133565-20-5 Usage
Chemical structure
A complex structure with a dibenzocyclooctadiene core, featuring six methoxy groups, two hydroxy groups, and two methyl groups.
Classification
A lignan, which is a type of polyphenolic compound found in plants.
Natural occurrence
Found in certain plants, making it a naturally occurring compound.
Medicinal properties
Studied for its potential medicinal properties, including antioxidant and anti-inflammatory activities.
Disease treatment potential
Investigated for its potential use in the treatment of various diseases due to its biological activities.
Research interest
A subject of interest for researchers in the fields of natural product chemistry and pharmacology, due to its unique chemical structure and biological activities.
Antioxidant properties
Capable of neutralizing free radicals, which can help protect cells from damage and reduce the risk of certain diseases.
Anti-inflammatory properties
May help reduce inflammation in the body, which can be beneficial for treating conditions associated with chronic inflammation.
Molecular weight
Approximately 504.58 g/mol
Appearance
The compound is likely to be a solid, with a specific color and texture that may vary depending on its purity and form.
Solubility
The solubility of the compound in various solvents is not explicitly mentioned, but it is likely to be influenced by its polar and nonpolar functional groups.
Stability
The stability of the compound under different conditions (e.g., temperature, pH, light exposure) is not provided, but it may be affected by its chemical structure and functional groups.
Synthesis
The synthesis of 1,2,3,10,11,12-hexamethoxy-6,7-dihydroxy-6,7-dimethyldibenzocyclooctadiene may involve multiple steps, including the formation of the dibenzocyclooctadiene core and the subsequent introduction of methoxy, hydroxy, and methyl groups.
Purification
The purification of the compound may involve techniques such as chromatography, crystallization, or distillation, depending on the specific requirements and the scale of the synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 133565-20-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,5,6 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 133565-20:
(8*1)+(7*3)+(6*3)+(5*5)+(4*6)+(3*5)+(2*2)+(1*0)=115
115 % 10 = 5
So 133565-20-5 is a valid CAS Registry Number.
InChI:InChI=1/C24H32O8/c1-23(25)11-13-9-15(27-3)19(29-5)21(31-7)17(13)18-14(12-24(23,2)26)10-16(28-4)20(30-6)22(18)32-8/h9-10,25-26H,11-12H2,1-8H3
133565-20-5Relevant academic research and scientific papers
Ikeya,Sugama,Tanaka,Wakamatsu,Ono,Takeda,Oyama,Maruno
, p. 121 - 129 (1995)
After oral administration of schizandrin (1) to rat, the bile was collected and treated with β-glucuronidase and arylsulfatase. Eleven metabolites, SZ-M0 (3), SZ-M1 (4), SZ-M2 (5), SZ-M3 (6), SZ-M4 (7), SZ-MS (8), SZ M6 (9), SZ-M7 (10), SZ-M8 (11), SZ-M9 (12) and SZ-M10 (13) were isolated from the bile treated with the enzymes. The bile after oral administration of 1 to dog was collected and treated with enzymes in the same way, and eight metabolites, 3-8, 10 and SZ-MD2 (14) were isolated from the bile treated with enzymes. The structures of these metabolites were determined on the basis of chemical and spectral studies. The major metabolite in the bile of rat was 7 and the major metabolites in the bile of dog were 7 and 14.
