Abacavir sulfate presents itself as potent antiretroviral drug commonly utilized in the treatment of HIV infection. Chemically, it includes the compound abacavir, which functions as a nucleoside reverse transcriptase inhibitor (NRTI). Abacavir sulfate exhibits 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.
Additionally, more info abacavir sulfate exhibits a low melting point and experiences minimal decomposition at room temperature. Its physicochemical properties influence its effectiveness as an antiretroviral agent by permitting 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 treating 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 unique identifier, for Abarelix is 124630-58-4. This identifier allows for unambiguous specification of the compound in scientific literature and databases.
- Structural Features,, Abarelix comprises numerous rings and functional groups.
- The precise configuration of these components contributes to its binding affinity to the target receptor.
Additional information about Abarelix's structure and CAS number can be found from reliable sources such as PubChem, ChemSpider, and scientific journals.
Abiraterone Acetate: A Detailed Look at Its Chemical Profile
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. Key information includes its characteristics, formula, and potential applications. Abacavir Sulfate is a white powder often used in the treatment of HIV infection.
Recognizing Abarelix Through Its CAS Number (183552-38-7)
Abarelix is a pharmaceutical agent employed in the care of certain types of cancer. Its unique CAS number, 183552-38-7, operates as a distinct identifier. This code facilitates precise characterization of Abarelix within scientific and medical databases. Researchers can leverage 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 acetate, a pharmaceutical compound with CAS identifier 154229-18-2. Herein provides detailed information on its physical properties, including melting point.
Abiraterone acetate is a potent inhibitor of hormone production, chiefly used in the management of prostate cancer. Its chemical structure consists a specific arrangement of atoms, contributing its biological activity and clinical effects.
Additionally, 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 medical practices.