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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
33 Results for "
A16
" in MedChemExpress (MCE) Product Catalog:
Products (33)
33 Results for "A16" in MCE Product Catalog:
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DC07090 dihydrochloride is a low toxicity, potent, reversible and competitive non-peptidyl human enterovirus 71 3C protease inhibitor with an IC50 and a Ki value for 21.72 μM and 23.29 μM. DC07090 dihydrochloride could also inhibit coxsackievirus A16 (CVA16) replication with an EC50 value of 27.76 μM .
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GPX4-IN-9 (Compound A16) is a glutathione peroxidase 4 (GPX4) inhibitor that specifically targets GPX4 under both in vitro and in vivo conditions, inducing ferroptosis. GPX4-IN-9 exhibits cytotoxicity against pancreatic cancer cells and can be used in cancer research .
Cat. No.: HY-175830
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PROTAC AURKA degrader 1 (Compound A16 + X7) is a Aurora kinase A (AURKA) PROTAC degrader. PROTAC AURKA degrader 1 can be used for cancers research . Pink: AURKA ligand (HY-175827); Blue: CRBN ligase ligand (HY-W867704); Black: linker (HY-132208)
Cat. No.: HY-P4792
CAS No.: 1374694-00-4
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Cat. No.: HY-178801
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SDH-IN-39 (Compound A16) is a SDH inhibitor, with an IC50 value of 6.83 μg/mL. SDH-IN-39 is also an antifungal agent. SDH-IN-39 shows antifungal activity against Rhizoctonia solani (EC50 of 1.49 μg/mL), G. zeae, C. gloeosporioides, S. sclerotiorum and M. oryzae .
Cat. No.: HY-123517A
CAS No.: 879070-72-1
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DC07090 is a potent, reversible and competitive non-peptidyl human enterovirus 71 3C protease inhibitor with an IC50 and a Ki value for 21.72 μM and 23.29 μM. DC07090 could also inhibit coxsackievirus A16 (CVA16) replication with an EC50 value of 27.76 μM .
Cat. No.: HY-P10802
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Cat. No.: HY-170846
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FGFRs-IN-1 (Compound A16) is the orally active inhibitor for FGFR, that inhibits FGFR1/2/3/4 with IC50s of 2.3, 7, 11, and 163 nM, respectively. FGFRs-IN-1 also inhibits VEGFR1/2/3, Abl, and Flt3 with IC50s of 61, 176, 112, 26, and 353 nM, respectively. FGFRs-IN-1 exhibits weak inhibitory efficacy against CYP enzymes. FGFRs-IN-1 reduces the expression of α-SMA and collagen I, and inhibits epithelial-mesenchymal transition (EMT) in TGF-β1 stimulated A549 cell. FGFRs-IN-1 exhibits anti-inflammatory activity in Bleomycin (HY-17565)-induced mouse pulmonary fibrosis model and CCl4 (HY-Y0298)-induced mouse liver fibrosis model .
Cat. No.: HY-P76280
Purity: ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: Coxsackievirus A16 (Cox A16) (strain G-10) VP4 Protein; VP1 Protein; CV
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Cat. No.: HY-P76281
Purity: ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: Coxsackievirus A16 (Cox A16) (strain G-10) VP4 Protein; VP4 Protein; CV
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Cat. No.: HY-N13105
CAS No.: 87387-63-1
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Cat. No.: HY-CE00489
Synonyms: 16-Methyldocosanoyl-coenzyme A
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16-Methyldocosanoyl-CoA (16-Methyldocosanoyl-coenzyme A) is a coenzyme A derivative.
Cat. No.: HY-CE00491
Synonyms: 16-Methylhenicosanoyl-coenzyme A
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16-Methylhenicosanoyl-CoA (16-Methylhenicosanoyl-coenzyme A) is a coenzyme A derivative.
Cat. No.: HY-CE00492
Synonyms: 16-Methylheptadecanoyl-coenzyme A
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16-Methylheptadecanoyl-CoA (16-Methylheptadecanoyl-coenzyme A) is a coenzyme A derivative.
Cat. No.: HY-CE00494
Synonyms: 16-Methylicosanoyl-coenzyme A
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16-Methylicosanoyl-CoA (16-Methylicosanoyl-coenzyme A) is a coenzyme A derivative.
Cat. No.: HY-CE00498
Synonyms: 16-Methylpentacosanoyl-coenzyme A
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16-Methylpentacosanoyl-CoA (16-Methylpentacosanoyl-coenzyme A) is a coenzyme A derivative.
Cat. No.: HY-CE00499
Synonyms: 16-Methyltetracosanoyl-coenzyme A
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16-Methyltetracosanoyl-CoA (16-Methyltetracosanoyl-coenzyme A) is a coenzyme A derivative.
Cat. No.: HY-CE00501
Synonyms: 16-Methyltricosanoyl-coenzyme A
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16-Methyltricosanoyl-CoA (16-Methyltricosanoyl-coenzyme A) is a coenzyme A derivative.
Cat. No.: HY-CE00508
Synonyms: 16-Methylnonadecanoyl-coenzyme A
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16-Methylnonadecanoyl-CoA (16-Methylnonadecanoyl-coenzyme A) is a coenzyme A derivative.
Cat. No.: HY-RS12377
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S100A16 Human Pre-designed siRNA Set A contains three designed siRNAs for S100A16 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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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
