Abacavir Sulfate: A Look at its Chemistry
Abacavir sulfate is a potent antiretroviral drug commonly utilized in the treatment of HIV infection. Chemically, it consists of the compound abacavir, which resides as a nucleoside reverse transcriptase inhibitor (NRTI). Abacavir sulfate possesses 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.
Moreover, 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 enabling absorption, distribution, metabolism, and excretion within the body.
Abarelix: CAS Number and Structural Information
Abarelix is the gonadotropin-releasing hormone receptor antagonist used for treating advanced prostate cancer. Its chemical structure, defined as 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 identifier 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 affects its binding affinity to the target receptor.
Additional information about Abarelix's structure and CAS number can be found 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 AMPROLIUM HYDROCHLORIDE 137-88-2 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 database record contains detailed facts about Abacavir Sulfate, a chemical compound with the CAS number 188062-50-2. Important details includes its characteristics, chemical structure, and uses. Abacavir Sulfate is a white powder often used in the therapy of HIV infection.
Pinpointing Abarelix Through Its CAS Number (183552-38-7)
Abarelix represents a medicinal substance utilized in the management of certain categories of cancer. Its unique CAS number, 183552-38-7, operates as a universal identifier. This number allows precise identification of Abarelix within scientific and healthcare databases. Researchers can utilize this CAS number to obtain valuable information about Abarelix, including its chemical structure, properties, and potential applications.
Abiraterone Acetate CAS Number 154229-18-2: Detailed Specifications
These chemical specification outlines the features of abiraterone acetate, a medication compound with CAS number 154229-18-2. It provides detailed information on its chemical properties, including appearance.
The drug is a potent inhibitor of hormone production, chiefly used in the management of prostate cancer. Its composition features a unique arrangement of atoms, contributing its biological activity and clinical effects.
Furthermore, this specification explores the stability of abiraterone acetate under various conditions.
The provided data is intended for professionals working with this compound and requires understanding within the context of relevant regulatory guidelines.