officinale

Guaifenesin (Guaiphenesin) is an expectorant that also has some muscle relaxing action. It is used in many cough preparations.

Zingerone (Vanillylacetone) is a nontoxic methoxyphenol isolated from Zingiber officinale, with potent anti-inflammatory, antidiabetic, antidiarrhoeic, antilipolytic, antispasmodic, and anti-tumor properties. Zingerone (Gingerone) alleviates oxidative stress and inflammation, down-regulates NF-κB mediated signaling pathways, acts as an anti-mitotic agent, and inhibits the growth of neuroblastoma cells.

(Z)-Ligustilide (Ligustilide A) , an active ingredient isolated from the medicinal plants Angelica acutiloba and Cnidium officinale, inhibits benzo(a)pyrene-induced CYP1A1 upregulation in cultured human keratinocytes via ROS-dependent Nrf2 activation.

Isoviolanthin reduces the migratory and invasive capacities of TGF-β1-treated HCC cells without cytotoxic effects on normal live cells and has potential as a therapeutic agent for the treatment of advanced-stage metastatic HCC. Isoviolanthin is a flavonoid glycoside extracted from the leaves of Dendrobium Officinale.

Rhein (NSC 38629) is an anthraquinone compound extracted from Polygonaceae Rheum Officinale with anti-inflammation and antitumor activities.

Beauvericin A is a cyclodepsipeptide and derivative of beauvericin originally isolated fromB. bassianathat has diverse biological activities.1,2,3It is active againstM. tuberculosis(MIC = 25 μg/ml) andP. falciparum(IC50= 12 μg/ml).2Beauvericin A is toxic to brine shrimp (LD100= 32 μg/ml).3 1.Gupta, S., Montillor, C., and Hwang, Y.-S.Isolation of Novel Beauvericin Analogues from the Fungus Beauveria bassianaJ. Nat. Prod.58(5)733-738(1995) 2.Nilanonta, C., Isaka, M., Kittakoop, P., et al.Antimycobacterial and antiplasmodial cyclodepsipeptides from the insect pathogenic fungus Paecilomyces tenuipes BCC 1614Planta Med.66(8)756-758(2000) 3.Shi, S., Li, Y., Ming, Y., et al.Biological activity and chemical composition of the endophytic fungus Fusarium sp. TP-G1 obtained from the root of Dendrobium officinale Kimura et MigoRec. Nat. Prod.12(6)549-556(2018)

Taraxasterol (Taraxasterin) is compound with anti-inflammatory activity.

(-)-Rabdosiin, identified as a novel phenolic marker in Symphytum officinale L., exhibits antioxidant, neuroprotective, and anti-HIV activities [1].

Apigenin-6-C-β-D-xylopyranosyl-8-C-α-L-arabinopyranoside is a natural flavonoid discovered in Dendrobium officinale, possessing antioxidant activity.

Rhein (Standard) is a reference standard for research and analysis in studies involving Rhein. Rhein (NSC 38629) is an anthraquinone compound extracted from Polygonaceae Rheum Officinale with anti-inflammation and antitumor activities.

(Z)-Ligustilide (Standard) is a reference standard for research and analysis in studies involving (Z)-Ligustilide. (Z)-Ligustilide (Ligustilide A) , an active ingredient isolated from the medicinal plants Angelica acutiloba and Cnidium officinale, inhibits benzo(a)pyrene-induced CYP1A1 upregulation in cultured human keratinocytes via ROS-dependent Nrf2 activation.

Zingerone (Standard) is a reference standard for research and analysis in studies involving Zingerone. Zingerone (Vanillylacetone) is a nontoxic methoxyphenol isolated from Zingiber officinale, with potent anti-inflammatory, antidiabetic, antidiarrhoeic, antilipolytic, antispasmodic and anti-tumor properties. Zingerone(Gingerone) alleviates oxidative stress and inflammation, down-regulates NF-κB mediated signaling pathways. Zingerone(Gingerone) acts as an anti-mitotic agent, and inhibits the growth of neuroblastoma cells.

Taraxasterol (Standard) is a reference standard for research and analysis in studies involving Taraxasterol. Taraxasterol (Taraxasterin) is compound with anti-inflammatory activity.

Neonuezhenide is a phenolic compound isolated from Ligustrum officinale, which has strong antioxidant effects on free radical-induced hemolysis of red blood cells.

5-Methoxy-[8]-gingerol is a compound that can be isolated from ginger (Zingiber officinale).

Deoxygeraniol is a monoterpene compound that has been identified in tea trees (Camellia sinensis), Magnolia sieboldii, and ginger (Zingiber officinale), and is frequently utilized as an intermediate in the synthesis of fragrances or flavors.

Cnidilide is a natural alkyl phthalide compound that can be isolated from the rhizomes of Cnidium officinale. It reduces the production of NO and PGE2 by inhibiting LPS-induced expression of iNOS and COX-2. Additionally, Cnidilide suppresses the pro-inflammatory cytokines IL-1β, IL-6, and TNF-α. It specifically inhibits the phosphorylation of p38 MAPK and JNK, as well as the activation of downstream kinase MSK-1. Moreover, Cnidilide blocks signaling pathways by inhibiting the transcriptional activities of AP-1 and NF-κB. This compound is useful in the study of inflammatory diseases.

(–)-β-Sesquiphellandrene, a sesquiterpene identified in Z. officinale, exhibits antiviral and anticancer properties. It effectively inhibits rhinovirus IB virus replication in a plaque reduction assay with an IC50 of 0.44 µM. Additionally, at a concentration of 10 µM, it demonstrates cytotoxicity to HCT116 cells.

8-Gingerdione can be isolated from Ginger (Zingiber officinale). It does not significantly inhibit the production of the inflammatory mediators NO, TNF-α, and IL-6.