Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL28055271

Cc1ccccc1C.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.50

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
TSHR P16473 2/20 0.50
ACHE P22303 1/20 0.50
LMNA P02545 3/20 0.46
MAPK1 P28482 1/20 0.46
CYP2D6 P10635 1/20 0.42
SRC P12931 1/20 0.42
CES2 O00748 1/20 0.42
CES1 P23141 1/20 0.42
NPC1 O15118 1/20 0.41
RAB9A P51151 1/20 0.41
L3MBTL1 Q9Y468 1/20 0.41
HPGD P15428 3/20 0.41
MYC P01106 1/20 0.41
POLB P06746 1/20 0.41
HIF1A Q16665 1/20 0.41
KDM4E B2RXH2 1/20 0.41
ALDH1A1 P00352 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 SCHEMBL29071383 1.00 TSHR (0.50) TSHRACHELMNAMAPK1CYP2D6
Cadaverine Tartrate SCHEMBL9732307 0.85 LMNA (0.55) TSHRACHELMNAMAPK1CYP2D6
Cadaverine Tartrate SCHEMBL18586007 0.85 LMNA (0.55) TSHRACHELMNAMAPK1CYP2D6
Toluic Acid SCHEMBL27797922 0.85 ALDH1A1 (0.52) LMNAHPGDMYCPOLBHIF1A
SCHEMBL15552196 0.82 ACP3 (0.46) LMNAMAPK1CYP2D6SRCL3MBTL1
O-Xylene SCHEMBL27483991 0.82 L3MBTL1 (0.38) TSHRLMNAMAPK1CYP2D6L3MBTL1
O-Xylene SCHEMBL7498508 0.81 TSHR (0.67) TSHRACHECES2CES1NPC1
O-Xylene SCHEMBL28509799 0.81 TSHR (0.67) TSHRACHECES2CES1NPC1
Biphenyl SCHEMBL29071567 0.79 TSHR (0.56) TSHRLMNAMAPK1CYP2D6SRC
Cadaverine Tartrate SCHEMBL28055270 0.79 TSHR (0.56) TSHRACHELMNACES2CES1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111971270-B Dehydration and amination of alpha, beta-dihydroxycarbonyl compounds to alpha amino acids 阿彻丹尼尔斯米德兰德公司 2024-02-02 CN disclosed
CN-112074500-B Dehydration and cleavage of alpha, beta-dihydroxycarbonyl compounds to lactic acid and other products 阿彻丹尼尔斯米德兰德公司 2023-09-05 CN disclosed
CN-105492445-B Compounds (variants) and their use for the treatment of tumor diseases 国家制药技术有限责任公司 2018-02-13 CN disclosed
CN-107074807-A Compositions and methods for inhibiting histone demethylase 吉利德科学公司 2017-08-18 CN disclosed
CN-105492445-A Novel compounds (variants) and their use for the treatment of tumor diseases LTD LIABILITY COMPANY NAT PHARMACEUTICAL TECH 2016-04-13 CN disclosed