Abacavir Sulfate: A Look at its Chemistry
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 exhibits a molecular formula of C15H24N6O3S. The compound usually 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 affect 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 an gonadotropin-releasing hormone receptor antagonist used for controlling advanced prostate cancer. Its chemical structure, described with a complex arrangement of atoms, plays a crucial role in its therapeutic effects. The CAS Number, an identifying number, for Abarelix is 124630-58-4. This code allows for unambiguous specification of the compound in scientific literature and databases.
- The Structure of, Abarelix comprises numerous rings and functional groups.
- The precise design of these components affects 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: 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.
Chemical Database Entry: Abacavir Sulfate (188062-50-2)
This section contains detailed details about Abacavir Sulfate, a drug with the CAS number 188062-50-2. Key information includes its physical properties, formula, and purposes. 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 medicinal agent employed in the treatment of certain kinds of cancer. Its unique CAS number, 183552-38-7, operates as a universal identifier. This code enables precise recognition of Abarelix within scientific and medical databases. Professionals can employ this ALRESTATIN 51876-97-2 CAS number to obtain valuable data about Abarelix, including its chemical structure, properties, and potential applications.
Abiraterone Acetate CAS: 154229-18-2 - Chemical Specification
That chemical specification outlines the characteristics of abiraterone acetate, a pharmaceutical compound with CAS number 154229-18-2. Herein provides detailed information on its chemical properties, including boiling point.
This compound is a potent inhibitor of steroidogenesis, mainly used in the treatment of prostate cancer. Its molecular formula consists a specific arrangement of atoms, contributing its biological activity and clinical effects.
Moreover, this specification explores the durability of abiraterone acetate under various circumstances.
The provided data is intended for professionals working with this molecule and requires interpretation within the context of relevant regulatory guidelines.