Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL506352

O.O.O.O.O=C([O-])C(O)C(O)C(=O)[O-].[K+].[K+].[NaH].[NaH]

nearest known ligand 0.44

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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 13)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.41
LMNA P02545 2/20 0.40
CA4 P22748 5/20 0.38
FAHD1 Q6P587 1/20 0.38
BLM P54132 2/20 0.33
OR51E2 Q9H255 1/20 0.33
CYP3A4 P08684 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
PMP22 Q01453 1/20 0.33
TP53 P04637 1/20 0.32
MEN1 O00255 1/20 0.32
LDHA P00338 1/20 0.32
KMT2A Q03164 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 SCHEMBL5893261 0.96 TSHR (0.44) TSHRLMNACA4FAHD1BLM
Cadaverine Tartrate SCHEMBL7781114 0.96 TSHR (0.44) TSHRLMNACA4FAHD1BLM
Cadaverine Tartrate SCHEMBL29249913 0.96 TSHR (0.44) TSHRLMNACA4FAHD1BLM
Cadaverine Tartrate SCHEMBL2821640 0.96 TSHR (0.44) TSHRLMNACA4FAHD1BLM
Cadaverine Tartrate SCHEMBL188156 0.96 TSHR (0.44) TSHRLMNACA4FAHD1BLM
Cadaverine Tartrate SCHEMBL6937868 0.96 TSHR (0.44) TSHRLMNACA4FAHD1BLM
Cadaverine Tartrate SCHEMBL1434088 0.96 TSHR (0.44) TSHRLMNACA4FAHD1BLM
Cadaverine Tartrate SCHEMBL29098547 0.96 TSHR (0.44) TSHRLMNACA4FAHD1BLM
Cadaverine Tartrate SCHEMBL504364 0.93 TSHR (0.41) TSHRLMNACA4FAHD1BLM
Cadaverine Tartrate SCHEMBL440871 0.93 CA4 (0.47) TSHRLMNACA4FAHD1BLM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2183363-B1 FUNGAL XYLANASE DANISCO US INC (US) 2016-06-08 EP disclosed
CN-101611001-B Utilize the method for hydrosulphite Intermediate Preparation 6,6-dimethyl-3-azabicyclo-[3.1.0]-hexane compound MERCK SHARP & DOHME CORP. (US) 2015-11-25 CN disclosed
CN-104781213-A Pressure process WZR ceramic solutions GmbH 2015-07-15 CN disclosed
CN-103214483-B Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as janus kinase inhibitors INCYTE CORP 2014-12-17 CN disclosed
CN-104136432-A Industrial process for producing 1, 2-dihydroquinoline derivative or salt thereof and intermediate for producing the same SANTEN PHARMACEUTICAL CO LTD 2014-11-05 CN disclosed
CN-103254190-A Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as janus kinase inhibitors INCYTE CORP 2013-08-21 CN disclosed
CN-103214484-A Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as janus kinase inhibitors INCYTE CORP A DELAWARE CORP 2013-07-24 CN disclosed
CN-103214483-A Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as janus kinase inhibitors INCYTE CORP 2013-07-24 CN disclosed
CN-102803481-A Methods for reducing blue saccharide DANISCO US INC 2012-11-28 CN disclosed
CN-1474803-B Amide derivatives and their use for the preparation of medicaments MITSUBISHI TANABE PHARMA CORP 2012-11-21 CN disclosed
CN-1474803-A Novel amide derivative and medical use thereof ������ҩ��ʽ���� 2004-02-11 CN disclosed
CN-1428404-A Combustion agent composition for generating colour brilliance lamp, and its mking method JIN-MAN IM (KR) 2003-07-09 CN disclosed
CN-1100056-C Compound for inhibition of gastric acid secretion ASTRA AB (SE) 2003-01-29 CN disclosed
CN-1384222-A Electroplating liquor without electrolytic copper and high-frequency electronic element MURATA MANUFACTURING CO (JP) 2002-12-11 CN disclosed
CN-1272842-A 2-acylaminopropanamines as tachykinin receptor antagonists LILLY CO ELI (US) 2000-11-08 CN disclosed
CN-1259138-A 17 'beta'-allyloxy (thio) alkyl-androstane derivatives for the modulation of meiosis AKZO NOBEL NV (NL) 2000-07-05 CN disclosed
CN-1248257-A Compound for inhibition of gastric acid secretion ASTRA AB (SE) 2000-03-22 CN disclosed
EP-0327057-B1 Process for metalizing fibrous materials TEXMET SPA (IT) 1994-04-13 EP disclosed
US-5035924-A Process for metallizing fibrous materials HIMONT ITALIA S.R.L. (IT) 1991-07-30 US disclosed
EP-0327057-A1 Process for metalizing fibrous materials TEXMET S.p.A. (IT) 1989-08-09 EP disclosed