Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL11841907

CCCCN(CC(O)COc1ccccc1OCc1ccccc1)CC(O)Cn1c(=O)c2c(ncn2C)n(C)c1=O.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.46

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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
▸ HTR2A known ✓ P28223 1/20 0.39
▸ ADORA2B P29275 4/20 0.40
▸ POLB P06746 1/20 0.40
▸ NPSR1 Q6W5P4 1/20 0.40
▸ LDHA P00338 1/20 0.39
▸ TNF P01375 4/20 0.39
▸ MEN1 O00255 1/20 0.38
▸ KMT2A Q03164 1/20 0.38
▸ USP2 O75604 1/20 0.38
▸ LMNA P02545 1/20 0.38
▸ CYP1A2 P05177 1/20 0.38
▸ TSHR P16473 1/20 0.38
▸ NFKB1 P19838 1/20 0.38
▸ ACHE P22303 1/20 0.38
▸ PDE4A P27815 1/20 0.38
▸ PMP22 Q01453 1/20 0.38
▸ PDE4B Q07343 1/20 0.38
▸ PDE4C Q08493 1/20 0.38
▸ PDE4D Q08499 1/20 0.38
▸ SMN1; SMN2 Q16637 1/20 0.38

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 SCHEMBL11851019 0.91 ADORA2B (0.43) ADORA2BLDHATNFLMNASMN1; SMN2
Cadaverine Tartrate SCHEMBL11840590 0.86 KMT2A (0.43) POLBNPSR1MEN1KMT2ASMN1; SMN2
Cadaverine Tartrate SCHEMBL11853045 0.84 TSHR (0.49) ADORA2BPOLBNPSR1MEN1KMT2A
Hydrochloric Acid SCHEMBL11872388 0.81 HTR2A (0.45) ADORA2BPOLBHTR2ATNFUSP2
SCHEMBL11843030 0.79 CNOT7 (0.44) POLBNPSR1MEN1KMT2ASMN1; SMN2
Hydrochloric Acid SCHEMBL11859555 0.79 RXFP1 (0.51) ADORA2BPOLBNPSR1LDHAMEN1
Cadaverine Tartrate SCHEMBL11848587 0.77 KMT2A (0.46) POLBNPSR1MEN1KMT2AUSP2
SCHEMBL11841911 0.76 POLB (0.38) POLBNPSR1LDHAMEN1KMT2A
SCHEMBL11859590 0.76 ALDH1A1 (0.53) ADORA2BPOLBLDHALMNATSHR
Hydrochloric Acid SCHEMBL11848882 0.76 RXFP1 (0.51) ADORA2BPOLBLDHALMNATSHR

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
US-3998953-A 1,3,7-Trisubstitued xanthine peripheral vasodilators BOEHRINGER INGELHEIM GMBH (DT) 1976-12-21 — — US disclosed
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