59888-49-2 Usage
Uses
Used in Pharmaceutical Research:
2,3,10,10-tetramethyl-2,3-dihydro-10H-3,10a-epidithiopyrazino[1,2-a]indole-1,4-dione is utilized as a research compound for exploring its potential biological activities and therapeutic effects. Its unique structure and dithiopyrazinoindole backbone may contribute to novel pharmacological properties, making it a valuable candidate for drug discovery and development.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,3,10,10-tetramethyl-2,3-dihydro-10H-3,10a-epidithiopyrazino[1,2-a]indole-1,4-dione serves as a key intermediate or building block for the synthesis of more complex molecules with potential therapeutic applications. Its chemical properties and reactivity can be harnessed to create new drug candidates with improved efficacy and selectivity.
Note: Since the provided materials do not specify particular applications or industries for 2,3,10,10-tetramethyl-2,3-dihydro-10H-3,10a-epidithiopyrazino[1,2-a]indole-1,4-dione, the uses listed above are general and based on the potential of the compound in pharmaceutical research and medicinal chemistry. Further research and development may reveal more specific applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 59888-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,8 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59888-49:
(7*5)+(6*9)+(5*8)+(4*8)+(3*8)+(2*4)+(1*9)=202
202 % 10 = 2
So 59888-49-2 is a valid CAS Registry Number.
59888-49-2Relevant academic research and scientific papers
Gliotoxin analogues as inhibitors of reverse transcriptase. 1. Effect of lipophilicity.
Ottenheijm,H.C.J. et al.
, p. 796 - 799 (2007/10/08)
The reaction scheme, developed for the synthesis of the gliotoxin analogue 2, was found to be of general applicability for analogues with varying substituents at N(1) and C(2). Analogues 11b-g prepared by this method are inhibitors of reverse transcriptase (RNA-directed DNA polymerase). Their inhibitory activity seems to be related to the lipophilicity of the effector molecules: the most lipophilic compound is the most active inhibitor. The techniques of reversed-phase thin-layer chromatography with silylated, precoated plates as well as reversed-phase high-performance liquid chromatography were used to measure the relative lipophilicities; both techniques gave analogous results.
