Abacavir sulfate acts as a potent antiretroviral drug commonly utilized in the treatment of HIV infection. Chemically, it comprises the compound abacavir, which resides as a nucleoside reverse transcriptase inhibitor (NRTI). Abacavir sulfate displays a molecular formula of C15H24N6O3S. The compound usually appears as a white to off-white crystalline powder, identified by its solubility in water and limited solubility in organic solvents.
Furthermore, abacavir sulfate exhibits a low melting point and experiences 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.
About Abarelix: CAS Number and Structural Details
Abarelix is an gonadotropin-releasing hormone receptor antagonist used for managing advanced prostate cancer. Its chemical structure, characterized by 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 code allows for unambiguous recognition of the compound in scientific literature and databases.
- Structural Features,, Abarelix comprises numerous rings and functional groups.
- The precise arrangement of these components affects 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.
Abiraterone Acetate: A Detailed Look at Its Chemical Profile
Abiraterone acetate is a synthetic compound with the chemical formula C29H38O6. It/This/That belongs to a class of ANHYDROVINBLASTINE 38390-45-3 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 entry contains detailed details about Abacavir Sulfate, a drug with the CAS number 188062-50-2. Important details includes its physical properties, formula, and uses. Abacavir Sulfate is a crystalline solid often used in the therapy of HIV infection.
Identifying Abarelix Through Its CAS Number (183552-38-7)
Abarelix represents a pharmaceutical substance utilized in the management of certain types of cancer. Its individual CAS number, 183552-38-7, functions as a universal identifier. This number facilitates precise characterization of Abarelix within scientific and pharmaceutical databases. Scientists can employ this CAS number to obtain valuable data about Abarelix, including its chemical structure, properties, and potential applications.
Abiraterone Acetate (CAS 154229-18-2) - Chemical Properties
These chemical specification outlines the characteristics of abiraterone acetate, a drug compound with CAS code 154229-18-2. Herein provides detailed details on its chemical properties, including boiling point.
Abiraterone acetate is a potent inhibitor of enzyme activity, chiefly used in the management of prostate cancer. Its composition includes a unique arrangement of atoms, determining its biological activity and medical effects.
Moreover, this specification examines the stability of abiraterone acetate under various conditions.
The provided data is intended for scientists working with this compound and requires understanding within the context of relevant safety protocols.