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Filtered Search Results
Enzo Life Sciences GEA 3162 (10mg). CAS: 144575-47-3
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Water soluble nitric oxide donor and potent inhibitor of ADP-induced platelet aggregation in platelet rich plasma (PRP). Stimulates cGMP production in platelets, granulocytes and polymorphonuclear leukocytes. Vasodepressant. Alternative name: 1,2,3,4-Oxatriazolium, 5-amino-3-(3,4-dichlorophenyl)-, chloride. Purity: ≥97% (TLC). Solubility: Soluble in water, methanol or DMSO. Long Term Storage: -20°C.
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eMolecules Medchem Express / Eptapirone / 5mg / 446270576 / HY-19946 / / 179756-58-2 / MFCD08690608 / 345.407 / C16H23N7O2
Medchem Express / Eptapirone / 5mg / 446270576 / HY-19946 / / 179756-58-2 / MFCD08690608 / 345.407 / C16H23N7O2
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Medchemexpress LLC 4-hydroperoxy cyclophosphamide-d4 | 1246816-71-6 | MFCD34567216 | 95.0% | 297.11 g·mol⁻¹ | C7H11D4Cl2N2O4P | 1 MG
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4-Hydroperoxy cyclophosphamide-d4 is the deuterium-labeled stable isotope analog of 4-hydroperoxy cyclophosphamide, provided as a solid for analytical and research use in studies of drug metabolism and mechanism. It is intended for use as an internal standard and research reagent in small-quantity analytical workflows.
- Deuterium-labeled (d4) analog for use as an internal standard in analytical assays.
- Suitable for studies of cyclophosphamide metabolism and mechanism.
- Molecular weight 297.11 g·mol⁻¹.
- Molecular formula C7H11D4Cl2N2O4P.
- Available in 1 mg, 5 mg, and 10 mg sizes.
- Supplied as a solid; follow SDS handling instructions for storage and safety.
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Medchemexpress LLC PKC-theta inhibitor 2 | 736048-65-0 | 99.9% | 454.45 | 100 MG
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PKC-theta inhibitor 2 is a potent and selective inhibitor of PKC-θ, exhibiting an IC50 value of 18 nM. This compound is identified as a 2,4-diamino-5-nitropyrimidine, characterized by a trifluoromethoxy substitution at the 2-position.
- Potent and selective inhibition of PKC-θ.
- Exhibits an IC50 value of 18 nM.
- Characterized as a 2,4-diamino-5-nitropyrimidine compound.
- Features an o-trifluoromethoxy substitution at the 2-position.
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Medchemexpress LLC D-α-Hydroxyglutaric acid | 13095-47-1 | 148.11 | 10MG
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D-α-Hydroxyglutaric acid is the primary metabolite accumulating in D-2-hydroxyglutaric aciduria, a neurometabolic disease. It acts as a weak competitive antagonist of α-ketoglutarate (α-KG) and inhibits multiple α-KG-dependent dioxygenases. This compound also enhances reactive oxygen species (ROS) production, binds to and inhibits ATP synthase, and suppresses mTOR signaling. It accumulates in human cancers with specific mutations in IDH1 and IDH2 genes.
- Primary metabolite in D-2-hydroxyglutaric aciduria
- Weak competitive antagonist of α-ketoglutarate (α-KG)
- Inhibits multiple α-KG-dependent dioxygenases
- Increases reactive oxygen species (ROS) production
- Binds and inhibits ATP synthase
- Inhibits mTOR signaling
- Accumulates in human cancers with IDH1 and IDH2 mutations
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Selleck Chemical LLC L-methionine
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L-Methionine is an essential sulfur-containing free-form amino acid acts as an antioxidant promoter and contributes to the synthesis of S-adenosyl-L-methionine (SAMe)
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Medchemexpress LLC Vorinostat-d5 1mg | 1132749-48-4 | 1 MG
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Vorinostat-d5 is the deuterium-labeled analogue of vorinostat (suberoylanilide hydroxamic acid) supplied as a stable-isotope internal standard for quantitative NMR and mass spectrometry. It is provided as a white to off-white solid with high purity suitable for analytical tracer use.
- Deuterium-labeled internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
- High purity suitable for analytical reference standards and tracer work.
- Supplied in small, milligram quantities for method development and calibration.
- Stable solid form with white to off-white appearance for easy handling and storage.
- Chemical formula C14H15D5N2O3 and molecular weight 269.35 g/mol.
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Crescent Chemical Co Inc AMPICILLINTRIHYDRATE RES.GRADE
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Ampicillin trihydrate research grade, Ph. Eur. Semi-synthetic derivative of penicillin. Inhibitor of cell wall synthesis in E. coli. Soluble 1 part in 150 parts H2O as well as in diluted acids and bases. Insoluble in alcohol. Size - 100G Storage Conditions - +
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Lkt Laboratories CAS 1197-18-8, ≥98%, Plasminogen inhibitor used to decrease blood loss in cardiac surgery and trauma.
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Tranexamic acid is clinically used to decrease blood loss in cardiac surgery and trauma; it inhibits plasmin/plasminogen. In vivo, tranexamic acid inhibits fibrinolysis, decreases bleeding time, and increases thrombus formation. Additionally, tranexamic acid accelerates skin barrier recovery and upregulates occluding expression in UV-damaged skin.
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Apexbio Technology LLC Streptomycin sulfate 3810-74-0 10mM (in 1mL H2O)
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Streptomycin sulfate is an aminoglycoside antibiotic targeting the bacterial 30S ribosomal subunit It is designed to inhibit bacterial protein synthesis thereby suppressing bacterial proliferation Streptomycin sulfate exerts its biological activity primarily through inhibition of mRNA translation by binding to the 30S subunit which impairs initiation and elongation processes during protein synthesis and disrupts the ribosome mRNA complex Based on these pharmacological properties streptomycin sulfate holds research potential in microbiological experimentation susceptibility assays bacterial resistance profiling microbial genetics studies and screening of transgenic cells expressing antibiotic-resistance markers
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Apexbio Technology LLC Roxithromycin 80214-83-1 10mM (in 1mL DMSO)
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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 HY-10045 5mg Medchemexpress, AEE788 CAS:497839-62-0 Purity:>98%
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Medchemexpress, HY-10045 5mg AEE788 CAS:497839-62-0 AEE788 is an inhibitor of the EGFR and ErbB2 with IC 50 values of 2 and 6 nM, respectively. 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-100611 5mg Medchemexpress, CaCCinh-A01 CAS:407587-33-1 Purity:>98%
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Medchemexpress, HY-100611 5mg CaCCinh-A01 CAS:407587-33-1 CaCCinh-A01 is an inhibitor of both TMEM16A and calcium-activated chloride channel ( CaCC ) with IC 50 s of 2.1 and 10 μM, respectively. 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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Selleck Chemical LLC Carbenicillin disodium 50mg 4800-94-6 BRL-2064
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Carbenicillin (BRL-2064) is a semi-synthetic penicillin antibiotic which interferes with cell wall synthesis of gram-negative bacteria while displaying low toxicity. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
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Medchemexpress LLC Amphotericin B methyl ester | 36148-89-7 | MFCD30719782 | 83.4% | 938.11 | C48H75NO17 | 5 MG
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Amphotericin B methyl ester is the methyl ester derivative of the polyene antibiotic Amphotericin B. It is a cholesterol-binding antifungal compound reported to disrupt HIV-1 particle production and inhibit HIV-1 replication. The material is supplied as a solid for research use.
- Methyl ester derivative of Amphotericin B.
- Cholesterol-binding antifungal activity.
- Reported to disrupt HIV-1 particle production and inhibit replication.
- Solid, light yellow to yellow appearance.
- Molecular weight approximately 938.11; formula C48H75NO17.
- Purity approximately 83.4%.
- Store at -20°C and protect from light; in solvent store at -80°C up to 6 months.
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