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Filtered Search Results
Apexbio Technology LLC Roxithromycin 80214-83-1 5g
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Roxithromycin (80214-83-1) is a semisynthetic macrolide antibiotic that acts by binding to the bacterial ribosomal 50S subunit thereby inhibiting peptide chain elongation and disrupting protein synthesis Roxithromycin exerts its biological activity primarily through this mechanism of action In both in vitro and in vivo models Roxithromycin demonstrates inhibitory effects on cell proliferation inflammation pathways and tumor angiogenesis Reported IC50 values typically vary depending on the cell type and assay methodology Based on these pharmacological properties Roxithromycin holds research potential in studies of inflammation-associated pathologies cancer biology and lung injury
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Medchemexpress LLC Lenampicillin hydrochloride | 80734-02-7 | MFCD01745174 | >99.0% | 497.95 | C21H24ClN3O7S | 10 MG
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Lenampicillin hydrochloride is an orally active prodrug of ampicillin used as a research reagent. As a beta-lactam antibacterial, it exhibits improved oral absorption and reduced adverse effects compared with ampicillin and is commonly used in studies of suppurative skin and soft tissue infections.
- Orally active prodrug of ampicillin.
- Improved absorption and reduced side effects compared with ampicillin.
- Beta-lactam antibacterial that inhibits penicillin-binding proteins.
- Supplied as the hydrochloride salt for enhanced solubility.
- Suitable for in vitro and in vivo research on suppurative infections.
- Available in small research pack sizes.
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Enzo Life Sciences Ryanodine (high purity) (5mg). CAS: 15662-33-6
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Induces the release of intracellular Ca2+ . Ryanodine receptors mediate adenine nucleotide, Ca2+ and caffeine-sensitive release of Ca2+ from sarcoplasmic reticulum of cardiac and skeletal muscle and may also mediate intracellular Ca2+ release in neurons. Biphasic effect on sarcoplasmic reticulum calcium channels; Nanomolar levels open the channel and micromolar levels close it. Purity: ≥99% (HPLC). Appearance: White to off-white solid. Solubility: Soluble in methanol or DMSO (>29mg/ml), in 100% ethanol (16mg/ml); slightly soluble in water (warm). Long Term Storage: -20°C.
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Medchemexpress LLC Polygalasaponin V | 162857-65-0 | 5 MG
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Polygalasaponin V is a triterpenoid saponin isolated from the aerial parts of *Polygala japonica*. This compound has been studied for its potential expectorant, anti-inflammatory, antibacterial, and antidepressant properties, reflecting its traditional use in folk medicine.
- Isolated from *Polygala japonica*
- Molecular formula: C58H94O27
- Molecular weight: 1223.35
- Purity: 99.94%
- Appearance: White to off-white solid
- Classified as a triterpenoid saponin
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eMolecules 4382-63-2 | Medchem Express | PFK-015 | 5mg | 446260823 | HY-12204 | MFCD28099813 | 260.296 | C17H12N2O
Medchem Express | SJ000063181 | 5mg | 784544050 | HY-147372 | 945189-68-4 | 296.730 | C14H14ClFN2O2
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eMolecules 362003-83-6 | Medchem Express | NVP 231 | 10mg | 446263735 | HY-13945 | 431.55 | C25H25N3O2S
Pharmablock | 2-1-[(benzyloxy)carbonyl]piperidin-3-ylacetic acid | 50mg | 551212158 | PB06551 | 86827-10-3 | MFCD02179002 | 277.320 | C15H19NO4
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Enzo Life Sciences R-Sulforaphane (10mg). CAS: 142825-10-3
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Potent, selective inducer of phase II detoxification enzymes. Inhibits chemically induced mammary tumor formation in rats. Alternative name: L-Sulforaphane, (-)-1-Isothiocyanato-4R-(methylsulfinyl)-butane. Purity: ≥98% (UHPLC). Solubility: Soluble in methanol, 100% ethanol, DMSO or ethyl acetate. Long Term Storage: -20°C.
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MOLTOX Molecular Toxicology Inc Mitomycin C, 20 ug/vial, 5 vials/pack, Store in Refrigerator
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For use in Ames test with TA102 tester strain. Dose 0.5 µg/plate. Reconstitute with organic solvents such as DMSO or sterile dH2O as applicable. Direct acting mutagens do not require the use of S9 metabolic activation to cause mutagenicity. CONTROLCHEM™ chemicals are obtained from major suppliers of research chemicals and are employed without further characterization or purification. Packaged quantities are precise within 1%. Please Note: CONTROLCHEM™ chemicals are known mutagens/carcinogens/toxins and are sold only to those experienced in the safe handling and disposal of hazardous materials. Consult your Institutional Safety Officer before ordering.
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Selleck Chemical LLC Nitroxoline 100mg 4008-48-4 8-Hydroxy-5-nitroquinoline, 5-nitroquinolin-8-ol, 5-Nitro-8-quinolinol, 5-Nitro-8-hydroxyquinoline
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Nitroxoline (8-Hydroxy-5-nitroquinoline, 5-nitroquinolin-8-ol, 5-Nitro-8-quinolinol, 5-Nitro-8-hydroxyquinoline) is a urinary antibacterial agent active against susceptible gram-positive and gram-negative organisms commonly found in urinary tract infections. Nitroxoline impairs tumor progression in vitro and in vivo by inhibiting cathepsin B activity. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
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Medchemexpress LLC L-glutamic acid, 4-methyl-, (4R)- | 31137-74-3 | MFCD00937765 | 98.0% | 161.16 | C6H11NO4 | 10 MG
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SYM 2081 is a selective kainate receptor agonist used as a research reagent to investigate glutamate receptor function, excitatory neurotransmission, and neuroprotective signaling. It has documented activity in cellular and animal models of hypoxic-ischemic injury and inflammatory or neuropathic pain, and affects glutamate transport mechanisms.
- Selective kainate receptor agonist for receptor pharmacology studies.
- Modulates glutamate transport (EAAT1 substrate, EAAT2 inhibitor).
- Demonstrates neuroprotective effects in cellular and animal models.
- High purity suitable for research applications.
- Supplied in small milligram quantities with defined storage conditions.
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Medchemexpress LLC Cl-amidine hydrochloride | 1373232-26-8 | 99.8% | 347.24 | C14H20Cl2N4O2 | 25 MG
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Cl-amidine hydrochloride is an orally active peptidylarginine deiminase (PAD) inhibitor used in biomedical research to block protein citrullination and study PAD-mediated processes such as histone deimination and neutrophil extracellular trap formation. Supplied as a white to light-yellow solid in small vial quantities, it is intended for research use and requires appropriate low-temperature storage for long-term stability.
- Orally active PAD inhibitor for research applications.
- Blocks histone citrullination and neutrophil extracellular trap formation.
- High purity suitable for biochemical and cellular assays.
- Available in small solid aliquots for dosing flexibility.
- Stable when stored at -20°C under inert atmosphere; longer stability in solvent at -80°C.
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Medchemexpress LLC HY-15985 100mg Medchemexpress, CTX-0294885 CAS:1439934-41-4 Purity:98%
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Medchemexpress,HY-15985 100mg CTX-0294885 CAS:1439934-41-4 Formula:C22H24ClN7O Purity:98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Enzo Life Sciences Rufloxacin . hydrochloride (250mg). CAS: 106017-08-7
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Fluoroquinolone antibacterial agent. Structurally similar to ofloxacin. Specific inhibitor of bacterial DNA gyrase (topoisomerase). Inhibits B-cell differentiation. Shows photosensitizing effects. Alternative name: 6-Fluoro-2,3-dihydro-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzothia zine-6-carboxylic acid . hydrochloride, MF-934 . hydrochloride. Purity: ≥98% (Assay). Appearance: Off-white to light green crystalline solid. Solubility: Sparingly soluble in water; very slightly soluble in methanol; almost insoluble in chloroform or acetic acid. Long Term Storage: -20°C.
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Selleck Chemical LLC NE 52-QQ57
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NE 52-QQ57 is a selective and orally available antagonist of G-protein coupled receptor 4 (GPR4) with IC50 of 0 07 M NE 52-QQ57 effectively blocks GPR4-mediated cAMP accumulation with IC50 of 26 8 nM in HEK293 cells The antagonism of GPR4 with NE 52-QQ57 significantly inhibits the AGE-induced increased expression of several key inflammatory cytokines and signaling molecules including tumor necrosis factor- (TNF- ) interleukin (IL)-1 IL-6 inducible nitric oxide synthase (iNOS) nitric oxide (NO) cyclooxygenase 2 (COX2) and prostaglandin E2 (PGE2)
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Medchemexpress LLC D-Cl-amidine hydrochloride | 2985338-61-0 | 99.9% | 347.24 | C14H20Cl2N4O2 | 25 MG
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D-Cl-amidine hydrochloride is the hydrochloride salt of a selective protein arginine deiminase 1 (PAD1) inhibitor for research use. It is supplied as a solid or as a DMSO solution and includes documented solubility and storage recommendations to support laboratory handling.
- Selective PAD1 inhibitor with documented biological activity.
- Hydrochloride salt form improves aqueous solubility.
- High purity (99.91%) suitable for research applications.
- Available as small solid quantities and as a 10 mM solution in DMSO.
- Soluble in DMSO and water; sonication and warming recommended for dissolution.
- Store protected from light under inert atmosphere at -20 °C; in solution, store at -80 °C for long-term stability.
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