Abacavir Sulphate: Chemical Description and Attributes
Abacavir sulfate acts as a potent antiretroviral drug commonly utilized in the treatment of HIV infection. Chemically, it consists of the compound abacavir, which exists as get more info a nucleoside reverse transcriptase inhibitor (NRTI). Abacavir sulfate displays a molecular formula of C15H24N6O3S. The compound typically appears 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 undergoes minimal decomposition at room temperature. Its physicochemical properties contribute its effectiveness as an antiretroviral agent by allowing absorption, distribution, metabolism, and excretion within the body.
About Abarelix: CAS Number and Structural Details
Abarelix is the 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, an identifying number, for Abarelix is 124630-58-4. This identifier allows for unambiguous identification of the compound in scientific literature and databases.
- Structural Features,, Abarelix comprises several rings and functional groups.
- The precise design of these components affects its binding affinity to the target receptor.
More 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.
Chemical Database Entry: Abacavir Sulfate (188062-50-2)
This section contains detailed facts about Abacavir Sulfate, a drug with the CAS number 188062-50-2. Fundamental data includes its characteristics, formula, and purposes. Abacavir Sulfate is a crystalline solid often used in the management of HIV infection.
Recognizing Abarelix Through Its CAS Number (183552-38-7)
Abarelix represents a pharmaceutical agent utilized in the care of certain categories of cancer. Its individual CAS number, 183552-38-7, acts as a distinct identifier. This code facilitates precise recognition of Abarelix within scientific and healthcare databases. Researchers can employ this CAS number to access valuable details about Abarelix, including its chemical structure, properties, and potential applications.
Abiraterone Acetate (CAS 154229-18-2) - Chemical Properties
These chemical specification outlines the properties of abiraterone acetate, a medication compound with CAS code 154229-18-2. It provides detailed data on its physical properties, including appearance.
This compound is a potent inhibitor of hormone production, chiefly used in the treatment of prostate cancer. Its composition consists a complex arrangement of atoms, contributing its biological activity and clinical effects.
Furthermore, this specification delves into the stability of abiraterone acetate under various environments.
The provided data is intended for researchers working with this substance and requires understanding within the context of relevant regulatory guidelines.