Abacavir sulfate is a potent antiretroviral drug commonly utilized in the treatment of HIV infection. Chemically, it consists of the compound abacavir, which resides as a nucleoside reverse transcriptase inhibitor (NRTI). Abacavir sulfate displays a molecular formula of C15H24N6O3S. The compound often shows up as a white to off-white crystalline powder, defined by its solubility in water and limited solubility in organic solvents.
Additionally, abacavir sulfate exhibits a low melting point and suffers minimal decomposition at room temperature. Its physicochemical properties affect its effectiveness as an antiretroviral agent by allowing absorption, distribution, metabolism, and excretion within the ALLOPURINOL 315-30-0 body.
Abarelix: CAS Number and Structural Information
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 number allows for unambiguous specification 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.
Further information about Abarelix's structure and CAS number can be found 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.
Abacavir Sulfate Chemical Data
This database record contains detailed information about Abacavir Sulfate, a substance with the CAS number 188062-50-2. Fundamental data includes its characteristics, formula, and uses. Abacavir Sulfate is a fine substance often used in the therapy of HIV infection.
Identifying Abarelix Through Its CAS Number (183552-38-7)
Abarelix is a therapeutic agent employed in the care of certain types of cancer. Its unique CAS number, 183552-38-7, operates as a specific identifier. This code enables precise characterization of Abarelix within scientific and medical databases. Researchers can employ this CAS number to retrieve valuable information about Abarelix, including its chemical structure, properties, and potential applications.
Abiraterone Acetate (CAS 154229-18-2) - Chemical Properties
These chemical specification outlines the features of abiraterone acetate, a medication compound with CAS code 154229-18-2. This document provides detailed details on its physical properties, including boiling point.
The drug is a potent inhibitor of hormone production, primarily used in the treatment of prostate cancer. Its composition features a complex arrangement of atoms, influencing its biological activity and medical effects.
Moreover, this specification explores the stability of abiraterone acetate under various circumstances.
The provided data is intended for professionals working with this compound and requires understanding within the context of relevant medical practices.