CAS 57420-46-9

Barlerin

Description:

Barlerin, identified by the CAS number 57420-46-9, is a chemical compound that belongs to the class of natural products known as alkaloids. It is primarily derived from certain plant species and is noted for its potential biological activities, including antimicrobial and anti-inflammatory properties. Barlerin's structure features a complex arrangement of carbon, hydrogen, nitrogen, and oxygen atoms, which contributes to its unique chemical behavior and interactions. The compound is often studied for its pharmacological potential, particularly in the context of traditional medicine. Its solubility and stability can vary depending on the solvent and environmental conditions, which is important for its application in research and potential therapeutic uses. As with many natural products, the extraction and purification processes are crucial for obtaining Barlerin in a form suitable for scientific investigation. Further research is ongoing to fully elucidate its mechanisms of action and potential applications in medicine and pharmacology.

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

Synonyms:

• 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

Purity: 98%

Molecular weight: 448.4184

Ref: IN-DA00IKLH

Barlerin

CAS: 57420-46-9

Barlerin

Purity: ≥95%

Molecular weight: 448.42g/mol

Ref: 54-BUP04611

8-O-Acetyl shanzhiside methyl ester

CAS: 57420-46-9

Formula: C₁₉H₂₈O₁₂

Molecular weight: 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

Purity: 95%~99%

Color and Shape: Powder

Molecular weight: 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

Purity: 99.83% - ≥95%

Color and Shape: Solid

Molecular weight: 448.42

Ref: TM-T5S1632

8-acetylshanzhiside methyl ester

CAS: 57420-46-9

Natural glycoside

Formula: C₁₉H₂₈O₁₂

Purity: ≥ 90.0 % (HPLC)

Color and Shape: Powder

Molecular weight: 448.42

Ref: 5G-82461