Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL6834294

COC(=O)C(N)c1ccccc1Cl.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 20)

geneUniProtsupporting neighboursconfidence
CHRM2 known ✓ P08172 1/20 0.39
ADRA2A known ✓ P08913 1/20 0.39
HTR2A known ✓ P28223 1/20 0.39
OPRM1 known ✓ P35372 1/20 0.39
OPRK1 known ✓ P41145 1/20 0.39
ADRB2 known ✓ P07550 2/20 0.38
ADRB1 known ✓ P08588 2/20 0.38
CASP1 P29466 1/20 0.42
KMT2A Q03164 2/20 0.40
CXCL8 P10145 1/20 0.40
ROCK2 O75116 1/20 0.39
ROCK1 Q13464 1/20 0.39
MEN1 O00255 1/20 0.39
CYP1A2 P05177 1/20 0.39
CYP3A4 P08684 1/20 0.39
THRB P10828 1/20 0.39
NR1I2 O75469 1/20 0.39
ABCB11 O95342 1/20 0.39
CYP2B6 P20813 1/20 0.39
DRD1 P21728 1/20 0.39

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
Tartaric Acid SCHEMBL30358002 1.00 CASP1 (0.42) CASP1KMT2ACXCL8ROCK2ROCK1
Cadaverine Tartrate SCHEMBL29771995 1.00 CASP1 (0.42) CASP1KMT2ACXCL8ROCK2ROCK1
SCHEMBL1159853 0.91 CASP1 (0.44) CASP1KMT2ACXCL8ROCK2ROCK1
SCHEMBL13306848 0.91 CASP1 (0.44) CASP1KMT2ACXCL8ROCK2ROCK1
SCHEMBL29557046 0.91 CASP1 (0.44) CASP1KMT2ACXCL8ROCK2ROCK1
SCHEMBL29975235 0.91 CASP1 (0.44) CASP1KMT2ACXCL8ROCK2ROCK1
SCHEMBL5101666 0.91 CASP1 (0.44) CASP1KMT2ACXCL8ROCK2ROCK1
Hydrochloric Acid SCHEMBL30832053 0.89 CASP1 (0.43) CASP1KMT2ACXCL8ROCK2ROCK1
Hydrochloric Acid SCHEMBL28793542 0.89 CASP1 (0.43) CASP1KMT2ACXCL8ROCK2ROCK1
Hydrochloric Acid SCHEMBL29772137 0.89 CASP1 (0.43) CASP1KMT2ACXCL8ROCK2ROCK1

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
US-6812363-B2 HEATING WITH THIONYL CHLORIDE; CREATING MATERIAL WITH NEARLY EQUAL STEREOISOMER AMOUNTS FROM WASTE ENRICHED WITH UNWANTED ISOMERS USV LIMITED (IN) 2004-11-02 US disclosed
US-20040073057-A1 Racemization of optically active 2-substituted phenyl glycine esters USV. LTD. (CORPORATION OF INDIA) (IN) 2004-04-15 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 (1 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-20040073057-A1 Racemization of optically active 2-substituted phenyl glycine esters GLO1, SLC6A5, SLC6A9 CHRM2 4422/4885ADRA2A 3613/4885HTR2A 2448/4885

“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.