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Filtered Search Results
Cell Signaling Technology Ruxolitinib 5 mg
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Ruxolitinib 5 mg
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Cell Signaling Technology CDDO-Me 5 mg
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CDDO-Me 5 mg
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Medchemexpress LLC Cytochrome P450 1B1 | 50UL
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Cytochrome P450 1B1 | 50UL
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TARGETMOL CHEMICALS INC CALCIUM CHANNEL-MODULATO 5MG
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Calcium channel-modulator-1 is a calcium channel-modulator (IC500.8 uM) with specialisation to block aortic constriction. purity: 99%
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Medchemexpress LLC Sirtuin modulator 3 5mg | 5mg
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Sirtuin modulator 3 (compound 129) is a N-phenyl benzamide derivative acts as a sirtuin modulator[1]
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Medchemexpress LLC (+)-LRH-1 modulator-1 | 99.38% | 464.66 | 1 MG
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(+)-LRH-1 modulator-1 is a stereoisomer of LRH-1 modulator-1, which is a potent LRH-1 (liver receptor homolog-1) modulator/agonist. It exhibits anti-inflammatory effects in intestinal organoids by inducing the anti-inflammatory cytokine IL-10 and reducing the inflammatory cytokines IL-1b and TNFa.
- Potent LRH-1 modulator/agonist
- Demonstrates anti-inflammatory effects
- Induces IL-10 cytokine
- Reduces IL-1b and TNFa cytokines
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Medchemexpress LLC Promethazine sulfoxide | 7640-51-9 | MFCD08063694 | 10mg
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Promethazine sulfoxide is a metabolite of the histamine H1 receptor antagonist Promethazine (HY-B1296) It is formed from promethazine by the cytochrome P450 (CYP) isoform CYP2D6
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Medchemexpress LLC Glp-1r modulator l7-028 | 2648317-95-5 | 99.5% | C24H28N2O3 | 1 ML
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GLP-1R modulator L7-028 is an allosteric modulator that enhances GLP-1 binding to GLP-1R through a transmembrane site, with an EC50 of 11.01 ± 2.73 μM.
- Allosteric modulator
- Enhances GLP-1 binding to GLP-1R via a transmembrane site
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Medchemexpress LLC IL-17 modulator 1 (disodium) | 2446803-91-2 | 98.4% | C28H35N6Na2O6P | 25 MG
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IL-17 modulator 1 disodium is an orally active, highly efficacious small molecule IL-17 modulator. It is designed for research into diseases such as psoriasis, ankylosing spondylitis, and psoriatic arthritis. The disodium salt form provides enhanced water solubility and stability, making it suitable for various research applications.
- Orally active and highly efficacious small molecule
- Enhanced water solubility and stability
- Useful for research into psoriasis
- Useful for research into ankylosing spondylitis
- Useful for research into psoriatic arthritis
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Cell Signaling Technology A23187 Calcimycin 5 mg
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A23187 (Calcimycin) 5 mg
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Cell Signaling Technology NVP-BEZ235 5 mg
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NVP-BEZ235 5 mg
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Medchemexpress LLC Mutant p53 modulator-1 | 2746371-35-5 | 99.9% | C27H32F4N8O2 | 50 MG
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Mutant p53 modulator-1 is a mutant p53 modulator that reduces the progression of cancers containing a p53 mutation.
- Molecular weight: 576.59
- Appearance: Solid
- Color: Light yellow to brown
- Solubility in DMSO: 100 mg/mL (173.43 mM)
- Storage (powder): -20°C for 3 years, 4°C for 2 years
- Storage (in solvent): -80°C for 6 months, -20°C for 1 month
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Cell Signaling Technology Iodoacetamide, PTMScan(R) Qualified 5 g
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Iodoacetamide, PTMScan(R) Qualified 5 g
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Medchemexpress LLC Hsp110/sGC-modulator-1 | 99.6% | 490.86 g·mol⁻1 | C24H18ClF3N2O4 | 10 MG
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Hsp110/sGC-modulator-1 is an orally active small-molecule regulator that modulates Hsp110 and soluble guanylate cyclase (sGC). It demonstrates potent dual-target activity, produces vasodilatory effects, and attenuates pulmonary vascular remodeling and right ventricular hypertrophy in preclinical studies. Supplied in milligram quantities for research use only. Molecular formula C24H18ClF3N2O4; molecular weight 490.86 g·mol⁻1; reported purity 99.58%.
- Dual-target activity against Hsp110 and sGC.
- Demonstrated vasodilatory and antiproliferative effects in preclinical models.
- Suitable for in vitro and in vivo preclinical research.
- Supplied in milligram quantities for screening and lead optimization.
- Reported purity 99.58% and characterized by HRMS.
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Research Products International Corp 4Meth BDGalact 6 Sulf Sod 50MG
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Fluorescent substrate for Morquio A Sulphatase.
- 4-Methylumbelliferone: <100PPM
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