Abacavir sulfate acts as a potent antiretroviral drug commonly utilized in the treatment of HIV infection. Chemically, it includes the compound abacavir, which exists as a nucleoside reverse transcriptase inhibitor (NRTI). Abacavir sulfate displays a molecular formula of C15H24N6O3S. The compound usually shows up as a white to off-white crystalline powder, characterized its solubility in water and limited solubility in organic solvents.
Additionally, abacavir sulfate exhibits a low melting point and undergoes minimal decomposition at room temperature. Its physicochemical properties contribute its effectiveness as an antiretroviral agent by allowing absorption, distribution, metabolism, and excretion within the body.
Discovering Abarelix: CAS Number & Structure
Abarelix is a gonadotropin-releasing hormone receptor antagonist used for treating advanced prostate cancer. Its chemical structure, characterized by a complex arrangement of atoms, plays a crucial role in its therapeutic effects. The CAS Number, a unique identifier, for Abarelix is 124630-58-4. This identifier allows for unambiguous identification of the compound in scientific literature and databases.
- Structural Features,, Abarelix comprises numerous rings and functional groups.
- The precise design of these components contributes to its binding affinity to the target receptor.
Further information about Abarelix's structure and CAS number can be obtained from reliable sources such as PubChem, ChemSpider, and scientific journals.
Abiraterone Acetate: Diving into Its Chemical Composition
Abiraterone acetate is a synthetic compound with the chemical formula C29H38O6. It/This/That belongs to a class of drugs known as androgen synthesis inhibitors, which are primarily used in the treatment of prostate cancer. The/Its/This molecule exhibits a complex structure, featuring a steroid nucleus with several functional groups attached. One/Several/Key of these functional groups is a carboxyl group, responsible for its/the/that ability to inhibit the enzyme 17α-hydroxylase/C17,20 lyase. This/That/It enzymatic inhibition blocks the production of androgens, hormones/chemicals/substances that fuel the growth of prostate cancer cells.
- Amongst/Within/Throughout the various functional groups present in abiraterone acetate are a ketone group, an ether linkage, and two hydroxyl groups.
- These/This/That groups contribute to the molecule's overall polarity and its/their/these interactions with target enzymes.
The chemical structure of abiraterone acetate allows it to effectively bind to the active site of 17α-hydroxylase/C17,20 lyase, effectively/efficiently/successfully blocking the conversion of cholesterol into androgens. This mechanism of action makes it a valuable therapeutic agent in the management of prostate cancer.
Chemical Database Entry: Abacavir Sulfate (188062-50-2)
This database record contains detailed information about Abacavir Sulfate, a substance with the CAS number 188062-50-2. Important details includes its characteristics, chemical structure, and purposes. Abacavir Sulfate is a white powder often used in the treatment of HIV infection.
Recognizing Abarelix Through Its CAS Number (183552-38-7)
Abarelix serves as a pharmaceutical substance used in the treatment of certain categories of prostatetumors. Its unique CAS number, 183552-38-7, operates as a distinct identifier. This number enables precise identification of Abarelix within scientific and pharmaceutical databases. Researchers can leverage this CAS number to retrieve valuable information about Abarelix, including its chemical structure, properties, and potential applications.
Abiraterone Acetate CAS Number 154229-18-2: Detailed Specifications
That chemical specification outlines the characteristics of abiraterone acetate, a drug compound with CAS identifier 154229-18-2. Herein provides detailed data on its molecular properties, including melting point.
The drug is click here a potent inhibitor of steroidogenesis, primarily used in the therapy of prostate cancer. Its chemical structure consists a specific arrangement of atoms, influencing its biological activity and therapeutic effects.
Furthermore, this specification examines the stability of abiraterone acetate under various environments.
The provided data is intended for researchers working with this compound and requires interpretation within the context of relevant regulatory guidelines.