Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL5874353

CC[N+](CC)(CC)CC.O=C([O-])C(O)C(O)C(=O)O

nearest known ligand 0.46

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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 17)

geneUniProtsupporting neighboursconfidence
CHRM2 known ✓ P08172 1/20 0.32
CHRM1 known ✓ P11229 1/20 0.32
CHRM3 known ✓ P20309 1/20 0.32
TSHR P16473 6/20 0.46
CYP3A4 P08684 3/20 0.44
PMP22 Q01453 2/20 0.44
LMNA P02545 2/20 0.44
TDP1 Q9NUW8 1/20 0.44
BLM P54132 1/20 0.44
NFKB1 P19838 3/20 0.36
KCNA1 Q09470 1/20 0.36
KDM4E B2RXH2 1/20 0.35
ATM Q13315 1/20 0.35
NPSR1 Q6W5P4 2/20 0.34
CYP2C9 P11712 1/20 0.32
PDE4A P27815 1/20 0.32
TP53 P04637 1/20 0.32

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 SCHEMBL5874349 0.93 TSHR (0.42) TSHRCYP3A4PMP22LMNATDP1
Tetrapropylammonium SCHEMBL5874101 0.83 TSHR (0.42) TSHRCYP3A4PMP22LMNATDP1
Cadaverine Tartrate SCHEMBL3810388 0.80 TSHR (0.56) TSHRCYP3A4PMP22LMNATDP1
Tetrabuthylammonium SCHEMBL5874528 0.79 SLC22A1 (0.46) TSHRCYP3A4PMP22LMNATDP1
Tetrylammonium SCHEMBL36648 0.78 TSHR (0.42) TSHRCYP3A4PMP22NFKB1KCNA1
Tetrylammonium SCHEMBL5874502 0.77 TSHR (0.36) TSHRCYP3A4PMP22TDP1NFKB1
Cadaverine Tartrate SCHEMBL3209520 0.77 TSHR (0.67) TSHRCYP3A4PMP22LMNATDP1
Cadaverine Tartrate SCHEMBL21569383 0.77 TSHR (0.67) TSHRCYP3A4PMP22LMNATDP1
Cadaverine Tartrate SCHEMBL7510054 0.77 TSHR (0.67) TSHRCYP3A4PMP22LMNATDP1
Cadaverine Tartrate SCHEMBL21569402 0.77 TSHR (0.67) TSHRCYP3A4PMP22LMNATDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119684381-A Crystalline forms of nicotinamide riboside furanoside salts and nutritional supplements and pharmaceutical compositions containing same 生物合成股份公司 2025-03-25 CN disclosed
CN-119462782-A Method for producing nicotinamide riboside salts, nicotinamide riboside salts per se and use thereof 生物合成股份公司 2025-02-18 CN disclosed
US-11485915-B2 Methods of using ionic liquids as corrosion inhibitors BAKER HUGHES HOLDINGS LLC (US) 2022-11-01 US disclosed
CN-114423771-A Method for producing nicotinamide ribofuranoside salts, nicotinamide ribofuranoside salts themselves and use thereof 生物合成股份公司 2022-04-29 CN disclosed
US-20220098494-A1 METHODS OF USING IONIC LIQUIDS AS CORROSION INHIBITORS BAKER HUGHES HOLDINGS LLC 2022-03-31 US 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