Abacavir Sulfate: Chemical Identification and Properties
Abacavir sulfate presents itself as potent antiretroviral drug commonly utilized in the treatment of HIV infection. Chemically, it comprises the compound abacavir, which resides as a nucleoside reverse transcriptase inhibitor (NRTI). Abacavir sulfate displays a molecular formula of C15H24N6O3S. The compound often presents as a white to off-white crystalline powder, identified by its solubility in water and limited solubility in organic solvents.
Furthermore, abacavir sulfate exhibits a low melting point and suffers 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.
Discovering Abarelix: CAS Number & Structure
Abarelix is a gonadotropin-releasing hormone receptor antagonist used for managing advanced prostate cancer. Its chemical structure, described with a complex arrangement of atoms, influences a crucial role in its therapeutic effects. The CAS Number, a specific code, for Abarelix is 124630-58-4. This code allows for unambiguous identification of the compound in scientific literature and databases.
- Structure,, Abarelix comprises a multitude of rings and functional groups.
- The precise design of these components influences its binding affinity to the target receptor.
Additional information about Abarelix's structure and CAS number can be accessed 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 details about Abacavir Sulfate, a substance with the CAS number 188062-50-2. Fundamental data includes its physical properties, formula, and uses. Abacavir Sulfate is a white powder often used in the treatment of HIV infection.
Identifying Abarelix Through Its CAS Number (183552-38-7)
Abarelix is a pharmaceutical compound employed in the treatment of certain categories of cancer. Its individual CAS number, 183552-38-7, operates as a distinct identifier. This code allows precise recognition of Abarelix within scientific and healthcare databases. Professionals can utilize this CAS number to access valuable data about Abarelix, including its chemical structure, properties, and potential applications.
Abiraterone Acetate CAS: 154229-18-2 - Chemical Specification
These chemical specification outlines the features of abiraterone ALOGLIPTIN BENZOATE 850649-62-6 acetate, a medication compound with CAS identifier 154229-18-2. It provides detailed details on its physical properties, including boiling point.
The drug is a potent inhibitor of steroidogenesis, primarily used in the therapy of prostate cancer. Its molecular formula features a unique arrangement of atoms, influencing its biological activity and therapeutic effects.
Furthermore, this specification explores the stability of abiraterone acetate under various environments.
The provided data is intended for professionals working with this compound and requires understanding within the context of relevant safety protocols.