Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL5849599

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

nearest known ligand 0.62

Full drug profile on Sugi Atlas →

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 5/20 0.62
LMNA P02545 2/20 0.44
CYP3A4 P08684 2/20 0.44
TDP1 Q9NUW8 1/20 0.44
BLM P54132 1/20 0.44
PMP22 Q01453 1/20 0.44
CA4 P22748 3/20 0.38
TP53 P04637 1/20 0.35
CYP2C9 P11712 1/20 0.35
PDE4A P27815 1/20 0.35
NFKB1 P19838 2/20 0.33
FAHD1 Q6P587 1/20 0.33
CYP2C19 P33261 1/20 0.33
CA1 P00915 1/20 0.32
NPSR1 Q6W5P4 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 SCHEMBL9474227 0.97 TSHR (0.67) TSHRLMNACYP3A4TDP1BLM
Cadaverine Tartrate SCHEMBL191753 0.97 TSHR (0.67) TSHRLMNACYP3A4TDP1BLM
Cadaverine Tartrate SCHEMBL6332969 0.97 TSHR (0.67) TSHRLMNACYP3A4TDP1BLM
Cadaverine Tartrate SCHEMBL11054858 0.97 TSHR (0.67) TSHRLMNACYP3A4TDP1BLM
Cadaverine Tartrate SCHEMBL8467361 0.97 TSHR (0.67) TSHRLMNACYP3A4TDP1BLM
Cadaverine Tartrate SCHEMBL263200 0.97 TSHR (0.67) TSHRLMNACYP3A4TDP1BLM
Cadaverine Tartrate SCHEMBL4111185 0.97 TSHR (0.67) TSHRLMNACYP3A4TDP1BLM
Cadaverine Tartrate SCHEMBL29824737 0.97 TSHR (0.67) TSHRLMNACYP3A4TDP1BLM
Cadaverine Tartrate SCHEMBL263201 0.97 TSHR (0.67) TSHRLMNACYP3A4TDP1BLM
Cadaverine Tartrate SCHEMBL7804046 0.94 TSHR (0.62) TSHRLMNACYP3A4TDP1BLM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111547705-B Preparation method of porous carbon electrode material 中国计量大学 2022-03-29 CN claimed
CN-111547705-A Preparation method of porous carbon electrode material 中国计量大学 2020-08-18 CN claimed
US-20150374597-A1 DENTAL BLEACHING COMPOSITION OSSTEMIMPLANT CO., LTD (KR) 2015-12-31 US claimed
EP-2957276-A1 DENTAL BLEACHING COMPOSITION Osstem Implant Co., Ltd. (KR) 2015-12-23 EP claimed
CN-105025871-A Dental bleaching composition OSSTEM IMPLANT CO LTD 2015-11-04 CN claimed
CN-101723473-A Preparation method of multivariate doping spherical alpha-Ni(OH)2 with nanometer secondary structure UNIV BEIJING CHEMICAL 2010-06-09 CN claimed
JP-58187167-A None JP disclosed
JP-58187166-A None JP disclosed
CN-119950500-A Tobacco pest-reducing and pain-relieving products and methods thereof 瑞迪美天然有限公司 2025-05-09 CN disclosed
WO-2025058941-A1 TOBACCO HARM REDUCTION AND PAIN RELIEF PRODUCTS AND METHODS THEREOF Ready Mix Naturals, LLC (US) 2025-03-20 WO disclosed
US-20250082627-A1 TOBACCO HARM REDUCTION AND PAIN RELIEF PRODUCTS AND METHODS THEREOF Ready Mix Naturals, LLC (US) 2025-03-13 US disclosed
CN-118146418-A Raceme resolution method based on selective dissolution and chiral polymer used by same 西安交通大学 2024-06-07 CN disclosed
CN-115236156-A PAN-BSA (PAN-bovine serum albumin) compound modified electrode for chiral recognition of tryptophan enantiomer as well as preparation method and application of PAN-BSA compound modified electrode 常州大学 2022-10-25 CN disclosed
US-4329533-A Shape selective reactions with zeolite catalysts modified with group IA metals MOBIL OIL CORPORATION (US) 1982-05-11 US disclosed
US-4324681-A Chiral supports for resolution of racemates UOP INC. (US) 1982-04-13 US disclosed
US-4322310-A Chiral supports for resolution of racemates UOP INC. (US) 1982-03-30 US disclosed
US-4318819-A Chiral supports for resolution of racemates UOP INC. (US) 1982-03-09 US disclosed
US-4318820-A Chiral supports for resolution of racemates UOP INC. (US) 1982-03-09 US disclosed
EP-0039536-A1 Shape selective reactions with zeolite catalysts modified with group 1A metals MOBIL OIL CORPORATION (US) 1981-11-11 EP disclosed
US-3953504-A Racemization of optically active tartaric acid NIPPON PEROXIDE CO., LTD. (JA) 1976-04-27 US 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-20250082627-A1 TOBACCO HARM REDUCTION AND PAIN RELIEF PRODUCTS AND METHODS THEREOF OPRK1, SYMPK, TAS2R9 TSHR 306/4885LMNA 4012/4885CYP3A4 1266/4885

“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.