Abacavir sulfate is 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 possesses a molecular formula of C15H24N6O3S. The compound usually shows up as a white to off-white crystalline powder, characterized 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 influence its effectiveness as an antiretroviral agent by permitting absorption, distribution, metabolism, and excretion within the body.
Abarelix: CAS Number and Structural Information
Abarelix is the gonadotropin-releasing hormone receptor antagonist used for controlling advanced prostate cancer. Its chemical structure, defined as 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 number allows for unambiguous identification of the compound in scientific literature and databases.
- Structure,, Abarelix comprises several rings and functional groups.
- The precise arrangement of these components contributes to its binding affinity to the target receptor.
Additional 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.
Chemical Database Entry: Abacavir Sulfate (188062-50-2)
This database record contains detailed facts about Abacavir Sulfate, a drug with the CAS number 188062-50-2. Key information includes its attributes, formula, and potential applications. Abacavir Sulfate is a fine substance often used in the treatment of HIV infection.
Pinpointing Abarelix Through Its CAS Number (183552-38-7)
Abarelix serves as a pharmaceutical agent used in the treatment of certain kinds of prostatecancer. Its individual CAS number, 183552-38-7, functions as a specific identifier. This number facilitates precise recognition ANAGRELIDE HCL 58579-51-4 of Abarelix within scientific and medical databases. Scientists can employ 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
That chemical specification outlines the characteristics of abiraterone acetate, a medication compound with CAS identifier 154229-18-2. This document 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 features a specific arrangement of atoms, influencing its biological activity and clinical effects.
Moreover, this specification examines the stability of abiraterone acetate under various environments.
The provided data is intended for scientists working with this substance and requires analysis within the context of relevant regulatory guidelines.