Abacavir sulfate acts as a potent antiretroviral drug commonly utilized in the treatment of HIV infection. Chemically, it comprises the compound abacavir, which exists as a nucleoside reverse transcriptase inhibitor (NRTI). Abacavir sulfate possesses a molecular formula of C15H24N6O3S. The compound typically appears as a white to off-white crystalline powder, defined by its solubility in water and limited solubility in organic solvents.
Furthermore, abacavir sulfate exhibits a low melting point and undergoes minimal decomposition at room temperature. Its physicochemical properties influence its effectiveness as an antiretroviral agent by allowing absorption, distribution, metabolism, and excretion within the body.
Abarelix: CAS Number and Structural Information
Abarelix is an 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 identification of the compound in scientific literature and databases.
- Structure,, Abarelix comprises numerous rings and functional groups.
- The precise configuration of these components contributes to its binding affinity to the target receptor.
More 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.
Information on: Abacavir Sulfate
This section contains detailed details about Abacavir Sulfate, a substance with the CAS number 188062-50-2. Fundamental data includes its physical properties, composition, and purposes. website Abacavir Sulfate is a crystalline solid often used in the management of HIV infection.
Identifying Abarelix Through Its CAS Number (183552-38-7)
Abarelix serves as a medicinal substance employed in the treatment of certain kinds of prostatecancer. Its unique CAS number, 183552-38-7, functions as a specific identifier. This code allows precise recognition of Abarelix within scientific and healthcare databases. Professionals can leverage this CAS number to retrieve valuable data about Abarelix, including its chemical structure, properties, and potential applications.
Abiraterone Acetate (CAS 154229-18-2) - Chemical Properties
This chemical specification outlines the features of abiraterone acetate, a drug compound with CAS number 154229-18-2. This document provides detailed information on its physical properties, including appearance.
This compound is a potent inhibitor of steroidogenesis, primarily used in the management of prostate cancer. Its chemical structure consists a complex arrangement of atoms, determining its biological activity and clinical effects.
Additionally, this specification explores the stability of abiraterone acetate under various environments.
The provided data is intended for scientists working with this molecule and requires understanding within the context of relevant medical practices.