6678-00-8 Usage
Description
11beta,17,21-trihydroxypregn-4-ene-3,20-dione 21-valerate, also known as Hydrocortisone 21-Valerate, is a derivative of Hydrocortisone, a steroid hormone and a glucocorticoid produced by the zona fasciculata of the adrenal gland. It is involved in various physiological processes, including the regulation of blood sugar, immune system suppression, and metabolism of fat, protein, and carbohydrates.
Uses
Used in Pharmaceutical Industry:
11beta,17,21-trihydroxypregn-4-ene-3,20-dione 21-valerate is used as a pharmaceutical agent for its anti-inflammatory and immunosuppressive properties. It is particularly effective in treating various inflammatory and autoimmune conditions, such as rheumatoid arthritis, lupus, and asthma, by reducing inflammation and suppressing the immune system.
Used in Cosmetic Industry:
In the cosmetic industry, 11beta,17,21-trihydroxypregn-4-ene-3,20-dione 21-valerate is used as an ingredient in skincare products for its anti-inflammatory and skin-soothing properties. It helps to reduce redness, swelling, and irritation, making it suitable for sensitive and inflamed skin types.
Used in Veterinary Medicine:
11beta,17,21-trihydroxypregn-4-ene-3,20-dione 21-valerate is also used in veterinary medicine as an anti-inflammatory and immunosuppressive agent for the treatment of various conditions in animals, such as allergies, skin conditions, and inflammatory bowel disease.
Overall, 11beta,17,21-trihydroxypregn-4-ene-3,20-dione 21-valerate is a versatile compound with applications in various industries, primarily due to its anti-inflammatory and immunosuppressive properties.
Check Digit Verification of cas no
The CAS Registry Mumber 6678-00-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,7 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6678-00:
(6*6)+(5*6)+(4*7)+(3*8)+(2*0)+(1*0)=118
118 % 10 = 8
So 6678-00-8 is a valid CAS Registry Number.
6678-00-8Relevant articles and documents
Relative affinity of 17α-and/or 21-esters and 17α,21-diesters of cortisol for a glucocorticoid receptor from rat thymocytes
Solo,Tramposch,Szeto,Suto
, p. 747 - 749 (2007/10/02)
The affinity, relative to cortisol, of 17α- and 21-esters and 17α,21-diesters of cortisol for the glucocorticoid receptor of rat thymus cytosol was determined by a competitive binding assay which used [3H]dexamethasone. Esterification of the 21-hydroxy group of cortisol caused a loss of relative affinity to 0.046 for acetate and 0.32 for valerate. Esterification of the 17α-hydroxy group resulted in an increase in relative affinity to 1.14 for acetate, 12.4 for butyrate, and 11.5 for valerate. Diesters had relative affinities which reflected both trends. Thus, the 21-acetate, 21-propionate, 21-butyrate, and 21-valerate of cortisol 17-acetate had relative affinities of 0.036, 0.093, 0.152, and 0.272. The 21-acetate, 21-propionate, and 21-butyrate of cortisol 17-valerate had relative affinities of 0.76, 1.17, and 1.33.