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Verbascoside

CAT: 0013-GTR19158715-01Size: 200 mgDry Ice: NoHazardous: No
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CAT#:0013-GTR19158715-01Size:200 mg
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Description
Verbascoside is a novel Inhibitor of the Oligomerization of Pneumolysin. (In Vitro) :Verbascoside acts as an ATP-competitive inhibitor of PKC, with an IC50 of 25 μM. Verbascoside shows Kis of 22 and 28 μM with respect to ATP and histone, respectively. Verbascoside has potent antitumor activity against L-1210 cells, with an IC50 of 13 μM. Verbascoside (5, 10 μM) suppresses 2,4-dinitrochlorobenzene (DNCB) -induced T cell costimulatory factors CD86 and CD54, proinflammatory cytokines, and NFκB pathway activation in THP-1 cells. (In Vivo) :Verbascoside (1%) reduces the overall scratching behavior incidence as well as the severity of the skin lesions in 2,4-dinitrochlorobenzene (DNCB) -induced atopic dermatitis (AD) mice model. Verbascoside also blocks DNCB-induced expression of proinflammatory cytokine TNF-α, IL-6, and IL-4 mRNA in skin lesions. Verbascoside (50, 100 mg/kg, i.p.) does not modify chronic constriction injury (CCI) -induced cold allodynia. Verbascoside (200 mg/kg, i.p.) decreases hyper-sensitivity to cold stimulus, acetone, on day 3 in rats. Verbascoside also significantly reduces behavioral changes associated with neuropathy. Moreover, Verbascoside decreases Bax and increases Bcl-2 on day 3.
CAS Number
61276-17-3
Product Name Alternative
Verbascoside | Acetoside | Kusaginin
Purity
>98% (HPLC)
Solubility
DMSO : ≥ 6.3 mg/mL; 10.09 mM
Smiles
O ([C@H]1[C@H] (OC (=O) /C=C/c2cc (O) c (O) cc2) [C@H] (O[C@@H] (OCCc2ccc (c (c2) O) O) [C@@H]1O) CO) [C@@H]1O[C@H] ([C@H] (O) [C@@H] (O) [C@H]1O) C
Molecular Formula
C29H36O15
Molecular Weight
624.59
Storage Conditions
Storage temperature: -20°C. Stability: ≥ 2 years
Notes
For research use only.
Other Product Names
[ (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

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