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Results for "

nd 01

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    8
    TargetMol | Inhibitors_Agonists
  • Natural Products
    8
    TargetMol | Natural_Products
Compound 0166-0008
T131682
Compound 0166-0008 is a useful organic compound for research related to life sciences and the catalog number is T131682.
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Compound 0120-0020
T131683
Compound 0120-0020 is a useful organic compound for research related to life sciences and the catalog number is T131683.
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Compound 0120-0018
T131684
Compound 0120-0018 is a useful organic compound for research related to life sciences and the catalog number is T131684.
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Compound 0118-0250
T131685
Compound 0118-0250 is a useful organic compound for research related to life sciences and the catalog number is T131685.
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Compound 0118-0244
T131686
Compound 0118-0244 is a useful organic compound for research related to life sciences and the catalog number is T131686.
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Compound 0115-0004
T131688
Compound 0115-0004 is a useful organic compound for research related to life sciences and the catalog number is T131688.
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Compound 0115-0003
T131689
Compound 0115-0003 is a useful organic compound for research related to life sciences and the catalog number is T131689.
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Barlerin
ND01, 8-O-Acetylshanzhiside methyl ester
T5S163257420-46-9
Barlerin (8-O-Acetylshanzhiside methyl ester) has potential against cerebral ischemic injury, and its protective effect on oxygen-glucose deprivation-induced injury might be due to the suppression of intracellular Ca2+ elevation and caspase-3 activity, and improvement of mitochondrial energy metabolism.8-O-Acetylshanzhiside methylester can increase angiogenesis and improve functional recovery after stroke.8-O-Acetylshanzhiside methylester has protective effects on experimental myocardial ischemia injury, the effects might be due to block of myocardial inflammatory cascades through an HMGB1-dependent NF-κB signaling pathway.8-O-Acetylshanzhiside methylester protects diabetic brain against I R injury by alleviating diabetic cerebral I R injury and attenuating blood–brain barrier (BBB) breakdown, and its protective effects may involve HMGB-1 and NF-κB signalling pathway.
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