Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL5866450

NO.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.83

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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 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 4/20 0.83
TP53 P04637 1/20 0.44
CYP2C9 P11712 1/20 0.41
PDE4A P27815 1/20 0.41
NFKB1 P19838 2/20 0.39
CYP2C19 P33261 2/20 0.39
LMNA P02545 2/20 0.38
RECQL P46063 2/20 0.38
ALDH1A1 P00352 2/20 0.38
THRB P10828 1/20 0.38
HIF1A Q16665 2/20 0.37
OR51E2 Q9H255 1/20 0.37
ACHE P22303 1/20 0.36
KDM4E B2RXH2 3/20 0.35
BLM P54132 2/20 0.35
PMP22 Q01453 2/20 0.35
HSD17B10 Q99714 2/20 0.35
MAPT P10636 2/20 0.35
TDP1 Q9NUW8 2/20 0.35
MAPK1 P28482 1/20 0.35

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 SCHEMBL28932383 1.00 TSHR (0.83) TSHRTP53CYP2C9PDE4ANFKB1
Cadaverine Tartrate SCHEMBL28636687 0.92 TSHR (0.83) TSHRTP53CYP2C9PDE4ANFKB1
Cadaverine Tartrate SCHEMBL15660786 0.92 TSHR (0.83) TSHRTP53CYP2C9PDE4ANFKB1
Cadaverine Tartrate SCHEMBL2276011 0.92 TSHR (0.83) TSHRTP53CYP2C9PDE4ANFKB1
Cadaverine Tartrate SCHEMBL1431070 0.91 TSHR (1.00) TSHRTP53CYP2C9PDE4ANFKB1
Tartaric Acid SCHEMBL5762 0.91 TSHR (1.00) TSHRTP53CYP2C9PDE4ANFKB1
Cadaverine Tartrate SCHEMBL1062721 0.91 TSHR (1.00) TSHRTP53CYP2C9PDE4ANFKB1
Cadaverine Tartrate SCHEMBL22768 0.91 TSHR (1.00) TSHRTP53CYP2C9PDE4ANFKB1
Cadaverine Tartrate SCHEMBL848 0.91 TSHR (1.00) TSHRTP53CYP2C9PDE4ANFKB1
Cadaverine Tartrate SCHEMBL116846 0.91 TSHR (1.00) TSHRTP53CYP2C9PDE4ANFKB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-104098478-A Aminoalcohol resolution method ANHUI BIOCHEM UNITED PHARMACEUTICAL CO LTD 2014-10-15 CN claimed
CN-115998677-A Meta-hydroxylamine bitartrate injection and preparation method thereof 北京世桥生物制药有限公司 2023-04-25 CN disclosed
CN-218231844-U Tartaric acid bitartrate hydroxylamine injection configuration partial shipment device 北京市永康药业有限公司 2023-01-06 CN disclosed
CN-112245387-B Composition and preparation method of m-hydroxylamine bitartrate injection 南京泽恒医药技术开发有限公司 2022-05-10 CN disclosed
CN-112326810-A Pretreatment of m-hydroxylamine bitartrate injection and separation and determination of enantiomer 南京斯泰尔医药科技有限公司 2021-02-05 CN disclosed
CN-112245387-A Composition and preparation method of m-hydroxylamine bitartrate injection 南京泽恒医药技术开发有限公司 2021-01-22 CN disclosed
CN-104098478-B Aminoalcohol resolution method 安徽贝克联合制药有限公司 2017-05-17 CN disclosed
CN-104072381-B Preparation method for optically pure aminoalcohol hydrochloride 安徽贝克联合制药有限公司 2017-04-12 CN disclosed
CN-104098478-A Aminoalcohol resolution method ANHUI BIOCHEM UNITED PHARMACEUTICAL CO LTD 2014-10-15 CN disclosed
CN-104098478-A Aminoalcohol resolution method ANHUI BIOCHEM UNITED PHARMACEUTICAL CO LTD 2014-10-15 CN disclosed
US-5534525-A Lactam derivatives ZENECA LIMITED (GB) 1996-07-09 US disclosed
EP-0714392-A1 HETEROCYCLES USEFUL AS NEUROKININ ANTAGONISTS ZENECA LIMITED (GB) 1996-06-05 EP disclosed
EP-0667858-A1 4-CARBOXOAMIDO PIPERIDINE DERIVATIVES, INTERMEDIATES AND USE AS NEUROKININ ANTAGONISTS ZENECA LIMITED (GB) 1995-08-23 EP disclosed
WO-1995015961-A1 BICYCLIC HETEROCYCLES AS NEUROKININ A ANTAGONISTS ZENECA LIMITED (GB) 1995-06-15 WO disclosed
WO-1995012577-A1 NOVEL 4-PIPERIDINYL SUBSTITUTED LACTAMES AS NEUROKININ 2 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF ASTHMA ZENECA LIMITED (GB) 1995-05-11 WO disclosed
WO-1995005377-A1 HETEROCYCLES USEFUL AS NEUROKININ ANTAGONISTS ZENECA LIMITED (GB) 1995-02-23 WO disclosed
CN-1098094-A The heterocycle that aryl replaces ZENECA LTD (GB) 1995-02-01 CN disclosed
EP-0630887-A1 4-(aryl-substituted)-piperidines as neurokinin receptor antagonists ZENECA LIMITED (GB) 1994-12-28 EP disclosed
CN-1094723-A Carboxamide derivative ZENECA LTD (GB) 1994-11-09 CN disclosed
WO-1994010146-A1 4-CARBOXOAMIDO PIPERIDINE DERIVATIVES, INTERMEDIATES AND USE AS NEUROKININ ANTAGONISTS ZENECA LIMITED (GB) 1994-05-11 WO disclosed