P-Nitrophenol

P-Nitrophenol

SCHEMBL27623918

Cl.O=P(O)(O)O.O=P(O)(O)O.O=[N+]([O-])c1ccc(O)cc1

nearest known ligand 0.78

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of P-Nitrophenol. 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
CA1 P00915 3/20 0.55
CA2 P00918 3/20 0.55
CES1 P23141 2/20 0.55
CES2 O00748 1/20 0.55
AKR1C3 P42330 1/20 0.55
CA12 O43570 2/20 0.50
MMP2 P08253 2/20 0.50
MMP9 P14780 1/20 0.50
MMP8 P22894 1/20 0.50
MMP14 P50281 1/20 0.50
PTGS2 P35354 2/20 0.47
PTGS1 P23219 1/20 0.47
TDP1 Q9NUW8 1/20 0.47
ALDH1A1 P00352 2/20 0.46
ACHE P22303 1/20 0.46
HSD17B10 Q99714 1/20 0.46
MEN1 O00255 2/20 0.46
KMT2A Q03164 2/20 0.46
GAA P10253 1/20 0.46
MAPT P10636 1/20 0.46

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
P-Nitrophenol SCHEMBL161007 0.98 CA1 (0.57) CA1CA2CES1CES2AKR1C3
P-Nitrophenol SCHEMBL28493361 0.98 CA1 (0.57) CA1CA2CES1CES2AKR1C3
P-Nitrophenol SCHEMBL407205 0.96 CA1 (0.55) CA1CA2CES1CES2AKR1C3
P-Nitrophenol SCHEMBL6681729 0.96 CA1 (0.55) CA1CA2CES1CES2AKR1C3
P-Nitrophenol SCHEMBL6760441 0.91 CES1 (0.56) CA1CA2CES1PTGS2PTGS1
P-Nitrophenol SCHEMBL17512809 0.89 CA1 (0.53) CA1CA2CES1CES2AKR1C3
P-Nitrophenol SCHEMBL9684585 0.89 CA1 (0.53) CA1CA2CES1CES2AKR1C3
P-Nitrophenol SCHEMBL407206 0.89 CA1 (0.53) CA1CA2CES1CES2AKR1C3
P-Nitrophenol SCHEMBL16554130 0.89 CA1 (0.53) CA1CA2CES1CES2AKR1C3
P-Nitrophenol SCHEMBL11048842 0.89 CES1 (0.58) CA1CA2CES1PTGS2PTGS1

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-1711278-A Novel cytosine arabinoside monophosphate medicine precursor METABASIS THERAPEUTICS INC (US) 2005-12-21 CN disclosed