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Streptokinase Recombinant,produced in E.Coli is a non-glycosylated polypeptide chain containing 414 amino acids and having a molecular weight of 47 kd.
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(3S,4S)-Tofacitinib is the S-enantiomer of the JAK inhibitor tofacitinib and is provided as a research reference compound for biochemical and cellular studies. It is reported to be less active than the clinical racemate and is characterized by CAS 1092578-47-6, formula C16H20N6O, and molecular weight 312.37 g/mol.
Enantiomeric reference for JAK signaling studies.
High purity (99.75%) suitable for analytical and biochemical assays.
Molecular formula C16H20N6O and molecular weight 312.37 g/mol.
Supplied as a 10 mg research quantity.
Useful as a reference standard for selectivity and potency comparisons.
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Triamcinolone acetonide is a synthetic glucocorticoid steroid characterized by potent anti-inflammatory activity Its molecular structure allows it to penetrate cells effectively facilitating modulation of inflammatory processes by suppressing IgE-dependent histamine release from human basophils This effect interferes with mast cell-mediated allergic response pathways reducing inflammation in affected tissues Additionally Triamcinolone acetonide inhibits proliferation of specific human cell lines including the NEL-M1 melanoma cells making it particularly useful in oncology research settings involving cell growth regulation It is widely applied in biomedical investigation for studying inflammatory signaling pathways immune cell functions and cellular proliferation mechanisms relevant to dermatological autoimmune and tumor-associated inflammatory conditions
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If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link: eMolecules Building Block Tool
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Moxifloxacin HCl (186826-86-8) is a small-molecule inhibitor targeting bacterial DNA gyrase (topoisomerase II) and topoisomerase IV It is designed to inhibit these enzymes thereby disrupting essential bacterial DNA replication transcription and repair processes Moxifloxacin HCl exerts its biological activity primarily through inhibition of DNA gyrase and topoisomerase IV It demonstrates antibacterial activity against both Gram-positive and Gram-negative bacteria including ciprofloxacin-resistant strains with MIC90 values for ciprofloxacin-susceptible strains up to 0 6 g/mL Additionally moxifloxacin inhibits human serum paraoxonase-1 (hPON1) with a Ki value of 2 641 0 004 mM Based on these pharmacological properties Moxifloxacin HCl holds research potential in studying antibacterial mechanisms and enzyme-inhibitor interactions
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Gonadorelin Acetate is a synthetic peptide agonist targeting gonadotropin-releasing hormone (GnRH) receptors It is designed to bind specifically to GnRH receptors on pituitary gonadotrophs thereby modulating secretion of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) Gonadorelin Acetate exerts its biological activity primarily through receptor-mediated regulation of the reproductive hormone axis Based on these pharmacological properties Gonadorelin Acetate holds research potential in studies of reproductive hormone signaling pathways endocrine regulation associated with infertility disorders and characterization of gonadotropin responses in cellular or animal models
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Encorafenib (LGX818) is a highly potent RAF inhibitor with selective anti-proliferative and apoptotic activity in cells expressing B-RAF(V600E) with EC50 of 4 nM. Phase 3. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
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