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Filtered Search Results
Apexbio Technology LLC IK-930-25MG
IK-930 (CAS No 2563892-44-2) is a small-molecule inhibitor predominantly utilized in cancer research Originating from targeted therapy development it functions by modulating specific signaling pathways involved in tumor proliferation such as the PI3K/AKT/mTOR pathway Its in vitro activity is observed in the nanomolar to low micromolar range which underscores its potency in inhibiting cancer cell growth IK-930 is commonly used in cell models and animal studies to investigate its therapeutic potential and mechanism of action as well as in drug screening processes Experimental concentrations typically depend on the specific research design
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Chemscene CHEMSCENE
5000578244 1-BUTYL-1-METHYLIMIDAZOL 100MG
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Chemscene CHEMSCENE
5000579609 6-CHLORO-2-FLUORO-9H-PURINE 5G
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Cell Signaling Technology CELL SIGNALING TECHNOLOGY INC
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5000561068 BETA-CRYSTALLIN B1/CRYBB1 F6Y9
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Gold Biotechnology Inc Imidazole Recrystallized
Imidazole is a planar 5-membered ring It is a highly polar highly water soluble amphoteric compound Imidazole is often used to elute tagged proteins bound to metal ions attached to the surface of beads in a chromatography column by displacing the His-tag from the metal ion and freeing the His-tagged proteins
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Medchemexpress LLC Imidazole | 288-32-4 | 99.96% | 100 G
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Imidazole | 288-32-4 | 99.96% | 100 G
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Medchemexpress LLC Imidazole | 288-32-4 | 99.96% | 10 G
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Imidazole (Glyoxaline) is a heterocyclic aromatic compound. It is utilized as an inhibitor for corrosion, acetylcholinesterase (AChEI), and xanthine oxidase (XO). Imidazole demonstrates various biological activities including antifungal, antituberculosis, anti-inflammatory, antioxidant, and analgesic properties.
- Inhibits enzymatic conversion of endoperoxides to thromboxane A2
- Derivatives show inhibition of the SARS-CoV-2 3CLPro enzyme
- Potential for research in Alzheimer's disease, gout, and COVID-19
- Suitable for laboratory centrifugation and storage
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Medchemexpress LLC 3- 2-THIENYL -L-ALAN 10G
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3- 2-THIENYL -L-ALAN 10G
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Medchemexpress LLC 3- 2-THIENYL -D-ALAN 10G
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3- 2-THIENYL -D-ALAN 10G
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eMolecules 288-32-4 | Imidazole, ACS grade | Oakwood Chemical | MFCD00005183 | 68.079 | C3H4N2 | 99.000 | c1c[nH]cn1 | 500g | 788479283
Imidazole, ACS grade | Oakwood Chemical | 288-32-4 | MFCD00005183 | 68.079 | C3H4N2 | 99.000 | c1c[nH]cn1 | 500g | 788479283
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eMolecules 91524-96-8 | 2-Chlorothiazolo[5,4-b]pyridine | Combi-Blocks | MFCD13190222 | 170.610 | C6H3ClN2S | 97.000 | Clc1nc2cccnc2s1 | 10g | 448003055
2-Chlorothiazolo[5,4-b]pyridine | Combi-Blocks | 91524-96-8 | MFCD13190222 | 170.610 | C6H3ClN2S | 97.000 | Clc1nc2cccnc2s1 | 10g | 448003055
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eMolecules 57090-88-7 | 4-Cyanoimidazole | Ambeed | MFCD00233358 | 93.089 | C4H3N3 | 98.000 | N#Cc1c[nH]cn1 | 10g | 525042677
4-Cyanoimidazole | Ambeed | 57090-88-7 | MFCD00233358 | 93.089 | C4H3N3 | 98.000 | N#Cc1c[nH]cn1 | 10g | 525042677
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Medchemexpress LLC VRT-534 | 926664-32-6 | 98.3% | 497.99 | 25 MG
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VRT-534 is a chemical chaperone that specifically targets connexin 26 (Cx26). It demonstrates dose-responsive binding to recombinant wild-type Cx26 and mutant Cx26 K188N. This compound can be utilized in research pertaining to hearing impairment and has shown restorative effects on Cx26 mutants in HeLa cells.
- Exhibits dose-responsive binding to Cx26
- Restores vitality of HeLa cells
- Useful in research for hearing impairment
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Medchemexpress LLC CP-289,503 | 1349637-14-4 | 98.2% | 491.06 | 100 MG
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CP-289,503 is an inhibitor of the complement C5a receptor with an IC50 of 1 μM. C5a activates leukocytes and phagocytes during complement system activation. The C5a receptor binds to C5a, stimulating the upregulation of cell surface integrins and degranulation of inflammatory cells, leading to endothelial cell damage. C5a receptor inhibitors can block C5a signaling and inhibit a variety of inflammatory diseases.
- C5a receptor inhibitor
- For research use only
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Medchemexpress LLC HWY-289 | 908001-51-4 | 98.0% | 562.49 | 5 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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HWY-289 is a semisynthetic protoberberine derivative that exhibits broad-spectrum and potent activities against phytopathogenic fungi, especially *Botrytis cinerea*. It works by altering the morphology of the mycelium and the internal structure of fungal cells, and it also reduces ATP content, ATPase activities, and key enzyme activities within the TCA cycle.
- Exhibits broad-spectrum and potent activity against phytopathogenic fungi.
- Particularly effective against *Botrytis cinerea*.
- Alters the morphology of the mycelium and internal structure of fungal cells.
- Reduces ATP content, ATPase activities, and key enzyme activities in the TCA cycle.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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