Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL9110378

CC(C)N(CC[C@H](c1ccccc1)c1cc(Cl)ccc1O)C(C)C.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.79

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
CHRM3 known ✓ P20309 10/20 0.79
ADRB2 known ✓ P07550 9/20 0.79
CHRM2 known ✓ P08172 3/20 0.79
CHRM1 known ✓ P11229 3/20 0.79
HRH1 known ✓ P35367 2/20 0.79
ESR1 known ✓ P03372 1/20 0.65
CHRM4 known ✓ P08173 1/20 0.65
HTR2A known ✓ P28223 1/20 0.65
ADRA1A known ✓ P35348 1/20 0.65
OPRK1 known ✓ P41145 1/20 0.65
CHRM5 P08912 2/20 0.79
CX3CR1 P49238 1/20 0.79
TMEM97 Q5BJF2 1/20 0.79
FFAR4 Q5NUL3 1/20 0.79
SIGMAR1 Q99720 1/20 0.79
LMNA P02545 5/20 0.65
MAPT P10636 4/20 0.65
KCNE1 P15382 1/20 0.65
PTGS1 P23219 1/20 0.65
HRH2 P25021 1/20 0.65

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 SCHEMBL9111161 1.00 CHRM3 (0.79) CHRM3ADRB2CHRM2CHRM1CHRM5
SCHEMBL9224718 0.93 CHRM3 (0.74) CHRM3ADRB2CHRM2CHRM1CHRM5
SCHEMBL4663940 0.93 CHRM3 (0.74) CHRM3ADRB2CHRM2CHRM1CHRM5
Tolterodine SCHEMBL110955 0.88 CHRM3 (1.00) CHRM3ADRB2CHRM2CHRM1CHRM5
Tolterodine SCHEMBL2403972 0.88 CHRM3 (1.00) CHRM3ADRB2CHRM2CHRM1CHRM5
Tolterodine SCHEMBL1560185 0.88 CHRM3 (1.00) CHRM3ADRB2CHRM2CHRM1CHRM5
Tolterodine SCHEMBL36881 0.88 CHRM3 (1.00) CHRM3ADRB2CHRM2CHRM1CHRM5
Tolterodine SCHEMBL467372 0.88 CHRM3 (1.00) CHRM3ADRB2CHRM2CHRM1CHRM5
Tolterodine SCHEMBL3098149 0.88 CHRM3 (1.00) CHRM3ADRB2CHRM2CHRM1CHRM5
Tolterodine SCHEMBL29873356 0.88 CHRM3 (1.00) CHRM3ADRB2CHRM2CHRM1CHRM5

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-2044001-B1 PROCESS FOR PREPARATION OF 3-(2-HYDROXY-5-SUBSTITUTED PHENYL)-N-ALKYL-3-PHENYLPROPYLAMINES LEK PHARMACEUTICALS (SI) 2016-11-23 EP disclosed
US-8193391-B2 Process for preparation of 3-(2-hydroxy-5-substituted phenyl)-N-alkyl-3-phenylpropylamines LEK PHARMACEUTICALS, D.D. (SI) 2012-06-05 US disclosed