Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL13736620

Cc1nc2ccc(Oc3ccccc3)cc2c2c1CCN2CCc1ccccc1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.40

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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
MEN1 O00255 1/20 0.40
KMT2A Q03164 1/20 0.40
PLA2G2A P14555 3/20 0.39
EGLN2 Q96KS0 2/20 0.38
EGLN1 Q9GZT9 2/20 0.38
PTGER4 P35408 1/20 0.37
PTGER2 P43116 1/20 0.37
ALDH1A1 P00352 2/20 0.36
CYP1A2 P05177 2/20 0.36
TSHR P16473 2/20 0.36
USP2 O75604 1/20 0.36
CYP3A4 P08684 1/20 0.36
CYP2C19 P33261 1/20 0.36
NR1H4 Q96RI1 3/20 0.36
P2RX3 P56373 1/20 0.36
CHEK2 O96017 1/20 0.36
PPARG P37231 1/20 0.35
JAK2 O60674 1/20 0.35
INSR P06213 1/20 0.35
IGF1R P08069 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
Acetic Acid SCHEMBL20422024 0.93 MEN1 (0.41) MEN1KMT2APLA2G2APTGER4PTGER2
SCHEMBL29750185 0.92 MEN1 (0.44) MEN1KMT2AALDH1A1CYP1A2TSHR
SCHEMBL456750 0.92 MEN1 (0.44) MEN1KMT2AALDH1A1CYP1A2TSHR
Succinic Acid SCHEMBL13739526 0.91 FFAR1 (0.40) MEN1KMT2APLA2G2AEGLN2EGLN1
Hydrochloric Acid SCHEMBL574759 0.91 MEN1 (0.43) MEN1KMT2AALDH1A1CYP1A2TSHR
Bromide SCHEMBL13737447 0.91 MEN1 (0.43) MEN1KMT2AALDH1A1CYP1A2TSHR
Methane SCHEMBL13736906 0.91 MEN1 (0.43) MEN1KMT2AALDH1A1CYP1A2TSHR
Sulfuric Acid SCHEMBL13737697 0.90 MEN1 (0.40) MEN1KMT2APLA2G2APTGER4PTGER2
Trifluoroacetic Acid SCHEMBL4717787 0.89 MEN1 (0.38) MEN1KMT2APLA2G2AEGLN2EGLN1
SCHEMBL571991 0.89 GRIN1 (0.40) MEN1KMT2APLA2G2AALDH1A1CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2012153130-A1 SALTS OF 4 -ETHYL-1-(2 - PHENYLETHYL) - 8 -PHENOXY - 2, 3 - DIHYDRO - 1H - PYRROLO [3, 2 -C] QUINOLINE AND THEIR USE FOR TREATING INFECTIONS HELPERBY THERAPEUTICS LIMITED (GB) 2012-11-15 WO disclosed