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Filtered Search Results
MEDCHEMEXPRESS LLC SAR-260301 5MG
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501873374 SAR-260301 5MG
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MEDCHEMEXPRESS LLC MPTP HYDROCHLORIDE 10MG
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501873305 MPTP HYDROCHLORIDE 10MG
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Medchemexpress LLC HY-100574A 10mg Medchemexpress, Cl-amidine (hydrochloride) CAS:1373232-26-8 Purity:>98%
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Medchemexpress, HY-100574A 10mg Cl-amidine (hydrochloride) CAS:1373232-26-8 Cl-amidine (hydrochloride) is a peptidylarginine deminase (PAD) inhibitor, with an IC 50 5.9 μM for PAD4. 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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Medchemexpress LLC HY-100358 5mg Medchemexpress, AQ-13 dihydrochloride CAS:169815-40-1 Purity:>98%
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Medchemexpress, HY-100358 5mg AQ-13 dihydrochloride CAS:169815-40-1 AQ-13 dihydrochloride is an aminoquinoline antimalarial drug that is effective against chloroquine-resistant strains of Plasmodium falciparum. 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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Bioworld Erythromycin, 10 g
Erythromycin A macrolide antibiotic against Gram-positive bacteria. It binds to 50S ribosomal subunit and blocks bacterial protein synthesis.USP GradeA macrolide antibiotic protein synthesis inhibitorPotency >850 μg/mgWater <10.0%Residue on ignition <2.0%.For in vitro lab use only. Not for human use or consumption.Appearance: SolidBoiling Point : 818.4 °C at 760 mmHg (Predicted)Density : 1.2 g/cm3 (Predicted)Melting Point: 135-140 °C (lit.)RTECS Number: KF4375000
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Apexbio Technology LLC Dapsone 80-08-0 1g
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Dapsone (80-08-0) is a small-molecule inhibitor targeting dihydropteroate synthase (DHPS) It is designed to interfere with folate synthesis pathways thereby impeding bacterial nucleic acid production Dapsone exerts its biological activity primarily through DHPS inhibition In in vitro studies dapsone demonstrates inhibitory activity with IC50 values typically ranging between 0 1 1 M dependent on organism strain and experimental conditions Based on these pharmacological properties dapsone holds research potential in leprosy drug development adjunctive antimicrobial therapy investigation antimicrobial resistance profiling and in studies targeting protozoal parasites such as Plasmodium falciparum
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Apexbio Technology LLC 3CAI 28755-03-5 5mg
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3CAI (CAS 28755-03-5) is a small molecule allosteric inhibitor selectively targeting AKT serine/threonine kinases Acting via an ATP-noncompetitive mechanism 3CAI binds directly to AKT1 and AKT2 exhibiting an IC50 of 1 M and suppressing 60% of AKT1 kinase activity at this concentration In vitro 3CAI reduces the expression of downstream AKT targets such as mTOR and GSK3 and at 4 M induces growth inhibition and apoptosis in HCT116 and HCT29 colon cancer cells Oral administration at 30 mg/kg significantly inhibits tumor growth and AKT substrate expression in mouse xenograft models 3CAI is valuable for studying AKT signaling and its implications in cancer research
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Apexbio Technology LLC Quinacrine (hydrochloride hydrate),100mg
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Quinacrine, also commonly known as atebrine, is a compound which is commonly used as an anti-protozoal agent. It inhibits voltage-dependent sodium channels with an IC50 value of 3.3 μM and suppresses aldehyde oxidase with an IC50 value of 3.3 μM. Quinacrine prevents misfolding of prion protein with an EC50 value of 0.3 μM. As an effective riboflavin antagonist, quinacrine associates with the riboflavin-binding protein with a Ki value of 6.7 μM. Voltage-dependent sodium channels play a vital role in action potential initiation and propagation in excitable cells, including muscle, nerve, and neuroendocrine cell types. Other sizes are also available. Please inqury us for quote.
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Apexbio Technology LLC Azithromycin Dihydrate 117772-70-0 25mg
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Azithromycin Dihydrate (CAS 117772-70-0) is a macrolide antibiotic targeting the bacterial 50S ribosomal subunit It is designed to inhibit bacterial protein synthesis thereby disrupting bacterial growth and replication Azithromycin Dihydrate exerts its biological activity primarily through reversible binding to the 50S ribosomal subunit inhibiting protein synthesis In in vitro assays Azithromycin Dihydrate demonstrates inhibitory activity against susceptible bacterial strains with reported IC50 values typically in the micromolar range Based on these pharmacological properties Azithromycin Dihydrate holds research potential in investigating mechanisms of antibiotic resistance bacterial susceptibility and developing therapeutic strategies against bacterial infections
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Medchemexpress LLC HY-W017162 100mg Medchemexpress, DL-3-Phenyllactic acid CAS:828-01-3 Purity:>98%
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Medchemexpress, HY-W017162 100mg DL-3-Phenyllactic acid CAS:828-01-3 DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound. 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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Medchemexpress LLC Geneticin disulphate | 50 ML
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MCE G418 Selective Antibiotic, Sterile (50 mg/mL) is an aminoglycoside antibiotic produced by Micromonospora rhodorangea. It functions by binding to the 80S subunit of the bacterial ribosome, thereby inhibiting protein synthesis in both prokaryotic and eukaryotic cells. Resistance to G418 selective antibiotic is conferred by the E. coli APH (3) I and APH (3) II resistance genes. The gene becomes APH (3) II on Tn5 and APH (3) I on Tn601. Consequently, G-418 selective antibiotic can be utilized to select and maintain prokaryotic or eukaryotic cells that carry the G418 resistance gene.
- Aminoglycoside antibiotic.
- Produced by Micromonospora rhodorangea.
- Inhibits protein synthesis in both prokaryotic and eukaryotic cells.
- Binds to the 80S subunit of the bacterial ribosome.
- Can be used to select and maintain prokaryotic or eukaryotic cells carrying the G418 resistance gene.
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![eMolecules Medchem Express / Flubendazole-d3 / 1mg / 784544313 / HY-B0294S / / 1173021-08-3 / [null] / 316.307 / C16H12FN3O3](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502463307.JPG-250.jpg)
eMolecules Medchem Express / Flubendazole-d3 / 1mg / 784544313 / HY-B0294S / / 1173021-08-3 / [null] / 316.307 / C16H12FN3O3
Medchem Express / Flubendazole-d3 / 1mg / 784544313 / HY-B0294S / / 1173021-08-3 / [null] / 316.307 / C16H12FN3O3
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Apexbio Technology LLC Tioconazole 65899-73-2 5g
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Tioconazole (65899-73-2) is a small-molecule inhibitor targeting the fungal cytochrome P450-dependent enzyme lanosterol 14 -demethylase It is designed to inhibit ergosterol biosynthesis thereby disrupting fungal cell membrane stability and cellular integrity Tioconazole exerts its biological activity primarily through interference with ergosterol biosynthesis within fungal cell membranes In in vitro studies Tioconazole demonstrates inhibitory activity with MIC50 values below 3 12 mg/L for dermatophyte strains and below 9 mg/L for yeast species Based on these pharmacological properties Tioconazole holds research potential in the study of antifungal mechanisms and in vitro antifungal screening assays
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Sigma Aldrich Fine Chemicals Biosciences Pleuromutilin >=95% | 125-65-5 | 25MG
Pleuromutilin >=95% | Purity: >=95% | Mol Wt: 378.5 | 125-65-5 | 25MG
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Medchemexpress LLC HY-10004 10mg Medchemexpress, Faropenem daloxate CAS:141702-36-5 Purity:>98%
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Medchemexpress, HY-10004 10mg Faropenem daloxate CAS:141702-36-5 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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