Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL28355308

O=C(O)C(O)C(O)C(=O)O.O=[N+]([O-])c1cccc(B(O)O)c1

nearest known ligand 0.76

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 17)

geneUniProtsupporting neighboursconfidence
TP53 P04637 1/20 0.49
TSHR P16473 4/20 0.47
LMNA P02545 1/20 0.47
CES2 O00748 1/20 0.46
CES1 P23141 1/20 0.46
ALDH1A1 P00352 4/20 0.45
TDP1 Q9NUW8 1/20 0.45
ALOX15 P16050 1/20 0.45
KMO O15229 1/20 0.45
HTT P42858 2/20 0.43
KMT2A Q03164 2/20 0.43
MEN1 O00255 1/20 0.43
DDX3X O00571 1/20 0.43
POLB P06746 1/20 0.43
MAPT P10636 1/20 0.43
CTDSP1 Q9GZU7 1/20 0.43
GAA P10253 1/20 0.42

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
SCHEMBL29758194 0.87 TSHR (0.61) TP53TSHRLMNACES2CES1
SCHEMBL127723 0.87 TSHR (0.61) TP53TSHRLMNACES2CES1
Hydrochloric Acid SCHEMBL28382242 0.85 TSHR (0.59) TP53TSHRLMNACES2CES1
SCHEMBL6981176 0.81 ALDH1A1 (0.66) TP53TSHRLMNACES2CES1
Phosphoric Acid SCHEMBL28445592 0.81 TSHR (0.53) TP53TSHRLMNACES2CES1
SCHEMBL1668771 0.79 TSHR (0.47) TP53TSHRLMNACES2CES1
SCHEMBL28355307 0.77 TSHR (0.44) TP53TSHRLMNACES2CES1
SCHEMBL6701294 0.75 TSHR (0.46) TP53TSHRLMNACES2CES1
Cadaverine Tartrate SCHEMBL28015424 0.74 TDP1 (0.59) TSHRLMNACES2CES1ALDH1A1
SCHEMBL13857813 0.74 TP53 (0.50) TP53TSHRLMNACES2CES1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115632164-A Additive for positive electrolyte, electrolyte containing additive and application of additive 哈尔滨工业大学 2023-01-20 CN claimed
CN-111154273-A Flexible high-temperature-resistant wire and cable material and processing method thereof 何先鹏 2020-05-15 CN claimed
CN-110746885-A Sound-insulation weather-resistant waterproof coating and preparation method thereof 湖南辰砾新材料有限公司 2020-02-04 CN claimed
CN-115632164-A Additive for positive electrolyte, electrolyte containing additive and application of additive 哈尔滨工业大学 2023-01-20 CN disclosed
CN-111154273-A Flexible high-temperature-resistant wire and cable material and processing method thereof 何先鹏 2020-05-15 CN disclosed
CN-110746885-A Sound-insulation weather-resistant waterproof coating and preparation method thereof 湖南辰砾新材料有限公司 2020-02-04 CN disclosed