Abacavir sulfate presents itself as potent antiretroviral drug commonly utilized in the treatment of HIV infection. Chemically, it consists of the compound abacavir, which exists as a nucleoside reverse transcriptase inhibitor (NRTI). Abacavir sulfate exhibits a molecular formula of C15H24N6O3S. The compound typically presents as a white to off-white crystalline powder, defined by 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 influence its effectiveness as an antiretroviral agent by enabling absorption, distribution, metabolism, and excretion within the body.
Discovering Abarelix: CAS Number & Structure
Abarelix is the 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 unique identifier, for Abarelix is 124630-58-4. This identifier 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 design of these components affects its binding affinity to the target receptor.
More information about Abarelix's structure and CAS number can be obtained 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 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 section contains detailed facts about Abacavir Sulfate, a chemical compound with the CAS number 188062-50-2. Fundamental data includes its physical properties, composition, and uses. Abacavir Sulfate is a fine ADEFOVIR DIPIVOXIL 142340-99-6 substance often used in the therapy of HIV infection.
Recognizing Abarelix Through Its CAS Number (183552-38-7)
Abarelix represents a medicinal substance utilized in the care of certain types of prostatecancer. Its specific CAS number, 183552-38-7, functions as a universal identifier. This designation allows precise recognition of Abarelix within scientific and healthcare databases. Scientists can employ 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
This chemical specification outlines the characteristics of abiraterone acetate, a medication compound with CAS code 154229-18-2. Herein provides detailed data on its molecular properties, including boiling point.
This compound is a potent inhibitor of steroidogenesis, primarily used in the therapy of prostate cancer. Its composition consists a unique arrangement of atoms, determining its biological activity and clinical effects.
Moreover, this specification explores the stability of abiraterone acetate under various circumstances.
The provided data is intended for researchers working with this compound and requires analysis within the context of relevant regulatory guidelines.