Abacavir sulfate acts as a potent antiretroviral drug commonly utilized in the treatment of HIV infection. Chemically, it comprises the compound abacavir, which exists as a nucleoside reverse transcriptase inhibitor (NRTI). Abacavir sulfate displays a molecular formula of C15H24N6O3S. The compound often appears 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 contribute its effectiveness as an antiretroviral agent by permitting absorption, distribution, metabolism, and excretion within the body.
About Abarelix: CAS Number and Structural Details
Abarelix is AMITRIPTYLINE HYDROCHLORIDE 549-18-8 the gonadotropin-releasing hormone receptor antagonist used for treating advanced prostate cancer. Its chemical structure, characterized by 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 recognition 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 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 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 entry contains detailed details about Abacavir Sulfate, a substance with the CAS number 188062-50-2. Key information includes its attributes, formula, and purposes. Abacavir Sulfate is a crystalline solid often used in the therapy of HIV infection.
Recognizing Abarelix Through Its CAS Number (183552-38-7)
Abarelix serves as a medicinal substance employed in the treatment of certain kinds of prostatecancer. Its individual CAS number, 183552-38-7, operates as a distinct identifier. This code facilitates precise characterization of Abarelix within scientific and medical databases. Scientists can utilize 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
These chemical specification outlines the features of abiraterone acetate, a drug compound with CAS number 154229-18-2. Herein provides detailed data on its chemical properties, including melting point.
The drug is a potent inhibitor of enzyme activity, mainly used in the therapy of prostate cancer. Its molecular formula includes a complex arrangement of atoms, contributing its biological activity and therapeutic effects.
Furthermore, this specification explores the stability of abiraterone acetate under various circumstances.
The provided data is intended for researchers working with this molecule and requires interpretation within the context of relevant safety protocols.