486430-93-7 Usage
General Description
O-Acetylcycloalopin A is a natural chemical compound derived from the aerial parts of the Chinese medicinal herb Schisandra sphaerandra. This bioactive compound has been found to exhibit a range of pharmacological activities, including anti-inflammatory, anti-tumor, and anti-hypoxia effects. O-Acetylcycloalopin A has also been shown to inhibit the growth of certain cancer cell lines, making it a potentially promising candidate for the development of new anticancer drugs. Additionally, it has been reported to have hepatoprotective and antioxidant properties, making it a valuable natural product with potential therapeutic applications in the treatment of various diseases and health conditions. Further research on O-Acetylcycloalopin A may lead to the development of novel pharmaceuticals and therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 486430-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,6,4,3 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 486430-93:
(8*4)+(7*8)+(6*6)+(5*4)+(4*3)+(3*0)+(2*9)+(1*3)=177
177 % 10 = 7
So 486430-93-7 is a valid CAS Registry Number.
486430-93-7Relevant articles and documents
Calopins and cyclocalopins - Bitter principles from Boletus calupos and related mushrooms
Hellwig, Veronika,Dasenbrock, Johannes,Graef, Claudia,Kahner, Lydia,Schumann, Susanne,Steglich, Wolfgang
, p. 2895 - 2904 (2007/10/03)
Boletus calopus and closely related mushrooms of the Boletus section Calopodes are characterized by their bitter taste, which is caused mainly by O-acetylcyclocalopin A (6a), a member of a series of unique δ-lactone derivatives. Besides the simple lactone calopin (1b) and its O-acetyl derivative la, the more complex cyclocalopins 6-12 have been isolated and their structures elucidated. Cyclocalopin D (10a) is an unprecedented α-glucoside in which the sugar residue is bound to an enolic hydroxy group., The chemical conversion of 6b into la established the same stereochemistry for the calopin and cyclocalopin types of metabolites. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.
