Emodin API Manufacturers
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Looking for Emodin API 518-82-1?
- Description:
- Here you will find a list of producers, manufacturers and distributors of Emodin. You can filter on certificates such as GMP, FDA, CEP, Written Confirmation and more. Send inquiries for free and get in direct contact with the supplier of your choice.
- API | Excipient name:
- Emodin
- Synonyms:
- 1,3,8-trihydroxy-6-methyl-9,10-anthracenedione , 1,3,8-trihydroxy-6-methyl-9,10-anthraquinone , Schuttgelb
- Cas Number:
- 518-82-1
- DrugBank number:
- DB07715
- Unique Ingredient Identifier:
- KA46RNI6HN
General Description:
Emodin, identified by CAS number 518-82-1, is a notable compound with significant therapeutic applications. Emodin has been investigated for the treatment of Polycystic Kidney.
Classification:
Emodin belongs to the class of organic compounds known as hydroxyanthraquinones. These are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group, classified under the direct parent group Hydroxyanthraquinones. This compound is a part of the Organic compounds, falling under the Benzenoids superclass, and categorized within the Anthracenes class, specifically within the Anthraquinones subclass.
Categories:
Emodin is categorized under the following therapeutic classes: Anthracenes, Anthraquinones, Biological Products, Enzyme Inhibitors, Gastrointestinal Agents, Laxatives, Plant Extracts, Plant Preparations, Protein Kinase Inhibitors, Quinones. These classifications highlight the drug's diverse therapeutic applications and its importance in treating various conditions.
Emodin is a type of Enzyme Replacements/modifiers
Enzyme replacements/modifiers are a crucial category of pharmaceutical active pharmaceutical ingredients (APIs) utilized in the treatment of various enzyme-related disorders. Enzymes play a vital role in the normal functioning of the body by catalyzing specific biochemical reactions. However, in certain medical conditions, the body may lack or produce dysfunctional enzymes, leading to serious health complications.
Enzyme replacement therapy (ERT) involves administering exogenous enzymes to compensate for the enzyme deficiency in patients. These enzymes are typically derived from natural sources or produced using recombinant DNA technology. By introducing these enzymes into the body, they can effectively substitute the missing or defective enzymes, thereby restoring normal metabolic processes.
On the other hand, enzyme modifiers are API substances that regulate the activity of specific enzymes within the body. These modifiers can either enhance or inhibit the enzyme's function, depending on the therapeutic objective. By modulating enzyme activity, these APIs can restore the balance of enzymatic reactions, leading to improved physiological outcomes.
Enzyme replacements/modifiers have shown remarkable success in treating various genetic disorders, such as Gaucher disease, Fabry disease, and lysosomal storage disorders. Additionally, they have demonstrated potential in managing enzyme deficiencies associated with rare diseases and certain types of cancer.
The development and production of enzyme replacements/modifiers involve rigorous research, formulation optimization, and adherence to stringent quality control measures. Pharmaceutical companies invest substantial resources in developing these APIs to ensure their safety, efficacy, and compliance with regulatory standards.
Overall, enzyme replacements/modifiers represent a vital therapeutic category in modern medicine, offering hope and improved quality of life for patients with enzyme-related disorders.
