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Thiamine disulfide
CAS No. 67-16-3
Thiamine disulfide( Algoneurina | Daiomin | TDS )
Catalog No. M27222 CAS No. 67-16-3
Thiamine, also known as thiamin or vitamin B1, is a vitamin found in food and manufactured as a dietary supplement and medication. Thiamine also acts as a cofactor for many centrally metabolizing enzymes.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 28 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | 32 | In Stock |
|
Biological Information
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Product NameThiamine disulfide
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NoteResearch use only, not for human use.
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Brief DescriptionThiamine, also known as thiamin or vitamin B1, is a vitamin found in food and manufactured as a dietary supplement and medication. Thiamine also acts as a cofactor for many centrally metabolizing enzymes.
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DescriptionThiamine, also known as thiamin or vitamin B1, is a vitamin found in food and manufactured as a dietary supplement and medication. Thiamine also acts as a cofactor for many centrally metabolizing enzymes.
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In VitroThiamine disulfide markedly inhibits production of progeny HIV-1 in acute and chronic HIV-1-infected CEM at nontoxic concentrations of 500-1000 μM. Thiamine disulfide (500 μM) blocks 99.7% of HIV-1 production after 96 hours culture in acute HIV-1 (LAV-1) infection, whereas it inhibits 90-98% of HIV-1 production in chronic-infected cells (CEM/LAV-1, H9/MN, and Molt-4/IIIB).
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In Vivo——
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SynonymsAlgoneurina | Daiomin | TDS
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PathwayMicrobiology/Virology
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TargetHIV
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RecptorGRK5
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Research Area——
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Indication——
Chemical Information
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CAS Number67-16-3
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Formula Weight562.71
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Molecular FormulaC24H34N8O4S2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (444.28 mM)
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SMILESC\C(N(Cc1cnc(C)nc1N)C=O)=C(\CCO)SS\C(CCO)=C(/C)N(Cc1cnc(C)nc1N)C=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Krause M, Foks H, Gobis K. Pharmacological Potential and Synthetic Approaches of Imidazo[4,5-b]pyridine and Imidazo[4,5-c]pyridine Derivatives. Molecules. 2017;22(3):399.
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