Cadaverine Tartrate

Cadaverine Tartrate

SCHEMBL5550872

Cc1ccc(O)cc1.Cc1ccc(O)cc1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.59

Full drug profile on Sugi Atlas →

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
ACHE P22303 1/20 0.59
TSHR P16473 1/20 0.46
ALDH1A1 P00352 4/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
MAPT P10636 2/20 0.43
RAB9A P51151 2/20 0.43
POLB P06746 1/20 0.43
MAOA P21397 1/20 0.43
MAOB P27338 1/20 0.43
LMNA P02545 2/20 0.42
HIF1A Q16665 1/20 0.42
KDM4E B2RXH2 1/20 0.42
NPC1 O15118 1/20 0.42
GAA P10253 1/20 0.41
CES2 O00748 2/20 0.41
CES1 P23141 2/20 0.41
CA12 O43570 1/20 0.41
CA1 P00915 1/20 0.41
CA2 P00918 1/20 0.41
CA3 P07451 1/20 0.41

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 SCHEMBL28055270 0.91 TSHR (0.56) ACHETSHRALDH1A1SMN1; SMN2MAPT
Cadaverine Tartrate SCHEMBL28066769 0.88 TSHR (0.59) TSHRALDH1A1MAPTRAB9APOLB
P-Cresol SCHEMBL25273489 0.84 ACHE (0.62) ACHEALDH1A1SMN1; SMN2MAPTRAB9A
P-Cresol SCHEMBL27541413 0.83 ACHE (0.77) ACHEALDH1A1SMN1; SMN2MAPTRAB9A
Cadaverine Tartrate SCHEMBL9732307 0.81 LMNA (0.55) ACHETSHRALDH1A1SMN1; SMN2MAPT
Cadaverine Tartrate SCHEMBL18586007 0.81 LMNA (0.55) ACHETSHRALDH1A1SMN1; SMN2MAPT
Gluconic Acid SCHEMBL29209873 0.80 PDE4A (0.61) ACHETSHRALDH1A1SMN1; SMN2MAPT
Glucuronic Acid SCHEMBL28944953 0.80 ACHE (0.42) ACHEALDH1A1SMN1; SMN2MAPTRAB9A
P-Cresol SCHEMBL9330932 0.80 ACHE (0.72) ACHETSHRALDH1A1SMN1; SMN2MAPT
P-Cresol SCHEMBL6684218 0.80 ACHE (0.72) ACHETSHRALDH1A1SMN1; SMN2MAPT

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-110590602-B Resolution refining method of racemic citalopram diol 浙江海森药业股份有限公司 2022-04-05 CN disclosed
JP-2007106987-A COMPOSITION AND THERMOSENSITIVE ADHESIVE MATERIAL RICOH CO LTD 2007-04-26 JP disclosed