Abacavir Sulphate: Chemical Description and Attributes
Abacavir sulfate presents itself as potent antiretroviral drug commonly utilized in the treatment of HIV infection. Chemically, it includes the compound abacavir, which resides as a nucleoside reverse transcriptase inhibitor (NRTI). Abacavir sulfate displays a molecular formula of C15H24N6O3S. The compound usually presents as a white to off-white crystalline powder, characterized its solubility in water and limited solubility in organic solvents.
Moreover, abacavir sulfate exhibits a low melting point and suffers minimal decomposition at room temperature. Its physicochemical properties contribute its effectiveness as an antiretroviral agent by permitting absorption, distribution, metabolism, and excretion within the body.
Discovering Abarelix: CAS Number & Structure
Abarelix is a gonadotropin-releasing hormone receptor antagonist used for controlling advanced prostate cancer. Its chemical structure, described with a complex arrangement of atoms, influences a crucial role in its therapeutic effects. The CAS Number, an identifying number, for Abarelix is 124630-58-4. This code allows for unambiguous recognition of the compound in scientific literature and databases.
- Structural Features,, Abarelix comprises a multitude of rings and functional groups.
- The precise configuration 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.
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 ALLOPURINOL 315-30-0 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 entry contains detailed facts about Abacavir Sulfate, a substance with the CAS number 188062-50-2. Key information includes its characteristics, formula, and uses. Abacavir Sulfate is a white powder often used in the therapy of HIV infection.
Recognizing Abarelix Through Its CAS Number (183552-38-7)
Abarelix represents a therapeutic compound employed in the care of certain categories of cancer. Its specific CAS number, 183552-38-7, operates as a specific identifier. This code allows precise recognition of Abarelix within scientific and healthcare databases. Researchers can leverage this CAS number to access valuable details about Abarelix, including its chemical structure, properties, and potential applications.
Abiraterone Acetate CAS Number 154229-18-2: Detailed Specifications
These chemical specification outlines the characteristics of abiraterone acetate, a pharmaceutical compound with CAS number 154229-18-2. Herein provides detailed data on its chemical properties, including melting point.
This compound is a potent inhibitor of hormone production, mainly used in the therapy of prostate cancer. Its molecular formula includes a complex arrangement of atoms, determining its biological activity and medical effects.
Moreover, this specification examines the stability of abiraterone acetate under various environments.
The provided data is intended for professionals working with this molecule and requires analysis within the context of relevant medical practices.