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Filtered Search Results
eMolecules 6130-64-9 | Medchem Express | Penicillin G procaine (hydrate) | 25mg | 527573625 | HY-N7120 | MFCD00150771 | 588.72 | C29H40N4O7S
Medchem Express | Penicillin G procaine (hydrate) | 25mg | 527573625 | HY-N7120 | 6130-64-9 | MFCD00150771 | 588.720 | C29H40N4O7S
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eMolecules 1215721-40-6 | Medchem Express | CP-809101 (hydrochloride) | 10mg | 446265942 | HY-15543A | MFCD10687106 | 341.24 | C15H18Cl2N4O
AstaTech | 4-CYANO-3-ETHYLPYRIDINE | 0.25g | 449757179 | CL0167 | 95.000 | 13341-18-9 | MFCD13175867 | 132.166 | C8H8N2
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eMolecules 1469988-75-7 | Medchem Express | QL47 | 5mg | 446271617 | HY-80003 | MFCD22124682 | 447.498 | C27H21N5O2
Medchem Express | P-gp inhibitor 1 | 5mg | 721309271 | HY-101791 | 2050747-49-2 | 517.633 | C32H31N5O2
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Medchemexpress LLC Vancomycin hydrochloride | 1404-93-9 | 99.4% | 1485.71 | 1 ML
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Vancomycin hydrochloride is an antibiotic used for treating bacterial infections. Its mechanism of action involves inhibiting the second stage of cell wall synthesis in susceptible bacteria. Additionally, vancomycin modifies the permeability of the cell membrane and selectively prevents ribonucleic acid synthesis. This product is for research use only and has not been fully validated for medical applications.
- Inhibits bacterial cell wall synthesis
- Modifies cell membrane permeability
- Selectively inhibits ribonucleic acid synthesis
- Acts as an antibiotic
- Relevant for autophagy research
- Applicable in infection research
- Used in cancer research
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Medchemexpress LLC HY-103315 10mg Medchemexpress, Bepridil hydrochloride CAS:68099-86-5 Purity:>98%
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Medchemexpress, HY-103315 10mg Bepridil HCl CAS:68099-86-5 Bepridil hydrochloride (CERM 1978) is a calcium channel blocker, with antianginal activity. 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 DHODH-IN-17 | 16344-26-6 | 99.9% | 10 MG
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DHODH-IN-17 is a 2-anilino nicotinic acid and a human DHODH inhibitor with an IC50 value of 0.40 μM. It is intended for research purposes, specifically in the study of acute myeloid leukemia (AML). Its molecular weight is 248.67, with a chemical formula of C12H9ClN2O2, and it appears as an off-white to gray solid.
- Inhibits human DHODH with an IC50 of 0.4 μM.
- Induces differentiation in bone marrow cells (EC50 of 3 μM).
- Induces differentiation in THP-1 cells (EC50 of 10.7 μM).
- Induces differentiation in U-937 cells (EC50 of 6.1 μM).
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Medchemexpress LLC VU0463271 | 1391737-01-1 | 99.8% | 382.50 | 10 MG
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VU0463271 is a selective and potent KCC2 antagonist. It demonstrates high selectivity over NKCC1 and no activity against a broad panel of GPCRs, ion channels, and transporters. In vitro, it is rapidly cleared. In vivo studies in rats show it is a moderate-to-high clearance compound.
- IC50 of 61 nM for KCC2.
- >100-fold selectivity over NKCC1.
- No activity against GPCRs, ion channels, and transporters.
- Rapidly cleared in vitro.
- Significantly increased firing rates in Drosophila CNS.
- Moderate-to-high clearance (CL=57 mL/min/kg) in rats after intravenous administration.
- Low volume of distribution at steady state (Vss 0.4 L/kg) in rats.
- Relatively short t1/2 (9 min) in rats.
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Medchemexpress LLC HY-10388A 10mg Medchemexpress, TTA-Q6(isomer) CAS:910484-32-1 Purity:>98%
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Medchemexpress, HY-10388A 10mg TTA-Q6(isomer) CAS:910484-32-1 TTA-Q6(isomer) is an isomer of TTA-Q6. TTA-Q6 is a selective T-type Ca2+ channel antagonist. 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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eMolecules 177355-84-9 | N2,N4-Dibenzylquinazoline-2,4-diamine | MFCD03691820 | 50mg
Ambeed | Methyl 3-bromothiophene-2-carboxylate | 5g | 552678498 | A255746 | 26137-08-6 | MFCD00173839 | 221.070 | C6H5BrO2S
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Medchemexpress LLC HY-107433 10mg Medchemexpress, U18666A CAS:3039-71-2 Purity:>98%
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Medchemexpress, HY-107433 10mg U18666A CAS:3039-71-2 U18666A, a cell permeable drug, is a cholesterol synthesis and transport inhibitor. 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 GSK4112 (SR6452) | 1216744-19-2 | 99.9% | C18H21ClN2O4S | 100 MG
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GSK4112, also known as SR6452, is identified as a Rev-erbα agonist with an EC50 value of 0.4 μM. It serves as a valuable chemical tool for investigating the role of Rev-erbα in various biological processes, including transcriptional repression, the regulation of circadian rhythms, and metabolic pathways.
- Interacts with Rev-erbα with an EC50 of 0.4 μM.
- Represses the expression of bmal1 and target genes associated with gluconeogenesis, recruits HDAC3, and modulates Rev-erbα's effect on hepatic gene expression oscillation.
- Reduces glucose output in murine hepatocytes.
- Attenuates Fas-induced hepatic damage in male C57BL/6 mice.
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Medchemexpress LLC HY-101792 10mg Medchemexpress, RG7800 CAS:1449598-06-4 Purity:>98%
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Medchemexpress, HY-101792 10mg RG7800 CAS:1449598-06-4 RG7800 is a SMN2 splicing modifier. RG7800 has the potential for spinal muscular atrophy treatment. 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 4-(2′-aminoethyl)amino-1,8-dimethylimidazo[1,2-a]quinoxaline | 445430-58-0 | MFCD18089812 | 99.7% | 255.32 g·mol⁻1 | C14H17N5 | 25 MG
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BMS-345541 is a small-molecule research reagent that selectively inhibits the catalytic subunits of IκB kinase (IKK). It binds an allosteric site on IKK and is used to probe NF-κB signaling pathways in biochemical and cellular studies. The compound is supplied with analytical characterization for research use only.
- Selective inhibition of IKK catalytic subunits, with greater potency for IKK-2
- Binds an allosteric site on the IKK enzyme
- Reported IC50 values: IKK-2 = 0.3 μM; IKK-1 = 4 μM
- High analytical purity suitable for research applications
- Available in multiple pack sizes, including 25 MG
- Molecular formula C14H17N5 and molecular weight 255.32 g·mol⁻1
- Offered as solid and as ready-to-use DMSO solution formats
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Apexbio Technology LLC OLIGOMYCIN COMPLEX 5MG
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OLIGOMYCIN COMPLEX 5MG APEXBIO TECHNOLOGIES
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Medchemexpress LLC Anhydrotetracycline hydrochloride | 13803-65-1 | ≥98.0% | 462.88 | C22H23ClN2O7 | 10 MG
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Anhydrotetracycline hydrochloride is a tetracycline-family antibiotic supplied as an analytical reference standard for laboratory research. It is commonly used as an effector in tetracycline-regulated gene expression systems and for analytical method development. The material is provided as the hydrochloride salt with molecular weight 462.88 g·mol⁻1 and chemical formula C22H23ClN2O7.
- Reference standard for research and analytical applications.
- Acts as an effector in tetracycline-regulated gene expression systems.
- Supplied as a hydrochloride salt; formula C22H23ClN2O7 and MW 462.88 g·mol⁻1.
- High reported purity (≥98%) suitable for analytical work.
- Available in small laboratory pack sizes (e.g., 10 MG, 50 MG).
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