Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL27875442

N#Cc1cccc2cc[nH]c12.O=C(O)C(O)C(O)C(=O)O.c1ccc2ncccc2c1

nearest known ligand 0.38

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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
▸ ALDH1A1 P00352 3/20 0.38
▸ KEAP1 Q14145 1/20 0.37
▸ ADORA2A P29274 3/20 0.36
▸ GRM5 P41594 1/20 0.34
▸ PDPK1 O15530 1/20 0.34
▸ SLC40A1 Q9NP59 1/20 0.34
▸ DYRK1A Q13627 2/20 0.33
▸ HCRTR1 O43613 1/20 0.32
▸ HCRTR2 O43614 1/20 0.32
▸ HPGD P15428 2/20 0.32
▸ DOT1L Q8TEK3 1/20 0.32
▸ AXL P30530 1/20 0.32
▸ NUDT1 P36639 1/20 0.32
▸ CYP1A2 P05177 1/20 0.32
▸ CYP2C9 P11712 1/20 0.32
▸ CYP2C19 P33261 1/20 0.32
▸ HIF1A Q16665 1/20 0.32
▸ HSD17B10 Q99714 1/20 0.32
▸ PABPC1 P11940 1/20 0.32
▸ LMNA P02545 1/20 0.31

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
Quinoline SCHEMBL27950148 0.88 ALDH1A1 (0.49) ALDH1A1ADORA2ASLC40A1DYRK1AHPGD
Cadaverine Tartrate SCHEMBL28147371 0.87 KEAP1 (0.47) KEAP1GRM5PDPK1
Quinoline SCHEMBL27875441 0.79 DYRK1A (0.37) ALDH1A1ADORA2ADYRK1ALMNANFATC1
Cadaverine Tartrate SCHEMBL28081412 0.78 ALDH1A1 (0.63) ALDH1A1HPGDCYP1A2CYP2C9CYP2C19
Cadaverine Tartrate SCHEMBL5874237 0.78 ALDH1A1 (0.63) ALDH1A1HPGDCYP1A2CYP2C9CYP2C19
Cadaverine Tartrate SCHEMBL5874249 0.78 ALDH1A1 (0.63) ALDH1A1HPGDCYP1A2CYP2C9CYP2C19
Quinoline SCHEMBL28040754 0.76 ALDH1A1 (0.49) ALDH1A1KEAP1ADORA2AGRM5PDPK1
SCHEMBL29361477 0.73 AHR (0.50) KEAP1PDPK1DYRK1ANFATC1GSK3B
SCHEMBL1420318 0.73 AHR (0.50) KEAP1PDPK1DYRK1ANFATC1GSK3B
Trifluoroacetic Acid SCHEMBL29364273 0.72 KEAP1 (0.47) KEAP1GRM5PDPK1

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
CN-102702067-A Novel intermediate for synthesizing silodosin as well as preparation method and purpose of novel intermediate BEIJING LIANBEN MEDICAL CHEMICAL TECHNOLOGY CO LTD 2012-10-03 — — CN disclosed
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