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Filtered Search Results
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000283051 N-ETHYLGLYCINE 5G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000283824 GLYCOFUROL 25G
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Medchemexpress LLC N-ACETYLSULFANILAMID 5G
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N-ACETYLSULFANILAMID 5G
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Medchemexpress LLC 2-ETHYLPYRAZINE 50G
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2-ETHYLPYRAZINE 50G
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Medchemexpress LLC GRP75-IN-1 dihydrochloride | 99.75% | 539.60 | 25 MG
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GRP75-IN-1 hydrochloride (compound 33) is an anti-endometrial cancer (EC) agent that induces apoptosis. It reduces Ca2+ levels in mitochondria by targeting GRP75 and disrupting its interaction with IP3R. This product is for research use only and not for sale to patients.
- Antitumor agent
- Induces apoptosis
- Targets GRP75
- Disrupts interaction with IP3R
- Reduces mitochondrial Ca2+ levels
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000742707 N-SUCCINIMIDYL BROMO 5G
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Medchemexpress LLC N-BENZOYLIMIDAZOLE 5G
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N-BENZOYLIMIDAZOLE 5G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000744924 2 2-OXYBISETHYLAMIN 100G
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Medchemexpress LLC Norcyclizine | 841-77-0 | 99.7% | 252.35 | 25 G
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Norcyclizine is a piperazine compound used for the synthesis of antimicrobial and anticancer agents. It enhances the antibacterial activity of β-lactam antibiotics against Methicillin-resistant Staphylococcus aureus (MRSA) by inhibiting the allosteric site of PBP2a.
- Used for the synthesis of antimicrobial agents
- Enhances antibacterial activity of β-lactam antibiotics against MRSA
- Inhibits the allosteric site of PBP2a
- Serves as a pharmacological scaffold for synthesizing anticancer agents
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000760563 MIL-101CR F FREE 5G
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Medchemexpress LLC Bromo-PEG1-C2-azide | 1144106-65-9 | 99.5% | C4H8BrN3O | 25MG
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Bromo-PEG1-C2-azide is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. It functions as a click chemistry reagent due to its azide group, enabling it to undergo copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with molecules containing alkyne groups. It can also participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules possessing DBCO or BCN groups. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Functions as a click chemistry reagent
- Contains an azide group
- Undergoes copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc)
- Participates in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions
- Utilizes the intracellular ubiquitin-proteasome system
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Medchemexpress LLC TETRALIN 100G
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TETRALIN 100G
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Medchemexpress LLC PTX-35 1 mg
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PTX-35 1MG
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Medchemexpress LLC BSJ-02-162 | 2139329-47-6 | 98.1% | C43H49N11O7 | 1 ML
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BSJ-02-162, also known as CDK4/6-IN-11, is a potent PROTAC CDK4/6 degrader. It is specifically designed with a thalidomide-based E3 ligase ligand, Palbociclib as a target protein ligand, and a PROTAC linker, making it suitable for targeted protein degradation studies.
- Potent PROTAC CDK4/6 degrader
- Composed of a thalidomide-based E3 ligase ligand
- Includes a target protein ligand
- Features a PROTAC linker
- Available in solid and solution formats
- Soluble in DMSO
- Store powder at -20°C for 3 years, 4°C for 2 years
- Store in solvent at -80°C for 6 months, -20°C for 1 month
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000747238 VUTRISIRAN SODIUM 1MG
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