Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL28783254

Nc1ccc[nH]1.Nc1ccc[nH]1.Nc1ccc[nH]1.Nc1ccc[nH]1.Nc1ccc[nH]1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.42

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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
▸ ESR2 known ✓ Q92731 1/20 0.34
▸ TSHR P16473 3/20 0.40
▸ NAPRT Q6XQN6 1/20 0.38
▸ AURKA O14965 1/20 0.38
▸ AURKB Q96GD4 1/20 0.38
▸ INCENP Q9NQS7 1/20 0.38
▸ KDM4E B2RXH2 5/20 0.37
▸ MAPT P10636 2/20 0.37
▸ GAA P10253 1/20 0.37
▸ LMNA P02545 4/20 0.36
▸ HIF1A Q16665 2/20 0.36
▸ MAPK1 P28482 2/20 0.34
▸ BLM P54132 3/20 0.34
▸ POLB P06746 2/20 0.34
▸ PKM P14618 1/20 0.34
▸ PTPN1 P18031 1/20 0.34
▸ PTPN7 P35236 1/20 0.34
▸ KMT2A Q03164 1/20 0.34
▸ L3MBTL1 Q9Y468 1/20 0.34
▸ PMP22 Q01453 2/20 0.34

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
Maleic Acid SCHEMBL31158052 0.78 MAPT (0.41) TSHRNAPRTAURKAAURKBINCENP
SCHEMBL73934 0.78 — —
Ammonia Solution, Strong SCHEMBL29014480 0.75 — —
SCHEMBL19838559 0.75 — —
Hydrochloric Acid SCHEMBL29144528 0.75 — —
Hydrochloric Acid SCHEMBL5652646 0.75 — —
SCHEMBL15577261 0.73 — —
SCHEMBL487186 0.73 TSHR (0.44) TSHRNAPRTAURKAAURKBINCENP
Formamide SCHEMBL28513591 0.72 — —
Cadaverine Tartrate SCHEMBL21145114 0.72 TSHR (0.55) TSHRKDM4EMAPTLMNAHIF1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-104800862-A Efficient synthesis, compositions and uses of chelators for nuclear imaging and radiotherapy UNIV TEXAS 2015-07-29 — — CN disclosed
CN-101678118-A Efficient synthesis of chelators for nuclear imaging and radiotherapy: composition and use UNIV TEXAS 2010-03-24 — — CN disclosed
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