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Filtered Search Results
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000283776 BENZYL 5-HYDROXYPEN 500MG
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Medchemexpress LLC Azido-PEG4-alcohol | 86770-67-4 | 98.9% | 219.24 | 25 G
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Azido-PEG4-alcohol is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. It functions as a click chemistry reagent, featuring an Azide group capable of undergoing copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules possessing Alkyne groups. It can also participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Click chemistry reagent
- Contains an azide group
- Undergoes copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with alkyne groups
- Undergoes strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups
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Medchemexpress LLC 3-chlorogentisyl alcohol | 32744-80-2 | 99.7% | 174.58 g/mol | C7H7ClO3 | 10 MG
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3-Chlorogentisyl alcohol is a small-molecule inhibitor of E. coli β-glucuronidase with reported antiproliferative activity. It is provided as a high-purity solid for biochemical and enzyme inhibition research.
- Potent E. coli β-glucuronidase inhibitor (IC50 0.74 μM; Ki 0.58 μM).
- Molecular formula C7H7ClO3; molecular weight 174.58 g/mol.
- Purity 99.7%.
- Available as solid quantities (including 10 mg) and as a 10 mM solution in DMSO.
- Appearance off-white to light yellow solid.
- Storage: powder -20°C; in solvent -80°C for 6 months, -20°C for 1 month.
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eMolecules 4-Bromo-3-iodobenzyl alcohol | 1261776-05-9 | MFCD18391657 | 1g
Apollo Scientific | 4-Bromo-3-iodobenzyl alcohol | 1g | 562429305 | OR400084 | | 1261776-05-9 | MFCD18391657 | 312.932 | C7H6BrIO
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eMolecules 2-Bromo-3-methoxybenzyl alcohol | 199436-55-0 | MFCD18391884 | 1g
Apollo Scientific | 2-Bromo-3-methoxybenzyl alcohol | 1g | 562429527 | OR400088 | | 199436-55-0 | MFCD18391884 | 217.062 | C8H9BrO2
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Apexbio Technology LLC APEXBIO TECHNOLOGY LLC
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5000569937 VERATRYL-ALCOHOL-200MG
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eMolecules 3-Chloro-5-iodobenzyl alcohol | 912343-40-9 | MFCD18393356 | 1g
Apollo Scientific | 3-Chloro-5-iodobenzyl alcohol | 1g | 591806637 | OR400250 | 95.000 | 912343-40-9 | MFCD18393356 | 268.480 | C7H6ClIO
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eMolecules 2,4-Dibromo-6-fluorobenzyl alcohol | 497181-22-3 | MFCD03094090 | 1g
Apollo Scientific | 2,4-Dibromo-6-fluorobenzyl alcohol | 1g | 591806670 | PC0744 | 95.000 | 497181-22-3 | MFCD03094090 | 283.922 | C7H5Br2FO
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eMolecules 2-Bromo-6-iodobenzyl alcohol | 1261850-41-2 | MFCD11520412 | 1g
Apollo Scientific | 2-Bromo-6-iodobenzyl alcohol | 1g | 562428664 | OR400119 | 95.000 | 1261850-41-2 | MFCD11520412 | 312.932 | C7H6BrIO
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Sigma Aldrich Fine Chemicals Biosciences Benzyl alcohol ACS reagent
Benzyl alcohol (BnOH) is a monoaromatic primary alcohol widely used as a solvent and an intermediate in cosmetic formulations pharmaceutical and flavor/fragrance industries. It shows bacteriostatic property. Commercial method for its synthesis is by the alkaline hydrolysis of benzyl chloride. Conformational studies by ab initio calculations shows gauche cis conformation around the alcoholic group.
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Medchemexpress LLC Aminooxy-PEG2-alcohol | 185022-12-2 | MFCD30182047 | 95.0% | 121.14 g·mol⁻¹ | C4H11NO3 | 250 MG
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Aminooxy-PEG2-alcohol is a short, bifunctional polyethylene glycol (PEG) linker bearing an aminooxy functional group and a terminal alcohol. It is used as a non-cleavable linker in antibody-drug conjugate (ADC) synthesis and as a PEG-based linker for PROTAC and other bioconjugation applications. Lot-specific purity and handling details are provided in the certificate of analysis.
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eMolecules Ambeed / 4-Methylbenzyl Phenyl Ketone / 1g / 600847504 / A771498 / / 2430-99-1 / MFCD00017513 / 210.276 / C15H14O
Ambeed / 4-Methylbenzyl Phenyl Ketone / 1g / 600847504 / A771498 / / 2430-99-1 / MFCD00017513 / 210.276 / C15H14O
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Medchemexpress LLC 1H-Indole-3-methanol, 1-(phenylmethyl)- | 60941-76-6 | 237.30 | 5 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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1-Benzyl-I3C is an E1/E2/E3 enzyme inhibitor, specifically a NEDD4-1 inhibitor, demonstrating significant anticancer activity. It directly inhibits the ubiquitination activity of NEDD4-1 with an IC50 of 12.3μM, which is considerably more potent than its precursor compound I3C. In vitro ubiquitination experiments and thermal stability analysis indicate that 1-Benzyl-I3C binds to the catalytic HECT domain of NEDD4-1. This product is for research use only.
- Inhibits E1/E2/E3 enzymes
- Shows significant anticancer activity
- Binds to the catalytic HECT domain of NEDD4-1
- High purity of 99.68%
- White to off-white solid appearance
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eMolecules N-(3,4-dimethoxybenzyl)-6-chloropyridazin-3-amine | 1155466-26-4 | MFCD12478964 | 1g
Broadpharm | N-(3,4-dimethoxybenzyl)-6-chloropyridazin-3-amine | 1g | 112542162 | BP-20043 | 97.000 | 1155466-26-4 | MFCD12478964 | 279.720 | C13H14ClN3O2
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![eMolecules Ambeed / (S)-2-Nitro-6-((4-(trifluoromethoxy)benzyl)oxy)-67-dihydro-5H-imidazo[21-b][13]oxazine / 1mg / 525120839 / A204906 / / 187235-37-6 / MFCD06809939 / 359.261 / C14H12F3N3O5](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502431628.PNG-250.jpg)
eMolecules Ambeed / (S)-2-Nitro-6-((4-(trifluoromethoxy)benzyl)oxy)-67-dihydro-5H-imidazo[21-b][13]oxazine / 1mg / 525120839 / A204906 / / 187235-37-6 / MFCD06809939 / 359.261 / C14H12F3N3O5
Ambeed / (S)-2-Nitro-6-((4-(trifluoromethoxy)benzyl)oxy)-67-dihydro-5H-imidazo[21-b][13]oxazine / 1mg / 525120839 / A204906 / / 187235-37-6 / MFCD06809939 / 359.261 / C14H12F3N3O5
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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