Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL3065246

O=C(O)C(O)C(O)C(=O)O.OO

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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
TSHR P16473 3/20 1.00
TP53 P04637 1/20 0.50
CYP2C9 P11712 2/20 0.45
PDE4A P27815 1/20 0.45
LMNA P02545 2/20 0.43
ALDH1A1 P00352 2/20 0.43
THRB P10828 1/20 0.43
RECQL P46063 1/20 0.43
CYP2C19 P33261 2/20 0.42
NFKB1 P19838 1/20 0.42
OR51E2 Q9H255 1/20 0.41
HPGD P15428 2/20 0.40
HSD17B10 Q99714 2/20 0.40
TDP1 Q9NUW8 2/20 0.40
ABCB11 O95342 1/20 0.40
F2 P00734 1/20 0.40
KDM4E B2RXH2 1/20 0.40
MEN1 O00255 1/20 0.40
MAPT P10636 1/20 0.40
ALOX15 P16050 1/20 0.40

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 SCHEMBL30689288 1.00 TSHR (1.00) TSHRTP53CYP2C9PDE4ALMNA
Cadaverine Tartrate SCHEMBL848 1.00 TSHR (1.00) TSHRTP53CYP2C9PDE4ALMNA
Tartaric Acid SCHEMBL29430365 1.00 TSHR (1.00) TSHRTP53CYP2C9PDE4ALMNA
Cadaverine Tartrate SCHEMBL1062721 1.00 TSHR (1.00) TSHRTP53CYP2C9PDE4ALMNA
Cadaverine Tartrate SCHEMBL22768 1.00 TSHR (1.00) TSHRTP53CYP2C9PDE4ALMNA
Cadaverine Tartrate SCHEMBL116846 1.00 TSHR (1.00) TSHRTP53CYP2C9PDE4ALMNA
Cadaverine Tartrate SCHEMBL29382062 1.00 TSHR (1.00) TSHRTP53CYP2C9PDE4ALMNA
Cadaverine Tartrate SCHEMBL31427568 1.00 TSHR (1.00) TSHRTP53CYP2C9PDE4ALMNA
Tartaric Acid SCHEMBL5762 1.00 TSHR (1.00) TSHRTP53CYP2C9PDE4ALMNA
Cadaverine Tartrate SCHEMBL1431070 1.00 TSHR (1.00) TSHRTP53CYP2C9PDE4ALMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112142589-A Method for synthesizing cobalt oxalate dihydrate from leaching solution of positive active material of waste lithium battery 厦门理工学院 2020-12-29 CN claimed
CN-104390954-B Method for determining rhenium in smelting waste acid by complexing separation of tartaric acid and hydrogen peroxide 西北矿冶研究院 2017-05-17 CN claimed
CN-104390954-A Method for determining rhenium in smelting waste acid by complexing separation of tartaric acid and hydrogen peroxide NORTHWEAT RES INST OF MINING & METALLURG INST 2015-03-04 CN claimed
CN-103965815-A Ultralow-viscosity pressure-sensitive adhesive and ultralow-viscosity protective film ZHANGJIAGANG KANGDE XIN PHOTOELECTRIC MATERIAL CO LTD 2014-08-06 CN claimed
CN-113692651-B Method for manufacturing electronic device 信越半导体株式会社 2024-08-16 CN disclosed
US-11996496-B2 Semiconductor light-emitting device DOWA ELECTRONICS MATERIALS CO., LTD. (JP) 2024-05-28 US disclosed
WO-2024048538-A1 III-V COMPOUND SEMICONDUCTOR LIGHT-EMITTING ELEMENT AND METHOD FOR PRODUCING III-V COMPOUND SEMICONDUCTOR LIGHT-EMITTING ELEMENT DOWAエレクトロニクス株式会社 2024-03-07 WO disclosed
US-11894502-B2 Method of manufacturing semiconductor optical device and intermediate article of semiconductor optical device DOWA ELECTRONICS MATERIALS CO., LTD. (JP) 2024-02-06 US disclosed
US-11888090-B2 Semiconductor light-emitting element and method of producing semiconductor light-emitting element DOWA ELECTRONICS MATERIALS CO., LTD. (JP) 2024-01-30 US disclosed
WO-2024019098-A1 SEMICONDUCTOR LIGHT-EMITTING ELEMENT AND METHOD FOR MANUFACTURING SEMICONDUCTOR LIGHT-EMITTING ELEMENT DOWAエレクトロニクス株式会社 2024-01-25 WO disclosed
CN-116806843-A Antibacterial composite powder material and preparation method thereof 广州市科瑨材料科技有限公司 2023-09-29 CN disclosed
CN-111492494-B Semiconductor light emitting device and method for manufacturing the same 同和电子科技有限公司 2023-08-01 CN disclosed
EP-0154831-B1 ROD-SHAPED POLYMER LATEX, ROD-SHAPED POLYMER FINE POWER AND DISPERSION COMPRISING THE FINE POWDER DISPERSED IN NON-AQUEOUS MEDIUM Kao Corporation (JP) 1990-12-19 EP disclosed
US-4798721-A LATEX, WATER INSOLUBLE MONOMERS KAO CORPORATION (JP) 1989-01-17 US disclosed
US-4746455-A SHRINK RESISTANCE FOR FELTS KAO CORPORATION (JP) 1988-05-24 US disclosed
EP-0251188-A2 Liquid detergent composition for clothing articles Kao Corporation (JP) 1988-01-07 EP disclosed
EP-0214626-A2 Hair cosmetic composition Kao Corporation (JP) 1987-03-18 EP disclosed
US-4634725-A SOLUBILIZING MONOMER IN MICELLES KAO CORPORATION (JP) 1987-01-06 US disclosed
EP-0154831-A2 Rod-shaped polymer latex, rod-shaped polymer fine power and dispersion comprising the fine powder dispersed in non-aqueous medium Kao Corporation (JP) 1985-09-18 EP disclosed
US-4432920-A FORMING A MEMBRANE FROM DISPERSION BLEND OF WAXY OR FATTY SUBSTANCE AND HIGH POLYMER, THEN SOLVENT EXTRACTION DAIDO-MARUTA FINISHING CO., LTD. (JP) 1984-02-21 US disclosed