Abacavir sulfate is a potent antiretroviral drug commonly utilized in the treatment of HIV infection. Chemically, it consists of the compound abacavir, which exists as a nucleoside reverse transcriptase inhibitor (NRTI). Abacavir sulfate displays a molecular formula of C15H24N6O3S. The compound typically presents 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 experiences minimal decomposition at room temperature. Its physicochemical properties affect its effectiveness as an antiretroviral agent by enabling absorption, distribution, metabolism, and excretion within the body.
About Abarelix: CAS Number and Structural Details
Abarelix is a gonadotropin-releasing hormone receptor antagonist used for managing advanced prostate cancer. Its chemical structure, defined as a complex arrangement of atoms, contributes a crucial role in its therapeutic effects. The CAS Number, an identifying number, for Abarelix is 124630-58-4. This identifier allows for unambiguous recognition of the compound in scientific literature and databases.
- The Structure of, Abarelix comprises numerous rings and functional groups.
- The precise configuration of these components affects its binding affinity to the target receptor.
Additional information about Abarelix's structure and CAS number can be obtained from reliable sources such as PubChem, ChemSpider, and scientific journals.
Exploring Abiraterone Acetate's Chemical Structure
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 section contains detailed information about Abacavir Sulfate, a chemical compound with the CAS number 188062-50-2. Important details includes its attributes, formula, and potential applications. Abacavir Sulfate is a white powder often used in the management of HIV infection. ARFORMOTEROL TARTRATE 200815-49-2
Identifying Abarelix Through Its CAS Number (183552-38-7)
Abarelix represents a medicinal compound utilized in the care of certain kinds of prostatetumors. Its individual CAS number, 183552-38-7, operates as a universal identifier. This number enables precise identification of Abarelix within scientific and healthcare databases. Scientists can employ this CAS number to access valuable information about Abarelix, including its chemical structure, properties, and potential applications.
Abiraterone Acetate (CAS 154229-18-2) - Chemical Properties
This chemical specification outlines the properties of abiraterone acetate, a pharmaceutical compound with CAS identifier 154229-18-2. It provides detailed information on its molecular properties, including melting point.
Abiraterone acetate is a potent inhibitor of steroidogenesis, chiefly used in the treatment of prostate cancer. Its molecular formula consists a specific arrangement of atoms, contributing its biological activity and clinical effects.
Additionally, this specification explores the stability of abiraterone acetate under various environments.
The provided data is intended for professionals working with this substance and requires interpretation within the context of relevant safety protocols.