77248-65-8 Usage
Uses
Used in Pharmaceutical Synthesis:
5-METHYLSULFANYL-1H-INDOLE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic benefits.
Used in Antifungal Applications:
In the field of antifungal agents, 5-METHYLSULFANYL-1H-INDOLE is utilized for its potential to combat fungal infections, providing a valuable tool in the treatment of various fungal diseases.
Used in Anticancer Applications:
5-METHYLSULFANYL-1H-INDOLE is employed as an anticancer agent, leveraging its biological activity to target and inhibit the growth of cancer cells, offering a promising avenue for cancer treatment and research.
Used in Drug Development:
In the realm of drug development, 5-METHYLSULFANYL-1H-INDOLE serves as a crucial component in the creation of novel therapeutics, with ongoing research aimed at harnessing its properties to improve patient outcomes and address unmet medical needs.
Used in Medicinal Chemistry Research:
5-METHYLSULFANYL-1H-INDOLE is used in medicinal chemistry research to explore its potential interactions with biological targets, furthering understanding of its mechanisms of action and paving the way for the design of more effective drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 77248-65-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,4 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77248-65:
(7*7)+(6*7)+(5*2)+(4*4)+(3*8)+(2*6)+(1*5)=158
158 % 10 = 8
So 77248-65-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NS/c1-11-8-2-3-9-7(6-8)4-5-10-9/h2-6,10H,1H3
77248-65-8Relevant academic research and scientific papers
COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH STING ACTIVITY
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Page/Page column 224; 225, (2021/07/10)
This disclosure features chemical entities (e.g., a compound or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound) that inhibit (e.g., antagonize) Stimulator of Interferon Genes (STING). Said che
SYNTHESIS OF SOME 5-SUBSTITUTED INDOLES
Yang, Youhua,Martin, Arnold R.,Nelson, David L.,Regan, John
, p. 1169 - 1175 (2007/10/02)
A halogen-metal exchange strategy was employed to prepare several 5-substituted indoles from 5-bromoindole.Additional derivatives were elaborated from the formyl, acetyl, thiomethyl, boronic acid and trimethylstannyl analogues thus prepared.
Antipsychotic tetrahydropyridinyl-indoles, compositions and method of use
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, (2008/06/13)
Novel tetranydro-pyridinyl-indoles of the formula STR1 wherein X is selected from the group consisting of alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 5 carbon atoms, alkynyl of 3 to 5 carbon atoms, cycloalkyl of 5 to 6 carbon atoms, cycloalkylalkyl of 4
