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Filtered Search Results
Medchemexpress LLC HY-14181 5mg Medchemexpress, Cinaciguat CAS:329773-35-5 Purity:>98%
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Medchemexpress, HY-14181 5mg Cinaciguat CAS:329773-35-5 Cinaciguat is an activator of guanylate cyclase (sGC), and used for acute decompensated heart failure. 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 GT 949 | 50MG
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GT 949 is a selective excitatory amino acid transporter-2 (EAAT2) positive allosteric modulator with an EC50 of 0 26 nM[1]
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Medchemexpress LLC (E)-3-(3-(2-chlorophenyl)acryloyl)-2H-chromen-2-one | 1253978-24-3 | 99.1% | 310.73 g/mol | C18H11ClO3 | 5 MG
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MAO-B-IN-2 is a small-molecule, selective and competitive inhibitor of monoamine oxidase B (MAO-B) and butyrylcholinesterase (BChE). It is provided for research use and is available as a solid and as a 10 mM solution in DMSO for biochemical and cell-based studies.
- Selective MAO-B and BChE inhibition (IC50 MAO-B = 0.51 μM; BChE = 7.00 μM).
- Molecular formula C18H11ClO3; molecular weight 310.73 g/mol.
- High purity (99.05% by supplier analysis).
- Available as solid and 10 mM solution in DMSO.
- Suitable for enzymatic assays, inhibitor screening, and cell-based studies.
- Research use only; not for human therapeutic use.
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Medchemexpress LLC HY-12037A 5mg Medchemexpress, Rigosertib CAS:592542-59-1 Purity:>98%
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Medchemexpress, HY-12037A 5mg Rigosertib CAS:592542-59-1 Rigosertib (ON-01910) is a multi-kinase inhibitor and a selective anti-cancer agent, which induces apoptosis by inhibition the PI3 kinase/Akt pathway, promots the phosphorylation of histone H2AX and induces G2/M arrest in cell cycle[2]. Rigosertib is a selective and non-ATP-competitive inhibitor of PLK1 with an IC50 of 9 nM[3]. 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 Talampanel >=97% (HPLC) | 161832-65-1 | MFCD00871406 | 5MG
Talampanel >=97% (HPLC) | Purity: >=97% (HPLC) | Mol Wt: 337.37 | 161832-65-1 | MFCD00871406 | 5MG
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eMolecules 122-99-6 | 2-Phenoxyethanol | Ambeed | MFCD00002857 | 138.166 | C8H10O2 | 94.000 | OCCOc1ccccc1 | 100g | 570567668
2-Phenoxyethanol | Ambeed | 122-99-6 | MFCD00002857 | 138.166 | C8H10O2 | 94.000 | OCCOc1ccccc1 | 100g | 570567668
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eMolecules 105512-79-6 | 4-(4-Trifluoromethylphenyl)thiazol-2-ylamine | Oakwood Chemical | MFCD03094298 | 244.240 | C10H7F3N2S | 98.000 | Nc1nc(cs1)-c1ccc(cc1)C(F)(F)F | 100mg | 537674379
4-(4-Trifluoromethylphenyl)thiazol-2-ylamine | Oakwood Chemical | 105512-79-6 | MFCD03094298 | 244.240 | C10H7F3N2S | 98.000 | Nc1nc(cs1)-c1ccc(cc1)C(F)(F)F | 100mg | 537674379
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Echelon Biosciences Research Labs 306OI10 100MG
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306Oi10, 95% 100mg CAS#2322290-93-5 C59H115N3O8 MW:994.58
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Medchemexpress LLC JAK-IN-5 hydrochloride | 2751323-21-2 | 99.5% | 511.03 | 50 MG
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JAK-IN-5 hydrochloride is an inhibitor of JAK, extracted from patent US20170121327A1. It is intended for research use only.
- Inhibits JAK.
- Inhibits STAT6 phosphorylation by 60% in IL-13-induced lung tissue in a mouse model of pSTAT6 induction at 0.5 mg/mL (oral aspirate, 50 μL).
- Inhibits 88% of BALF eosinophils in a male C57 mice model of Alternaria alternata-induced eosinophilic inflammation of the lung at 0.1-1.0 mg/mL (oral aspirate, 50 μL).
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Medchemexpress LLC HY-N0700 1g Medchemexpress, alpha-Asarone CAS:2883-98-9 Purity:>98%
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Medchemexpress, HY-N0700 1g alpha-Asarone CAS:2883-98-9 alpha-Asarone (α-Asarone) is one of the main psychoactive compounds, and possesses an antidepressant-like activity in mice. 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 133229-11-5 | Medchem Express | AM-92016 (hydrochloride) | 5mg | 482203787 | HY-101253 | MFCD00673947 | 483.83 | C19H25Cl3N2O4S
Medchem Express | ML401 | 5mg | 495799946 | HY-116814 | 1597489-14-9 | 419.750 | C20H20BrClN2O
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![eMolecules 100286-90-6 | Irinotecan HCl | Broadpharm590.721 | C33H42N4O6 | 0.000 | CCc1c2CN3C(CC4C(COC(=O)[C@]4(O)CC)C3=O)c2nc2ccc(OC(=O)N3CCC(CC3)N3CCCCC3)cc12 | 100mg | 724438162](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502461873.JPG-250.jpg)
eMolecules 100286-90-6 | Irinotecan HCl | Broadpharm590.721 | C33H42N4O6 | 0.000 | CCc1c2CN3C(CC4C(COC(=O)[C@]4(O)CC)C3=O)c2nc2ccc(OC(=O)N3CCC(CC3)N3CCCCC3)cc12 | 100mg | 724438162
Irinotecan HCl | Broadpharm | 100286-90-6590.721 | C33H42N4O6 | 0.000 | CCc1c2CN3C(CC4C(COC(=O)[C@]4(O)CC)C3=O)c2nc2ccc(OC(=O)N3CCC(CC3)N3CCCCC3)cc12 | 100mg | 724438162
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Medchemexpress LLC HY-18936 10mg Medchemexpress, Alda-1 CAS:349438-38-6 Purity:>98%
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Medchemexpress, HY-18936 10mg Alda-1 CAS:349438-38-6 Alda-1 is a potent ALDH2 agonist, which activates wild-type ALDH2 and restores near wild-type activity to ALDH2*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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Selleck Chemical LLC JNJ0966
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JNJ0966 is a highly selective compound that inhibits activation of MMP-9 zymogen and subsequent generation of catalytically active enzyme It has no effect on MMP-1 MMP-2 MMP-3 MMP-9 or MMP-14 catalytic activity and did not inhibit activation of the highly related MMP-2 zymogen
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Apexbio Technology LLC Phenoxybenzamine HCl 63-92-3 10mM (in 1mL DMSO)
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Phenoxybenzamine HCl (CAS number 63-92-3) is an irreversible nonselective antagonist of alpha-adrenergic receptors It covalently binds to these receptors producing sustained blockage and therefore preventing receptor-mediated vasoconstriction Due to this prolonged alpha-receptor antagonism phenoxybenzamine hydrochloride is frequently utilized in biomedical research to study sympathetic nervous system functions receptor pharmacology and cardiovascular-related pathophysiology
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