Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL3586505

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-].O=C([O-])C(O)C(O)C(=O)[O-].O=C([O-])C(O)C(O)C(=O)[O-].[V+5].[V+5]

nearest known ligand 0.50

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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 15)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.47
LMNA P02545 2/20 0.43
CA4 P22748 3/20 0.40
CYP3A4 P08684 2/20 0.35
TDP1 Q9NUW8 1/20 0.35
BLM P54132 1/20 0.35
PMP22 Q01453 1/20 0.35
TP53 P04637 1/20 0.35
CA1 P00915 3/20 0.33
FAHD1 Q6P587 1/20 0.33
NFKB1 P19838 1/20 0.32
NPSR1 Q6W5P4 1/20 0.32
SLC22A6 Q4U2R8 1/20 0.32
CA2 P00918 1/20 0.31
CA9 Q16790 1/20 0.31

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 SCHEMBL2376153 0.96 LMNA (0.48) TSHRLMNACA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL3591252 0.92 TSHR (0.47) TSHRLMNACA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL119095 0.92 TSHR (0.47) TSHRLMNACA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL223358 0.92 TSHR (0.47) TSHRLMNACA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL5141545 0.92 TSHR (0.47) TSHRLMNACA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL23855755 0.92 TSHR (0.47) TSHRLMNACA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL1985645 0.92 TSHR (0.47) TSHRLMNACA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL16527654 0.92 TSHR (0.47) TSHRLMNACA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL813951 0.92 TSHR (0.47) TSHRLMNACA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL6355357 0.92 TSHR (0.47) TSHRLMNACA4CYP3A4TDP1

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 82 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111135829-B Ammonia oxidation catalyst and preparation method and application thereof 万华化学集团股份有限公司 2022-09-20 CN claimed
CN-109847744-B Ammoxidation catalyst, process for producing the same and process for producing isophthalonitrile 万华化学集团股份有限公司 2022-02-15 CN claimed
CN-112703055-A Selective oxidation catalyst and oxidation of C in the presence of a selective oxidation catalyst2Process for the production of hydrocarbons 沙特基础工业全球技术公司 2021-04-23 CN claimed
CN-111135829-A Ammonia oxidation catalyst and preparation method and application thereof 万华化学集团股份有限公司 2020-05-12 CN claimed
CN-119985456-A Method for detecting content of niobium element in iron-nickel-based superalloy 西安热工研究院有限公司 2025-05-13 CN disclosed
EP-3650120-B1 FLUIDIZED-BED CATALYST APPLICABLE TO HALOARYLNITRILE PRODUCTION, AND PREPARATION AND APPLICATION THEREOF CHINA PETROLEUM & CHEM CORP (CN) 2024-09-18 EP disclosed
CN-117917273-A Ammonia oxidation catalyst, preparation method thereof and method for co-producing m-methylbenzonitrile and m-phthalonitrile by m-xylene gas-phase ammonia oxidation 中国石油化工股份有限公司 2024-04-23 CN disclosed
CN-115518688-B Catalyst for producing 2, 6-dichlorobenzonitrile and preparation method thereof 中国石油化工股份有限公司 2024-01-26 CN disclosed
CN-112457214-B Synthesis method of 4-nitrophthalonitrile 鞍山七彩化学股份有限公司 2023-11-24 CN disclosed
CN-114471645-B Catalyst for producing isophthalonitrile by gas phase ammoxidation and preparation method and application thereof 中国石油化工股份有限公司 2023-08-29 CN disclosed
CN-115518688-A Catalyst for producing 2, 6-dichlorobenzonitrile and preparation method thereof 中国石油化工股份有限公司 2022-12-27 CN disclosed
CN-112473569-B Fluidized bed reactor and reaction method thereof 鞍山七彩化学股份有限公司 2022-11-18 CN disclosed
EP-0339680-B1 Process for producing cyanopyridines MITSUBISHI GAS CHEMICAL CO (JP) 1996-03-06 EP disclosed
US-5407878-A Magnesium, lanthanum, aluminum oxides and oxidation promoters W. R. GRACE & CO.-CONN. (US) 1995-04-18 US disclosed
US-5338759-A Oral therapy for diabetes YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) 1994-08-16 US disclosed
EP-0554968-A1 Metal passivation/SOx control compositions for FCC W.R. Grace & Co.-Conn. (US) 1993-08-11 EP disclosed
WO-1993007155-A1 VANADYL COMPLEXES OF HYDROXAMATE CHELATORS AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEM YEDA RESEARCH AND DEVELOPMENT CO., LTD. (IL) 1993-04-15 WO disclosed
US-4963687-A Process for producing cyanopyridines MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1990-10-16 US disclosed
EP-0339680-A2 Process for producing cyanopyridines MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1989-11-02 EP disclosed
US-4002653-A Manufacture of anthraquinone BASF AKTIENGESELLSCHAFT (DT) 1977-01-11 US disclosed