Abacavir sulfate presents itself as potent antiretroviral drug commonly utilized in the treatment of HIV infection. Chemically, it includes the compound abacavir, which exists as a nucleoside reverse transcriptase inhibitor (NRTI). Abacavir sulfate displays a molecular formula of C15H24N6O3S. The compound typically 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 suffers minimal decomposition at room temperature. Its physicochemical properties influence its effectiveness as an antiretroviral agent by allowing 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, described with 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 specification of the compound in scientific literature and databases.
- The Structure of, Abarelix comprises numerous 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 obtained 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 ALRESTATIN 51876-97-2 of action makes it a valuable therapeutic agent in the management of prostate cancer.
Information on: Abacavir Sulfate
This section contains detailed details about Abacavir Sulfate, a drug with the CAS number 188062-50-2. Important details includes its attributes, chemical structure, and purposes. Abacavir Sulfate is a fine substance often used in the therapy of HIV infection.
Recognizing Abarelix Through Its CAS Number (183552-38-7)
Abarelix is a medicinal agent used in the care of certain kinds of prostatecancer. Its specific CAS number, 183552-38-7, operates as a distinct identifier. This code facilitates precise recognition of Abarelix within scientific and healthcare databases. Researchers can utilize this CAS number to access valuable information about Abarelix, including its chemical structure, properties, and potential applications.
Abiraterone Acetate CAS: 154229-18-2 - Chemical Specification
These chemical specification outlines the properties of abiraterone acetate, a drug compound with CAS number 154229-18-2. This document provides detailed information on its physical properties, including melting point.
The drug is a potent inhibitor of enzyme activity, mainly used in the therapy of prostate cancer. Its chemical structure includes a unique arrangement of atoms, contributing its biological activity and medical effects.
Moreover, this specification delves into the shelf life of abiraterone acetate under various environments.
The provided data is intended for scientists working with this substance and requires interpretation within the context of relevant safety protocols.