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| Product | Description | |
|---|---|---|
| 1,2-Naphthoquinone | 1,2-Naphthoquinone. Group: Ligands for functional metal complexes. Alternative Names: 1,2-Naphthalenedione; 1,2-NAPHTHOQUINONE. CAS No. 524-42-5. Product ID: naphthalene-1,2-dione. Molecular formula: 158.15. Mole weight: C10< / sub>H6< / sub>O2< / sub>. C1=CC=C2C(=C1)C=CC(=O)C2=O. KETQAJRQOHHATG-UHFFFAOYSA-N. PRACTICAL. |  |
| 1,2-Naphthoquinone | 5g Pack Size. Group: Aroma Chemicals, Building Blocks, Organics. Formula: C10H6O2. CAS No. 524-42-5. Prepack ID 42251673-5g. Molecular Weight 158.15. See USA prepack pricing. |  |
| 1,2-Naphthoquinone-4-sulfonic acid sodium salt | 1,2-Naphthoquinone-4-sulfonic acid sodium salt. Group: Biochemicals. Grades: Highly Purified. CAS No. 521-24-4. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C10H5O5S·Na. US Biological Life Sciences. |  Worldwide |
| 1,2-Naphthoquinone (90%) | 1,2-Naphthquinone is a highly reactive quinone species which aids in modulating cellular homeostasis and electrophilic signal transduction pathways. Group: Biochemicals. Grades: Highly Purified. CAS No. 524-42-5. Pack Sizes: 1g, 2.5g. Molecular Formula: C10H6O2. US Biological Life Sciences. | Worldwide |
| Potassium 1,2-naphthoquinone-4-sulphonate | Potassium 1,2-naphthoquinone-4-sulphonate (Compound 16) is a 6-phosphogluconate dehydrogenase ( 6PGDH ) inhibitor with an IC 50 of 53 μM. Potassium 1,2-naphthoquinone-4-sulphonate can be used in the study of human African trypanosomiasis [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 5908-27-0. Pack Sizes: 1 mg. Product ID: HY-W726137. |  |
| 1,2-Naphthalenedione,4-amino- | 1,2-Naphthalenedione,4-amino-. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4-AMINONAPHTHALENE-1,2-DIONE;4-azanylnaphthalene-1,2-dione. Product Category: Heterocyclic Organic Compound. CAS No. 5460-35-5. Molecular formula: C10H7NO2. Mole weight: 173.1681. Purity: 0.96. IUPACName: 4-aminonaphthalene-1,2-dione. Canonical SMILES: C1=CC=C2C(=C1)C(=CC(=O)C2=O)N. Density: 1.351 g/cm³. Product ID: ACM5460355. Alfa Chemistry ISO 9001:2015 Certified. Categories: 4-Amino-1,2-naphthoquinone. |  |
| 3,4-Dihydro-3,4-dioxo-1-naphthalenesulfonic acid ammonium salt | 3,4-Dihydro-3,4-dioxo-1-naphthalenesulfonic acid ammonium salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3,4-Dihydro-3,4-dioxo-1-naphthalenesulfonic acid ammonium salt;1,2-Naphthoquinone -4-Sulfonic Acid Ammonium Salt. Product Category: Heterocyclic Organic Compound. CAS No. 53684-60-9. Product ID: ACM53684609. Alfa Chemistry ISO 9001:2015 Certified. | |
| 4-(4-Hydroxyanilino)-1,2-dihydronaphthalene-1,2-dione | 4-(4-Hydroxyanilino)-1,2-dihydronaphthalene-1,2-dione. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4-(4-HYDROXYANILINO)-1,2-DIHYDRONAPHTHALENE-1,2-DIONE;4-(4-HYDROXYANILINO)-1,2-DIHYDRONAPHTHALENE-1,2-DIONE , 01;4-(4-HYDROXYANILINO)-1,2-NAPHTHOQUINONE. Product Category: Heterocyclic Organic Compound. CAS No. 75140-07-7. Molecular formula: C16H11NO3. Mole weight: 265.26. Purity: 0.96. IUPACName: 4-(4-hydroxyanilino)naphthalene-1,2-dione. Canonical SMILES: C1=CC=C2C(=C1)C(=CC(=O)C2=O)NC3=CC=C(C=C3)O. Density: 1.442g/cm³. Product ID: ACM75140077. Alfa Chemistry ISO 9001:2015 Certified. | |
| Aflatoxin B1 aldehyde reductase member 2 from Human, Recombinant | Aflatoxin B1 aldehyde reductase member 2 catalyzes the NADPH-dependent reduction of succinic semialdehyde to gamma-hydroxybutyrate. May have an important role in producing the neuromodulator gamma-hydroxybutyrate (GHB). Has broad substrate specificity. Has NADPH-dependent aldehyde reductase activity towards 2-carboxybenzaldehyde, 2-nitrobenzaldehyde and pyridine-2-aldehyde (in vitro). Can reduce 1,2-naphthoquinone and 9,10-phenanthrenequinone (in vitro). Can reduce the dialdehyde protein-binding form of aflatoxin B1 (AFB1) to the non-binding AFB1 dialcohol. May be involved in protection of liver against the toxic and carcinogenic effects of AFB1, a potent hepatocarcinogen. Group: Enzymes. Synonyms: AFB1 aldehyde reductase 1; AFB1-AR 1; Aldoketoreductase 7; Succinic semialdehyde reductase. Enzyme Commission Number: EC 1.1.1.n11. AKR7A2. Mole weight: 39588.9 Da. Source: Human. AFB1 aldehyde reductase 1; AFB1-AR 1; Aldoketoreductase 7; Succinic semialdehyde reductase; EC 1.1.1.n11; AKR7A2; Aflatoxin B1 aldehyde reductase member 2. Cat No: NATE-1196. |  |
| NADPH:quinone reductase | A zinc enzyme, specific for NADPH. Catalyses the one-electron reduction of certain quinones, with the orthoquinones 1,2-naphthoquinone and 9,10-phenanthrenequinone being the best substrates. Dicoumarol [cf. EC 1.6.5.2 NAD(P)H dehydrogenase (quinone)] and nitrofurantoin are competitive inhibitors with respect to the quinone substrate. The semiquinonefree-radical product may be non-enzymically reduced to the hydroquinone or oxidized back to quinone in the presence of O2. In some mammals, the enzyme is abundant in the lens of the eye, where it is identified with the protein ζ-crystallin. Group: Enzymes. Synonyms: NADPH2:quinone reductase. Enzyme Commission Number: EC 1.6.5.5. CAS No. 9032-20-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1594; NADPH:quinone reductase; EC 1.6.5.5; 9032-20-6; NADPH2:quinone reductase. Cat No: EXWM-1594. | |
| Pigment Green 8 | Pigment Green 8. Uses: Designed for use in research and industrial production. Additional or Alternative Names: sodium tris(1,2-naphthoquinone 1-oximato-O,O')ferrate(1-);CI 10006;Ferrate(1-), tris(1,2-naphthalenedione-.kappa.O2) 1-(oximato-.kappa.O)-, sodium;SODIUMFERRICCOMPLEXOF1-NITROSO-2-HYDROXYNAPHTHALENE;Pigment green 8 (C.I. 10006);Ferrate(1-), tris(1,2-naph. Product Category: Pigments. CAS No. 16143-80-9. Molecular formula: C30H18FeN3NaO6. Mole weight: 595.3222. Product ID: ACM16143809. Alfa Chemistry ISO 9001:2015 Certified. Categories: Pigment Green 7. | |
| quinaldate 4-oxidoreductase | The enzyme from Pseudomonas sp. AK2 also acts on quinoline-8-carboxylate, whereas that from Serratia marcescens 2CC-1 will oxidize nicotinate; quinaldate is a substrate for both of these enzymes. 2,4,6-Trinitrobenzene sulfonate, 1,4-benzoquinone, 1,2-naphthoquinone, nitroblue tetrazolium, thionine and menadione will serve as an electron acceptor for the former enzyme and ferricyanide for the latter; Meldola blue, iodonitrotetrazolium chloride, phenazine methosulfate, 2,6-dichlorophenolindophenol and cytochrome c will act as electron acceptors for both. Group: Enzymes. Synonyms: quinaldic acid 4-oxidoreductase. Enzyme Commission Number: EC 1.3.99.18. CAS No. 149885-77-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1423; quinaldate 4-oxidoreductase; EC 1.3.99.18; 149885-77-8; quinaldic acid 4-oxidoreductase. Cat No: EXWM-1423. | |
| Sodium 1,2-Napthoquinone-4-sulfonate | Sodium 1,2-Napthoquinone-4-sulfonate. Group: Biochemicals. Alternative Names: 3,4-Dihydro-3,4-dioxo-1-naphthalenesulfonic Acid Sodium Salt; 3,4-Dihydro-3,4-dioxo-1-naphthalenesulfonic Acid Sodium Salt; 1,2-Naphthoquinone-4-sodium Sulfonate; 1,2-Naphthoquinone-4-sulfonic Acid Sodium Salt; Sodium 1,2-Naphthoquinone-4-sulfonate; Sodium 3,4-dihydro-3,4-dioxo-1-naphthalenesulfonate; Sodium 3,4-dioxo-1-naphthalenesulfonate; Sodium β-naphthoquinone-4-sulfonate; Sodium β -Naphthoquinonesulfonat e; β-Naphthoquinone-4-sulfonate Sodium Salt. Grades: Highly Purified. CAS No. 521-24-4. Pack Sizes: 100mg. Molecular Formula: C10H8NaO5S, Molecular Weight: 263.22. US Biological Life Sciences. | Worldwide |
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