Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL164158

CC=O.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.67

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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 14)

geneUniProtsupporting neighboursconfidence
TSHR P16473 5/20 0.67
TP53 P04637 1/20 0.44
NFKB1 P19838 1/20 0.39
CYP2C19 P33261 1/20 0.39
CYP2C9 P11712 1/20 0.36
PDE4A P27815 1/20 0.36
PGD P52209 1/20 0.34
CYP3A4 P08684 1/20 0.32
TDP1 Q9NUW8 1/20 0.32
LMNA P02545 1/20 0.32
BLM P54132 1/20 0.32
PMP22 Q01453 1/20 0.32
GRIK1 P39086 3/20 0.32
GRIK2 Q13002 3/20 0.32

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 SCHEMBL4655414 0.83 TSHR (0.71) TSHRTP53NFKB1CYP2C19CYP2C9
Cadaverine Tartrate SCHEMBL8945831 0.82 TSHR (0.83) TSHRTP53NFKB1CYP2C19CYP2C9
Cadaverine Tartrate SCHEMBL4778934 0.82 TSHR (0.83) TSHRTP53NFKB1CYP2C19CYP2C9
Cadaverine Tartrate SCHEMBL1431070 0.82 TSHR (1.00) TSHRTP53NFKB1CYP2C19CYP2C9
Cadaverine Tartrate SCHEMBL116846 0.82 TSHR (1.00) TSHRTP53NFKB1CYP2C19CYP2C9
Cadaverine Tartrate SCHEMBL848 0.82 TSHR (1.00) TSHRTP53NFKB1CYP2C19CYP2C9
Cadaverine Tartrate SCHEMBL31427568 0.82 TSHR (1.00) TSHRTP53NFKB1CYP2C19CYP2C9
Cadaverine Tartrate SCHEMBL1062721 0.82 TSHR (1.00) TSHRTP53NFKB1CYP2C19CYP2C9
Cadaverine Tartrate SCHEMBL22768 0.82 TSHR (1.00) TSHRTP53NFKB1CYP2C19CYP2C9
Tartaric Acid SCHEMBL5762 0.82 TSHR (1.00) TSHRTP53NFKB1CYP2C19CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106232636-B Ceramics forming with or conductive paste binder and their purposes 株式会社可乐丽 2018-12-21 CN disclosed
EP-2611444-A1 HETEROCYCLYL COMPOUNDS AS HISTAMINE H3 RECEPTOR LIGANDS Suven Life Sciences Limited (IN) 2013-07-10 EP disclosed
WO-2012029070-A1 HETEROCYCLYL COMPOUNDS AS HISTAMINE H3 RECEPTOR LIGANDS SUVEN LIFE SCIENCES LIMITED (IN) 2012-03-08 WO disclosed