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AG23080

5119-48-2 | Withaferin a

Packsize Purity Availability Price Discounted Price    Quantity
1mg 98% in stock $36.00 $25.00 -   +
5mg 98% in stock $72.00 $50.00 -   +
10mg 98% in stock $118.00 $82.00 -   +
25mg 98% in stock $242.00 $169.00 -   +
100mg 98% in stock $733.00 $513.00 -   +
250mg 98% in stock $1,529.00 $1,070.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AG23080
Chemical Name: Withaferin a
CAS Number: 5119-48-2
Molecular Formula: C28H38O6
Molecular Weight: 470.5977199999999
MDL Number: MFCD10687098
SMILES: OCC1=C(C)C[C@@H](OC1=O)[C@H]([C@H]1CC[C@@H]2[C@]1(C)CC[C@H]1[C@H]2C[C@@H]2[C@]3([C@]1(C)C(=O)C=C[C@@H]3O)O2)C

 

Upstream Synthesis Route
  • Withaferin A is a potent bioactive compound isolated from the Withania somnifera plant, also known as Ashwagandha. In chemical synthesis, Withaferin A is widely used as a versatile building block due to its unique chemical structure and diverse reactivity. Its ability to form covalent bonds with various nucleophiles makes it a valuable tool for the construction of complex molecular architectures.One key application of Withaferin A in chemical synthesis is its utility as a Michael acceptor in the synthesis of heterocyclic compounds. By acting as a Michael acceptor, Withaferin A undergoes nucleophilic addition reactions with a range of nucleophiles, such as thiols and amines, leading to the formation of new carbon-carbon and carbon-heteroatom bonds. This reactivity enables the synthesis of structurally diverse compounds with potential biological activities.Additionally, Withaferin A has been employed in the development of novel synthetic methodologies, such as cascade reactions and multicomponent reactions. These strategies harness the unique reactivity of Withaferin A to rapidly assemble complex molecular frameworks in an efficient and cost-effective manner.Overall, the versatile reactivity of Withaferin A in chemical synthesis makes it an invaluable building block for the construction of natural product analogs, drug-like molecules, and other biologically active compounds. Its application continues to inspire innovative approaches in synthetic organic chemistry and drug discovery efforts.
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