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Filtered Search Results
eMolecules 59674-85-0 | 7-Aminoquinazoline-2,4(1H,3H)-dione | MFCD13191696 | 100mg
Ambeed | 7-Aminoquinazoline-2,4(1H,3H)-dione | 100mg | 506391219 | A532977 | 59674-85-0 | MFCD13191696 | 177.163 | C8H7N3O2
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Medchemexpress LLC Tucatinib hemiethanolate | 1429755-56-5 | 98.8% | 503.57 | 50 MG
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Tucatinib hemiethanolate is a potent, orally active, and selective HER2 inhibitor. It demonstrates nanomolar activity against purified HER2 enzyme and is approximately 500-fold selective for HER2 versus EGFR in cell-based assays. It selectively inhibits the receptor tyrosine kinase HER2 relative to EGFR, blocking proliferation and phosphorylation of HER2 and its downstream effector, Akt in HER2 overexpressing cell lines. It is intended for research use only.
- Potent and selective HER2 inhibition (IC50 of 8 nM)
- Antiproliferative effects in HER2 overexpressing cell lines
- Reduced EGFR-related toxicities
- Anti-tumor activity and survival benefit in animal models
- Significant reduction in brain pErbB2 (80%)
- Dose-related tumor growth inhibition
- Enhanced tumor growth inhibition when combined with trastuzumab
- Studied in various clinical trials
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Accela Chembio Inc Bis(pentafluorophenyl) Carbonate | 25g | 59483-84-0 | MFCD00368353 | 97+% | Shelf Life: 1440 Days | +4
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Bis(pentafluorophenyl) Carbonate | 25g | 59483-84-0 | MFCD00368353 | 97+% | Shelf Life: 1440 Days | +4
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Medchemexpress LLC Tucatinib hemiethanolate | 1429755-56-5 | 98.8% | 503.57 | 100 MG
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Tucatinib hemiethanolate is a potent, orally active, and selective HER2 inhibitor. With an IC50 of 8 nM, it selectively targets HER2, showing approximately 500-fold selectivity over EGFR in cell-based assays. This compound is intended for research use only.
- Potent, orally active, and selective HER2 inhibitor
- Selectively inhibits receptor tyrosine kinase HER2 relative to EGFR
- Blocks proliferation and phosphorylation of HER2 and its downstream effector Akt
- Demonstrated anti-tumor activity and improved survival in animal models
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eMolecules 131179-95-8 | Medchem Express | Efaproxiral | 50mg | 446263211 | HY-13619 | MFCD00899086 | 341.407 | C20H23NO4
Ambeed | Benzyl 5-aminopentanoate hydrochloride | 5g | 572859746 | A1037243 | 154407-91-7 | MFCD25371665 | 243.730 | C12H18ClNO2
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Medchemexpress LLC AMTB hydrochloride | 926023-82-7 | 99.2% | 430.99 | C23H27ClN2O2S | 5 MG
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AMTB hydrochloride is a research-grade small molecule that selectively blocks TRPM8 ion channels and also inhibits voltage-gated sodium channels. Supplied as a white to off-white solid with high chemical purity, it is intended for in-vitro and in-vivo research applications investigating TRPM8-mediated physiology and pharmacology.
- Selective TRPM8 channel blocker and non-selective voltage-gated sodium channel inhibitor.
- High purity: 99.18%.
- White to off-white solid form suitable for formulation.
- Soluble in DMSO (up to 100 mg/mL) with sonication.
- In vivo formulation protocols available for concentrations ≥ 2.5 mg/mL.
- Supplied in small research pack sizes, including 5 mg.
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eMolecules 63019-39-6 | 3-Hydroxychrysene | Toronto Research Chemicals | MFCD01736446 | 244.293 | C18H12OOc1ccc2ccc3c4ccccc4ccc3c2c1 | 100mg | 483412499
3-Hydroxychrysene | Toronto Research Chemicals | 63019-39-6 | MFCD01736446 | 244.293 | C18H12OOc1ccc2ccc3c4ccccc4ccc3c2c1 | 100mg | 483412499
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Medchemexpress LLC PARP14 inhibitor H10 | 2084811-68-5 | 99.5% | 557.58 | C24H27N7O7S | 10 MG
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A selective small-molecule inhibitor of PARP14 designed for biochemical and cellular research targeting PARP14-mediated pathways and apoptosis.
- Selective PARP14 inhibitor with reported IC50 of 490 nM.
- High reported purity (99.46% as supplied).
- Molecular weight 557.58 and formula C24H27N7O7S.
- Supplied as a solid (off-white to yellow) or as a 10 mM solution in DMSO for easy reconstitution.
- Available in small research quantities, including 10 mg.
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Medchemexpress LLC 1,4-dimethoxybenzene | 150-78-7 | MFCD00008401 | 100.0% | 138.16 g/mol | C8H10O2 | 50 MG
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Analytical reference standard of 1,4-dimethoxybenzene (CAS 150-78-7) supplied as a high-purity crystalline solid for research and analytical applications. It is intended for instrument calibration, method development, and quality control where a well-characterized reference compound is required.
- High purity (99.99%) for analytical reliability.
- Molecular formula C8H10O2, molecular weight 138.16 g/mol.
- White to colorless crystalline solid with melting point ~55-60 °C.
- Suitable for calibration, method development, and quality control.
- Provided in small, measured quantities for laboratory use.
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Medchemexpress LLC KRAS G12C inhibitor 15 | 2349393-21-9 | 98.5% | 498.91 g/mol | C25H21ClF2N4O3 | 100MG
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KRAS G12C inhibitor 15 is a research-grade small-molecule inhibitor selective for the KRAS G12C mutant, derived from patent WO2019110751A1 (compound 22). It is reported to inhibit KRAS G12C with an IC50 of 5 nM and is supplied as a solid for laboratory research use only.
- Potent KRAS G12C inhibition (IC50 5 nM).
- High purity (~98.5%).
- Molecular weight 498.91 g/mol; formula C25H21ClF2N4O3.
- White to yellow solid suitable for biochemical and cellular assays.
- Supplied as 100 MG for research use only.
- Derived from patent WO2019110751A1 (compound 22).
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Selleck Chemical LLC Schisandrin B S3600-10mg
Schisandrin B is the most abundant dibenzocyclooctadiene lignan present in the traditional Chinese medicinal herb Schisandra chinensis (Turcz ) Baill It is a kind of ATR and P-gp inhibitor with high safety
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Selleck Chemical LLC LY2109761 S2704-200mg
LY2109761 is a novel selective TGF- receptor type I/II (T RI/II) dual inhibitor with Ki of 38 nM and 300 nM in a cell-free assay respectively shown to negatively affect the phosphorylation of Smad2 LY2109761 blocks autophagy and induces apoptosis
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eMolecules 101526-62-9 | Medchem Express | Sematilide (hydrochloride) | 5mg | 713704199 | HY-101436A | MFCD01667315 | 349.87 | C14H24ClN3O3S
Pharmablock | methyl 2-bromo-13-benzothiazole-6-carboxylate | 25mg | 784547251 | PBT8584 | 1024583-33-2 | MFCD16660646 | 272.120 | C9H6BrNO2S
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eMolecules 947914-18-3 | Medchem Express | ML365 | 5mg | 446261098 | HY-12345 | MFCD09204310 | 360.413 | C22H20N2O3
Medchem Express | ML365 | 5mg | 446261098 | HY-12345 | 947914-18-3 | MFCD09204310 | 360.413 | C22H20N2O3
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Medchemexpress LLC DSM705 hydrochloride | 2989908-08-7 | 99.6% | C19H20ClF3N6O | 10MG
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DSM705 hydrochloride is the hydrochloride salt of DSM705, a pyrrole-based dihydroorotate dehydrogenase (DHODH) inhibitor with oral antimalarial activity. It shows nanomolar potency against Plasmodium DHODH (IC50 ≈95 nM for P. falciparum and ≈52 nM for P. vivax) and activity against Plasmodium parasites, with minimal inhibition of mammalian DHODHs.
- Pyrrole-based DHODH inhibitor with nanomolar potency.
- Orally active antimalarial compound.
- Selective for Plasmodium DHODH over mammalian DHODHs.
- Hydrochloride salt form for improved solubility and handling.
- Available in multiple solid and solution pack sizes for research use.
- Reported purity approximately 99.6%.
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