8-O-acetylharpagide CAS 6926-14-3

Introduction:Basic information about 8-O-acetylharpagide CAS 6926-14-3, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

8-O-acetylharpagide Basic information

Product Name:8-O-acetylharpagide
Synonyms:b-D-Glucopyranoside,(1S,4aS,5R,7S,7aS)-7-(acetyloxy)-1,4a,5,6,7,7a-hexahydro-4a,5-dihydroxy-7-methylcyclopenta[c]pyran-1-yl;8-O-Acetylharpagide Acetylharpagide;Acetylharpagide(8-O-Acetylharpagide);3-Acetylharpagide;beta-D-Glucopyranoside, (1S,4aS,5R,7S,7aS)-7-(acetyloxy)-1,4a,5,6,7,7a-hexahydro-4a,5-dihydroxy-7-methylcyclopenta[c]pyran-1-yl;Harpagide 7-acetate;(1S,4aS,5R,7S,7aS)-1-(hexopyranosyloxy)-4a,5-dihydroxy-7-Methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-ylacetate;8-O-acetylharpagide
CAS:6926-14-3
MF:C17H26O11
MW:406.38
EINECS:
Product Categories:chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract
Mol File:6926-14-3.mol

8-O-acetylharpagide Chemical Properties

Melting point 227-229℃
Boiling point 607.2±55.0 °C(Predicted)
density 1.58
storage temp. Sealed in dry,Store in freezer, under -20°C
solubility Soluble in DMSO and methanol;
form Powder
pka11.88±0.70(Predicted)
color White to off-white
Water Solubility insoluble in water
InChIKeyCAFTUQNGDROXEZ-XBDCZORHSA-N
SMILESCC(=O)O[C@@]1(C)C[C@@H](O)[C@]2(O)C=CO[C@@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]12

Safety Information

Safety Statements 24/25
WGK Germany 3
HS Code 29389090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral

8-O-acetylharpagide Usage And Synthesis

Chemical PropertiesWhite crystalline powder, easily soluble in water and methanol, from the whole herb of Ajuga decumbens Thunb. in the genus Sinews, family Labiatae, and Scrophularia ningpoensis Hemsl in the family Genseng.
Uses3-Acetylharpagide is an iridoid glycoside displaying antibacterial, antiinflammatory and antiviral effects.
SynthesisDried and pulverized whole grass of Solanum vulgare (3.0 kg) was soaked in acetone (20 L) at room temperature for 48 h. The filtrate was extracted three times in the same way by recovering the solvent under reduced pressure to obtain 92.0 .g acetone extract. The residue of the herb continued to be soaked in methanol (12 L) for 72 h, the filtrate was decompressed to recover the solvent, and extracted twice in the same way to obtain 222.6 g of methanol extract.g methanol extract. The acetone extract and methanol extract were combined, dissolved in 90% methanol, and extracted with hexane and dichloromethane sequentially to obtain 71.0 g of hexane extract, 30.4 of dichloromethane extract and 197.5 g of aqueous parts.The aqueous part (197.5 g) was extracted by D101 macromolecule.g) was passed through a D101 macroporous resin and eluted sequentially with water, 20%, 40%, 60% and 80% ethanol-water in a gradient to obtain the aqueous eluted site Fr.W1 (about 160 ), the 20% ethanol-water eluted site Fr.g), 20% ethanol site Fr. W2 (13.2 g), 40% ethanol site Fr. W3 (15.0 g), 60% ethanol site Fr. W4 (ca. 3.0 ) and 80% ethanol site Fr. W4 (ca. 3.0 ).g), 60% ethanol site Fr.W4 (ca. 3.0 ) and 80% ethanol site Fr.W5 (ca. 2.0 g). Fr.W2 was chromatographed on a Sephadex LH-20 column.LH-20 column chromatography, eluting with 50% methanol to give 8 flow fractions (Fr. W2a to W2h). Fr. W2d was purified by silica gel column chromatography and semi-preparative HPLC to give compound l (16.4 ).mg).

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