Name | Description | Size | Catalog # | Supplier | |
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88255-01-0 | Purity ≥98%. MW: 420.46 | 100 mg, 500 mg | MBS132338 |
![]() MYBIOSOURCE INC. |
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95343-20-7 | Purity ≥98%. MW: 664.1 | 100 mg, 500 mg | MBS130215 |
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666-15 | An inhibitor of CREB-mediated gene transcription (IC50 = 81 nM in a cell-b… | 10 mg | 30780-10 |
![]() CAYMAN CHEMICAL COMPANY |
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666-15 | An inhibitor of CREB-mediated gene transcription (IC50 = 81 nM in a cell-b… | 25 mg | 30780-25 |
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666-15 | An inhibitor of CREB-mediated gene transcription (IC50 = 81 nM in a cell-b… | 5 mg | 30780-5 |
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666-15 | An inhibitor of CREB-mediated gene transcription (IC50 = 81 nM in a cell-b… | 50 mg | 30780-50 |
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92.1 | Tissue: uvea; Tumor: melanoma, melanin production. | 1 vial | ABC-TC444S |
![]() ACCEGEN BIOTECH |
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380 | Tissue: peripheral blood; Tumor: leukemia, pre-B cell; Derived from a pati… | 1 vial | ABC-TC442S |
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1301 | Human T-cell leukaemia. 1301 Is a sub-line of CCRF-CEM. It has unusually l… | 1 vial | ABC-TC0001 |
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5637 | 5637 Cell line was established from the primary bladder carcinoma of a 68-… | 1 vial | ABC-TC0015 |
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1360900-71-5 | MW: 228.0427 | 100 mg | orb1146568 |
![]() BIORBYT LTD. |
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666-15 | MW: 620.52 | 100 mg, 250 mg, 1 g | orb401883 |
![]() BIORBYT LTD. |
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293 | n/a | n/a | 103 |
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A 205804 | Purity ≥98%. MW: 300.39 | 100 mg, 500 mg | MBS132392 |
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A 66 | Purity ≥98%. MW: 393.52 | 100 mg, 500 mg | MBS132169 |
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A 740003 | Purity ≥98%. MW: 474.565 | 100 mg, 500 mg | MBS132187 |
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A 740003 | Purity >98%. A 740003 is a novel competitive antagonist of P2X7 receptors… | 10 mg, 25 mg, 50 mg | MBS384091 |
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A 769662 | Purity ≥98%. MW: 360.39 | 100 mg, 500 mg | MBS130892 |
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A 769662 | Purity 97%+. MW: 360.39 | 5 mg, 1ml/10mM (in DMSO), 10 mg | MBS576261 |
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A 803467 | Purity >98%. A 803467 is a selective blocker of NaV1.8 channels (IC50 valu… | 10 mg, 1 mL (in DMSO), 25 mg | MBS384093 |
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A 83-01 | Purity ≥98% by HPLC. Background: A selective inhibitor of TGF-beta type… | 1 mg | MBS842636 |
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A 83-01 | Purity ≥98%. MW: 421.52 | 100 mg, 500 mg | MBS132328 |
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A 83-01 | Purity >98%. A83-01 is a TGF-β kinase / activin receptor like kinase… | 5 mg, 10 mg, 25 mg | MBS384095 |
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A 922500 | MW: 428.48 | 5 mg | MBS8506458 |
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A 922500 | Purity ≥98%. MW: 428.488 | 100 mg, 500 mg | MBS130245 |
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A 967079 | Purity >98%. A 967079 is a selective TRPA1 channel blocker (IC50 values ar… | 10 mg, 25 mg, 50 mg | MBS384097 |
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A-1155463 | Purity >98%. A-1155463 is a highly potent and selective BCL-XL inhibitor,… | 5 mg, 10 mg, 50 mg | MBS384082 |
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A-1210477 | Purity ≥98%. MW: 886.51 | 100 mg, 500 mg | MBS131280 |
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A-1210477 | Purity ≥99%. MW: 850.04 | 2 mg, 5 mg, 10 mg | MBS575263 |
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A-1210477 | Purity >98%. A-1210477 is a potent and selective MCL-1 inhibitor. A-121047… | 5 mg, 10 mg, 25 mg | MBS384084 |
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A-1331852 | Purity ≥98%. MW: 658.82 | 100 mg, 500 mg | MBS131656 |
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A-196 | Purity ≥99%. A-196 is a potent and selective inhibitor of SUV420 h1 and… | 2 mg, 1ml/10mM (in DMSO), 5 mg | MBS5750478 |
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A-205804 | Purity 97%+. MW: 300.41 | 5 mg, 10 mg, 1ml/10mM (in DMSO) | MBS576130 |
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A23187 | Purity >98% by TLC. Background: A calcium ionophore. Causes rapid influx o… | 10 mg | MBS843148 |
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A-366 | Purity ≥98% by HPLC. Background: A-366 is a potent and selective G9a /… | 1 mg, 5 mg | MBS842453 |
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A-366 | Purity ≥98%. MW: 329.444 | 100 mg, 500 mg | MBS131198 |
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A-366 | Purity >98%. A-366 is a potent and selective G9a / GLP histone lysine meth… | 10 mg, 25 mg, 50 mg | MBS384085 |
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A427 | A427 cells are derived from human lung epithelial carcinoma taken from a 5… | 0.1 mg, 0.2 mg, 0.5 mg | MBS201043 |
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A431 | A431 cells were established from an epidermoid carcinoma in the skin / epi… | 0.1 mg, 0.2 mg, 0.5 mg | MBS201022 |
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A-443654 | Purity >98%. A-443654, a specific Akt inhibitor with Ki value of 160 pM, i… | 2 mg, 5 mg, 10 mg | MBS384086 |
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A-484954 | Purity >98%. A-484954 is a potent, selective inhibitor of eukaryotic longa… | 10 mg, 25 mg, 50 mg | MBS384087 |
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A549 | A549 cells are adenocarcinomic human alveolar basal epithelial cells. The… | 0.1 mg, 0.2 mg, 0.5 mg | MBS201023 |
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A66 | MW: 393.53 | 10 mg | MBS8506193 |
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A66 | Purity >98%. The S-enantiomer of A66 is a potent inhibitor of the p110alph… | 5 mg, 1 mL (in DMSO), 10 mg | MBS384089 |
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A66 | Purity 97%+. MW: 393.53 | 2 mg, 5 mg, 1ml/10mM (in DMSO) | MBS575616 |
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A-674563 | MW: 358.44 | 2 mg | MBS8506244 |
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A-674563 | Purity ≥98%. A-674563 is an Akt1 inhibitor with Ki of 11 nM, modest pot… | 1 mg, 2 mg, 5 mg | MBS578707 |
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A-674563 | Purity ≥98%. MW: 358.445 | 100 mg, 500 mg | MBS131746 |
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A-674563 | Purity >98%. A-674563 is a B / Akt inhibitor with an IC50 of 14 nM and als… | 5 mg, 1 mL (in DMSO), 10 mg | MBS384090 |
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A-769662 | Purity ≥98% by HPLC. Background: Cell-permeable. A potent AMPK activato… | 5 mg | MBS842018 |
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