Tenidap

≥98%

Reagent Code: #63021
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CAS Number 120210-48-2

science Other reagents with same CAS 120210-48-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 320.75 g/mol
Formula C₁₄H₉ClN₂O₃S
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Tenidap is a synthetic organic compound and dual inhibitor of cyclooxygenase (COX) and 5-lipoxygenase (LOX) enzymes, primarily used as a research reagent in pharmaceutical studies on rheumatoid arthritis due to its anti-inflammatory and analgesic properties. It inhibits the biosynthesis of prostaglandins and leukotrienes, key mediators of inflammation and pain, making it effective in experimental models for reducing joint swelling, stiffness, and discomfort. It has also been investigated for osteoarthritis and ankylosing spondylitis. Typically supplied as a high-purity solid (≥98%) for laboratory use. Note: For research purposes only; not intended for human or veterinary therapeutic use. Clinical development was limited due to potential hepatotoxicity.

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Test Parameter Specification
Appearance solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿13,900.00
inventory 10mg
10-20 days ฿25,880.00

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Tenidap
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Tenidap is a synthetic organic compound and dual inhibitor of cyclooxygenase (COX) and 5-lipoxygenase (LOX) enzymes, primarily used as a research reagent in pharmaceutical studies on rheumatoid arthritis due to its anti-inflammatory and analgesic properties. It inhibits the biosynthesis of prostaglandins and leukotrienes, key mediators of inflammation and pain, making it effective in experimental models for reducing joint swelling, stiffness, and discomfort. It has also been investigated for osteoarthrit

Tenidap is a synthetic organic compound and dual inhibitor of cyclooxygenase (COX) and 5-lipoxygenase (LOX) enzymes, primarily used as a research reagent in pharmaceutical studies on rheumatoid arthritis due to its anti-inflammatory and analgesic properties. It inhibits the biosynthesis of prostaglandins and leukotrienes, key mediators of inflammation and pain, making it effective in experimental models for reducing joint swelling, stiffness, and discomfort. It has also been investigated for osteoarthritis and ankylosing spondylitis. Typically supplied as a high-purity solid (≥98%) for laboratory use. Note: For research purposes only; not intended for human or veterinary therapeutic use. Clinical development was limited due to potential hepatotoxicity.

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