You Searched For: 1,2-Naphthoquinone


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Supplier: TCI America
Description: CAS Number: 521-24-4
MDL Number: MFCD00001700
Molecular Formula: C10H6O5S
Molecular Weight: 260.19
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Supplier: TCI America
Description: CAS Number: 524-42-5
MDL Number: MFCD00001698
Molecular Formula: C10H6O2
Molecular Weight: 158.16
Purity/Analysis Method: >95.0% (HPLC,W)
Form: Crystal
Melting point (°C): 133
Storage Temperature: 0-10°C
Supplier: Thermo Scientific Chemicals
Description: Colorimetric determination of amino acids and amines.
Catalog Number: (10431-480)
Supplier: Bioss
Description: May be involved in the generation of reactive oxygen species (ROS). Has low NADPH-dependent beta-naphthoquinone reductase activity, with a preference for 1,2-beta-naphthoquinone over 1,4-beta-naphthoquinone. Has low NADPH-dependent diamine reductase activity (in vitro).


Catalog Number: (10431-502)
Supplier: Bioss
Description: May be involved in the generation of reactive oxygen species (ROS). Has low NADPH-dependent beta-naphthoquinone reductase activity, with a preference for 1,2-beta-naphthoquinone over 1,4-beta-naphthoquinone. Has low NADPH-dependent diamine reductase activity (in vitro).


Catalog Number: (10431-494)
Supplier: Bioss
Description: May be involved in the generation of reactive oxygen species (ROS). Has low NADPH-dependent beta-naphthoquinone reductase activity, with a preference for 1,2-beta-naphthoquinone over 1,4-beta-naphthoquinone. Has low NADPH-dependent diamine reductase activity (in vitro).


Catalog Number: (76117-130)
Supplier: Bioss
Description: May be involved in the generation of reactive oxygen species (ROS). Has low NADPH-dependent beta-naphthoquinone reductase activity, with a preference for 1,2-beta-naphthoquinone over 1,4-beta-naphthoquinone. Has low NADPH-dependent diamine reductase activity (<i>in vitro</i>).


Catalog Number: (10431-496)
Supplier: Bioss
Description: May be involved in the generation of reactive oxygen species (ROS). Has low NADPH-dependent beta-naphthoquinone reductase activity, with a preference for 1,2-beta-naphthoquinone over 1,4-beta-naphthoquinone. Has low NADPH-dependent diamine reductase activity (in vitro).


Catalog Number: (76117-128)
Supplier: Bioss
Description: May be involved in the generation of reactive oxygen species (ROS). Has low NADPH-dependent beta-naphthoquinone reductase activity, with a preference for 1,2-beta-naphthoquinone over 1,4-beta-naphthoquinone. Has low NADPH-dependent diamine reductase activity (<i>in vitro</i>).


Catalog Number: (10431-498)
Supplier: Bioss
Description: May be involved in the generation of reactive oxygen species (ROS). Has low NADPH-dependent beta-naphthoquinone reductase activity, with a preference for 1,2-beta-naphthoquinone over 1,4-beta-naphthoquinone. Has low NADPH-dependent diamine reductase activity (in vitro).


Catalog Number: (10431-500)
Supplier: Bioss
Description: May be involved in the generation of reactive oxygen species (ROS). Has low NADPH-dependent beta-naphthoquinone reductase activity, with a preference for 1,2-beta-naphthoquinone over 1,4-beta-naphthoquinone. Has low NADPH-dependent diamine reductase activity (in vitro).


Catalog Number: (10431-492)
Supplier: Bioss
Description: May be involved in the generation of reactive oxygen species (ROS). Has low NADPH-dependent beta-naphthoquinone reductase activity, with a preference for 1,2-beta-naphthoquinone over 1,4-beta-naphthoquinone. Has low NADPH-dependent diamine reductase activity (in vitro).


Catalog Number: (10473-592)
Supplier: Bioss
Description: Catalyzes the NADPH-dependent reduction of a variety of aromatic and aliphatic aldehydes to their corresponding alcohols. Catalyzes the reduction of mevaldate to mevalonic acid and of glyceraldehyde to glycerol. Has broad substrate specificity. In vitro substrates include succinic semialdehyde, 4-nitrobenzaldehyde, 1,2-naphthoquinone, methylglyoxal, and D-glucuronic acid. Plays a role in the activation of procarcinogens, such as polycyclic aromatic hydrocarbon trans-dihydrodiols, and in the metabolism of various xenobiotics and drugs, including the anthracyclines doxorubicin (DOX) and daunorubicin (DAUN).


Catalog Number: (10473-614)
Supplier: Bioss
Description: Catalyzes the NADPH-dependent reduction of a variety of aromatic and aliphatic aldehydes to their corresponding alcohols. Catalyzes the reduction of mevaldate to mevalonic acid and of glyceraldehyde to glycerol. Has broad substrate specificity. In vitro substrates include succinic semialdehyde, 4-nitrobenzaldehyde, 1,2-naphthoquinone, methylglyoxal, and D-glucuronic acid. Plays a role in the activation of procarcinogens, such as polycyclic aromatic hydrocarbon trans-dihydrodiols, and in the metabolism of various xenobiotics and drugs, including the anthracyclines doxorubicin (DOX) and daunorubicin (DAUN).


Supplier: TCI America
Description: CAS Number: 14918-69-5
MDL Number: MFCD00075261
Molecular Formula: C10H4Cl2O4
Molecular Weight: 259.04
Purity/Analysis Method: >97.0% (HPLC,T)
Form: Crystal
Melting point (°C): 201
Catalog Number: (TCD2070-001G)
Supplier: TCI America
Description: CAS Number: 475-38-7
MDL Number: MFCD00001685
Molecular Formula: C10H6O4
Molecular Weight: 190.15
Purity/Analysis Method: >75.0% (HPLC)
Form: Crystal
Melting point (°C): 230

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