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Filtered Search Results
Aqua Solutions TBC 10 000 UG/ML MEOH 100ML
TBC 10 000 UG/ML MEOH 100ML ..
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Aqua Solutions Silver Nitrate 0.02 Normal NIST Traceable, Solution (1L)
Silver Nitrate 0.02 Normal NIST Traceable, Solution (1L)
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Aqua Solutions CDTA Titrant 0.00200 Normal NIST Traceable Solution (10L)
CDTA Titrant 0.00200 Normal NIST Traceable Solution (10L)
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Aqua Solutions SILVER NITRATE,.02% 4L
Silver Nitrate 0.02 Normal Aqueous Solution N.i.s.t. Traceable
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Aqua Solutions Potassium Thiocyanate (500ML)
Potassium Thiocyanate (500ML)
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Aqua Solutions Potassium Iodide 10% w/v Solution (500ML)
Potassium Iodide 10% w/v Solution (500ML)
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Aqua Solutions Hydrazine Standard 1,000 ppm as N₂H₂ Preserved with 3.5% HNO₃ (500ML)
Hydrazine Standard 1,000 ppm as N₂H₂ Preserved with 3.5% HNO₃ (500ML)
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Medchemexpress LLC RIP1 kinase inhibitor 1 | 2095515-38-9 | 99.96% | 461.90 | 10 MG
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RIP1 kinase inhibitor 1 (compound 22) is a highly potent, orally available, and brain-penetrating RIP1 kinase inhibitor with a pKi of 9.04. It strongly suppresses necroptotic cell death and phosphorylation of MLKL in human colorectal adenocarcinoma HT-29 cells and mouse L-cells NCTC 929.
- Highly potent and orally available
- Brain-penetrating RIP1 kinase inhibitor
- Suppresses necroptotic cell death
- Inhibits phosphorylation of MLKL
- Effective in human colorectal adenocarcinoma HT-29 cells
- Effective in mouse L-cells NCTC 929
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LaMarKa Chemical Company Hydrochloric Acid 1.0N Phenolphthalein Endpoint, 500ml
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Hydrochloric Acid 1.0N Phenolphthalein Endpoint, 500ml Plastic Bottle
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Sigma Aldrich Fine Chemicals Biosciences Chromeceptin >=98% (HPLC), solid | 331859-86-0 | MFCD00815850 | 5MG
Chromeceptin >=98% (HPLC), solid | Purity: >=98% (HPLC) | Mol Wt: 359.35 | 331859-86-0 | MFCD00815850 | 5MG
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Apexbio Technology LLC Dynamin inhibitory peptide 251634-21-6 10mg
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Dynamin inhibitory peptide (CAS 251634-21-6) is a peptide-based inhibitor targeting the GTPase dynamin It is designed to competitively block the interaction between dynamin and amphiphysin proteins thereby inhibiting dynamin-dependent internalization pathways Dynamin inhibitory peptide exerts its biological activity primarily by disrupting dynamin amphiphysin binding This mechanism effectively inhibits endocytic processes and reduces receptor internalization including the cellular uptake of GABA receptors in neuronal models Based on these pharmacological properties Dynamin inhibitory peptide holds research potential in the study of vesicle trafficking inhibition of endocytic pathways and modulation of receptor internalization
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![Medchemexpress LLC Glycine, N,N-bis[2-(2,6-dioxo-4-morpholinyl)ethyl]- | 23911-26-4 | ≥97.0% | 357.32 | 25 G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000366890-logo.png-250.jpg){kind=logo}
Medchemexpress LLC Glycine, N,N-bis[2-(2,6-dioxo-4-morpholinyl)ethyl]- | 23911-26-4 | ≥97.0% | 357.32 | 25 G
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DTPA anhydride is a bifunctional chelator whose anhydride can react with amino groups in proteins (such as lysine residues) to form stable amide bonds. It can also bind to radionuclides to synthesize radionuclide-labeled drug conjugates (RDCs). RDCs have the ability to specifically target biomolecules and can be used in medical imaging or therapy.
- Bifunctional chelator
- Reacts with amino groups in proteins
- Forms stable amide bonds
- Binds to radionuclides
- Synthesizes radionuclide-labeled drug conjugates (RDCs)
- RDCs can specifically target biomolecules
- Used in medical imaging or therapy
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Medchemexpress LLC LDN-27219 | 312946-37-5 | 99.6% | 408.50 | 1 ML
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LDN-27219 | 312946-37-5 | 99.6% | 408.50 | 1 ML
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Sigma Aldrich Fine Chemicals Biosciences Poly(acrylic acid) partial potassium salt <1000 mum particle size | 25608-12-2 | MFCD00217695 | 1KG
Poly(acrylic acid) partial potassium salt <1000 mum particle size | 25608-12-2 | MFCD00217695 | 1KG
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Medchemexpress LLC Grazoprevir potassium salt | 1206524-86-8 | C38H49KN6O9S | 50 MG
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Grazoprevir potassium salt is a selective inhibitor of Hepatitis C virus (HCV) NS3/4a protease, demonstrating broad activity across various genotypes and resistant variants. It also inhibits SARS-CoV-2 3CLpro activity. This compound has shown efficacy in vivo against chronic-HCV-infected chimpanzees and good plasma and liver exposure in dogs, highlighting its potential as an antiviral agent.
- Selective inhibitor of Hepatitis C virus NS3/4a protease
- Broad activity across genotypes and resistant variants
- Effective against major genotypes and common resistant mutations
- Inhibits SARS-CoV-2 3CLpro activity
- Demonstrates subnanomolar to low-nanomolar EC50s against genotypes 1a, 1b, and 2a
- Maintains excellent potency against HCV replication mutants
- Shows efficacy against chronic-HCV-infected chimpanzees
- Achieves good plasma and high liver exposure in dogs
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