Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL5961178

N.O=C(O)C(O)C(O)C(=O)O.[Sb]

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 3/20 0.83
TP53 P04637 1/20 0.44
CYP2C9 P11712 2/20 0.41
PDE4A P27815 1/20 0.41
CYP2C19 P33261 2/20 0.39
NFKB1 P19838 1/20 0.39
LMNA P02545 2/20 0.38
ALDH1A1 P00352 2/20 0.38
THRB P10828 1/20 0.38
RECQL P46063 1/20 0.38
TDP1 Q9NUW8 3/20 0.37
OR51E2 Q9H255 1/20 0.37
HPGD P15428 2/20 0.35
HSD17B10 Q99714 2/20 0.35
ABCB11 O95342 1/20 0.35
F2 P00734 1/20 0.35
KDM4E B2RXH2 1/20 0.35
MEN1 O00255 1/20 0.35
MAPT P10636 1/20 0.35
ALOX15 P16050 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 SCHEMBL2005530 0.96 TSHR (0.91) TSHRTP53CYP2C9PDE4ACYP2C19
Cadaverine Tartrate SCHEMBL30692300 0.96 TSHR (0.91) TSHRTP53CYP2C9PDE4ACYP2C19
Tartaric Acid SCHEMBL29368126 0.96 TSHR (0.91) TSHRTP53CYP2C9PDE4ACYP2C19
Cadaverine Tartrate SCHEMBL218603 0.96 TSHR (0.91) TSHRTP53CYP2C9PDE4ACYP2C19
Cadaverine Tartrate SCHEMBL41453 0.96 TSHR (0.91) TSHRTP53CYP2C9PDE4ACYP2C19
Cadaverine Tartrate SCHEMBL30692284 0.96 TSHR (0.91) TSHRTP53CYP2C9PDE4ACYP2C19
Cadaverine Tartrate SCHEMBL9602705 0.96 TSHR (0.91) TSHRTP53CYP2C9PDE4ACYP2C19
Cadaverine Tartrate SCHEMBL41454 0.96 TSHR (0.91) TSHRTP53CYP2C9PDE4ACYP2C19
Cadaverine Tartrate SCHEMBL5961170 0.92 TSHR (0.83) TSHRTP53CYP2C9PDE4ACYP2C19
Cadaverine Tartrate SCHEMBL1938732 0.92 TSHR (0.83) TSHRTP53CYP2C9PDE4ACYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7049466-B2 Contacting in reaction zone an alkane with a catalyst containing a mixed metal oxide under conditions which produce product gas comprising unsaturated carboxylic acid, unreacted alkane and alkene ROHM AND HAAS COMPANY (US) 2006-05-23 US disclosed
US-6989460-B2 Methods for producing unsaturated carboxylic acids and unsaturated nitriles ROHM AND HAAS COMPANY (US) 2006-01-24 US disclosed
US-20040210086-A1 Methods for producing unsaturated carboxylic acids and unsaturated nitriles BOGAN LEONARD EDWARD (US) 2004-10-21 US disclosed
US-6710207-B2 CATALYTIC OXIDATION OF MIXTURES OF ALKENES AND ALKANES IN PRESENCE OF MIXED METAL OXIDE CONTAINING MOLYBDENUM OR TUNGSTEN ROHM AND HAAS COMPANY 2004-03-23 US disclosed
US-20030187297-A1 Methods for producing unsaturated carboxylic acids and unsaturated nitriles ROHM AND HAAS COMPANY 2003-10-02 US disclosed
US-20020123647-A1 Recycle process ROHM AND HAAS COMPANY 2002-09-05 US disclosed
EP-1201636-A2 Method for producing unsaturated carboxylic acids and unsaturated nitriles ROHM AND HAAS COMPANY (US) 2002-05-02 EP 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
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
EP-0529853-A2 Catalyst and process for producing nitriles Mitsubishi Chemical Corporation (JP) 1993-03-03 EP disclosed