Cyclotriazadisulfonamide structure
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Common Name | Cyclotriazadisulfonamide | ||
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CAS Number | 182316-44-5 | Molecular Weight | 581.78900 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C31H39N3O4S2 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of CyclotriazadisulfonamideCyclotriazadisulfonamide (CADA) is a specific CD4-targeted HIV entry inhibitors. Cyclotriazadisulfonamide (CADA) inhibits the co-translational translocation of human CD4 (huCD4) into the ER lumen in a signal peptide (SP)-dependent way[1][2]. |
Name | 9-benzyl-3-methylene-1,5-ditosyl-1,5,9-triazacyclododecane (CADA) |
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Synonym | More Synonyms |
Description | Cyclotriazadisulfonamide (CADA) is a specific CD4-targeted HIV entry inhibitors. Cyclotriazadisulfonamide (CADA) inhibits the co-translational translocation of human CD4 (huCD4) into the ER lumen in a signal peptide (SP)-dependent way[1][2]. |
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Related Catalog | |
In Vitro | Cyclotriazadisulfonamide (CADA) significantly decreases the amount of cell surface CD4 -the main receptor for HIV -without altering the expression of any other cellular receptor examined so far[1]. Cyclotriazadisulfonamide (CADA) exhibits an EC50 of 0.4 μg/mL for CD4 in MO-DC cells. Treatment of MO-DC with 10 μg/mL of CADA results in 83% downregulation of cell surface CD4, an effect that is similar to that observed for CADA treatment of CD4+ T cells[1]. CADA prevents MT-4 cells from HIV-1 and SIV infection (EC50 are 0.7 and 1.2 g/ml, respectively)[1]. Western Blot Analysis[1] Cell Line: MO-DCs. Concentration: 0.4 μg/mL. Incubation Time: 24 h. Result: A 50% reduction in CD4 expression was obtained. |
References |
Molecular Formula | C31H39N3O4S2 |
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Molecular Weight | 581.78900 |
Exact Mass | 581.23800 |
PSA | 94.76000 |
LogP | 6.81250 |
Hazard Codes | Xi |
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9-benzyl-3-methylene-1,5-ditosyl-1,5,9-triazacyclododecane |
CADA |
9-Benzyl-3-methylene-1,5-bis-(toluene-4-sulfonyl)-1,5,9-triaza-cyclododecane |
9-benzyl-3-methylene-1,5-bis(4-methylbenzenesulfonyl)-1,5,9-triazacyclododecane |