Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL5874849

O=C(O)C(O)C(O)C(=O)O.OCCN(CCO)CCO.OCCN(CCO)CCO

nearest known ligand 0.53

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
▸ GBA1 known ✓ P04062 1/20 0.37
▸ CHRM2 known ✓ P08172 1/20 0.36
▸ ADRA2A known ✓ P08913 1/20 0.36
▸ SLC6A2 known ✓ P23975 1/20 0.36
▸ ADRA1A known ✓ P35348 1/20 0.36
▸ SLC6A3 known ✓ Q01959 1/20 0.36
▸ TSHR P16473 4/20 0.53
▸ CYP2C9 P11712 1/20 0.41
▸ PDE4A P27815 1/20 0.41
▸ KDM4E B2RXH2 4/20 0.38
▸ ALOX15 P16050 2/20 0.38
▸ MAPT P10636 2/20 0.38
▸ SMN1; SMN2 Q16637 2/20 0.38
▸ TDP1 Q9NUW8 2/20 0.38
▸ OR51E2 Q9H255 1/20 0.38
▸ EYA2 O00167 1/20 0.38
▸ APP P05067 1/20 0.38
▸ ACE P12821 1/20 0.38
▸ LMNA P02545 1/20 0.36
▸ DRD1 P21728 1/20 0.36

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 SCHEMBL8339185 1.00 TSHR (0.53) TSHRCYP2C9PDE4AKDM4EALOX15
Cadaverine Tartrate SCHEMBL8830362 1.00 TSHR (0.53) TSHRCYP2C9PDE4AKDM4EALOX15
Mucic Acid SCHEMBL9324826 0.90 PDE4A (0.54) TSHRCYP2C9PDE4AKDM4EALOX15
Cadaverine Tartrate SCHEMBL1131873 0.85 KDM5A (0.41) TSHRMAPT
Cadaverine Tartrate SCHEMBL1132209 0.85 KDM5A (0.41) TSHRMAPT
Cadaverine Tartrate SCHEMBL8830361 0.84 TSHR (0.37) TSHRCYP2C9PDE4ASMN1; SMN2GBA1
Trolamine SCHEMBL338255 0.82 TP53 (0.55) KDM4EALOX15MAPTSMN1; SMN2OR51E2
Trolamine SCHEMBL31438317 0.82 TP53 (0.55) KDM4EALOX15MAPTSMN1; SMN2OR51E2
Gluconic Acid SCHEMBL290784 0.81 PDE4A (0.73) TSHRCYP2C9PDE4AKDM4EALOX15
Gluconic Acid SCHEMBL27994593 0.81 PDE4A (0.73) TSHRCYP2C9PDE4AKDM4EALOX15

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
US-20240138403-A1 Synergistic Combinations for Reducing Volatility of Auxin Herbicides ETHOX CHEMICALS, LLC 2024-05-02 — — US disclosed
US-20230021295-A1 Synergistic Combinations for Reducing Volatility of Auxin Herbicides ETHOX CHEMICALS, LLC 2023-01-19 — — US disclosed
WO-2023278670-A1 SYNERGISTIC COMBINATIONS FOR REDUCING VOLATILITY OF AUXIN HERBICIDES ETHOX CHEMICALS, LLC (US) 2023-01-05 — — WO disclosed
EP-3518878-A1 IMPROVED CONDITIONING HAIR TREATMENT PRODUCT WITH WASHOUT PROTECTION Henkel AG & Co. KGaA (DE) 2019-08-07 — — EP disclosed
US-7128976-B2 Composition for film formation, method of film formation, and silica-based film JSR CORPORATION (JP) 2006-10-31 — — US disclosed
US-20030091838-A1 Composition for film formation, method of film formation, and silica-based film JSR CORPORATION (JP) 2003-05-15 — — US disclosed
EP-0077674-A2 Viscous compositions containing amidobetaines and salts UNILEVER PLC (GB) 1983-04-27 — — EP disclosed
US-4375421-A COSMETICS, CLEANING COMPOUNDS LEVER BROTHERS COMPANY (US) 1983-03-01 — — US disclosed
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