Organo-Metalloid Compounds
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Filtered Search Results
Aobchem 5-Bromo-2-(ethylthio)benzo[d]thiazole | 95% | CAS 1286195-84-3 | C9H8BrNS2 | 250mg
5-Bromo-2-(ethylthio)benzo[d]thiazole | 95% | CAS 1286195-84-3 | C9H8BrNS2 | 250mg
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Aobchem Methyl 2-[2-(trimethylsilyl)ethynyl]benzoate | ≥95% | CAS 107793-07-7 | C13H16O2Si | 1g
Methyl 2-[2-(trimethylsilyl)ethynyl]benzoate | ≥95% | CAS 107793-07-7 | C13H16O2Si | 1g
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Aobchem 3-(Ethylthio)-4-methylbenzonitrile | 95% | CAS 1824585-70-7 | C10H11NS | 500mg
3-(Ethylthio)-4-methylbenzonitrile | 95% | CAS 1824585-70-7 | C10H11NS | 500mg
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Aobchem Ethyl 2-(2-(ethylthio)phenyl)-2-oxoacetate | 95% | CAS 2565806-75-7 | C12H14O3S | 500mg
Ethyl 2-(2-(ethylthio)phenyl)-2-oxoacetate | 95% | CAS 2565806-75-7 | C12H14O3S | 500mg
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Aobchem 6-(Ethylthio)-2-fluoronicotinic acid | 95% | CAS 3002478-04-5 | C8H8FNO2S | 1g
6-(Ethylthio)-2-fluoronicotinic acid | 95% | CAS 3002478-04-5 | C8H8FNO2S | 1g
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Aobchem 6-(Ethylthio)-4-methylnicotinic acid | 95% | CAS 2918921-26-1 | C9H11NO2S | 1g
6-(Ethylthio)-4-methylnicotinic acid | 95% | CAS 2918921-26-1 | C9H11NO2S | 1g
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Aobchem (2-(Ethylthio)phenyl)(phenyl)methanone | 95% | CAS 192586-25-7 | C15H14OS | 1g
(2-(Ethylthio)phenyl)(phenyl)methanone | 95% | CAS 192586-25-7 | C15H14OS | 1g
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Aobchem 2-Bromo-5-(ethylthio)-3-methylthiophene | 95% | C7H9BrS2 | 500mg
2-Bromo-5-(ethylthio)-3-methylthiophene | 95% | C7H9BrS2 | 500mg
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Aobchem (2-Ethoxy-5-ethylphenyl)trimethylsilane | 95% | C13H22OSi | 250mg
(2-Ethoxy-5-ethylphenyl)trimethylsilane | 95% | C13H22OSi | 250mg
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Aobchem 1-(2-(Ethylthio)phenyl)-2 2 2-trifluoroethanone | 95% | CAS 2565806-59-7 | C10H9F3OS | 500mg
1-(2-(Ethylthio)phenyl)-2 2 2-trifluoroethanone | 95% | CAS 2565806-59-7 | C10H9F3OS | 500mg
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Medchemexpress LLC Pepinh-TRIF TFA | 99.4% | 3875.54 | 10 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Pepinh-TRIF (TFA) is a 30 amino acid peptide designed to inhibit TIR-domain-containing adapter-inducing interferon-β (TRIF) signaling by disrupting the interaction between TLR and TRIF. This product is intended for research use only.
- Inhibits TIR-domain-containing adapter-inducing interferon-β (TRIF) signaling
- Disrupts interaction between TLR and TRIF
- Blocks expression and production of IL-33 stimulated by polyI:C or flagellin
- Suppresses stimulated IκB-α phosphorylation and degradation in HCECs
- Suppresses NF-κB activation with p65 protein nuclear translocation
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Medchemexpress LLC (S,R,S)-AHPC-C2-amide-benzofuranylmethyl-pyridine | 2347517-69-3 | 98.6% | C41H46N6O6S | 10MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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(S,R,S)-AHPC-C2-amide-benzofuranylmethyl-pyridine is a PROTAC small-molecule research reagent that induces ubiquitination and degradation of Smad3 while modulating HIF-α protein levels. It is intended for preclinical studies of anti-fibrosis, renal protection, and oncology mechanisms and is supplied as a high-purity solid.
- High purity (98.6%) for reliable experimental results.
- Dual-target PROTAC mechanism induces Smad3 degradation and modulates HIF-α levels.
- Suitable for preclinical research in fibrosis, renal protection, and oncology.
- Supplied as a solid and available in small research pack sizes for screening and synthesis.
- High solubility in DMSO (≥170 mg/mL) for convenient stock preparation.
- Stable under recommended storage conditions to preserve activity.
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Medchemexpress LLC (S,R,S)-AHPC-C2-amide-benzofuranylmethyl-pyridine | 2347517-69-3 | MFCD34676915 | 98.6% | 750.91 | 1 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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(S,R,S)-AHPC-C2-amide-benzofuranylmethyl-pyridine is a dual-target PROTAC that functions by facilitating the ubiquitination and degradation of Smad3, and by increasing HIF-α protein levels. This compound exhibits multi-path anti-fibrosis activity and renal protection functions.
- Suitable for research on renal anemia, prostate cancer, and other cancers
- Facilitates ubiquitination and degradation of Smad3
- Increases HIF-α protein levels
- Exhibits multi-path anti-fibrosis function
- Provides renal protection
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eMolecules 1313712-18-3 | 6-Bromo-1-(2-trimethylsilanyl-ethoxymethyl)-1H-[1,2,3]triazolo[4,5-b]pyridine | Combi-Blocks | MFCD19441852 | 329.273 | C11H17BrN4OSi | 95.000 | C[Si](C)(C)CCOCn1nnc2ncc(Br)cc12 | 1g | 388718197
6-Bromo-1-(2-trimethylsilanyl-ethoxymethyl)-1H-[1,2,3]triazolo[4,5-b]pyridine | Combi-Blocks | 1313712-18-3 | MFCD19441852 | 329.273 | C11H17BrN4OSi | 95.000 | C[Si](C)(C)CCOCn1nnc2ncc(Br)cc12 | 1g | 388718197
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Apexbio Technology LLC OSI-930 728033-96-3 10mM (in 1mL DMSO)
OSI-930 (CAS 728033-96-3) is a small molecule inhibitor targeting multiple receptor tyrosine kinases including Flt1 (IC 8 nM) KDR/VEGFR2 (IC 9 nM) CSF-1R (IC 15 nM) Lck c-Raf and Kit (IC 80 nM) In cellular studies OSI-930 inhibits proliferation and induces apoptosis in HMC-1 cells whose survival is dependent on Kit signaling while exhibiting minimal effects on COLO-205 cells under standard conditions Additionally OSI-930 inactivates cytochrome P450 3A4 in a time- and concentration-dependent manner and alters its spectral properties These characteristics make OSI-930 a valuable tool compound for investigating receptor tyrosine kinase signaling pathways and related cellular processes in cancer research
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