Pyridoxal

Pyridoxal

SCHEMBL5498057

Cc1ncc(CO)c(C=O)c1O.Cc1ncc(CO)c(C=O)c1O.O=P(O)(O)O

nearest known ligand 0.88

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Pyridoxal. 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
KDM4E B2RXH2 10/20 0.88
ALDH1A1 P00352 8/20 0.88
LMNA P02545 6/20 0.88
HPGD P15428 5/20 0.88
MEN1 O00255 3/20 0.88
KMT2A Q03164 3/20 0.88
AOX1 Q06278 1/20 0.88
TRIM24 O15164 1/20 0.85
TRIM33 Q9UPN9 1/20 0.85
ESR1 P03372 1/20 0.68
PTGS1 P23219 1/20 0.68
ACP1 P24666 1/20 0.68
PDE4A P27815 1/20 0.68
P2RX1 P51575 1/20 0.68
P2RX2 Q9UBL9 1/20 0.68
PDXK O00764 1/20 0.62
HSD17B10 Q99714 1/20 0.51
HTT P42858 6/20 0.50
MAPT P10636 5/20 0.50
L3MBTL1 Q9Y468 4/20 0.50

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
Pyridoxal SCHEMBL9559097 1.00 KDM4E (0.88) KDM4EALDH1A1LMNAHPGDMEN1
Pyridoxal SCHEMBL27627958 1.00 KDM4E (0.88) KDM4EALDH1A1LMNAHPGDMEN1
Pyridoxal SCHEMBL28454700 1.00 KDM4E (0.88) KDM4EALDH1A1LMNAHPGDMEN1
Pyridoxal SCHEMBL18726347 1.00 KDM4E (0.88) KDM4EALDH1A1LMNAHPGDMEN1
Pyridoxal SCHEMBL5051301 1.00 KDM4E (0.88) KDM4EALDH1A1LMNAHPGDMEN1
Pyridoxal SCHEMBL30616198 1.00 KDM4E (0.88) KDM4EALDH1A1LMNAHPGDMEN1
Pyridoxal SCHEMBL27131 1.00 KDM4E (0.88) KDM4EALDH1A1LMNAHPGDMEN1
Pyridoxal SCHEMBL8090165 0.98 KDM4E (0.85) KDM4EALDH1A1LMNAHPGDMEN1
Pyridoxal SCHEMBL1065056 0.98 KDM4E (0.85) KDM4EALDH1A1LMNAHPGDMEN1
Pyridoxal SCHEMBL6701817 0.98 KDM4E (0.85) KDM4EALDH1A1LMNAHPGDMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3333266-B1 METHOD FOR PRODUCING SELENONEINE KIKKOMAN CORP (JP) 2024-04-24 EP claimed
WO-2024090329-A1 COMPOSITION FOR AMELIORATING INFLAMMATION ASSOCIATED WITH CHRONIC HYPOXIA 国立大学法人東北大学 2024-05-02 WO disclosed
WO-2024013258-A1 PRODUCTION OF CYSTEINE OR CYSTINE FROM SERINE IN FERMENTATION MEDIUM CYSBIO APS (DK) 2024-01-18 WO disclosed
US-20070148154-A1 Use of superoxide dismutase mimetics and reductase gultatione in the form of anticancer drugs UNIVERSITE RENE DESCARTES (PARIS V) (FR) 2007-06-28 US disclosed
EP-1694338-A2 USE OF SUPEROXIDE DISMUTASE MIMETICS AND REDUCTASE GLUTATHIONE IN THE FORM OF ANTICANCER DRUGS UNIVERSITE RENE DESCARTES, (PARIS V) (FR) 2006-08-30 EP disclosed
WO-2005060976-A2 USE OF SUPEROXIDE DISMUTASE MIMETICS AND REDUCTASE GLUTATHIONE IN THE FORM OF ANTICANCER DRUGS UNIVERSITE RENE DESCARTES (PARIS V) (FR) 2005-07-07 WO disclosed