Welcome to LookChem.com Sign In|Join Free

CAS

  • or

17652-16-3

Post Buying Request

17652-16-3 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

17652-16-3 Usage

Description

4,9(11)-PREGNADIEN-3,20-DIONE, also known as prednisolone, is a synthetic steroid derived from cortisone and belongs to the class of glucocorticoids. It is commonly used as an anti-inflammatory and immunosuppressant medication, working by reducing inflammation and suppressing the immune system. Prednisolone is available in various forms, including tablets, syrups, and injections, and is prescribed for both short-term and long-term use depending on the individual's condition.

Uses

Used in Pharmaceutical Industry:
4,9(11)-PREGNADIEN-3,20-DIONE is used as an anti-inflammatory and immunosuppressant medication for the treatment of various conditions such as allergies, asthma, autoimmune diseases, and inflammatory disorders. Its ability to reduce inflammation and suppress the immune system makes it a valuable treatment option for these conditions.
Used in Allergy Treatment:
4,9(11)-PREGNADIEN-3,20-DIONE is used as an anti-inflammatory agent for the treatment of allergic reactions. It helps to reduce the symptoms of allergies by decreasing the body's immune response to allergens.
Used in Asthma Management:
4,9(11)-PREGNADIEN-3,20-DIONE is used as a medication to manage asthma symptoms. It helps to reduce inflammation in the airways, improving lung function and reducing the frequency of asthma attacks.
Used in Autoimmune Disease Treatment:
4,9(11)-PREGNADIEN-3,20-DIONE is used as an immunosuppressant in the treatment of autoimmune diseases. It helps to suppress the overactive immune response that causes damage to the body's own tissues in conditions such as rheumatoid arthritis, lupus, and multiple sclerosis.
Used in Inflammatory Disorder Treatment:
4,9(11)-PREGNADIEN-3,20-DIONE is used as an anti-inflammatory medication for the treatment of various inflammatory disorders. It helps to reduce inflammation and alleviate symptoms in conditions such as Crohn's disease, ulcerative colitis, and psoriasis.

Check Digit Verification of cas no

The CAS Registry Mumber 17652-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,5 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17652-16:
(7*1)+(6*7)+(5*6)+(4*5)+(3*2)+(2*1)+(1*6)=113
113 % 10 = 3
So 17652-16-3 is a valid CAS Registry Number.

17652-16-3Downstream Products

17652-16-3Relevant articles and documents

9α-hydroxy-17-methylene steroids, process for their preparation and their use in the preparation of corticosteroids

-

, (2008/06/13)

New 9α-hydroxy-17-methylene steroids are prepared by the introduction of a substituted 17-methylene group in 9α-hydroxyandrost-4-ene-3, 17-dione. The resulting compounds are useful starting compounds in the synthesis of corticosteroids.

9-Alpha-hydroxy-17-methylene steroids, process for their preparation and their use in the preparation of corticosteroids

-

, (2008/06/13)

New 9α-hydroxy-17-methylene steroids are prepared by the introduction of a substituted 17-methylene group in 9α-hydroxyandrost-4-ene-3,17-dione., The resulting compounds are useful starting compounds in the synthesis of corticosteroids.

Microbial hydroxylation of steroids. 10. Rearrangement during epoxidation and hydroxylation, and the stepwise nature of these enzymic reactions

Holland, Herbert L.,Riemland, Elly

, p. 1121 - 1126 (2007/10/02)

A series of unsaturated steroids has been incubated with fungi which are known to hydroxylate at a site corresponding to the allylic position in the analogous saturated steroids.In some cases, the anticipated hydroxylation occurred without rearrangement of the double bond.In a number of instances, however, products were obtained whose structures implied that allylic rearrangement had occurred during the reaction.The formation of these products is consistent with a stepwise mechanism of enzymatic oxidation.Possible routes for product formation are presented which incorporate this proposal.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 17652-16-3