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Documenti fondamentali

SBR00026

Sigma-Aldrich

Ligstroside

Nitric oxide inhibitor, ≥95%

Sinonimo/i:

(-)-ligstroside, Ligustroside

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About This Item

Formula empirica (notazione di Hill):
C25H32O12
Numero CAS:
Peso molecolare:
524.51
Codice UNSPSC:
12352200
NACRES:
NA.25

Origine biologica

plant

Livello qualitativo

Saggio

≥95%

Stato

lyophilized powder

PM

524.51

Solubilità

DMSO: ≥10 mg/mL (19 mM)
methanol: ≥10 mg/mL

applicazioni

metabolomics
vitamins, nutraceuticals, and natural products

Temperatura di conservazione

−20°C

InChI

1S/C25H32O12/c1-3-15-16(10-19(28)34-9-8-13-4-6-14(27)7-5-13)17(23(32)33-2)12-35-24(15)37-25-22(31)21(30)20(29)18(11-26)36-25/h3-7,12,16,18,20-22,24-27,29-31H,8-11H2,1-2H3/b15-3+/t16-,18+,20+,21-,22+,24-,25-/m0/s1
GMQXOLRKJQWPNB-MVVLSVRYSA-N

Descrizione generale

Ligstroside, also known as ligusroside, is a secoiridoid glycoside, a bioactive natural compound commonly derived from plants like Ligustrum lucidum, Jasminum officinale, and Osmanthus heterophyllus. Existing research suggests that this metabolite functions as an nitric oxide inhibitor and may exhibit diverse biological activities, including anti-neoplastic, antioxidant, antiviral, and anti-inflammatory properties.

Applicazioni

Ligstroside is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.

Azioni biochim/fisiol

Ligstroside is a natural product derived from leaves of Olea europaea. Ligstroside displays several potentially beneficial anti-inflammatory properties by exhibiting selective inhibition effect on COX-1 enzyme of arachidonate cascade metabolism. Ligstroside generates a reduction of the PGE2 (prostaglandin E2) levels in activated mouse macrophage (IC50 = 48.53 μM) and also reduction of the TXB2 (thromboxane B2) levels in human platelets (IC50 = 122.63 μM).[1] Moreover, Ligstroside exhibits inhibition activity of NO production in LPS-activated RAW264.7 macrophages (17.8% at 30 μM and 40.7% at 100 μM) without any cytotoxic effect in these cells.[2],[3] Additionally, Ligstroside exhibits in vitro antiviral activity against parainfluenza type 3 virus (IC50 = 15.6 μM).[4]

Caratteristiche e vantaggi

  • Suitable for Biochemical and Biomedical research
  • Versatile and adaptable for wide variety of laboratory and research applications

Stoccaggio e stabilità

Hygroscopic; store in dry place with desiccant

Altre note

For additional information on our range of Biochemicals, please complete this form.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Certificati d'analisi (COA)

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Chemical structures of constituents from the flowers of Osmanthus fragrans var. aurantiacus.
Liu, J., Nakamura, S., Xu, B., Matsumoto, T., Ohta, T., Fujimoto, K., ... & Matsuda, H.
Journal of Natural Medicines, 69(1), 135-141 (2015)
In African Natural Plant Products Volume II: Discoveries and Challenges in Chemistry, Health, and Nutrition.
Bai, N., He, K., Roller, M., Lai, C.S., Shao, X., Pan, M.H., & Ho, C.T.
Journal of the American Chemical Society, 2, 115-125 (2013)
In vitro evaluation of secoiridoid glucosides from the fruits of Ligustrum lucidum as antiviral agents.
Ma, S.C., He, Z.D., Deng, X.L., But, P.P.H., Ooi, V.E.C., Xu, H.X., ... & Lee, S.F.
Chemical & Pharmaceutical Bulletin, 49(11), 1471-1473 (2001)
In vitro anti-inflammatory activity of iridoids and triterpenoid compounds isolated from Phillyrea latifolia L.
Diaz, A.M., Abad, M.J., Fernandez, L., Recuero, C., Villaescusa, L., Silvan, A.M., & Bermejo, P.
Biological & Pharmaceutical Bulletin, 23(11), 1307-1313 (2000)

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Recensioni

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