نتایج جستجو برای: cox 2 inhibitory

تعداد نتایج: 2641865  

Journal: :Journal of immunology 2006
Elizabeth P Ryan Christine M Malboeuf Matthew Bernard Robert C Rose Richard P Phipps

Vaccination to generate protective humoral immunity against infectious disease is becoming increasingly important due to emerging strains of virus, poorly immunogenic vaccines, and the threat of bioterrorism. We demonstrate that cyclooxygenase-2 (Cox-2) is crucial for optimal Ab responses to a model vaccine, human papillomavirus type 16 virus-like particles (HPV 16 VLPs). Cox-2-deficient mice p...

Journal: :Archives of pharmacal research 2006
Se Jong Kim Meihua Jin Eunkyung Lee Tae Chul Moon Zhejiu Quan Ju Hye Yang Kun Ho Son Kil-Ung Kim Jong Kun Son Hyeun Wook Chang

Methyl gallate (MG) is a medicinal herbal product that is isolated from Paeonia lactiflora that inhibits cyclooxygenase-2 (COX-2) dependent phases of prostaglandin D2 (PGD2) generation in bone marrow-derived mast cells (BMMC) in a concentration-dependent manner with an IC50 values of 17.0 microM. This compound also found inhibited the COX-2-dependent conversion of the exogenous arachidonic acid...

Design of selective cyclooxygenase-2 (COX-2) inhibitors is still a challenging task because of active site similarities between COX isoenzymes. To help with this issue, we tried to generate a 3D-QSAR (3 dimensional quantitative structure activity relationship) model that might reflect the essential features of COX-2 active sites. Compounds in a series of resveratrol derivatives inhibitors with ...

Journal: :Cancer research 2000
J Lu C T Ho G Ghai K Y Chen

Theaflavin (TF-1), theaflavin-3-monogallate and theaflavin-3'-monogallate mixture (TF-2), and theaflavin-3,3'-digallate (TF-3) are the major black tea polyphenols. Here we compared the effects of these polyphenols on cell growth, apoptosis, and gene expression in normal and cancerous cells. We showed that TF-2 (10-50 microM) inhibited the growth of SV40 transformed WI38 human cells (WI38VA) and...

Journal: :In vivo 2005
Atsusi Hirata Yukio Murakami Toshiko Atsumi Masao Shoji Takako Ogiwara Kazutoshi Shibuya Shigeru Ito Ichro Yokoe Seiichiro Fujisawa

Phenylpropanoids may act as nonsteroidal anti-inflammatory drug (NSAID)-like compounds. 4-cis, 8-cis-Bis (4-hydroxy-3-methoxyphenyl)-3, 7-dioxabicyclo-[3.3.0]octane-2,6-dione (bis-FA, compound 2), a dimer of ferulic acid, was synthesized from ferulic acid (1), and its effect on lipopolysaccharide (LPS)-stimulated cyclooxygenase-2 (COX-2) expression in RAW 264.7 cells was compared with those of ...

Journal: :Molecular and cellular biology 2007
Xin Tong Rukiyah T Van Dross Adnan Abu-Yousif Aubrey R Morrison Jill C Pelling

Cyclooxygenase 2 (COX-2) is a key enzyme in the conversion of arachidonic acid to prostaglandins, and COX-2 overexpression plays an important role in carcinogenesis. Exposure to UVB strongly increased COX-2 protein expression in mouse 308 keratinocytes, and this induction was inhibited by apigenin, a nonmutagenic bioflavonoid that has been shown to prevent mouse skin carcinogenesis induced by b...

Journal: :African Journal of Pharmacy and Pharmacology 2023

Cyclooxygenase 2 (COX-2) is involved in the production of prostaglandins that sustain inflammatory process. Inflammatory cells release a number reactive species. Furthermore, oxygen species can initiate intracellular signaling cascades and enhance expression pro-inflammatory genes. The objective was to study cyclooxygenase protein denaturation inhibition antioxidant activity ten extracts from f...

Journal: :Planta medica 2002
A Suksamrarn S Kumpun K Kirtikara B Yingyongnarongkul S Suksamrarn

A new iridoid, pedunculariside, together with the known iridoid agnuside were isolated from the butanol extract of Vitex peduncularis stem bark. Both pedunculariside and agnuside showed preferential inhibition of COX-2, with IC50 values of 0.15 +/- 0.21 mg/ml and 0.026 +/- 0.015 mg/ml respectively, while having only small inhibitory effects on COX-1. Both compounds did not exhibit cytotoxicity ...

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