Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL6806779

O=C([O-])C(O)C(O)C(=O)[O-].O=C([O-])C(O)C(O)C(=O)[O-].O=C([O-])C(O)C(O)C(=O)[O-].[NH4+].[Nb+5]

nearest known ligand 0.48

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Known targets — ChEMBL curated mechanism

ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3BCHECHRM1CHRM2CHRM3CHRM4CHRNA3CHRNA4CHRNB2CHRNB4ESR1ESR2GABRA1GABRB1GABRG2GBA1GHSRHRH1HTR1DHTR2AMAOBOPRD1OPRK1OPRM1SLC6A2SLC6A3TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8UGCGrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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
LMNA P02545 2/20 0.48
TSHR P16473 3/20 0.44
CA4 P22748 3/20 0.38
CYP3A4 P08684 2/20 0.34
TDP1 Q9NUW8 1/20 0.34
BLM P54132 1/20 0.34
PMP22 Q01453 1/20 0.34
TP53 P04637 1/20 0.33
PDE4A P27815 1/20 0.33
CA1 P00915 1/20 0.31
FAHD1 Q6P587 1/20 0.31
NFKB1 P19838 1/20 0.30
NPSR1 Q6W5P4 1/20 0.30
SLC22A6 Q4U2R8 1/20 0.30

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 SCHEMBL223358 0.96 TSHR (0.47) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL11578822 0.92 LMNA (0.48) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL9551431 0.92 LMNA (0.48) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL3160195 0.92 LMNA (0.48) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL9551433 0.92 LMNA (0.48) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL3160181 0.92 LMNA (0.48) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL11578827 0.92 LMNA (0.48) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL5961174 0.92 LMNA (0.48) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL1938734 0.92 LMNA (0.48) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL2376153 0.92 LMNA (0.48) LMNATSHRCA4CYP3A4TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0895809-B1 Process Using Niobium-containing Aqueous Solution in Producing Niobium-containing Oxide Catalyst ASAHI CHEMICAL IND (JP) 2014-03-19 EP disclosed
CN-1216847-C Method for preparing acrylic acid from propane under the condition of free-dioxygen ATOPHINA CO (FR) 2005-08-31 CN disclosed
US-6833474-B2 Process for manufacturing acrylic acid from propane in the absence of molecular oxygen ARKEMA (FR) 2004-12-21 US disclosed
US-20040147393-A1 Preparation of a multimetal oxide composition BASF AKIENGESELLSCHAFT (DE) 2004-07-29 US disclosed
US-20030088124-A1 Process for manufacturing acrylic acid from propane in the absence of molecular oxygen ATOFINA (FR) 2003-05-08 US disclosed
CN-1375487-A Method for preparing acrylic acid from propane under the condition of free-dioxygen ATOPHINA CO (FR) 2002-10-23 CN disclosed
US-6036880-A AQUEOUS SOLUTION OF DICARBOXYLIC ACID, AN NB COMPOUND AND OPTIONALLY AMMONIA, WITH SPECIFIC DICARBOXYLIC ACID/NB MOLAR RATIO; CATALYST FOR OXIDATION OR AMMOXIDATION OR PROPANE OR ISOBUTANE TO (METH)ACRYLIC ACID OR (METH)ACRYLONITRILE ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 2000-03-14 US disclosed
EP-0895809-A1 Niobium-containing aqueous solution for use in producing niobium-containing oxide catalyst ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 1999-02-10 EP 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-20040147393-A1 Preparation of a multimetal oxide composition SOD1, SOD3, POLM LMNA 1294/4885TSHR 4238/4885CA4 141/4885

“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.