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Filtered Search Results
Medchemexpress LLC HY-111647 10mg Medchemexpress, N2-Methylguanosine CAS:2140-77-4 Purity:>98%
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Medchemexpress, HY-111647 10mg N2-Methylguanosine CAS:2140-77-4 N2-methylguanosine is a modified nucleoside that occurs at several specific locations in many tRNA's. 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 Contezolid (MRX-I) | 1112968-42-9 | 99.2% | 408.33 | 50 MG
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Contezolid (MRX-I) | 1112968-42-9 | 99.2% | 408.33 | 50 MG
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Medchemexpress LLC HY-100902 5mg Medchemexpress, CDD3506 CAS:197913-15-8 Purity:>98%
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Medchemexpress, HY-100902 5mg CDD3506 CAS:197913-15-8 CDD3506 is used for elevating high density lipoprotein cholesterol (HDL) by inducing hepatic cytochrome P450IIIA (CYP3A) 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 M-89 | 2363165-42-6 | 99.1% | 10 MG
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M-89 is a highly potent and specific menin inhibitor, with a Kd of 1.4 nM for binding to menin. M-89 inhibits the menin-mixed lineage leukemia (Menin-MLL) protein-protein interaction and has potential to study MLL leukemia. M-89 inhibits the cell growth in leukemia cell lines carrying MLL fusion.
- Inhibits the cell growth of MV4-11 cell line with an IC50 of 25 nM.
- Inhibits the cell growth of HL-60 cell line with an IC50 of 10.2 μM.
- Stabilized the cellular menin protein in both MV4-11 and MOLM-13 cells dose-dependently (3.7-300 nM).
- Induces a time- and dose-dependent apoptosis in MV4-11 cells (0.03-3 μM, 48 h).
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Medchemexpress LLC M-89 | 2363165-42-6 | 99.1% | 50 MG
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M-89 is a highly potent and specific menin inhibitor that targets the menin-mixed lineage leukemia (Menin-MLL) protein-protein interaction. It has potential for studying MLL leukemia by inhibiting cell growth in leukemia cell lines and inducing apoptosis. It is for research use only.
- Highly potent and specific menin inhibitor
- Inhibits menin-MLL protein-protein interaction
- Potential for studying MLL leukemia
- Inhibits cell growth in leukemia cell lines carrying MLL fusion
- Induces time- and dose-dependent apoptosis in MV4;11 cells
- Stabilizes cellular menin protein in MV4;11 and MOLM-13 cells
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Medchemexpress LLC SGC-CK2-1 | 2470424-39-4 | 99.7% | 375.43 | 50 MG
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SGC-CK2-1 is a highly potent, ATP-competitive, and cell-active CK2 chemical probe. It shows exclusive selectivity for both human CK2 isoforms, with IC50s of 36 nM for CK2α and 16 nM for CK2α′ in the nanoBRET assay. This compound can be utilized for research into neurodegenerative diseases.
- Highly potent, ATP-competitive, and cell-active
- Exclusive selectivity for human CK2 isoforms
- Useful for neurodegenerative disease research
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eMolecules AstaTech / DABIGATRAN ETEXILATE MESYLATE / 0.25g / 248482726 / 41056 / 98.000 / 872728-81-9 / [null] / 723.850 / C35H45N7O8S
AstaTech / DABIGATRAN ETEXILATE MESYLATE / 0.25g / 248482726 / 41056 / 98.000 / 872728-81-9 / [null] / 723.850 / C35H45N7O8S
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Medchemexpress LLC HY-11048 10mg Medchemexpress, NS11394 CAS:951650-22-9 Purity:>98%
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Medchemexpress, HY-11048 10mg NS11394 CAS:951650-22-9 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 N6-Methyl-2'-deoxyadenosine | 2002-35-9 | MFCD00055999 | 250mg
Combi-Blocks | N6-Methyl-2'-deoxyadenosine | 250mg | 277529486 | QC-4154 | 95.000 | 2002-35-9 | MFCD00055999 | 265.273 | C11H15N5O3
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Medchemexpress LLC Bilastine-d6 | 1215358-58-9 | 97.1% | C28H31D6N3O3 | 1 MG
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Bilastine-d6 is a deuterium-labeled Bilastine. Bilastine is a selective histamine H1 receptor antagonist used for the treatment of allergic rhinoconjunctivitis and urticaria.
- Used as a tracer.
- Functions as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
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Medchemexpress LLC HY-19488A 5mg Medchemexpress, Ribocil-C CAS:1825355-56-3 Purity:>98%
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Medchemexpress, HY-19488A 5mg Ribocil-C CAS:1825355-56-3 Ribocil-C is a highly selective inhibitor of bacterial riboflavin riboswitches . 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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Sigma Aldrich Fine Chemicals Biosciences Ganciclovir | 82410-32-0 | MFCD00870588 | 100mg
Ganciclovir | 99% | MW: 255.23 | 82410-32-0 | MFCD00870588 | 100mg
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eMolecules 1246560-33-7 | Medchem Express | VS-5584 | 5mg | 446267557 | HY-16585 | MFCD25372027 | 354.418 | C17H22N8O
Medchem Express | M-110 | 5mg | 446261904 | HY-12830 | 1395048-49-3 | MFCD28053523 | 445.950 | C22H28ClN5O3
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eMolecules 475110-96-4 | Medchem Express | ZSTK474 | 10mg | 446271120 | HY-50847 | MFCD08705334 | 417.421 | C19H21F2N7O2
Ambeed | 5101520-Tetrakis-(4-aminophenyl)-porphyrin-Fe-(III) chloride | 250mg | 633659549 | A1194369 | 99651-88-4 | 764.090 | C44H32ClFeN8
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Medchemexpress LLC Olmesartan methyl ester | 1347262-29-6 | MFCD24386461 | 95.0% | 460.53 g/mol | C25H28N6O3 | 5 MG
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Olmesartan methyl ester is a chemical intermediate used in the synthesis of olmesartan medoxomil, an angiotensin AT1 receptor antagonist. It is intended for research and synthetic applications and is supplied in small laboratory pack sizes.
- Intermediate in the synthesis of olmesartan medoxomil.
- CAS number 1347262-29-6 for unambiguous identification.
- Molecular formula C25H28N6O3 and molecular weight 460.53 g/mol.
- Supplied with stated purity of 95.0%.
- Available in small research pack sizes (5 mg).
- Typically accompanied by a certificate of analysis and analytical data for batch traceability.
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