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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
458 Results for "
O2
" in MedChemExpress (MCE) Product Catalog:
Products (458)
458 Results for "O2" in MCE Product Catalog:
Cat. No.: HY-N20734
CAS No.: 64527-08-8
Synonyms: Polygalacin
Target:
Cat. No.: HY-W587784
CAS No.: 542-40-5
Cat. No.: HY-N6595
CAS No.: 97653-92-4
Category:
Human Gut Microbiota Metabolites Microorganisms Terpenoids Diterpenoids Endogenous metabolite
Target:
Cat. No.: HY-P5883
CAS No.: 2126166-03-6
Synonyms: tatM2NX
Target:
Research Areas:
Cat. No.: HY-N16417
CAS No.: 24512-87-6
Category:
Cat. No.: HY-159485
Target:
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NFh-ALP is an alkaline phosphatase (ALP)-activatable photosensitizer. NFh-ALP could be activated by ALP in cells and generate 1O2 under 808 nm excitation, effectively killing tumor cells by inducing apoptosis and having good biocompatibility. The maximum absorption wavelength of NFh-ALP is about 656 nm .
Cat. No.: HY-D2986
CAS No.: 2634719-04-1
Cat. No.: HY-164926
CAS No.: 2640677-68-3
Target:
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PARP1-IN-33 (Example 6) is a PARP1 inhibitor (IC50: 0.41 nM). PARP1-IN-33 has retinal cytoprotective effect, with an EC50 of 0.02 nM (inhibition on MTS activity of H2O2 induced human retinal pigment epithelial cell) .
Cat. No.: HY-168031
CAS No.: 2756368-79-1
Target:
Histamine Receptor Calcium Channel Cholinesterase (ChE) Reactive Oxygen Species (ROS) Amyloid-β
Research Areas:
AChE/BChE-IN-21 is a histamine H3 receptor antagonist, calcium channel blocker, and acetylcholinesterase inhibitor. AChE/BChE-IN-21 exhibits neuroprotective activity against H2O2 and Aβ1-40, and can restore cognitive function in AD mice .
Cat. No.: HY-126841
CAS No.: 22897-08-1
Category:
Target:
Cat. No.: HY-N2203A
CAS No.: 1229437-79-9
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Cat. No.: HY-P2965
CAS No.: 70132-14-8
Target:
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L-Lysine α-oxidase is a potent anticancer agent. L-Lysine α-oxidase also a L-amino acid oxidase, deaminates L-lysine with the yield of H2O2, ammonia, and α-keto-ε-aminocaproate. L-Lysine α-oxidase shows cytotoxicity and anticancer activity [2].
Cat. No.: HY-175671
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LSD1/HDAC-IN-3 is a inhibitor targeting class I HDAC and LSD1 enzymes. LSD1/HDAC-IN-3 inhibits HDAC1, HDAC2, HDAC3, and LSD1 with IC50 values of 1702 nM, 842 nM, 358 nM, and 1074 nM, respectively. LSD1/HDAC-IN-3 exhibits antioxidant effects in H2O2-stressed ARPE-19 and 661W retinal cells, increasing levels of acetylated and methylated histone H3. LSD1/HDAC-IN-3 enhances photoreceptor survival in the rd10 mouse model of retinitis pigmentosa. LSD1/HDAC-IN-3 can be used for the study of inherited retinal diseases such as retinitis pigmentosa (RP) .
Cat. No.: HY-175675
CAS No.: 3104888-50-5
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P2Y1 antagonist 4 is a selective P2Y1 receptor antagonist with excellent blood-brain barrier (BBB) penetration.
P2Y1 antagonist 4 inhibits P2Y1 receptor-mediated cytosolic Ca 2+ increase (IC50 = 1.95 μM) and platelet aggregation (IC50 = 3.24 μM) induced by ADP in rabbit washed platelets. P2Y1 antagonist 4 significantly upregulates the level of nuclear Nrf2 protein in H2O2-treated HT22 cells. P2Y1 antagonist 4 reduces myocardial infarct size in a mouse acute myocardial infarction (MI) model. P2Y1 antagonist 4 can be used for the study of ischemic stroke and myocardial infarction .
Cat. No.: HY-18542
CAS No.: 1402612-58-1
Target:
Research Areas:
Neurological Disease Metabolic Disease Inflammation/Immunology Cancer
KT195 is a serine hydrolase inhibitor that targets ABHD6 (IC50 = 10 nM) and ABHD2, with no significant activity against DAGLβ. KT195 inhibits endoplasmic reticulum calcium release and mitochondrial calcium uptake by targeting ABHD2, thereby blocking A23187 (HY-N6687) and H2O2-induced necrotic cell death and apoptosis. By inhibiting ABHD6 activity, KT195 significantly induces 2-AG accumulation in Neuro2A cells and reduces IL-1β secretion in lipopolysaccharide-treated macrophages. KT195 has been used as a negative control probe for DAGLβ and can be applied in studies of ABHD6 and ABHD2 in calcium signaling, lipid metabolism, neuronal function, and inflammatory [2] .
Cat. No.: HY-D3139
CAS No.: 2245162-94-9
Cat. No.: HY-E70987
Target:
Research Areas:
Chloroperoxidase, Caldariomyces fumago (EC 1.11.1.10) is an extracellular heme glycoenzyme containing ferriprotoporphyrin IX as the prosthetic group. Chloroperoxidase, Caldariomyces fumago (EC 1.11.1.10) is a peroxide-dependent chlorinating enzyme. It also catalyzes peroxidase-, catalase-and cytochrome P450-type reactions of dehydrogenation, H2O2 decomposition and oxygen insertion, respectively.
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
