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Filtered Search Results
Medchemexpress LLC Samuraciclib hydroch 25mg | 1805789-54-1 | 25MG
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Samuraciclib hydrochloride (CT7001 hydrochloride) is a potent selective ATP-competitive and orally active CDK7 inhibitor with an IC50 of 41 nM Samuraciclib hydrochloride displays 45- 15- 230- and 30-fold selectivity over CDK1 CDK2 (IC50 of 578 nM) CDK5 and CDK9 respectively Samuraciclib hydrochloride inhibits the growth of breast cancer cell lines with GI50 values between 0 2-0 3 M Samuraciclib hydrochloride has anti-tumor effects[1 [2
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Medchemexpress LLC HIF-1a-IN-2 hydroch 25mg | 25MG
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HIF-1a-IN-2 hydroch 25mg | 25MG
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Medchemexpress LLC 3-Bromomethylpyridine hydrobromide | 4916-55-6 | 252.93 | 10 G
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3-Bromomethylpyridine hydrobromide is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
- Can be used as a biological material or organic compound
- Suitable for life science related research
- For research use only
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Medchemexpress LLC Norverapamil hydrochloride | 67812-42-4 | MFCD00078605 | 99.8% | 477.04 g/mol | C26H37ClN2O4 | 5 MG
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Norverapamil hydrochloride is the N-demethylated metabolite of verapamil used in pharmacological research. It functions as an L-type calcium channel blocker and a P-glycoprotein (P-gp) function inhibitor, supplied as a research-grade chemical for in vitro and in vivo studies.
- L-type calcium channel blocker and P-gp inhibitor.
- High purity (99.8%).
- Molecular formula C26H37ClN2O4; molecular weight 477.04 g/mol.
- Suitable for pharmacological and membrane transport studies.
- Provided as a solid hydrochloride salt for straightforward handling and dosing.
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Medchemexpress LLC 1R 2R-2-Pcca Hydroch 10Mg | HY-100013A1-10MG
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1R 2R-2-Pcca Hydroch 10Mg
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eMolecules 56962-01-7 | 3-Amino-2-chlorophenol | MFCD11044694 | 250mg
Ambeed | 3-Amino-2-chlorophenol | 250mg | 602850772 | A796202 | 56962-01-7 | MFCD11044694 | 143.570 | C6H6ClNO
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eMolecules 109-78-4 | Ambeed | 3-Hydroxypropionitrile | 100g | 533498540 | A141843 | MFCD00002826 | 71.079 | C3H5NO
Medchem Express | Aticaprant | 5mg | 446257108 | HY-101718 | 1174130-61-0 | MFCD22572355 | 418.512 | C26H27FN2O2
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Sigma Aldrich Fine Chemicals Biosciences 3-NN-Dimethylpalmitylammon5G
3-(N N-Dimethylpalmitylammonio)propanesulfonate is a zwitterionic detergent.
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Sigma Aldrich Fine Chemicals Biosciences Riboflavin 100G
Riboflavin belongs to the vitamin-B family and contains a pentose side chain ribitol.
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Medchemexpress LLC 3-phenoxybenzaldehyde | 39515-51-0 | MFCD00003353 | 99.2% | 198.22 g/mol | C13H10O2 | 50g
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3-Phenoxybenzaldehyde has weak complement classical pathway inhibition and hemolytic activity[1]
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eMolecules 58020-43-2 | Medchem Express | HOKU-81 | 5mg | 446270950 | HY-50291 | MFCD00900701 | 243.73 | C12H18ClNO2
Medchem Express | HOKU-81 | 5mg | 446270950 | HY-50291 | 58020-43-2 | MFCD00900701 | 243.730 | C12H18ClNO2
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Medchemexpress LLC Jnj-47117096 hydrochloride | 1610536-69-0 | 99.7% | 398.891 g/mol | C21H23ClN4O2 | 25MG
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JNJ-47117096 hydrochloride (MELK-T1 hydrochloride) is the hydrochloride salt of a small-molecule kinase inhibitor selective for MELK and active against FLT3. It is used as a research reagent to probe MELK biology and to evaluate antiproliferative effects in cellular assays.
- Potent MELK inhibition (IC50 23 nM)
- Also inhibits Flt3 (IC50 18 nM)
- Shows cellular antiproliferative activity (Ba/F3 cells IC50 ~1.5 μM without IL-3)
- Provided as a hydrochloride salt to aid solubility in biological assays
- High chemical purity (~99.7%) and documented CAS identifier (1610536-69-0)
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Medchemexpress LLC AMPK activator 2 hydrochloride | 00-00-0 | 99.7% | 337.77 | C13H19ClF3N5 | 5 MG
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AMPK activator 2 hydrochloride is a fluorine-containing proguanil derivative that activates AMP-activated protein kinase (AMPK), modulating downstream mTOR/4EBP1/p70S6K signaling. It is reported to inhibit proliferation and migration of human cancer cell lines and is provided as a research reagent for in vitro studies.
- Up-regulates AMPK signaling pathway.
- Downregulates mTOR/4EBP1/p70S6K signaling.
- Inhibits proliferation and migration in UMUC3, T24, and A549 cell lines.
- Available in small quantities suitable for assay development.
- High reported purity for biochemical experiments.
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Medchemexpress LLC Bay 61-3606 hydrochloride | 1615197-10-8 | MFCD29073361 | 98.1% | 426.86 | C20H19ClN6O3 | 10 MG
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BAY 61-3606 hydrochloride is the hydrochloride salt of BAY 61-3606, a selective ATP-competitive Syk inhibitor used for in vitro research on Syk-mediated signaling and apoptosis. The product is supplied as a solid with a reported CAS number 1615197-10-8, molecular formula C20H19ClN6O3, molecular weight 426.86, and high purity for research applications.
- Selective Syk inhibitor suitable for cell signaling studies.
- ATP-competitive and reversible mechanism of action.
- Hydrochloride salt form improves solubility for aqueous assays.
- High reported purity supports reproducible experimental results.
- Intended for research use only; not for human or veterinary use.
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Medchemexpress LLC Crinecerfont hydrochloride | 321839-75-2 | 98.0% | 519.50 | C27H29Cl2FN2OS | 5 MG
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Crinecerfont hydrochloride is the hydrochloride salt of crinecerfont (SSR-125543), a potent, orally active, non-peptide corticotropin-releasing factor 1 (CRF1) receptor antagonist supplied for preclinical pharmacology research. It is provided as a high-purity solid with documented solubility and storage recommendations for laboratory use.
- Potent CRF1 receptor antagonist for preclinical research.
- High purity (98.0%).
- Molecular weight 519.50 g/mol.
- Soluble in DMSO at 100 mg/mL; in vivo formulation protocols available.
- Available in small research quantities, such as 5 mg.
- Store sealed away from moisture and light; follow cold storage guidance for solutions.
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