CAS 57420-46-9
:Barlerin
Descrizione:
Barlerin, identificato dal numero CAS 57420-46-9, è un composto chimico che appartiene alla classe dei prodotti naturali noti come alcaloidi. È principalmente derivato da alcune specie vegetali ed è noto per le sue potenziali attività biologiche, comprese le proprietà antimicrobiche e anti-infiammatorie. La struttura di Barlerin presenta un complesso arrangiamento di atomi di carbonio, idrogeno, azoto e ossigeno, che contribuisce al suo comportamento chimico unico e alle interazioni. Il composto è spesso studiato per il suo potenziale farmacologico, in particolare nel contesto della medicina tradizionale. La sua solubilità e stabilità possono variare a seconda del solvente e delle condizioni ambientali, il che è importante per la sua applicazione nella ricerca e nei potenziali usi terapeutici. Come molti prodotti naturali, i processi di estrazione e purificazione sono cruciali per ottenere Barlerin in una forma adatta per l'indagine scientifica. Ulteriori ricerche sono in corso per chiarire completamente i suoi meccanismi d'azione e le potenziali applicazioni in medicina e farmacologia.
Formula: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
InChI key: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
Sinonimi:- 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
- Vedi altri sinonimi
Ordinare per
Purezza (%)
0
100
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0
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50
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90
|
95
|
100
6 prodotti.
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:Formula:C19H28O12Purezza:98%Peso molecolare: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.Formula:C19H28O12Purezza:95%~99%Colore e forma:PowderPeso molecolare: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>Formula:C19H28O12Purezza:99.83% - ≥95%Colore e forma:SolidPeso molecolare:448.428-acetylshanzhiside methyl ester
CAS:Natural glycosideFormula:C19H28O12Purezza:≥ 90.0 % (HPLC)Colore e forma:PowderPeso molecolare:448.42





