Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL17439178

NC1CCCC[C@@H]1N.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.50

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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 2/20 0.50
THRB P10828 1/20 0.50
MEN1 O00255 1/20 0.50
KMT2A Q03164 1/20 0.50
NFKB1 P19838 1/20 0.38
CYP2C19 P33261 1/20 0.38
MMP2 P08253 2/20 0.35
MMP9 P14780 2/20 0.35
CA12 O43570 2/20 0.35
CA1 P00915 2/20 0.35
CA2 P00918 2/20 0.35
CA9 Q16790 2/20 0.35
MMP1 P03956 1/20 0.35
MMP3 P08254 1/20 0.35
MMP8 P22894 1/20 0.35
MMP13 P45452 1/20 0.35
GABRR1 P24046 1/20 0.35
EPHX1 P07099 1/20 0.34
GRIN2D O15399 5/20 0.33
GRIN3B O60391 5/20 0.33

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 SCHEMBL30899743 1.00 TSHR (0.50) TSHRTHRBMEN1KMT2ANFKB1
Tartaric Acid SCHEMBL30276688 1.00 TSHR (0.50) TSHRTHRBMEN1KMT2ANFKB1
Cadaverine Tartrate SCHEMBL5804440 1.00 TSHR (0.50) TSHRTHRBMEN1KMT2ANFKB1
Cadaverine Tartrate SCHEMBL1155812 1.00 TSHR (0.50) TSHRTHRBMEN1KMT2ANFKB1
Cadaverine Tartrate SCHEMBL918361 1.00 TSHR (0.50) TSHRTHRBMEN1KMT2ANFKB1
Cadaverine Tartrate SCHEMBL30899742 1.00 TSHR (0.50) TSHRTHRBMEN1KMT2ANFKB1
Cadaverine Tartrate SCHEMBL2998062 0.83 TSHR (0.48) TSHRNFKB1CYP2C19MMP2MMP1
SCHEMBL11367816 0.83 THRB (0.48) THRBMEN1KMT2AMMP2MMP9
Cadaverine Tartrate SCHEMBL30432913 0.81 THRB (0.46) TSHRTHRBMEN1KMT2AMMP2
SCHEMBL8939281 0.81 THRB (0.46) THRBMEN1KMT2AMMP2MMP9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2977368-B1 METHOD FOR PRODUCING OPTICALLY ACTIVE TRANS-1,2-DIAMINOCYCLOHEXANE TORAY FINECHEMICALS CO LTD (JP) 2019-06-12 EP disclosed
EP-2977368-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE TRANS-1,2-DIAMINOCYCLOHEXANE Toray Fine Chemicals Co., Ltd. (JP) 2016-01-27 EP disclosed
US-20160016885-A1 METHOD OF PRODUCING OPTICALLY ACTIVE TRANS-1,2-DIAMINOCYCLOHEXANE TORAY FINE CHEMICALS CO., LTD. (JP) 2016-01-21 US disclosed