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SBR00026

Sigma-Aldrich

Ligstroside

Nitric oxide inhibitor, ≥95%

Synonyme(s) :

(-)-ligstroside, Ligustroside

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About This Item

Formule empirique (notation de Hill):
C25H32O12
Numéro CAS:
Poids moléculaire :
524.51
Code UNSPSC :
12352200
Nomenclature NACRES :
NA.25

Source biologique

plant

Niveau de qualité

Pureté

≥95%

Forme

lyophilized powder

Poids mol.

524.51

Solubilité

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

Application(s)

metabolomics
vitamins, nutraceuticals, and natural products

Température de stockage

−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

Clé InChI

GMQXOLRKJQWPNB-MVVLSVRYSA-N

Description générale

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.

Application

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

Actions biochimiques/physiologiques

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). 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., Additionally, Ligstroside exhibits in vitro antiviral activity against parainfluenza type 3 virus (IC50 = 15.6 μM).

Caractéristiques et avantages

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

Stockage et stabilité

Hygroscopic; store in dry place with desiccant

Autres remarques

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Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Certificats d'analyse (COA)

Lot/Batch Number

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

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)
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)

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