CAS 87085-00-5

Mulberrofuran G

Description:

Mulberrofuran G is a natural compound primarily derived from the Morus alba (white mulberry) plant. It belongs to the class of flavonoids and is characterized by its unique chemical structure, which includes multiple hydroxyl groups contributing to its potential antioxidant properties. This compound has garnered interest in the field of pharmacology due to its various biological activities, including anti-inflammatory, anti-cancer, and neuroprotective effects. Mulberrofuran G exhibits a relatively low toxicity profile, making it a candidate for further research in therapeutic applications. Its solubility in organic solvents and limited solubility in water can influence its bioavailability and efficacy in biological systems. Additionally, studies have indicated that Mulberrofuran G may interact with various cellular pathways, suggesting its potential role in modulating metabolic processes. Overall, the compound's diverse pharmacological properties and natural origin make it a subject of interest in both medicinal chemistry and natural product research.

Formula: C₃₄H₂₆O₈

InChI: InChI=1/C34H26O8/c1-16-8-23-22-6-4-21(37)15-30(22)41-34(25-7-5-19(35)13-26(25)38)33(23)24(9-16)32-27(39)10-18(12-31(32)42-34)28-11-17-2-3-20(36)14-29(17)40-28/h2-7,9-15,23-24,33,35-39H,8H2,1H3/t23-,24-,33-,34+/m1/s1

InChI key: InChIKey=MJJWBJFYYRAYKU-FJPSCYHJSA-N

SMILES: OC1=C([C@@]23[C@]4([C@@](C=5C(O2)=CC(=CC5O)C=6OC=7C(C6)=CC=C(O)C7)(C=C(C)C[C@@]4(C=8C(O3)=CC(O)=CC8)[H])[H])[H])C=CC(O)=C1

Synonyms:

• (3aS,8aS,13bS,13cR)-8a-(2,4-Dihydroxyphenyl)-1,8a,13b,13c-tetrahydro-6-(6-hydroxy-2-benzofuranyl)-2-methyl-3aH-benzo[3,4][2]benzopyrano[1,8-bc][1]benzopyran-4,11-diol
• 3aH-Benzo[3,4][2]benzopyrano[1,8-bc][1]benzopyran-4,11-diol, 8a-(2,4-dihydroxyphenyl)-1,8a,13b,13c-tetrahydro-6-(6-hydroxy-2-benzofuranyl)-2-methyl-, (3aS,8aS,13bS,13cR)-
• 3aH-Benzo[3,4][2]benzopyrano[1,8-bc][1]benzopyran-4,11-diol, 8a-(2,4-dihydroxyphenyl)-1,8a,13b,13c-tetrahydro-6-(6-hydroxy-2-benzofuranyl)-2-methyl-, [3aS-(3aα,8aα,13bβ,13cα)]-
• Mulberrofuran G
• albanol A
• Mulberrofuran G（(+)-Albanol A,Albanol A）

3aH-Benzo[3,4][2]benzopyrano[1,8-bc][1]benzopyran-4,11-diol,8a-(2,4-dihydroxyphenyl)-1,8a,13b,13c-tetrahydro-6-(6-hydroxy-2-benzofuranyl)-2-methyl-, (3aS,8aS,13bS,13cR)-

CAS: 87085-00-5

Formula: C₃₄H₂₆O₈

Purity: 90%

Color and Shape: Solid

Molecular weight: 562.5654

Ref: IN-DA00IECJ

Mulberrofuran G

CAS: 87085-00-5

Mulberrofuran G, from Morus alba L., is a dual inhibitor of PTP1B and α-glucosidase with anti-hcv activity and can be used in Alzheimer's disease research.

Formula: C₃₄H₂₆O₈

Purity: 95% - 99.97%

Color and Shape: Solid

Molecular weight: 562.57

Ref: TM-TN1956

Mulberrofuran G

CAS: 87085-00-5

Mulberrofuran G

Purity: ≥95%

Molecular weight: 562.57g/mol

Ref: 54-BUP20037

Mulberrofuran G

CAS: 87085-00-5

Formula: C₃₄H₂₆O₈

Purity: 95%~99%

Color and Shape: Powder

Molecular weight: 562.574

Ref: BP-SBP02868

Mulberrofuran G

Controlled Product

CAS: 87085-00-5

Mulberrofuran G is a natural compound that has been extracted from Mulberry leaves. It has been shown to have potent antimicrobial activity against Gram-positive bacteria, such as Staphylococcus aureus and Bacillus subtilis, and is active against Gram-negative bacteria such as Escherichia coli. Mulberrofuran G also inhibits the production of estrogen by inhibiting the enzyme aromatase. This inhibition reduces the risk of estrogen-related diseases such as breast cancer, uterine cancer, and endometrial cancer. Mulberrofuran G also inhibits uptake of cholesterol into cells by blocking the formation of cholesteryl esters in the liver cells, which may be useful for treating hypercholesterolemia.
Mulberrofuran G is a natural compound that has been extracted from Mulberry leaves. It has been shown to have potent antimicrobial activity against Gram-positive bacteria, such as Staphylococcus aure

Formula: C₃₄H₂₆O₈

Purity: Min. 95%

Molecular weight: 562.57 g/mol

Ref: 3D-MDA08500