[CAS NO. 106362-34-9]  Adaptavir (DAPTA)

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PRODUCTS SPECIFICATIONS [106362-34-9]

Catalog
SLK-S8501
Brand
Selleck
CAS
106362-34-9

DESCRIPTION [106362-34-9]

Overview

MDLMFCD00076838
Molecular Weight856.88
Molecular FormulaC35H56N10O15
SMILESOC1=CC=C(C[C@H](NC([C@@H](NC([C@H]([C@H](O)C)NC([C@@H](NC([C@H]([C@H](O)C)NC([C@@H](NC([C@H](N)C)=O)CO)=O)=O)[C@H](O)C)=O)=O)CC(N)=O)=O)C(N[C@H](C(N)=O)[C@H](O)C)=O)C=C1

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM1.1670 mL5.8351 mL11.6702 mL
5 mM0.2334 mL1.1670 mL2.3340 mL
10 mM0.1167 mL0.5835 mL1.1670 mL
50 mM0.0233 mL0.1167 mL0.2334 mL

Description

Adaptavir (DAPTA, D-Ala-peptide T-amide, peptide T) is a water soluble potent, selective antagonist which potently inhibits specific CD4-dependent binding of gp120 Bal (IC50 = 0.06 nM) and CM235 (IC50 = 0.32 nM) to CCR5.

Targets

gp120 Bal-CCR5 [1]
(Cell-free assay)
CM235-CCR5 [1]
(Cell-free assay)
0.06 nM0.32 nM

In vitro

DAPTA is a non-toxic experimental antiviral entry inhibitor. DAPTA potently inhibits specific CD4-dependent binding of gp120 Bal (IC50 = 0.06 nM) and CM235 (IC50 = 0.32 nM) to CCR5. In co-immunoprecipitation studies, DAPTA (1 nM) blocks formation of the gp120/sCD4 complex with CCR5. Confocal microscopic studies of direct FITC-DAPTA binding to CCR5+, but not CCR5−, cells show that CCR5 is a DAPTA receptor. DAPTA is an antagonist of CCR5-mediated chemotaxis and is most effective as an antiviral agent primarily against R5-tropic HIV-1 isolates, with reduced or absent effect for X4-tropic laboratory isolates. DAPTA does not inhibit fusion in typical assays, which use high local concentrations of virus and cells. The Th2 cytokines IL-4, IL-10,and IL-13, are increased by DAPTA and induce a potent virostatic state in infected macrophages in vitro, as well as inhibit production of the proinflammatory cytokines IL-1 and TNFα, which upregulate virus expression. Thus the elevation of Th2 cytokines by DAPTA treatment would favor less macrophage viral replication.

In vivo

The levels of inflammatory cytokines IL-1, IL-6, and TNFα decrease in plasma following DAPTA treatment. Peptide T(DAPTA) treatment prevents the neuronal cell death associated with gpl20. DAPTA prevents gpl20-associated neural deficits in vivo.