ChemicalBook Product Catalog Biochemical Engineering Natural Products Verbascoside

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Verbascoside

$ 1.00 /1KG

Min. Order1KG
Purity99%
Cas No61276-17-3
Supply Ability1000KGS
Update time2020-01-01

career henan chemical co

6YR

China

Chemical Properties

Product Name	Verbascoside
CAS No	61276-17-3
EC-No
Min. Order	1KG
Purity	99%
Supply Ability	1000KGS
Release date	2020/01/01

hanne 784

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Product Name:

Verbascoside

Synonyms:

glucopyranoside,2-(3,4-dihydroxyphenyl)ethyl3-o-(6-deoxy-alpha-l-mannopyranos;ACTEOSIDE :B-D-GLUCOPYRANOSIDE, 2-(3,4-DIHYDROXYPHENYL)ETHYL 3-O-(6-DEOXY-A-L-MANNOPYRANOSYL)-,4-[3-(3,4-DIHYDROXYPHENYL)-2-PROPENOATE],(E)-,;Acetoside;Extract from Verbena minutiflora (B864379);[(2R,3R,4R,5R,6R)-6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate;VERBASCOSIDE WITH HPLC;2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside 4-[(E)-3-(3,4-dihydroxyphenyl)propenoate];3,4-Dihydroxyphenethyl alcohol acteoside

CAS:

61276-17-3

MF:

C29H36O15

MW:

624.59

EINECS:

Product Categories:

-;Miscellaneous Natural Products;TCI-;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract

Mol File:

61276-17-3.mol

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Verbascoside Chemical Properties

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Melting point

232℃

Boiling point

908.8±65.0 °C(Predicted)

density

1.60±0.1 g/cm3(Predicted)

storage temp.

room temp

pka

9.31±0.10(Predicted)

InChIKey

FBSKJMQYURKNSU-ZLSOWSIRSA-N

CAS DataBase Reference

61276-17-3(CAS DataBase Reference)

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Safety Information

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Safety Statements

24/25

WGK Germany

RTECS

LZ5786000

HS Code

29389090

Toxicity

LD50 oral in rat: > 5gm/kg

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MSDS Information

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Verbascoside Usage And Synthesis

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Chemical Properties

White solid

Enzyme inhibitor

This plant glycoside and antioxidant (FW = 624.60 g/mol; CAS 61276-173), also known as verbascoside, inhibits TNFa-mediated apoptosis in LPSstimulated macrophages as well as 1-methyl-4-phenylpyridiniuminduced apoptosis in cerebellar granule neurons. It also inhibits proliferation of human promyelocytic HL-60 leukemia cells by inducing cell cycle arrest at the G0/G1 phase, followed by differentiation into monocytes. Acteoside inhibits PMA-induced invasion and migration of human fibrosarcoma cells by Ca2+-dependent CaMK/ERK and JNK/NFκB-signaling pathways. Acteoside thus shows the potential as antimetastatic agent. Another intriguing finding is that acteoside inhibits amyloid-β aggregation. Target(s): aldose reductase; protein kinase C; integrase, HIV-1; peptidyl-dipeptidase A, or angiotensin-converting enzyme; tyrosinase, or monophenol monooxygenase; 5-lipoxygenase, or arachidonate 5-lipoxygenase.

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