CAS 57420-46-9

Barlerin

Descrição:

Barlerin, identificado pelo número CAS 57420-46-9, é um composto químico que pertence à classe de produtos naturais conhecidos como alcaloides. É derivado principalmente de certas espécies de plantas e é notado por suas potenciais atividades biológicas, incluindo propriedades antimicrobianas e anti-inflamatórias. A estrutura de Barlerin apresenta uma disposição complexa de átomos de carbono, hidrogênio, nitrogênio e oxigênio, o que contribui para seu comportamento químico único e interações. O composto é frequentemente estudado por seu potencial farmacológico, particularmente no contexto da medicina tradicional. Sua solubilidade e estabilidade podem variar dependendo do solvente e das condições ambientais, o que é importante para sua aplicação em pesquisa e possíveis usos terapêuticos. Assim como muitos produtos naturais, os processos de extração e purificação são cruciais para obter Barlerin em uma forma adequada para investigação científica. Pesquisas adicionais estão em andamento para elucidar completamente seus mecanismos de ação e possíveis aplicações em medicina e farmacologia.

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

Chave 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

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

Fórmula: C₁₉H₂₈O₁₂

Pureza: 98%

Peso molecular: 448.4184

Ref: IN-DA00IKLH

Barlerin

CAS: 57420-46-9

Barlerin

Pureza: ≥95%

Peso molecular: 448.42g/mol

Ref: 54-BUP04611

8-O-Acetyl shanzhiside methyl ester

CAS: 57420-46-9

Fórmula: C₁₉H₂₈O₁₂

Peso molecular: 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.

Fórmula: C₁₉H₂₈O₁₂

Pureza: 95%~99%

Cor e Forma: Powder

Peso molecular: 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

Fórmula: C₁₉H₂₈O₁₂

Pureza: 99.83% - ≥95%

Cor e Forma: Solid

Peso molecular: 448.42

Ref: TM-T5S1632

8-acetylshanzhiside methyl ester

CAS: 57420-46-9

Natural glycoside

Fórmula: C₁₉H₂₈O₁₂

Pureza: ≥ 90.0 % (HPLC)

Cor e Forma: Powder

Peso molecular: 448.42

Ref: 5G-82461