1-Naphthol

1-Naphthol

SCHEMBL7714764

O=S(=O)(O)O.Oc1cccc2ccccc12

nearest known ligand 0.77

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of 1-Naphthol. 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
CYP1A2 P05177 1/20 0.77
CA1 P00915 1/20 0.52
CA2 P00918 1/20 0.52
CA9 Q16790 1/20 0.52
KDM4E B2RXH2 2/20 0.50
ALOX12 P18054 1/20 0.50
CDK2 P24941 1/20 0.50
ERN1 O75460 1/20 0.48
PTPN22 Q9Y2R2 1/20 0.46
HCRTR1 O43613 1/20 0.46
IDO1 P14902 1/20 0.46
PLAU P00749 1/20 0.45
LDHA P00338 1/20 0.45
MAPKAPK2 P49137 1/20 0.45
CTDSP1 Q9GZU7 1/20 0.45
NQO2 P16083 1/20 0.45
POLB P06746 2/20 0.44
MAPT P10636 2/20 0.44
TDP1 Q9NUW8 2/20 0.44
GAA P10253 2/20 0.44

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
1-Naphthol SCHEMBL30669386 1.00 CYP1A2 (0.77) CYP1A2CA1CA2CA9KDM4E
1-Naphthol SCHEMBL28395998 0.98 CYP1A2 (0.74) CYP1A2CA1CA2CA9KDM4E
1-Naphthol SCHEMBL10605017 0.98 CYP1A2 (0.74) CYP1A2CA1CA2CA9KDM4E
1-Naphthol SCHEMBL10605020 0.98 CYP1A2 (0.74) CYP1A2CA1CA2CA9KDM4E
1-Naphthol SCHEMBL27594854 0.93 CYP1A2 (0.74) CYP1A2CA1CA2CA9KDM4E
1-Naphthol SCHEMBL4591799 0.92 CYP1A2 (0.65) CYP1A2CA1CA2CA9KDM4E
1-Naphthol SCHEMBL29216682 0.91 CYP1A2 (0.71) CYP1A2CA1CA2CA9KDM4E
1-Naphthol SCHEMBL28825167 0.91 CYP1A2 (0.71) CYP1A2CA1CA2CA9KDM4E
1-Naphthol SCHEMBL28748211 0.89 CYP1A2 (0.74) CYP1A2CA1CA2CA9KDM4E
1-Naphthol SCHEMBL10486461 0.88 CYP1A2 (1.00) CYP1A2CA2KDM4EPTPN22IDO1

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 54 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107245113-B Stigma Maydis polysaccharide extract with anticancer effect and its preparation method 吉林化工学院 2020-12-11 CN claimed
CN-107245113-A Corn silk polysaccharide extract with antitumaous effect and preparation method thereof 吉林化工学院 2017-10-13 CN claimed
US-6475531-B1 Safe botanical drug for treatment and prevention of influenza and increasing immune function L.Y. (HK) BIOTECH LIMITED (HK) 2002-11-05 US claimed
EP-0331821-A1 Antiviral agent KUREHA KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1989-09-13 EP claimed
EP-0212501-A2 Therapeutic agent for treating hematopoietic diseases GREEN CROSS CORPORATION (JP) 1987-03-04 EP claimed
JP-60034186-A None JP disclosed
JP-63316730-A None JP disclosed
CN-113249419-B Method for synthesizing rhamnolipid by extracellular enzyme catalysis 南京工业大学 2023-10-27 CN disclosed
CN-115992064-A Sea monad and its application 山东大学威海工业技术研究院 2023-04-21 CN disclosed
CN-113481140-A Method for improving rhamnolipid yield and genetic engineering bacteria 南京工业大学 2021-10-08 CN disclosed
CN-109266640-B Method for preparing composite carrier by using modified carbon fiber and polyurethane as raw materials 河南工业大学 2021-09-24 CN disclosed
CN-113249419-A Method for synthesizing rhamnolipid by extracellular enzyme catalysis 南京工业大学 2021-08-13 CN disclosed
EP-0331821-A1 Antiviral agent KUREHA KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1989-09-13 EP disclosed
JP-S63316730-A ANTIVIRAL AGENT KUREHA CHEM IND CO LTD 1988-12-26 JP disclosed
EP-0295956-A2 Use of a protein-bound polysaccharide for making a drug for treating AIDS. KUREHA KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1988-12-21 EP disclosed
EP-0212501-A2 Therapeutic agent for treating hematopoietic diseases GREEN CROSS CORPORATION (JP) 1987-03-04 EP disclosed
JP-S6034186-A INHIBITORY SUBSTANCE AGAINST ENZYME CAPABLE OF CONVERTING ANGIOTENSIN I FUJIREBIO INC 1985-02-21 JP disclosed
US-4481137-A ANTITUMOR AGENTS FROM CELL CULTURES MOCHIDA PHARMACEUTICAL CO., LTD. (JP) 1984-11-06 US disclosed
US-4442181-A NICKEL, TIN, CHROMIUM, CORROSION RESISTANCE NIPPON STEEL CORPORATION (JP) 1984-04-10 US disclosed
JP-S0634186-A 0001-01-01 JP disclosed