CAS 57420-46-9
:Barlerin
Descripción:
Barlerin, identificado por el número CAS 57420-46-9, es un compuesto químico que pertenece a la clase de productos naturales conocidos como alcaloides. Se deriva principalmente de ciertas especies de plantas y se destaca por sus posibles actividades biológicas, incluyendo propiedades antimicrobianas y antiinflamatorias. La estructura de Barlerin presenta una disposición compleja de átomos de carbono, hidrógeno, nitrógeno y oxígeno, lo que contribuye a su comportamiento químico único e interacciones. El compuesto se estudia a menudo por su potencial farmacológico, particularmente en el contexto de la medicina tradicional. Su solubilidad y estabilidad pueden variar dependiendo del disolvente y las condiciones ambientales, lo cual es importante para su aplicación en la investigación y posibles usos terapéuticos. Al igual que con muchos productos naturales, los procesos de extracción y purificación son cruciales para obtener Barlerin en una forma adecuada para la investigación científica. Se están llevando a cabo más investigaciones para elucidar completamente sus mecanismos de acción y posibles aplicaciones en medicina y farmacología.
Fórmula:C19H28O12
InChI:InChI=1/C19H28O12/c1-7(21)31-19(2)4-9(22)11-8(16(26)27-3)6-28-17(12(11)19)30-18-15(25)14(24)13(23)10(5-20)29-18/h6,9-15,17-18,20,22-25H,4-5H2,1-3H3/t9-,10-,11+,12-,13-,14+,15-,17+,18+,19+/m1/s1
Clave InChI:InChIKey=ARFRZOLTIRQFCI-NGQYDJQZSA-N
SMILES:O([C@H]1[C@]2([C@@](C(C(OC)=O)=CO1)([C@H](O)C[C@@]2(OC(C)=O)C)[H])[H])[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O
Sinónimos:- 8-Acetylshanzhiside methyl ester
- 8-Acetylshanziside methyl ester
- 8-O-Acetyl Shanzhiside Methyl Ester
- 8-O-Acetylshanzhiside methyl ester
- Barlerin
- Cyclopenta[c]pyran-4-carboxylic acid, 7-(acetyloxy)-1-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-5-hydroxy-7-methyl-, methyl ester, (1S,4aS,5R,7S,7aS)-
- Cyclopenta[c]pyran-4-carboxylic acid, 7-(acetyloxy)-1-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-5-hydroxy-7-methyl-, methyl ester, [1S-(1α,4aα,5α,7α,7aα)]-
- Methyl (1S,4aS,5R,7S,7aS)-7-acetoxy-1-(beta-D-glucopyranosyloxy)-5-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate
- O-Acetyl Shanzhiside Methyl Ester, 8-
- Umbroside
- cyclopenta[c]pyran-4-carboxylic acid, 7-(acetyloxy)-1-(beta-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-5-hydroxy-7-methyl-, methyl ester, (1S,4aS,5R,7S,7aS)-
- Cyclopenta[c]pyran-4-carboxylic acid, 7-(acetyloxy)-1-(β-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-5-hydroxy-7-methyl-, methyl ester, (1S,4aS,5R,7S,7aS)-
- Cyclopenta[c]pyran-4-carboxylic acid, 7-(acetyloxy)-1-(β-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-5-hydroxy-7-methyl-, methyl ester, [1S-(1α,4aα,5α,7α,7aα)]-
- 7α-Acetoxy-1α-(β-D-glucopyranosyloxy)-1,4aα,5,6,7,7aα-hexahydro-5α-hydroxy-7-methylcyclopenta[c]pyran-4-carboxylic acid methyl ester
- ND01
- 8-O-Acetyl shanzhiside methyl ester, >98%
- (1S)-1α-(β-D-Glucopyranosyloxy)-5α-hydroxy-7α-acetoxy-7-methyl-1,4aα,5,6,7,7aα-hexahydrocyclopenta[c]pyran-4-carboxylic acid methyl ester
- methyl (1S,4aS,5R,7S,7aS)-7-acetyloxy-5-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate
- 1α-(β-D-Glucopyranosyloxy)-7α-acetoxy-5α-hydroxy-7-methyl-1,4aα,5,6,7,7aα-hexahydrocyclopenta[c]pyran-4-carboxylic acid methyl ester
- 8-O-Acetyl shanzhiside methyl ester, 98%, from Lamiophlomis rotata (Benth. ex Hook.f.) Kud
- 8-O-Acetyl shanzhiside methyl
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Pureza (%)
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100
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0
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50
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90
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95
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100
Encontrado 6 productos.
Cyclopenta[c]pyran-4-carboxylic acid,7-(acetyloxy)-1-(b-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-5-hydroxy-7-methyl-, methyl ester, (1S,4aS,5R,7S,7aS)-
CAS:Fórmula:C19H28O12Pureza:98%Peso molecular:448.41848-O-Acetyl shanzhiside methyl ester
CAS:8-O-acetyl shanzhiside methylester (ND01), an iridoid glucoside compound, was isolated from the leaves of Lamiophlomis rotata (Benth.) Kudo, ND01 has potential against cerebral ischemic injury, and its protective effect on oxygen–glucose deprivation-induced injury might be due to the suppression of intracellular Ca 2+ elevation and caspase-3 activity, and improvement of mitochondrial energy metabolism.Fórmula:C19H28O12Pureza:95%~99%Forma y color:PowderPeso molecular:448.421Barlerin
CAS:<p>Barlerin (8-O-Acetylshanzhiside methyl ester) has potential against cerebral ischemic injury, and protective effect on oxygen-glucose deprivation-induced injury</p>Fórmula:C19H28O12Pureza:99.83% - ≥95%Forma y color:SolidPeso molecular:448.428-acetylshanzhiside methyl ester
CAS:Natural glycosideFórmula:C19H28O12Pureza:≥ 90.0 % (HPLC)Forma y color:PowderPeso molecular:448.42





