
KCNH2 Q12809 1/20 0.38
CA1 P00915 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
SCHEMBL2902007 0.90 USP7 (0.49) ACKR3USP7USP30HTTLMNA
SCHEMBL12231304 0.83 USP7 (0.49) ACKR3USP7USP30HTTLMNA
Cadaverine Tartrate SCHEMBL3827865 0.82 NPC1 (0.49) NPC1RAB9ASMN1; SMN2POLBCASP3
SCHEMBL2896523 0.78 USP7 (0.55) USP7USP30HTTLMNAKMT2A
Hydrochloric Acid SCHEMBL3826936 0.77 USP7 (0.54) USP7USP30HTTLMNAKMT2A
SCHEMBL2893291 0.75 POLB (0.51) USP7USP30HTTLMNAKMT2A
SCHEMBL2902061 0.75 NPC1 (0.68) USP7USP30HTTLMNAKMT2A
SCHEMBL2896678 0.75 POLB (0.63) USP7USP30HTTLMNAKMT2A
SCHEMBL2899045 0.75 USP7 (0.56) USP7USP30HTTLMNAKMT2A
SCHEMBL10040509 0.75 USP30 (0.53) USP7USP30HTTLMNAKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1585515-B1 PIPERIDINE AND PYRROLIDINE DERIVATIVES AS ANTAGONISTS OF HISTAMINE H3 RECEPTOR HIGH POINT PHARMACEUTICALS LLC (US) 2009-09-16 EP claimed