Macrocarpal B - CAS 142698-60-0
Catalog number: B0005-166142
Not Intended for Therapeutic Use. For research use only.
Molecular Formula:
C28H40O6
Molecular Weight:
472.6
COA:
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Chemical Family:
Sesquiterpenoids
Description:
Macrocarpal B, which can be found in the branch of Eucalyptus globulus, shows antifouling activity.
Ordering Information
Catalog Number Size Price Stock Quantity
B0005-166142 1 mg $399 In stock
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Purity:
>98%
Appearance:
Yellow powder
MSDS:
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Application:
Antibacterial/antifouling
Quality Standard:
Enterprise Standard
Quantity:
Milligrams-Grams
1.Intestinal permeability of antivirus constituents from the fruits of Eucalyptus globulus Labill. in Caco-2 Cell Model.
Yang XW;Guo QM;Wang Y;Xu W;Tian L;Tian XJ Bioorg Med Chem Lett. 2007 Feb 15;17(4):1107-11. Epub 2006 Nov 10.
The uptake and transepithelial transport of the three main constituents macrocarpal A (M-A), macrocarpal B (M-B), and cypellocarpa C (Cy-C) from the fruits of Eucalyptus globulus Labill. were investigated. Monolayers of the human intestinal epithelial cancer cell line Caco-2 were incubated with M-A, M-B, and Cy-C to model its intestinal absorption and transport, respectively. The determination of compounds was performed by HPLC. The apparent permeability coefficients (P(app)) for M-A, M-B, and Cy-C in the apical-to-basolateral direction of a Caco-2 monolayer were (1.70+/-0.06)x10(-6), (1.99+/-0.10)x10(-6), and (6.08+/-0.41)x10(-6)cm/s, respectively. In the presence of iodoacetamide, the P(app) of Cy-C were both reducted in apical-to-basolateral and basolateral-to-apical directions. M-A and M-B appear to accumulate in the epithelial cells. The intestinal absorption of M-A, M-B, and Cy-C was passive diffusion as the dominating process and Cy-C was partly ATP-dependent.
2.[Studies on chemical constituents in fruits of Eucalyptus globulus].
Yang XW;Guo QM Zhongguo Zhong Yao Za Zhi. 2007 Mar;32(6):496-500.
OBJECTIVE: ;To study the chemical constituents in the fruits of Eucalyptus globulus Labill.;METHOD: ;The chemical constituents were isolated by various column chromatographic methods and structurally elucidated by IR, NMR and MS evidences.;RESULT: ;Fifteen compounds were obtained and identified as beta-sitosterol (1), betulinic acid (2), stigmasterol (3), euscaphic acid (4), 2a-Hydroxybetulinic acid (5), macrocarpal B (6), macrocarpal A (7), oleanolic acid (8), 3,4,3'-O-trimethylellagic acid (9), 3-O-methylellagic acid 4'-O-(2"-O-acetyl )-alpha-L-rhamnopyranoside (10), camaldulenside (cypellocarpin C, 11), 3-O-methylellagic acid 4'-O-alpha-L-rhamnopyranoside (12), 3-O-methylellagic acid (13), ellagic acid (14), and gallic acid (15).;CONCLUSION: ;Compounds 4 and 5 from genera Eucalyptus, 1, 3 and 11 from plant E. globulus, and 6, 7, 9 and 15 from the fruits of E. globulus were isolated for the first time.
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Chemical Structure

CAS 142698-60-0 Macrocarpal B

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