234-17-3 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The chemical structure describes the arrangement of atoms and bonds in the compound, highlighting its unique features.
Explanation
These properties suggest that the compound may have therapeutic applications in treating cancer and fighting infections.
Explanation
The compound is of interest to researchers in the field of medicinal chemistry due to its potential therapeutic applications.
Explanation
Further research is needed to fully understand the compound's potential applications in the pharmaceutical industry.
Explanation
The compound's antitumor and antimicrobial properties make it a promising candidate for the development of new drugs.
Explanation
The name follows the IUPAC nomenclature system, which provides a standardized way to name chemical compounds.
Explanation
These unique identifiers are used to locate information about the compound in chemical databases and literature.
Explanation
Ongoing research is necessary to determine the compound's effectiveness, safety, and optimal use in the pharmaceutical industry.
Chemical Structure
Heterocyclic compound with a dioxole ring fused to an isoquinoline ring
Potential Pharmaceutical Properties
Antitumor and antimicrobial activities
Field of Interest
Medicinal Chemistry
Current Status
Under investigation for biological and pharmacological activities
Research Focus
Development of new drug candidates
Nomenclature
1,3-Dioxolo[4,5-h]isoquinoline(8CI,9CI)
CAS Registry Numbers
8CI, 9CI
Further Studies Required
To fully understand its potential applications
Check Digit Verification of cas no
The CAS Registry Mumber 234-17-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,3 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 234-17:
(5*2)+(4*3)+(3*4)+(2*1)+(1*7)=43
43 % 10 = 3
So 234-17-3 is a valid CAS Registry Number.
234-17-3Relevant academic research and scientific papers
Gastric-mucous membrane protection activity of coptisine derivatives
Hirano,Osawa,Yamaoka,Yokoi
, p. 1277 - 1281 (2007/10/03)
Coptisine and 8-oxocoptisine were isolated as principles of the gastric-mucous membrane protection from Coptidis rhizoma. The two compounds showed stronger activity than cimetidine and sucralfate. We prepared several derivatives having a partial structure of coptisine from commercially available starting materials. The compounds obtained were tested for gastric-mucous membrane protective activity and a correlation between activity and structure was studied. Our results suggest that the partial charge of the catechol skeleton is related to activity.