Carboxylic acids and derivatives
Selleck Chemical LLC Menadiol Diacetate S4779-25mg
Menadiol Diacetate (Vitamin K4 Acetomenaphthone Kapilin) is a synthetic hydrophilic menadione compound which is clinically used as hemostasis medicine It induces caspase-3-related apoptosis pathway via mitochondrial dysfunction and DNA fragmentation
eMolecules 100957-85-5 | 1-Benzyl-3-(tert-butyl)-1h-pyrazole-5-carboxylic acid | Combi-Blocks | MFCD02090479 | 258.321 | C15H18N2O2 | 96.000 | CC(C)(C)c1cc(C(O)=O)n(Cc2ccccc2)n1 | 5g | 232313711
1-Benzyl-3-(tert-butyl)-1h-pyrazole-5-carboxylic acid | Combi-Blocks | 100957-85-5 | MFCD02090479 | 258.321 | C15H18N2O2 | 96.000 | CC(C)(C)c1cc(C(O)=O)n(Cc2ccccc2)n1 | 5g | 232313711
Teknova 20mM Sodium Citrate, 8% Sucrose, pH 6.0. 500mL, Endotoxin Tested, Sterile. 8 pack.
20mM Sodium Citrate, 8% Sucrose, pH 6.0. 500mL, Endotoxin Tested, Sterile. 8 pack.
Medchemexpress LLC Lei-101 hydrochloride | 2250025-91-1 | 99.4% | 508.99 | C23H26ClFN4O4S | 100MG
LEI-101 is a potent, selective cannabinoid CB2 receptor agonist used for biochemical and pharmacological research. It shows high selectivity for CB2 over CB1, is orally bioavailable, and is supplied as a solid for laboratory studies. Intended for research use only (not for human use).
- Selective CB2 receptor agonist with approximately 100-fold selectivity over CB1.
- Orally bioavailable, suitable for in vivo pharmacology studies.
- High purity (99.35%).
- Molecular weight 508.99 and formula C23H26ClFN4O4S.
- Soluble in DMSO (approx. 116.7 mg/mL).
- Intended for laboratory research use only, not for human consumption.
Medchemexpress LLC Filgotinib (maleate) | 1802998-75-9 | 99.88% | 541.58 | 1 ML
Filgotinib maleate (GLPG0634 maleate) is a selective, orally available JAK1 inhibitor with anti-inflammatory and antiviral activities. It can effectively inhibit the activities of JAK1, JAK2, JAK3, and TYK2. This compound also inhibits HIV-1 driven gene transcription and reduces proliferation of HIV-1 infected cells. It can be used in the study of rheumatoid arthritis and inflammatory bowel disease.
- Selective, orally available JAK1 inhibitor
- Anti-inflammatory and antiviral activities
- Inhibits activities of JAK1, JAK2, JAK3, and TYK2
- Inhibits HIV-1 driven gene transcription
- Reduces proliferation of HIV-1 infected cells
- Suitable for research in rheumatoid arthritis and inflammatory bowel disease
Chem-Impex International, Inc. 2-Cyanoacetamide | MFCD00008024 | 25G
2-Cyanoacetamide, MFCD00008024, 25G
Chem-Impex International, Inc. 2-Cyanoacetamide | MFCD00008024 | 1KG
2-Cyanoacetamide, MFCD00008024, 1KG
eMolecules 5447-60-9 | 5-Keto-d-gluconic acid potassium salt | MFCD00069562 | 1g
Combi-Blocks | 5-Keto-d-gluconic acid potassium salt | 1g | 232324007 | QB-5160 | 95.000 | 5447-60-9 | MFCD00069562 | 232.229 | C6H9KO7
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Medchemexpress LLC Cytidine 5'-triphosphate disodium salt | 36051-68-0 | MFCD00078193 | >97.0% | 527.12 g/mol | C9H14N3Na2O14P3 | 1ML
CTP disodium salt is a ready-to-use, PCR-grade 100 mM solution of cytidine-5'-triphosphate (disodium salt) supplied in a 1 mL vial. The formulation is qualified for molecular biology use and is intended as a nucleotide substrate for enzymatic reactions and nucleic acid synthesis.
Medchemexpress LLC 3-Methoxybenzamide | 5813-86-5 | 99.4% | 25 MG
3-methoxybenzamide is a small-molecule inhibitor of ADP-ribosyltransferases (ADPRTs) and poly(ADP-ribose) polymerases (PARPs), supplied as a high-purity solid for research use in biochemical assays and enzymatic studies.
- High purity (99.4%).
- Molecular weight 151.16 g/mol.
- Molecular formula C8H9NO2.
- Supplied as a solid powder with recommended cold storage.
- Available in small research sizes including a 25 mg vial.
eMolecules 10489-74-4 | Ethyl aminohydroxyiminoacetate | Combi-Blocks | MFCD03013442 | 132.119 | C4H8N2O3 | 98.000 | CCOC(=O)C(\N)=N/O | 25g | 335351474
Ethyl aminohydroxyiminoacetate | Combi-Blocks | 10489-74-4 | MFCD03013442 | 132.119 | C4H8N2O3 | 98.000 | CCOC(=O)C(\N)=N/O | 25g | 335351474
Medchemexpress LLC N-(3-(5-chloro-2-(difluoromethoxy)phenyl)-1-(2-(4-((2-cyanoethyl)(methyl)amino)piperidin-1-yl)-2-oxoet | 1831144-46-7 | 99.9% | 612.03 | C28H28ClF2N9O3 | 10MG
iJak-381 is a selective JAK1/2 inhibitor for laboratory research, used to study Janus kinase-mediated cytokine signaling and inflammatory responses. It has reported activity against IL-13, IL-4, and IL-6 pathways and has been evaluated in preclinical studies for lung-restricted inhalation delivery.
- Selective JAK1/2 inhibitor for research applications.
- Blocks IL-13, IL-4, and IL-6 signaling pathways.
- Lung-restricted profile suitable for respiratory disease models.
- High purity for reproducible experimental results.
- Supplied as a 10 mg research sample.
- Molecular formula C28H28ClF2N9O3, molecular weight 612.03.