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Filtered Search Results
Chem Service Inc 1,2-Dibromo-3-chloropropane | 96-12-8 | MFCD00039365 | 250mg
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This item has a minimum order quantity of 2 per supplier requirements
1,2-Dibromo-3-chloropropane | Putity: 99.5 | MW: 236.36 | 96-12-8 | MFCD00039365 | 250mg
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![eMolecules 2417979-24-7 | 3-Hydroxystearoylcarnitine Hydrochloride | Toronto Research Chemicals480.130 | C25H50ClNO5[Cl-].CCCCCCCCCCCCCCCC(O)CC(=O)O[C@H](CC(O)=O)C[N+](C)(C)C | 100mg | 483415273](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502177610.JPG-250.jpg)
eMolecules 2417979-24-7 | 3-Hydroxystearoylcarnitine Hydrochloride | Toronto Research Chemicals480.130 | C25H50ClNO5[Cl-].CCCCCCCCCCCCCCCC(O)CC(=O)O[C@H](CC(O)=O)C[N+](C)(C)C | 100mg | 483415273
3-Hydroxystearoylcarnitine Hydrochloride | Toronto Research Chemicals | 2417979-24-7480.130 | C25H50ClNO5[Cl-].CCCCCCCCCCCCCCCC(O)CC(=O)O[C@H](CC(O)=O)C[N+](C)(C)C | 100mg | 483415273
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Sigma Aldrich Fine Chemicals Biosciences KY02111 >=98% (HPLC) | 1118807-13-8 | 5MG
KY02111 >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 376.86 | 1118807-13-8 | 5MG
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Sigma Aldrich Fine Chemicals Biosciences Dafadine A >=98% (HPLC) | 1065506-69-5 | 25MG
Dafadine A >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 391.46 | 1065506-69-5 | 25MG
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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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Medchemexpress LLC HY-112569 5mg Medchemexpress, MAT2A inhibitor 2 CAS:13299-99-5 Purity:>98%
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Medchemexpress, HY-112569 5mg MAT2A inhibitor 2 CAS:13299-99-5 MAT2A inhibitor 2 is a methionine adenosyltransferase 2A (MAT2A) 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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Selleck Chemical LLC 1.4-Cineole S5419-25mg
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1 4-Cineole (Isocineole) is a widely distributed natural oxygenated monoterpene 1 4-Cineole present in eucalyptus oil activates both human TRPM8 and human TRPA1
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Medchemexpress LLC Erlotinib-d6 hydrochloride | 1189953-78-3 | 98.1% | 1 MG
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Erlotinib-d6 hydrochloride is a deuterium-labeled form of erlotinib hydrochloride used as an internal standard and analytical reagent for studies targeting the epidermal growth factor receptor (EGFR). Supplied as the hydrochloride salt to aid solubility, it is intended for research use only.
- Deuterium-labeled internal standard for quantitative analysis
- High purity suitable for LC-MS and analytical assays
- Molecular formula C22H18D6ClN3O4, molecular weight 435.93
- Available in 1 MG packs for small-scale experiments
- Intended for research use only; not for human consumption or clinical use
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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 HY-100544 5mg Medchemexpress, FLLL32 CAS:1226895-15-3 Purity:>98%
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Medchemexpress, HY-100544 5mg FLLL32 CAS:1226895-15-3 FLLL32, a synthetic analog of curcumina, is a JAK2/STAT3 dual inhibitor with anti-tumor activity [1] [2] . 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 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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