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1,4-Naphthoquinone is the parent structure of the 1,4-naphthoquinone family, with oxo groups at positions 1 and 4 of the naphthalene ring. Derivatives exhibit pharmacological properties and are derived from a naphthalene hydride.

CAS No.	130-15-4
Product Name	1,4-Naphthoquinone

Corrosive

Acute Toxic

Irritant

Health Hazard

Environmental Hazard

Signal Word:Danger

HCode:H301-H314-H315-H317-H318-H319-H330-H334-H335-H400-H410-H371-H373

PCode:P233-P260-P261-P264-P264+P265-P270-P271-P272-P273-P280-P284-P301+P316-P301+P330+P331-P302+P352-P302+P361+P354-P304+P340-P305+P351+P338-P305+P354+P338-P316-P317-P319-P320-P321-P330-P332+P317-P333+P317-P337+P317-P342+P316-P362+P364-P363-P391-P403-P403+P233-P405-P501-P308+P316

1,4-Naphthoquinone

CAS No.	130-15-4
MDL No.	MFCD00001676
MF	C₁₀H₆O₂
MW	158.15
InChI Key	FRASJONUBLZVQX-UHFFFAOYSA-N

CUSTOM SYNTHESIS PRECLINICAL SUPPORT

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Product Information

CAS No.	130-15-4
Product Name	1,4-Naphthoquinone

Corrosive

Acute Toxic

Irritant

Health Hazard

Environmental Hazard

Signal Word:Danger

HCode:H301-H314-H315-H317-H318-H319-H330-H334-H335-H400-H410-H371-H373

1,4-Naphthoquinone

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Properties

1,4-Naphthoquinone

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Documentation

1,4-Naphthoquinone

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Related Articles

Caspase-3-mediated cleavage of the NF-kappa B subunit p65 at the NH2 terminus potentiates naphthoquinone analog-induced apoptosis.

2- and 3-substituted 1,4-naphthoquinone derivatives as subversive substrates of trypanothione reductase and lipoamide dehydrogenase from Trypanosoma cruzi: synthesis and correlation between redox cycling activities and in vitro cytotoxicity.

In vitro and in vivo Leishmanicidal activity of 2-hydroxy-3-(3-methyl-2-butenyl)-1,4-naphthoquinone (lapachol).

NAD(P)H:menadione oxidoreductase of the amitochondriate eukaryote Giardia lamblia: a simpler homologue of the vertebrate enzyme.

1,4-Naphthoquinone

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Properties

Related Articles

Caspase-3-mediated cleavage of the NF-kappa B subunit p65 at the NH2 terminus potentiates naphthoquinone analog-induced apoptosis.

2- and 3-substituted 1,4-naphthoquinone derivatives as subversive substrates of trypanothione reductase and lipoamide dehydrogenase from Trypanosoma cruzi: synthesis and correlation between redox cycling activities and in vitro cytotoxicity.

In vitro and in vivo Leishmanicidal activity of 2-hydroxy-3-(3-methyl-2-butenyl)-1,4-naphthoquinone (lapachol).

NAD(P)H:menadione oxidoreductase of the amitochondriate eukaryote Giardia lamblia: a simpler homologue of the vertebrate enzyme.

Documentation