67920-52-9 Usage
Description
Danshensu is a salvianolic acid and the major component of S. miltiorrhiza (Danshen) and has diverse biological activities. It reduces expression of the autophagy-associated proteins p62, LC3-II, and Beclin-1 and the apoptosis-related proteins Bax and caspase-3, prevents cardiomyocyte damage, and increases heart rate, coronary flow (CF), and left ventricular developed pressure (LVDP) in an isolated rat heart model of ischemia and reperfusion injury. Danshensu (60 mg/kg per day) reduces infarct size and improves left ventricular function in a rat model of myocardial infarction. It enhances radiation-induced tumor cell death in a Lewis lung carcinoma mouse xenograft model. Danshensu also decreases infarct volume, neuronal apoptosis, production of TNF-α, IL-1β, and IL-6, and superoxide dismutase (SOD) and glutathione peroxidase (GPx) activity in a rat model of cerebral ischemia and reperfusion injury.
Chemical Properties
White to light brown powder
Uses
Sodium Danshensu is exhibits protective effects on the excitotoxicity of monosodium glutamate in the late stage of pregnancy on developing mouse fetal brain.
Check Digit Verification of cas no
The CAS Registry Mumber 67920-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,2 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67920-52:
(7*6)+(6*7)+(5*9)+(4*2)+(3*0)+(2*5)+(1*2)=149
149 % 10 = 9
So 67920-52-9 is a valid CAS Registry Number.
67920-52-9Relevant articles and documents
D-tyrosine a method for asymmetric synthesis of
-
, (2019/02/02)
A provided asymmetric syntheses method for D-tyrosine comprises the following steps: performing a condensation reaction on p-hydroxybenzaldehyde and acetylglycine, then performing hydrolysis or alcoholysis to obtain a dehyddroamino acid or ester; and then utilizing rhodium to perform catalytic asymmetric hydrogenation, and performing hydrolysis to obtain a key intermediate D-tyrosine. According to the method, the whole process has no complex separation steps, the preparation technology is simple, a chromatography column is not needed, the reaction steps can be further reduced by utilizing rhodium catalysis asymmetric hydrogenation technology, the production cost is reduced, and the method is extremely suitable for industrialized batch production.