Benzoxazines
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Filtered Search Results
eMolecules 238428-26-7 | 3-(Methylsulfonylamino)benzylamine hydrochloride | Combi-Blocks | MFCD09054706 | 236.710 | C8H13ClN2O2S | 97.000 | Cl.CS(=O)(=O)Nc1cccc(CN)c1 | 1g | 232336243
3-(Methylsulfonylamino)benzylamine hydrochloride | Combi-Blocks | 238428-26-7 | MFCD09054706 | 236.710 | C8H13ClN2O2S | 97.000 | Cl.CS(=O)(=O)Nc1cccc(CN)c1 | 1g | 232336243
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eMolecules 867062-95-1 | 1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13-tetraoxa-4-azahexadecan-16-oic acid | Synthonix | MFCD06656471 | 443.496 | C24H29NO7 | 95.000 | OC(=O)CCOCCOCCOCCNC(=O)OCC1c2ccccc2-c2ccccc12 | 50mg | 571832800
1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13-tetraoxa-4-azahexadecan-16-oic acid | Synthonix | 867062-95-1 | MFCD06656471 | 443.496 | C24H29NO7 | 95.000 | OC(=O)CCOCCOCCOCCNC(=O)OCC1c2ccccc2-c2ccccc12 | 50mg | 571832800
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TARGETMOL CHEMICALS INC IL-4-INHIBITOR-1 5MG
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. IL-4 inhibitor is an inhibitor of IL-4.1It binds to IL-4 with a Kdvalue of 1.8 uM and inhibits IL-4 activity in a cell-based reporter assay (EC50= 1.81 uM). It is selective for IL-4 over IL-13 (EC50= 18.2 uM). IL-4 inhibitor inhibits IL-4-induced STAT6 phosphorylation in THP-1 monocytes (EC50= 3.1 uM) indicating inhibition of the IL-4-JAK1-STAT6 signaling pathway. purity: 98%
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000760108 3 5-DIPHENYL-4H-1 2 250MG
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Leybold Vacuum Products Inc LEYBONOL LVO 130 20 LITER
NC3892119 LEYBONOL LVO 130 20 LITER
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Bradley Product Inc BRADLEY PRODUCT INC
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NC3894304 MARKING DYE 8OZ LIME
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UMICORE PRECIOUS METALS CHEMISTRY USA DIU-BROMOBIS1-METHYLNAPHTHY
NC3672725 DIU-BROMOBIS1-METHYLNAPHTHY
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TARGETMOL CHEMICALS INC Research Chemical 10mg
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Also available in 1 mg, 5 mg, 25 mg, 50 mg, 100 mg, 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. 9'''-Methyl salvianolate B is a natural product for research related to life sciences. The catalog number is T4589 and the CAS number is 1167424-32-9. purity: 99%
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Cell Signaling Technology Arginase-1 D4E3Mtm XPR R
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Arginase-1 (D4E3M(tm)) XP(R) Rabbit mAb (Alexa Fluor(R) 647 Conjugate) 100 ul
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Cell Signaling Technology HA-Tag (C29F4) Rabbit mAb (PE-Cy7(R) Conjugate) 100 ul
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HA-Tag (C29F4) Rabbit mAb (PE-Cy7(R) Conjugate) 100 ul
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TARGETMOL CHEMICALS INC VALEPOTRIATE 5MG
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Also available in 1 mg 10 mg 25 mg 50 mg and bulk. Please contact Fisher for quotes. Valepotriate (Valtrate) fraction can have sedative effects and affect behavioral parameters related to recognition memory. Valepotriates a new class of cytotoxic and antitumor agents they are very potent cytotoxic agents for the HTC hepatoma cells. Valepotriates may have a potential anxiolytic effect on the psychic symptoms of anxiety. purity: 99%
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Cell Signaling Technology Phospho-HS1 Tyr378/397 D12C
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Phospho-HS1 (Tyr378/397) (D12C1) XP(R) Rabbit mAb (PE Conjugate) 100 ul
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TARGETMOL CHEMICALS INC ML-SA1 25MG
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Also available in 5 mg 10 mg 50 mg 100 mg 200 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. ML-SA1 (Mucolipin synthetic agonist 1) is a selective TRPML agonist inhibits Dengue virus 2 (DENV2) and Zika virus (ZIKV) by promoting lysosomal acidification and protease activity. The IC50 value of ML-SA1 against DENV2 RNA and ZIKV RNA is 8.3 uM and 52.99 uM respectively[1]. purity: 99%
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TARGETMOL CHEMICALS INC JAK2 INHIBITOR V 25MG
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Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. JAK2 Inhibitor V (JAK2 Inhibitor V Z3) is a novel specific inhibitor of Jak2 inhibiting Jak2-V617F and Jak2-WT autophosphorylation in a dose-dependent manner. purity: 99%
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TARGETMOL CHEMICALS INC Research Chemical 25mg
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Also available in 5 mg, 10 mg, 50 mg, 100 mg, 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. 5,7,3',4'-Tetramethoxyflavone (TMF), a prominent polymethoxyflavone (PMF) derived from M. exotica, displays a range of notable bioactivities. These include anti-malarial, anti-fungal, anti-mycobacterial, and anti-inflammatory properties. Moreover, TMF specifically targets (beta)-catenin signaling to exhibit chondroprotective activity. purity: 99%
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