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Filtered Search Results
Medchemexpress LLC APX2039 | 2342606-49-7 | 98.4% | 362.36 | 100 MG
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APX2039 is an orally active and potent inhibitor of the fungal Gwt1 enzyme. It demonstrates extremely potent anticryptococcal activity against *C. neoformans* and *C. gattii*. It works by blocking the localization of GPI (glycosylphosphatidyl inositol)-anchored cell wall mannoproteins and can be used for Cryptococcal meningitis (CM) research.
- Orally active and potent inhibitor of the fungal Gwt1 enzyme
- Exhibits extremely potent anticryptococcal activity
- Blocks localization of GPI-anchored cell wall mannoproteins
- Useful for cryptococcal meningitis (CM) research
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Medchemexpress LLC Fidaxomicin | 873857-62-6 | MFCD27976367 | 99.9% | 1058.04 | C52H74Cl2O18 | 10 MG
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Fidaxomicin analytical standard supplied as a measured 10 MG quantity for research and analytical use. It is a macrocyclic antibiotic reference material intended for assay development, method validation, and qualitative or quantitative analyses by HPLC, GC, and MS. The material is provided at high purity suitable for laboratory analytical workflows.
- High purity suitable for quantitative analysis (99.9%).
- Intended for HPLC, GC, and MS method development and validation.
- Provided as a measured 10 MG quantity for analytical use.
- Useful as a reference standard in qualitative and quantitative assays.
- Includes CAS number 873857-62-6 for unambiguous identification.
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![Medchemexpress LLC 2-Chloro-N-[2-[[4-[methyl(4-phenylbutyl)amino]-6-(prop-2-ynylamino)-1,3,5-triazin-2-yl]amino]ethyl]acetamide | 2226201-97-2 | 99.9% | 429.95 g/mol | C21H28ClN7O | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000226771.png-250.jpg)
Medchemexpress LLC 2-Chloro-N-[2-[[4-[methyl(4-phenylbutyl)amino]-6-(prop-2-ynylamino)-1,3,5-triazin-2-yl]amino]ethyl]acetamide | 2226201-97-2 | 99.9% | 429.95 g/mol | C21H28ClN7O | 50 MG
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KSC-34 is a covalent modifier and selective inhibitor of protein disulfide isomerase A1 (PDIA1) used as a research reagent for biochemical and cell-based studies. It is supplied as a solid and intended for laboratory research use only; follow appropriate safety and storage guidelines.
- Selective PDIA1 a-site inhibitor with IC50 ≈3.5 μM.
- High purity (≈99.9%).
- Molecular weight 429.95 g/mol; formula C21H28ClN7O.
- White to off-white solid, packaged as 50 mg.
- Soluble in DMSO (100 mg/mL); in vivo formulation options documented.
- Storage: store at 4°C under nitrogen; in solution, store at -80°C for long-term preservation.
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Medchemexpress LLC Nordoxepin-d3 hydrochloride | 1331665-54-3 | 99.9% | C18H17D3ClNO | 10MG
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Nordoxepin-d3 hydrochloride is the deuterium-labeled form of nordoxepin hydrochloride, the active metabolite of doxepin. It is provided as a solid for use as a tracer and internal standard in quantitative analytical workflows, including NMR, GC-MS, and LC-MS.
- High chemical purity (99.9%).
- Deuterium-labeled for accurate internal standardization.
- Suitable for NMR, GC-MS, and LC-MS quantitation.
- Supplied as a stable solid for convenient handling and storage.
- Useful as a tracer in pharmacokinetic and metabolite studies.
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Medchemexpress LLC Acanthoside B | 7374-79-0 | 5 MG
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Acanthoside B is a potential bioactive lignan with anti-inflammatory and anti-amnesic activities, making it suitable for research into Alzheimer's disease and lung inflammation. It has been shown to attenuate scopolamine-inflicted AD-like amnesic traits in mice.
- Potential bioactive lignan
- Exhibits anti-inflammatory activities
- Exhibits anti-amnesic activities
- Applicable for Alzheimer's disease research
- Applicable for lung inflammation research
- Attenuates scopolamine-inflicted AD-like amnesic traits
- Restores cholinergic activity
- Decreases endogenous antioxidant status
- Suppresses neuroinflammation
- Activates the TrkB/CREB/BDNF pathway
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Medchemexpress LLC L-Carnosine | 305-84-0 | 99.94% | 226.24 | 10 MG
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L-Carnosine is a dipeptide composed of beta-alanine and histidine, naturally occurring in human brain, muscle, and gastrointestinal tissues. This endogenous metabolite acts as a non-enzymatic free radical scavenger and a natural antioxidant with anti-inflammatory and neuroprotective properties. It can inhibit biochemical changes associated with aging, attributed to its chelating effect against metal ions, superoxide dismutase (SOD)-like activity, and its ability to scavenge reactive oxygen species (ROS) and free radicals.
- Acts as a non-enzymatic free radical scavenger
- Functions as a natural antioxidant
- Exhibits anti-inflammatory properties
- Provides neuroprotective benefits
- Inhibits biochemical changes associated with aging
- Chelates metal ions
- Scavenges reactive oxygen species and free radicals
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eMolecules 25711-30-2 | ChemScene | 15-Dimethyl-1H-pyrazole-4-carbaldehyde | 1g | 582636477 | CS-0135588 | MFCD00159630 | 124.143 | C6H8N2O
Ambeed | Ethyl 4-bromothiophene-2-carboxylate | 1g | 525053049 | A143192 | 62224-17-3 | MFCD06204328 | 235.100 | C7H7BrO2S
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eMolecules 3769-41-3 | 3-(BENZYLOXY)PHENOL | AstaTech | MFCD00134682 | 200.237 | C13H12O2 | 97.000 | Oc1cccc(OCc2ccccc2)c1 | 1g | 411870168
3-(BENZYLOXY)PHENOL | AstaTech | 3769-41-3 | MFCD00134682 | 200.237 | C13H12O2 | 97.000 | Oc1cccc(OCc2ccccc2)c1 | 1g | 411870168
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![eMolecules 875515-76-7 | ChemScene | 4-Chlorothieno[32-d]pyrimidine-6-carboxylic acid | 100mg | 582650335 | CS-W006123 | MFCD11846188 | 214.62 | C7H3ClN2O2S](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502440933.PNG-250.jpg)
eMolecules 875515-76-7 | ChemScene | 4-Chlorothieno[32-d]pyrimidine-6-carboxylic acid | 100mg | 582650335 | CS-W006123 | MFCD11846188 | 214.62 | C7H3ClN2O2S
ChemScene | 4-Chlorothieno[32-d]pyrimidine-6-carboxylic acid | 100mg | 582650335 | CS-W006123 | 875515-76-7 | MFCD11846188 | 214.620 | C7H3ClN2O2S
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eMolecules 174972-79-3 | Medchem Express | Parishin B | 5mg | 495802508 | HY-N2124 | MFCD29048568 | 728.653 | C32H40O19
Ambeed | 1-(2-Fluorobenzyl)-1H-pyrazolo[34-b]pyridine-3-carboximidamide hydrochloride | 1g | 525107012 | A189655 | 256499-19-1 | MFCD18432772 | 305.740 | C14H13ClFN5
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eMolecules 2098890-15-2 | Medchem Express | SMS2-IN-1 | 5mg | 596114012 | HY-102041 | 681.676 | C34H37F6N3O5
Medchem Express | Bemesetron | 10mg | 441682037 | HY-B1541 | 40796-97-2 | MFCD00865533 | 314.210 | C15H17Cl2NO2
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eMolecules 2568073-22-1 | 6-(TRIFLUOROMETHYL)ISOQUINOLIN-5-OL | AstaTech213.159 | C10H6F3NO | 95.000 | Oc1c(ccc2cnccc12)C(F)(F)F | 0.1g | 562552067
6-(TRIFLUOROMETHYL)ISOQUINOLIN-5-OL | AstaTech | 2568073-22-1213.159 | C10H6F3NO | 95.000 | Oc1c(ccc2cnccc12)C(F)(F)F | 0.1g | 562552067
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Crescent Chemical Co Inc 1-PENTADECANOL 250 MG
1-Pentadecanol Hydrocarb./petrochem. (WS) CAS 629-76-5 Molecular Weight - 228.414 Storage - RT Catalog Num - DRE-C15973800 chemical
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Medchemexpress LLC Praliciguat | 1628730-49-3 | 99.4% | 534.36 | 1 ML
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Praliciguat (IW-1973) is a potent and orally active soluble guanylate cyclase (sGC) activator. It increases cGMP through the nitric oxide (NO)-sGC pathway. Praliciguat can also inhibit the expression of proinflammatory cytokines and apoptosis, and it promotes vasodilation. This compound can be used in research for metabolic diseases and cardiovascular diseases, including hypertension, diabetes, and heart failure.
- Potent and orally active soluble guanylate cyclase (sGC) activator.
- Increases cGMP via the nitric oxide (NO)-sGC pathway.
- Inhibits the expression of proinflammatory cytokines.
- Inhibits apoptosis.
- Promotes vasodilation.
- Useful for research in metabolic diseases and cardiovascular diseases, such as hypertension, diabetes, and heart failure.
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Medchemexpress LLC Samatasvir | 1312547-19-5 | 99.4% | 885.06 | 50 MG
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Samatasvir (IDX719) is a potent, orally active NS5A inhibitor that targets HCV replication. It demonstrates effectiveness and selectivity against infectious HCV and replicons, with EC50 values ranging from 2 to 24 pM across genotype 1 through 5 replicons.
- Potent, orally active NS5A inhibitor of HCV replication.
- Effective and selective against infectious HCV and replicons.
- Maintains full activity in the presence of HIV and hepatitis B virus (HBV) antivirals.
- Not cross-resistant with HCV protease, nucleotide, and nonnucleoside polymerase inhibitor classes.
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