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CAS RN: 22457-89-2 | 產品號碼: B4711
產品規格
Appearance | White to Almost white powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Purity(Neutralization titration) | min. 98.0 % |
性質
熔點 | 192 °C(dec.) |
GHS
相關法規
RTECS # | DH6910000 |
運輸資料
HS編碼* | 2933.59-000 |
Application
Paraptosis research
Reference
- Paraptosis Cell Death Induction by the Thiamine Analog Benfotiamine in Leukemia Cells
- Pharmacokinetics of thiamine derivatives, especially of benfotiamine (a review)
- D. Loew, Int. J. Clin. Pharmacol. Ther. 1996, 34, 47.
- Efficacy of benfotiamine versus thiamine on function and glycation products of peripheral nerves in diabetic rats
- Benfotiamine blocks three major pathways of hyperglycemic damage and prevents experimental diabetic retinopathy
- Benfotiamine prevents macro- and microvascular endothelial dysfunction and oxidative stress following a meal rich in advanced glycation end products in individuals with type 2 diabetes
- The multifaceted therapeutic potential of benfotiamine (a review)
Application
Benfotiamine: S-Acyl Derivative of Thiamine with High Bioavailability
S-benzoylthiamine O-monophoshate (benfotiamine) is a synthetic S-acyl derivative of thiamine (vitamin B1). Benfotiamine is absorbed in vivo much more than water soluble thiamine hydrochloride [T0181]. Benfotiamine increases the levels of intracellular thiamine diphosphate, a cofactor necessary for the activation transketolase, resulting in the reduction of tissue level of advanced glycation end products (AGEs) which can be a factor in the development or worsening of many degenerative diseases, such as diabetes, atherosclerosis, chronic renal failure and Alzheimer's disease.
References
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