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

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: 57420-46-9

Formula: C₁₉H₂₈O₁₂

Purezza: 98%

Peso molecolare: 448.4184

Ref: IN-DA00IKLH

Barlerin

CAS: 57420-46-9

Barlerin

Purezza: ≥95%

Peso molecolare: 448.42g/mol

Ref: 54-BUP04611

8-O-Acetyl shanzhiside methyl ester

CAS: 57420-46-9

Formula: C₁₉H₂₈O₁₂

Peso molecolare: 448.42

Ref: 7W-GY3466

8-O-Acetyl shanzhiside methyl ester

CAS: 57420-46-9

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: C₁₉H₂₈O₁₂

Purezza: 95%~99%

Colore e forma: Powder

Peso molecolare: 448.421

Ref: BP-BP0110

Barlerin

CAS: 57420-46-9

Barlerin (8-O-Acetylshanzhiside methyl ester) has potential against cerebral ischemic injury, and protective effect on oxygen-glucose deprivation-induced injury

Formula: C₁₉H₂₈O₁₂

Purezza: 99.83% - ≥95%

Colore e forma: Solid

Peso molecolare: 448.42

Ref: TM-T5S1632

8-acetylshanzhiside methyl ester

CAS: 57420-46-9

Natural glycoside

Formula: C₁₉H₂₈O₁₂

Purezza: ≥ 90.0 % (HPLC)

Colore e forma: Powder

Peso molecolare: 448.42

Ref: 5G-82461