CAS 364779-14-6: (2R,3S,4S,5R,6R)-2-(hidroximetil)-6-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hidroxi-4,4,8,10,14-pentametil-17-(5-metil-1-metileno-hex-4-enil)-2,3,5,6,7,9,11,12,13,15,16,17-dodecahidro-1H-ciclopenta[a]fenantren-3-il]oxi]tetrahidropirano-3,4,5-triol
Descripción:
La sustancia química con el nombre "(2R,3S,4S,5R,6R)-2-(hidroximetil)-6-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hidroxi-4,4,8,10,14-pentametil-17-(5-metil-1-metileno-hex-4-enil)-2,3,5,6,7,9,11,12,13,15,16,17-dodecahidro-1H-ciclopenta[a]fenantren-3-il]oxi]tetrahidropirano-3,4,5-triol" y el número CAS "364779-14-6" es una molécula orgánica compleja caracterizada por su intrincada estereoquímica y múltiples grupos funcionales. Presenta un anillo de tetrahidropirano, que es un éter cíclico de seis miembros, y contiene varios grupos hidroxilo (-OH) que contribuyen a su hidrofobicidad y potencial actividad biológica. La presencia de una estructura similar a un esteroide sugiere que puede interactuar con sistemas biológicos, posiblemente influyendo en vías hormonales o sirviendo como precursor para la síntesis de esteroides. La configuración estereoquímica del compuesto indica arreglos espaciales específicos de átomos, lo que puede afectar significativamente su reactividad e interacciones con otras moléculas. En general, esta sustancia probablemente exhiba propiedades físicas y químicas únicas, lo que la hace de interés en campos como la química medicinal y la bioquímica.
Fórmula:C36H60O7
InChI:InChI=1/C36H60O7/c1-20(2)10-9-11-21(3)22-12-16-36(8)28(22)23(38)18-26-34(6)15-14-27(33(4,5)25(34)13-17-35(26,36)7)43-32-31(41)30(40)29(39)24(19-37)42-32/h10,22-32,37-41H,3,9,11-19H2,1-2,4-8H3/t22-,23-,24-,25+,26-,27+,28+,29-,30+,31-,32+,34+,35-,36-/m1/s1
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Ginsenoside Rk2
CAS:Ginsenoside Rk1 has anti-tumor, and anti-platelet aggregation activities.Fórmula:C36H60O7Forma y color:SolidPeso molecular:604.869Ginsenoside Rk2
CAS:Ginsenoside Rk2 is a bioactive compound, specifically a saponin, which is extracted from the root of Panax ginseng, a plant traditionally used in Asian medicine. The mode of action of Ginsenoside Rk2 involves modulating various cellular pathways, including influencing gene expression and enzyme activity, which contribute to its diverse physiological effects. It has been studied for its potential to impact cell signaling mechanisms, including those involved in inflammation, oxidative stress, and apoptosis. Ginsenoside Rk2's primary applications center around its research potential in pharmacology and medicine. It is predominantly explored for its role in anti-cancer therapies, due to its ability to induce cell cycle arrest and promote apoptosis in cancer cells. Additionally, Rk2 is investigated for its neuroprotective effects, possibly offering insights into managing neurodegenerative disorders. Its anti-inflammatory properties are also of interest in studies related to chronic inflammatory diseases. As research continues, Ginsenoside Rk2 holds promise for contributing valuable insights into new therapeutic approaches targeting multiple biochemical pathways.Fórmula:C36H60O7Pureza:Min. 95%Forma y color:PowderPeso molecular:604.86 g/mol
