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编 号：F475358
分子式：C10H8KNO6S2
分子量：341.4
分子式：C10H8KNO6S2
分子量：341.4
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CAS No: 842-15-9
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生物活性：
2-Naphthylamine-6,8-disulfonic acid potassium is chemical that can be used for preparing dyestuff, medicine, agricultural chemicals etc.
体外研究：
2-Naphthylamine-6,8-disulfonic acid potassium (compound 20) can inhibit human immunodeficiency virus HIV-1 and HIV-2 by 11% and 13.6% at a concentration of 1369 μM, respectively.2-Naphthylamine-6,8-disulfonic acid potassium (ANDS) can directly analyze polyglycolic pyrophosphate-linked oligosaccharides in cell cultures and tissues.Guidelines (Following is our recommended protocol. This protocol only provides a guideline, and should be modified according to your specific needs).Labeling oligosaccharides:1. Prepared 0.15 M ANDS with 15% (v/v) acetic acid.2. Prepare 1M solution of sodium cyanoborohydride in dimethyl sulfoxide (DMSO).3. Add 5 μL ANDS reagent (1 μL if sample is below 200 pmol) to the sample.4. Add 5 μL sodium cyanoborohydride solution (1 μL if sample is below 200 pmol) to the sample.5. After mixing, the reaction was briefly centrifuged and allowed to dry for 18 hours at 37 °C.
2-Naphthylamine-6,8-disulfonic acid potassium is chemical that can be used for preparing dyestuff, medicine, agricultural chemicals etc.
体外研究：
2-Naphthylamine-6,8-disulfonic acid potassium (compound 20) can inhibit human immunodeficiency virus HIV-1 and HIV-2 by 11% and 13.6% at a concentration of 1369 μM, respectively.2-Naphthylamine-6,8-disulfonic acid potassium (ANDS) can directly analyze polyglycolic pyrophosphate-linked oligosaccharides in cell cultures and tissues.Guidelines (Following is our recommended protocol. This protocol only provides a guideline, and should be modified according to your specific needs).Labeling oligosaccharides:1. Prepared 0.15 M ANDS with 15% (v/v) acetic acid.2. Prepare 1M solution of sodium cyanoborohydride in dimethyl sulfoxide (DMSO).3. Add 5 μL ANDS reagent (1 μL if sample is below 200 pmol) to the sample.4. Add 5 μL sodium cyanoborohydride solution (1 μL if sample is below 200 pmol) to the sample.5. After mixing, the reaction was briefly centrifuged and allowed to dry for 18 hours at 37 °C.
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