Abacavir sulfate presents itself as potent antiretroviral drug commonly utilized in the treatment of HIV infection. Chemically, it comprises the compound abacavir, which functions as a nucleoside reverse transcriptase inhibitor (NRTI). Abacavir sulfate exhibits a molecular formula of C15H24N6O3S. The compound usually presents as a white to off-white crystalline powder, characterized its solubility in water and limited solubility in organic solvents.
Additionally, 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 enabling absorption, distribution, metabolism, and excretion within the body.
Abarelix: CAS Number and Structural Information
Abarelix is an gonadotropin-releasing hormone receptor antagonist used for treating 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 number allows for unambiguous identification of the compound in scientific literature and databases.
- Structural Features,, Abarelix comprises several rings and functional groups.
- The precise design of these components contributes to its binding affinity to the target receptor.
Additional information about Abarelix's structure and CAS number can be accessed ARECOLINE HYDROBROMIDE 300-08-3 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 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 chemical compound 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 treatment of HIV infection.
Identifying Abarelix Through Its CAS Number (183552-38-7)
Abarelix serves as a medicinal agent employed in the management of certain categories of cancer. Its unique CAS number, 183552-38-7, operates as a specific identifier. This code allows precise recognition of Abarelix within scientific and pharmaceutical databases. Professionals can utilize this CAS number to obtain valuable details 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. It provides detailed information on its physical properties, including melting point.
The drug is a potent inhibitor of enzyme activity, chiefly used in the therapy of prostate cancer. Its molecular formula features a complex arrangement of atoms, influencing its biological activity and therapeutic effects.
Additionally, this specification examines the stability of abiraterone acetate under various circumstances.
The provided data is intended for researchers working with this compound and requires understanding within the context of relevant safety protocols.