Abacavir Sulfate: A Look at its Chemistry
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 a nucleoside reverse transcriptase inhibitor (NRTI). Abacavir sulfate displays a molecular formula of C15H24N6O3S. The compound usually shows up as a white to off-white crystalline powder, identified by its solubility in water and limited solubility in organic solvents.
Additionally, abacavir sulfate exhibits a low melting point and experiences minimal decomposition at room temperature. Its physicochemical properties affect its effectiveness as an antiretroviral agent by enabling 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 controlling advanced prostate cancer. Its chemical structure, defined as a complex arrangement of atoms, contributes a crucial role in its therapeutic effects. The CAS Number, a unique identifier, for Abarelix is 124630-58-4. This code allows for unambiguous identification of the compound in scientific literature and databases.
- Structure,, Abarelix comprises a multitude of rings and functional groups.
- The precise arrangement of these components contributes to its binding affinity to the target receptor.
Further 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 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 section contains detailed information about Abacavir Sulfate, a drug with the CAS number 188062-50-2. Important details includes its characteristics, composition, and uses. Abacavir Sulfate is a fine substance often used ACRINOL 6402-23-9 in the treatment of HIV infection.
Pinpointing Abarelix Through Its CAS Number (183552-38-7)
Abarelix is a medicinal agent employed in the care of certain kinds of cancer. Its individual CAS number, 183552-38-7, functions as a distinct identifier. This number facilitates precise characterization of Abarelix within scientific and medical databases. Professionals can leverage this CAS number to access valuable information about Abarelix, including its chemical structure, properties, and potential applications.
Abiraterone Acetate CAS: 154229-18-2 - Chemical Specification
This chemical specification outlines the features of abiraterone acetate, a medication compound with CAS number 154229-18-2. Herein provides detailed information on its molecular properties, including boiling point.
The drug is a potent inhibitor of hormone production, primarily used in the management of prostate cancer. Its chemical structure consists a unique arrangement of atoms, influencing its biological activity and clinical effects.
Moreover, this specification explores the stability of abiraterone acetate under various conditions.
The provided data is intended for researchers working with this compound and requires analysis within the context of relevant regulatory guidelines.