Detail of > 79484-75-6
- CAS Number:
- 79484-75-6
- Name:
Eleutheroside D
- Formula:
- C34H46O18
- Molecular Structure:
- Synonyms:
- a-D-Glucopyranoside,[(1S,3aR,4S,6aS)-tetrahydro- 1H,3H-furo[3,4-c]furan-1,4-diyl]bis(2,- 6-dimethoxy-4,1-phenylene) bis-;
- Molecular Weight:
- 742.72
- Density:
- 1.475 g/cm3
- Boiling Point:
- 935.739 °C at 760 mmHg
- Flash Point:
- 519.716 °C
Related products
- 79484-75-6Eleutheroside D
- 39432-56-9b-D-Glucopyranoside,[(1R,3aR,4S,6aS)-tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl]bis(2,6-dimethoxy-4,1-phenylene)bis-
- 7374-79-0b-D-Glucopyranoside,2,6-dimethoxy-4-[(1S,3aR,4S,6aR)-tetrahydro-4-(4-hydroxy-3,5-dimethoxyphenyl)-1H,3H-furo[3,4-c]furan-1-yl]phenyl
- 118-34-3b-D-Glucopyranoside,4-[(1E)-3-hydroxy-1-propen-1-yl]-2,6-dimethoxyphenyl
- 474-58-8b-D-Glucopyranoside, (3b)-stigmast-5-en-3-yl
- 201136-45-0D-Glucose-1-13C-1-C-d(9CI)
- 201417-06-3D-Glucose-1-13C-2-C-d(9CI)
- 288846-89-9D-Xylose-1-C-d (9CI)
Refine Suppliers Do you want your product ranking ahead? Know what is 'Top Seller'!
- Supplier Location:
China (Mainland)(5)
- Business Type:
- Importer/Exporter(1)Lab/Research institutions(1)Manufacturers(1)
- Certificates:
- Production License(1) ISO (0)
Please post your buying leads,so that our qualified suppliers
will soon contact you!
*Required Fields
Reference
- Study of the pharmacokinetics and mechanism of action of Eleutherococcus glycosides
- Study of the pharmacokinetics and mechanism of action of Eleutherococcus glycosides. VII. Effect of the extract and of individual glycosides on protein biosynthesis. Todorov, I. N.; Sizova, S. T.; Mitrokhin, Yu. I.; German, A. V.; Dardymov, I. V.; Barenboim, G. M.; Shul'man, M. L. (Otd. Inst. Khim. Fiz., Chernogolovka, USSR). Khim.-Farm. Zh., 18(8), 920-4 (Russian) 1984. CODEN: KHFZAN. ISSN: 0023-1134. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) The effects of the water-alc. (33%) ext. of Eleutherococcus, its water-sol. ext. (sepd. using polymeric solubilizers), and of pure eleutheroside B (I) [118-34-3] and D (II) [79484-75-6] on protein biosynthesis were studied in cell-free rat liver microsomal and polyribosomal systems. The alc. ext. concn.-dependently inhibited protein synthesis in liver microsomal systems to a greater extent than in polyribosomal systems. The water ext. had less inhibitory activity. I and II inhibited protein synthesis 10-20 times more than did the alc. ext., when the inhibition was expressed per unit wt. of drug. Apparently, the inhibitory effects of Eleutherococcus ext. on protein synthesis are due to glycosides, particularly I and II.
- About us
- |
- Payment
- |
- Contact us
- |
- Links
- |
- Help Center
- |
- Disclaimer
- |
- Add to favorite
- | SiteMap
- |
- Product SiteMap
- |
- Manufacturers
- |
- Suppliers
©2008 LookChem.com,License:ICP NO.：Zhejiang10014259
[Hangzhou]86-571-85317600,85317603,85317620