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Filtered Search Results
Apexbio Technology LLC Prazosin HCl,100mg CAS# 19237-84-4
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α1 and α2B-adrenoceptor antagonist. Also a potent antagonist at the melatonin MT3 receptor (Ki = 10.2 nM). Also available as part of the α1-Adrenoceptor Tocriset™ and Mixed Adre. Other sizes are also available. Please inqury us for quote.
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Medchemexpress LLC BAY-293 10mg | 2244904-70-7 | 10 MG
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BAY-293 is a small-molecule chemical probe that inhibits the SOS1-KRAS interaction, reducing RAS activation (reported IC50 ≈ 21 nM). Supplied as a purified solid for research use; store at -20°C.
- Potent SOS1-KRAS interaction inhibitor (IC50 ≈ 21 nM).
- High purity, ≥98% by HPLC.
- Molecular weight 448.59 g·mol⁻1.
- Chemical formula C25H28N4O2S.
- Supplied as a milligram-scale solid; store at -20°C.
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eMolecules 1637735-84-2 | Medchem Express | FIIN-3 | 1mg | 446269123 | HY-18603 | MFCD28386554 | 691.61 | C34H36Cl2N8O4
Ambeed | Bis[(R)-1-phenylethyl]amine | 250mg | 632172738 | A212397 | 23294-41-9 | MFCD00243088 | 225.335 | C16H19N
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eMolecules 357-70-0 | Medchem Express | Galanthamine | 50mg | 446271480 | HY-76299 | MFCD00867189 | 287.359 | C17H21NO3
Ambeed | 5-Methyl-2-(4455-tetramethyl-132-dioxaborolan-2-yl)aniline | 100mg | 704973383 | A767206 | 863578-36-3 | MFCD06795679 | 233.120 | C13H20BNO2
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Active Motif RVX-208
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Active Motif's RVX-208 is a potent BET bromodomain antagonist with (IC50 = 0.51 uM for BD2) with approximately 170-fold selectivity over BD1 (ref 1,2). It increases apolipoprotein A-1 and HDL cholesterol in vitro and in vivo, and it reduces atherosclerosis.
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eMolecules 621-87-4 | Phenoxyacetone | ChemScene | MFCD00008767 | 150.177 | C9H10O2 | 98.000 | CC(=O)COc1ccccc1 | 10g | 686116656
Phenoxyacetone | ChemScene | 621-87-4 | MFCD00008767 | 150.177 | C9H10O2 | 98.000 | CC(=O)COc1ccccc1 | 10g | 686116656
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Medchemexpress LLC Alpha-Asarone | 2883-98-9 | 208.25 | 500 MG
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Alpha-Asarone (α-Asarone) is one of the main psychoactive compounds and possesses antidepressant-like activity in mice. It is for research use only.
- Purity: 99.89%
- Appearance: Solid
- Color: White to off-white
- Initial source: Plants (Araceae, Acorus tatarinowii Schott)
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Medchemexpress LLC HY-101634 5mg Medchemexpress, ABT-072 CAS:1132936-00-5 Purity:>98%
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Medchemexpress, HY-101634 5mg ABT-072 CAS:1132936-00-5 ABT-072 is a nonnucleoside NS5B polymerase inhibitor and a candidate drug evaluated for treatment of hepatitis C virus. 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 HY-101976 5mg Medchemexpress, JAK3-IN-6 CAS:1443235-95-7 Purity:>98%
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Medchemexpress, HY-101976 5mg JAK3-IN-6 CAS:1443235-95-7 JAK3-IN-6 is a potent, selective irreversible Janus Associated Kinase 3 (JAK3) inhibitor, with an IC50 of 0.15 nM. 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 HY-N0690 10mg Medchemexpress, Schisandrin C CAS:61301-33-5 Purity:>98%
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Medchemexpress, HY-N0690 10mg Schisandrin C CAS:61301-33-5 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 KU-57788 | 503468-95-9 | 100.0% | 413.49 | 1 ML
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KU-57788 (NU7441) is a highly potent and selective DNA-PK inhibitor with an IC50 of 14 nM. It acts as an NHEJ pathway inhibitor, and also inhibits PI3K and mTOR with IC50s of 5.0 μM and 1.7 μM, respectively.
- Highly potent and selective DNA-PK inhibitor (IC50 of 14 nM)
- NHEJ pathway inhibitor
- Inhibits PI3K (IC50 of 5.0 μM) and mTOR (IC50 of 1.7 μM)
- Inhibits the growth of liver cancer HepG2 cells dose- and time-dependently
- Reduces pDNA-PKcs (S2056) protein expression in liver cancer cells
- Affects DNA damage repair when double treated with 60Coγ IR
- Reduces the frequency of NHEJ and increases the rate of HDR following Cas9-mediated DNA cleavage
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Medchemexpress LLC HY-15338 10mg Medchemexpress, TG003 CAS:719277-26-6 Purity:>98%
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Medchemexpress, HY-15338 10mg TG003 CAS:719277-26-6 TG003 is a potent inhibitor of Clk1/Sty; inhibits Clk1 and Clk4 with IC50 values of 20 and 15 nM, respectively. 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 Carbamic acid, N-[(2R,3S)-2-methyl-4-oxo-3-oxetanyl]-, 5-phenylpentyl ester | 1439366-88-7 | 99.7% | 5MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000233666.png-250.jpg)
Medchemexpress LLC Carbamic acid, N-[(2R,3S)-2-methyl-4-oxo-3-oxetanyl]-, 5-phenylpentyl ester | 1439366-88-7 | 99.7% | 5MG
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Carbamic acid, N-[(2R,3S)-2-methyl-4-oxo-3-oxetanyl]-, 5-phenylpentyl ester | 1439366-88-7 | 99.7% | 5MG
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eMolecules 429653-73-6 | Medchem Express | Y16 | 5mg | 446261586 | HY-12649 | MFCD03083787 | 384.435 | C24H20N2O3
Ambeed | 246-Tris(3-(pyridin-3-yl)phenyl)-135-triazine | 100mg | 633419633 | A1156750 | 939430-26-9 | 540.630 | C36H24N6
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Aobchem AOBCHEM
5000951493 4-PHENOXY-2- TRIFLUOROMETHYL P
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