CAS 181701-06-4: Interiotherin A
Formula:C29H28O8
InChI:InChI=1S/C29H28O8/c1-15-10-18-11-20-25(35-13-33-20)27(31-3)22(18)23-19(12-21-26(28(23)32-4)36-14-34-21)24(16(15)2)37-29(30)17-8-6-5-7-9-17/h5-9,11-12,15-16,24H,10,13-14H2,1-4H3
InChI key:InChIKey=MBGKPRSARHEFAG-UHFFFAOYSA-N
SMILES:O(C)C1=C2C3=C(OC)C4=C(C=C3CC(C)C(C)C(OC(=O)C5=CC=CC=C5)C2=CC6=C1OCO6)OCO4
Synonyms:- Cycloocta[1,2-f:3,4-f′]bis[1,3]benzodioxol-5-ol, 5,6,7,8-tetrahydro-13,14-dimethoxy-6,7-dimethyl-, benzoate, (5R,6S,7S,13aS)-
- (-)-Interiotherin A
- Cycloocta[1,2-f:3,4-f′]bis[1,3]benzodioxol-5-ol, 5,6,7,8-tetrahydro-13,14-dimethoxy-6,7-dimethyl-, benzoate, stereoisomer
- Cycloocta[1,2-f:3,4-f′]bis[1,3]benzodioxol-5-ol, 5,6,7,8-tetrahydro-13,14-dimethoxy-6,7-dimethyl-, 5-benzoate, (5R,6S,7S,13aS)-
- Interiotherin A
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InteriotherinA
CAS:Interiotherin A inhibits HIV replication with the EC50 value of 3.1 micrograms/mL.Formula:C29H28O8Purity:98%Color and Shape:SolidMolecular weight:504.53InteriotherinA
CAS:InteriotherinA is a bioactive compound, which is derived from specific strains of bacteria. It operates through a sophisticated mode of action that involves modulating the activity of nerve cells by binding to particular receptors on their membranes. This interaction can alter ion channel function, thereby influencing the electrochemical signaling within these cells. InteriotherinA is primarily used in research settings to explore its effects on nervous system function. Its capacity to modify neuronal activity makes it a valuable tool for studying nerve cell behavior, neurophysiological pathways, and potential applications in neuromodulation research. This compound can also serve as a model for the development of novel therapeutics targeting neurological disorders. Furthermore, understanding its mechanism can provide insights into the fundamental processes of nervous system signaling.Formula:C29H28O8Purity:Min. 95%Molecular weight:504.5 g/mol
