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HYDROXYLAMINE HYDROCHLORIDE, 99.995% TRA
Кат. №: 379921-5G
Производитель: Sigma-Aldrich
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HYDROXYLAMINE HYDROCHLORIDE, 99.995% TRA
Main image
Кат. №: 379921-5G
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Main image
Печать
HYDROXYLAMINE HYDROCHLORIDE, 99.995% TRA
Кат. №: 379921-5G
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Description Application Reactant for preparation of: • Organosilane amines as potent inhibitors and structural probes of influenza A virus M2 proton channel • Lamellarin D analogues as inibitors of topoisomerase I and potential antitumor agents • Azapeptide tocolytic agents as inhibitors of prostaglandin F2α receptor for preventing preterm labor • Thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase B • Orally bioavailable quinoline-based antidiabetic dipeptidyl peptidase IV inhibitors targeting Lys554 • Pyrimidine nucleoside derivatives with nitric oxide donors as antiviral agents • Benzyladenosine compounds targeting adenosine A2A receptor and adenosine transporter for neuroprotection • Naphthol derivatives as inhibitors of the vanilloid receptor TRPV1 with improved potency in rat cystometry models of urinary incontinence Packaging 5, 25 g in poly bottle Biochem/physiol Actions MAO inhibitor; inhibits platelet aggregation.
Related Categories
C-X Bond Formation (Non-Halogen), Chemical Synthesis, Chemicals for the synthesis of candidate COVID-19 treatments, Hydroxychloroquine, Other Non-Halogen Reagents for C-X Bond Formation, Synthetic Reagents More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.
Description Application Reactant for preparation of: • Organosilane amines as potent inhibitors and structural probes of influenza A virus M2 proton channel • Lamellarin D analogues as inibitors of topoisomerase I and potential antitumor agents • Azapeptide tocolytic agents as inhibitors of prostaglandin F2α receptor for preventing preterm labor • Thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase B • Orally bioavailable quinoline-based antidiabetic dipeptidyl peptidase IV inhibitors targeting Lys554 • Pyrimidine nucleoside derivatives with nitric oxide donors as antiviral agents • Benzyladenosine compounds targeting adenosine A2A receptor and adenosine transporter for neuroprotection • Naphthol derivatives as inhibitors of the vanilloid receptor TRPV1 with improved potency in rat cystometry models of urinary incontinence Packaging 5, 25 g in poly bottle Biochem/physiol Actions MAO inhibitor; inhibits platelet aggregation.
Related Categories
C-X Bond Formation (Non-Halogen), Chemical Synthesis, Chemicals for the synthesis of candidate COVID-19 treatments, Hydroxychloroquine, Other Non-Halogen Reagents for C-X Bond Formation, Synthetic Reagents More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.