Isosakuranetin – 5 mg

Brand:
Cayman
CAS:
480-43-3
Storage:
-20
UN-No:
Non-Hazardous - /

Isosakuranetin is a flavanone that has been found in Citrus species and has diverse biological activities.{39812,39817,39813,39814,39815,39816,39818} It inhibits calcium uptake induced by pregnenolone sulfate (PregS; Item No. 21004) in HEK293 cells expressing mouse transient receptor potential melastatin 3 (TRPM3; IC50 = 50 nM).{39812} Isosakuranetin is selective for TRPM3 over TRPM1, TRPM8, and TRP vanilloid-related 1 (TRPV1) when used at a concentration of 10 μM. In vivo, isosakuranetin (2 mg/kg) increases latency to first pain-related response in mice in a hot plate test and reduces the number and duration of PregS-induced nocifensive responses, such as paw licking, shaking, or lifting, in mice. It also reduces systolic blood pressure in spontaneously hypertensive rats when administered at a dose of 10 mg/kg.{39817} Isosakuranetin (20 µM) inhibits UV-B-induced matrix metalloproteinase-1 (MMP-1) expression by 90% in HaCaT human keratinocyte cells, as well as phosphorylation of ERK1/2 when used at a concentration of 50 µM.{39813} It blocks hydrogen peroxide-induced increases in reactive oxygen species (ROS), intracellular calcium concentration, caspase-3 activity, and JNK phosphorylation, as well as decreases in catalase activity, in PC12 cells when used at a concentration of 0.8 µM.{39814} Isosakuranetin also has antibacterial and trypanocidal activity against M. tuberculosis, C. neoformans, and T. cruzi.{39815,39816,39818}  

 

Available on backorder

SKU: 25198 - 5 mg Category:

Description

A citrus flavanone with diverse biological activities; inhibits PregS-induced calcium uptake in HEK293 cells expressing mouse TRPM3 (IC50 = 50 nM); selective for TRPM3 over TRPM1, TRPM8, and TRPV1 at 10 µM; increases latency to first pain-related response in mice in a hot plate test and reduces the number and duration of PregS-induced nocifensive responses in mice at 2 mg/kg; reduces systolic blood pressure in spontaneously hypertensive rats at 10 mg/kg; inhibits UV-B-induced MMP-1 expression by 90% in HaCaT cells at 20 µM and inhibits phosphorylation of ERK1/2 at 50 µM; blocks hydrogen peroxide-induced increases in ROS, intracellular calcium concentration, caspase-3 activity, and JNK phosphorylation, as well as decreases in catalase activity, in PC12 cells at 0.8 µM; has antibacterial and trypanocidal activity against M. tuberculosis, C. neoformans, and T. cruzi,


Formal name: (2S)-2,3-dihydro-5,7-dihydroxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one

Synonyms: 

Molecular weight: 286.3

CAS: 480-43-3

Purity: ≥98%

Formulation: A crystalline solid


Product Type|Biochemicals|Antibiotics||Product Type|Biochemicals|Antiparasitics|Antiprotozoals||Product Type|Biochemicals|Ion Channel Modulation|Activators||Product Type|Biochemicals|Natural Products|Flavonoids||Product Type|Biochemicals|Ox Stress Reagents|Antioxidants||Research Area|Immunology & Inflammation||Research Area|Infectious Disease|Bacterial Diseases|Tuberculosis||Research Area|Infectious Disease|Parasitic Diseases|Chagas Disease||Research Area|Neuroscience|Pain Research||Research Area|Oxidative Stress & Reactive Species|Antioxidant Activity||Research Area|Oxidative Stress & Reactive Species|Reactive Oxygen