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Filtered Search Results
eMolecules 1261590-48-0 | Medchem Express | Duvelisib (R enantiomer) | 5mg | 446268210 | HY-17044A | MFCD30187518 | 416.87 | C22H17ClN6O
Ambeed | 2-Ethylhexyl 3-(35-di-tert-butyl-4-hydroxyphenyl)propanoate | 250mg | 696731383 | A1364274 | 144429-84-5 | 390.608 | C25H42O3
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Cayman Chemical ANTIBODY LysoFP-NO2 25mg
A turn-on lysosome-targeted fluorescent probe for CO; transformed into the highly fluorescent derivative lysoFP-NH2 in the presence of lysosomal CO; selective for CO over reactive nitrogen, oxygen, and sulfur species; ex/em = 440/528 nm, respectively; not cytotoxic to HepG2 cells for up to five hours at 30 µM
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eMolecules 935-69-3 | Ambeed | 7-Methyl-7H-purin-6-amine | 100mg | 600851603 | A574718 | MFCD00127790 | 149.157 | C6H7N5
Ambeed | 7-Methyl-7H-purin-6-amine | 100mg | 600851603 | A574718 | 935-69-3 | MFCD00127790 | 149.157 | C6H7N5
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Medchemexpress LLC Caerulomycin A 100mg | 21802-37-9 | 100 MG
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Caerulomycin A is a natural-product antifungal and antibiotic research compound (CAS 21802-37-9) that modulates immune signaling by enhancing TGF-β-Smad3 and suppressing interferon-γ-induced STAT1 pathways. It is supplied as a solid for laboratory research with reported purity ≥98% and molecular weight 229.23 g·mol-1.
- Antifungal and antibiotic activity.
- Modulates TGF-β-Smad3 and STAT1 signaling.
- Supplied as milligram-scale solid for research use only.
- Reported purity ≥98% (HPLC where reported).
- Soluble in DMSO; store refrigerated or frozen for long-term stability.
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eMolecules 2250025-92-2 | Medchem Express | DREADD agonist 21 (dihydrochloride) | 5mg | 761506071 | HY-100234A | 351.28 | C17H20Cl2N4
Ambeed | 22-Disulfanediyldiethanamine | 250mg | 716187862 | A1114607 | 51-85-4 | MFCD01002952 | 152.270 | C4H12N2S2
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Medchemexpress LLC Mi-389 | 2222635-92-7 | 99.3% | 654.69 g/mol | C35H35FN6O6 | 5 MG
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MI-389 is a proteolysis-targeting chimera (PROTAC) that degrades the translation termination factor GSPT1 through recruitment of the CRL4CRBN E3 ligase. It is provided as a research-grade small molecule with reported antiproliferative activity in leukemia cell lines and is intended for in vitro and cellular studies.
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Medchemexpress LLC HZX-02-059 | 2240205-30-3 | 99.4% | 487.48 | 100 MG
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HZX-02-059 is a potent methuosis inducer and a dual-target PIKfyve/tubulin inhibitor with anticancer activity. It primarily disrupts the balance of endocytosis and exocytosis, leading to the formation of numerous vesicles and inducing cell death. Additionally, HZX-02-059 promotes cell vacuolization, apoptosis, downregulates the p53 pathway, inhibits PI3K/AKT phosphorylation, and suppresses c-Myc and NF-κB transcription.
- Potent methuosis inducer.
- Dual-target PIKfyve/tubulin inhibitor.
- Exhibits anticancer activity.
- Induces cell vacuolization.
- Promotes apoptosis.
- Downregulates the p53 pathway.
- Inhibits PI3K/AKT phosphorylation.
- Inhibits c-Myc and NF-κB transcription.
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Medchemexpress LLC PF-4191834 50mg | 1029317-21-2 | 393.50 g·mol⁻¹ | C22H23N3O2S | 50 MG
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PF-4191834 is an orally active, non-iron-chelating, non-redox inhibitor of 5-lipoxygenase (5-LOX) used in research to probe leukotriene biosynthesis and 5-LOX-mediated pathways. It is supplied as a solid, characterized by high purity, and has documented solubility and storage recommendations for both powder and solution forms.
- Submicromolar potency against 5-LOX (reported IC50 ≈ 229 nM).
- High purity (reported 99.77%).
- Soluble in DMSO at approximately 100 mg/mL; in vivo formulation protocols documented.
- Stable as powder when stored at -20°C (up to 3 years) or 4°C (up to 2 years).
- Available in small research pack sizes including 50 mg.
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Research Products International Corp Bafilomycin B1, 1 MG
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Bafilomycin B1 is a naturally occurring macrolide antibiotic that is produced by certain strains of Streptomyces bacteria. It is a derivative of bafilomycin, a compound known for its inhibitory effects on the vacuolar-type H+-ATPase (V-ATPase) enzyme.
Similar to other members of the bafilomycin family, Bafilomycin B1 has gained attention in the field of life sciences for its ability to selectively inhibit V-ATPase. This enzyme is responsible for maintaining the acidic pH in various cellular compartments, including lysosomes and endosomes. By inhibiting V-ATPase, it disrupts the acidification process within these compartments. This disruption can have profound effects on various cellular processes and pathways that rely on proper pH regulation, such as protein degradation, autophagy, and vesicular trafficking.
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AdipoGen Lactacystin, 133343-34-7, MFCD01076525, 200 ug
MF: C15H24N2O7S, MW: 376.4, ≥98%, Appearance: White to off-white solid. Induces neuritogenesis, Apoptosis inducer, Anticancer compound, and Induces differentiation and inhibits cell cycle progression in several tumor cell lines.
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Medchemexpress LLC Ampicillin (Standard) | 69-53-4 | MFCD00005175 | 99.89% | 50 MG
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Ampicillin (Standard) is the analytical standard of ampicillin, a broad-spectrum beta-lactam antibiotic effective against various gram-positive and gram-negative bacteria. This product is specifically intended for research and analytical applications.
- Analytical standard for ampicillin
- Broad-spectrum beta-lactam antibiotic
- Effective against gram-positive and gram-negative bacteria
- Used in qualitative, quantitative, and methodological research experiments
- Commonly employed in HPLC, GC, and MS applications
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Sigma Aldrich Fine Chemicals Biosciences Vancomycin hydrochloride f100G
Chemical structure glycopeptide
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eMolecules 260415-63-2 | Medchem Express | PD173955 | 5mg | 446258406 | HY-10395 | MFCD16038305 | 443.35 | C21H16Cl2N4OS
Ambeed | Bis(cycloocta-15-diene)rhodium(I) hexafluorophosphate | 50mg | 632172965 | A378330 | 62793-31-1 | MFCD26793487 | 464.238 | C16H24F6PRh
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eMolecules 1332331-08-4 | Medchem Express | GSK2194069 | 5mg | 446261037 | HY-12325 | MFCD28167807 | 428.492 | C25H24N4O3
Pharmablock | cis-2-carbamoylcyclopropanecarboxylic acid | 25mg | 716543377 | PBGJ3031 | 15982-33-9 | 258.230 | C10H14N2O6
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Research Products International Corp Gentamicin Sulfate, 5 Grams
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Gentamicin Sulfate is an aminoglycoside antibiotic that inhibits bacterial protein synthesis by binding to the bacterial ribosome. This interference disrupts the translation process, leading to the production of faulty proteins and ultimately causing bacterial cell death.
It is frequently used as a selective agent in culture media to isolate bacteria that are sensitive to this antibiotic. Its inclusion in culture medium allows for the specific growth of bacteria lacking resistance to gentamicin.
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