Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL5961174

O=C([O-])C(O)C(O)C(=O)[O-].O=C([O-])C(O)C(O)C(=O)[O-].[NH4+].[Sb+3]

nearest known ligand 0.48

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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 14)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.48
TSHR P16473 3/20 0.44
CA4 P22748 3/20 0.38
CYP3A4 P08684 2/20 0.34
TDP1 Q9NUW8 1/20 0.34
BLM P54132 1/20 0.34
PMP22 Q01453 1/20 0.34
TP53 P04637 1/20 0.33
PDE4A P27815 1/20 0.33
CA1 P00915 1/20 0.31
FAHD1 Q6P587 1/20 0.31
NFKB1 P19838 1/20 0.30
NPSR1 Q6W5P4 1/20 0.30
SLC22A6 Q4U2R8 1/20 0.30

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 SCHEMBL31542424 0.96 TSHR (0.47) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL843543 0.96 TSHR (0.47) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL11578827 0.92 LMNA (0.48) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL3160181 0.92 LMNA (0.48) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL9551431 0.92 LMNA (0.48) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL6806779 0.92 LMNA (0.48) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL1938734 0.92 LMNA (0.48) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL330144 0.92 TSHR (0.44) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL9551433 0.92 LMNA (0.48) LMNATSHRCA4CYP3A4TDP1
Cadaverine Tartrate SCHEMBL970332 0.92 TSHR (0.44) LMNATSHRCA4CYP3A4TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110042380-A Zinc blackening agent for surface 祝亚琴 2019-07-23 CN claimed
CN-103739467-B Propylene oxidation prepares propenal method SINOPEC CORP. (CN) 2016-02-10 CN claimed
CN-102515260-A Method for producing nanometer tin oxide doped with antimony HEXIANG YI 2012-06-27 CN claimed
CN-101708820-A Method for manufacturing nano antimony doped tin oxide GANZHOU RUIDE CHEMICAL CO LTD 2010-05-19 CN claimed
CN-111558380-B Catalyst and preparation method thereof 赵玉平 2023-12-26 CN disclosed
CN-111545219-B Catalyst and preparation method thereof 陕西元亨医药科技有限责任公司 2023-04-28 CN disclosed
CN-111558380-A Catalyst for preparing acrolein by propylene oxidation and preparation method thereof 赵玉平 2020-08-21 CN disclosed
CN-111545219-A Catalyst for preparing acrolein by propylene oxidation and preparation method thereof 赵玉平 2020-08-18 CN disclosed
CN-110042380-A Zinc blackening agent for surface 祝亚琴 2019-07-23 CN disclosed
CN-103739467-B Propylene oxidation prepares propenal method SINOPEC CORP. (CN) 2016-02-10 CN disclosed
CN-103739467-B Propylene oxidation prepares propenal method SINOPEC CORP. (CN) 2016-02-10 CN disclosed
CN-102515260-A Method for producing nanometer tin oxide doped with antimony HEXIANG YI 2012-06-27 CN disclosed
CN-1346822-A Process for producing unsaturated carboxylic acid and unsaturated nitrile ROHM & HAAS (US) 2002-05-01 CN disclosed
EP-1193240-A1 Recycle process in the preparation of unsaturated carboxylic acids from alkane ROHM AND HAAS COMPANY (US) 2002-04-03 EP disclosed
CN-1031640-C Process for producing nitriles MITSUBISHI CHEM IND (JP) 1996-04-24 CN disclosed
EP-0529853-B1 Catalyst and process for producing nitriles MITSUBISHI CHEM CORP (JP) 1996-02-28 EP disclosed
US-5472925-A Coordination catalysts for producing a nitrile from an alkane comprising an oxide of molybdenum, vanadium, tellurium and one other metal; calcining in oxygen-free; catalyst selectivity MITSUBISHI CHEMICAL CORPORATION (JP) 1995-12-05 US disclosed
US-5281745-A Catayltic oxidation of an alkane and ammonia to prepare alpha, beta-ethylenically unsaturated nitrile MITSUBISHI KASEI CORPORATION (JP) 1994-01-25 US disclosed
CN-1069723-A The production method of nitrile MITSUBISHI CHEM IND (JP) 1993-03-10 CN disclosed
EP-0529853-A2 Catalyst and process for producing nitriles Mitsubishi Chemical Corporation (JP) 1993-03-03 EP disclosed