gitaloxin
- Product Name
- gitaloxin
- CAS No.
- 3261-53-8
- Chemical Name
- gitaloxin
- Synonyms
- gitaloxin;16-Formylgitoxin;3β-[[4-O-[4-O-(2,6-Dideoxy-β-D-ribo-hexopyranosyl)-2,6-dideoxy-β-D-ribo-hexopyranosyl]-2,6-dideoxy-β-D-ribo-hexopyranosyl]oxy]-16β-formyloxy-14-hydroxy-5β,14β-card-20(22)-enolide;Card-20(22)-enolide, 3-[(O-2,6-dideoxy-β-D-ribo-hexopyranosyl-(1→4)-O-2,6-dideoxy-β-D-ribo-hexopyranosyl-(1→4)-2,6-dideoxy-β-D-ribo-hexopyranosyl)oxy]-16-(formyloxy)-14-hydroxy-, (3β,5β,16β)-;[3-[5-[5-(4,5-dihydroxy-6-methyloxan-2-yl)oxy-4-hydroxy-6-methyloxan-2-yl]oxy-4-hydroxy-6-methyloxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] formate;[3-[5-[5-(4,5-dihydroxy-6-methyl-oxan-2-yl)oxy-4-hydroxy-6-methyl-oxan-2-yl]oxy-4-hydroxy-6-methyl-oxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] methanoate;formic acid [3-[5-[5-(4,5-dihydroxy-6-methyl-tetrahydropyran-2-yl)oxy-4-hydroxy-6-methyl-tetrahydropyran-2-yl]oxy-4-hydroxy-6-methyl-tetrahydropyran-2-yl]oxy-14-hydroxy-17-(5-keto-2H-furan-3-yl)-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] ester
- CBNumber
- CB6877110
- Molecular Formula
- C42H64O15
- Formula Weight
- 808.95
- MOL File
- 3261-53-8.mol
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gitaloxin Property
- Melting point:
- 251.5°C
- Boiling point:
- 674.74°C (rough estimate)
- Density
- 1.1231 (rough estimate)
- refractive index
- 1.5940 (estimate)
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N-Bromosuccinimide Price
American Custom Chemicals Corporation
- Product number
- TOX0000046
- Product name
- GITALOXIN
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $496.85
- Updated
- 2021/12/16
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gitaloxin Chemical Properties,Usage,Production
Originator
Gitaloxin,Shanghai Lansheng Corporation
Definition
ChEBI: A cardenolide glycoside that is gitoxin in which the 16beta-hydroxy group has been formylated.
Manufacturing Process
0.2 g gitoxin was dissolved in 15 ml of dimethylformamide and mixed with 2 ml of acetanhydride, 3 ml formic acid (98%) and 2 ml triethylamine or pyridine. The reaction mixture stood for 60 min. at room temperature, then it was diluted with water, a precipitated product was filtered off. A filtrate was shook with chloroform 2 times. Chloroform was distilled to dryness and the residue was added to the precipitate. 16-Formylgitoxin was isolated by fraction crystallization. MP: 250°-253°C, yield about 50%.
Therapeutic Function
Cardiotonic
gitaloxin Preparation Products And Raw materials
Raw materials
Preparation Products
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gitaloxin Suppliers
- Tel
- --
- Fax
- --
- enquiry@leancare.co.uk
- Country
- United Kingdom
- ProdList
- 6446
- Advantage
- 42
- Tel
- --
- Fax
- --
- sales@lanospharma.com
- Country
- China
- ProdList
- 6329
- Advantage
- 56
- Tel
- --
- Fax
- --
- sales@2apharmachem.com
- Country
- United States
- ProdList
- 6137
- Advantage
- 39
- Tel
- --
- Fax
- --
- zhou@pharmchemical.com
- Country
- China
- ProdList
- 2748
- Advantage
- 60
- Tel
- --
- Fax
- --
- sales@3bsc.com
- Country
- United States
- ProdList
- 6718
- Advantage
- 47