Non-Antibody Products — page 1 of 18,782



Non-Antibody Products
Page 1 of 18,782
  • Records 1 - 100 of 1,878,160
Name Description Size Catalog # Supplier
A-794278 An Antagonist of mGluR1 and mGluR5. Synthetic. Purity >98%. MW: 342.46 Da. 25 mg A-435 ALOMONE LABS
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A-794278 An Antagonist of mGluR1 and mGluR5. Synthetic. Purity >98%. MW: 342.46 Da. 50 mg A-435 ALOMONE LABS
ALOMONE LABS
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A-803467 A Potent and Selective Inhibitor of the TTX-Resistant NaV1.8 Channel. Synt… 10 mg A-105 ALOMONE LABS
ALOMONE LABS
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A-803467 A Potent and Selective Inhibitor of the TTX-Resistant NaV1.8 Channel. Synt… 25 mg A-105 ALOMONE LABS
ALOMONE LABS
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A-803467 A Potent and Selective Inhibitor of the TTX-Resistant NaV1.8 Channel. Synt… 50 mg A-105 ALOMONE LABS
ALOMONE LABS
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A-803467 A Potent and Selective Inhibitor of the TTX-Resistant NaV1.8 Channel. Synt… 100 mg A-105 ALOMONE LABS
ALOMONE LABS
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A-804598 A Potent and Selective Antagonist of P2X7 Receptors. Synthetic. Purity >99… 5 mg A-415 ALOMONE LABS
ALOMONE LABS
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A-804598 A Potent and Selective Antagonist of P2X7 Receptors. Synthetic. Purity >99… 10 mg A-415 ALOMONE LABS
ALOMONE LABS
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A-804598 A Potent and Selective Antagonist of P2X7 Receptors. Synthetic. Purity >99… 25 mg A-415 ALOMONE LABS
ALOMONE LABS
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A-804598 A Potent and Selective Antagonist of P2X7 Receptors. Synthetic. Purity >99… 50 mg A-415 ALOMONE LABS
ALOMONE LABS
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A-839977 A Potent and Selective Antagonist of P2X7 Receptors. Synthetic. Purity >96… 5 mg A-470 ALOMONE LABS
ALOMONE LABS
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A-839977 A Potent and Selective Antagonist of P2X7 Receptors. Synthetic. Purity >96… 10 mg A-470 ALOMONE LABS
ALOMONE LABS
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A-839977 A Potent and Selective Antagonist of P2X7 Receptors. Synthetic. Purity >96… 25 mg A-470 ALOMONE LABS
ALOMONE LABS
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A-839977 A Potent and Selective Antagonist of P2X7 Receptors. Synthetic. Purity >96… 50 mg A-470 ALOMONE LABS
ALOMONE LABS
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A-841720 An Antagonist of mGluR1 and mGluR5. Synthetic. Purity >98%. MW: 343.45 Da. 5 mg A-440 ALOMONE LABS
ALOMONE LABS
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A-841720 An Antagonist of mGluR1 and mGluR5. Synthetic. Purity >98%. MW: 343.45 Da. 10 mg A-440 ALOMONE LABS
ALOMONE LABS
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A-841720 An Antagonist of mGluR1 and mGluR5. Synthetic. Purity >98%. MW: 343.45 Da. 25 mg A-440 ALOMONE LABS
ALOMONE LABS
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A-841720 An Antagonist of mGluR1 and mGluR5. Synthetic. Purity >98%. MW: 343.45 Da. 50 mg A-440 ALOMONE LABS
ALOMONE LABS
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A-850002 A Selective and Potent Antagonist of mGluR1 Receptors. Synthetic. Purity >… 5 mg A-390 ALOMONE LABS
ALOMONE LABS
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A-850002 A Selective and Potent Antagonist of mGluR1 Receptors. Synthetic. Purity >… 10 mg A-390 ALOMONE LABS
ALOMONE LABS
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A-850002 A Selective and Potent Antagonist of mGluR1 Receptors. Synthetic. Purity >… 25 mg A-390 ALOMONE LABS
ALOMONE LABS
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A-850002 A Selective and Potent Antagonist of mGluR1 Receptors. Synthetic. Purity >… 50 mg A-390 ALOMONE LABS
ALOMONE LABS
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A-889425 A Blocker of TRPV1 Channels. Synthetic. Purity >99%. MW: 425.4 Da. 1 mg A-195 ALOMONE LABS
ALOMONE LABS
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A-889425 A Blocker of TRPV1 Channels. Synthetic. Purity >99%. MW: 425.4 Da. 5 mg A-195 ALOMONE LABS
ALOMONE LABS
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A-889425 A Blocker of TRPV1 Channels. Synthetic. Purity >99%. MW: 425.4 Da. 10 mg A-195 ALOMONE LABS
ALOMONE LABS
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A-889425 A Blocker of TRPV1 Channels. Synthetic. Purity >99%. MW: 425.4 Da. 25 mg A-195 ALOMONE LABS
ALOMONE LABS
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A-889425 A Blocker of TRPV1 Channels. Synthetic. Purity >99%. MW: 425.4 Da. 50 mg A-195 ALOMONE LABS
ALOMONE LABS
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A 205804 Purity ≥98%. MW: 300.39 100 mg, 500 mg MBS132392 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A 66 Purity ≥98%. MW: 393.52 100 mg, 500 mg MBS132169 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A 740003 Purity ≥98%. MW: 474.565 100 mg, 500 mg MBS132187 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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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 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A 769662 Purity ≥98%. MW: 360.39 100 mg, 500 mg MBS130892 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A 769662 Purity 97%+. MW: 360.39 5 mg, 1ml/10mM (in DMSO), 10 mg MBS576261 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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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 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A 83-01 Purity ≥98% by HPLC. Background: A selective inhibitor of TGF-beta type… 1 mg MBS842636 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A 83-01 Purity ≥98%. MW: 421.52 100 mg, 500 mg MBS132328 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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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 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A 922500 MW: 428.48 5 mg MBS8506458 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A 922500 Purity ≥98%. MW: 428.488 100 mg, 500 mg MBS130245 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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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 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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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 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-1210477 Purity ≥98%. MW: 886.51 100 mg, 500 mg MBS131280 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-1210477 Purity ≥99%. MW: 850.04 2 mg, 5 mg, 10 mg MBS575263 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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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 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-1331852 Purity ≥98%. MW: 658.82 100 mg, 500 mg MBS131656 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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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 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-205804 Purity 97%+. MW: 300.41 5 mg, 10 mg, 1ml/10mM (in DMSO) MBS576130 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A23187 Purity >98% by TLC. Background: A calcium ionophore. Causes rapid influx o… 10 mg MBS843148 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-366 Purity ≥98% by HPLC. Background: A-366 is a potent and selective G9a /… 1 mg, 5 mg MBS842453 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-366 Purity ≥98%. MW: 329.444 100 mg, 500 mg MBS131198 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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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 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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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 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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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 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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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 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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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 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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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 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A66 MW: 393.53 10 mg MBS8506193 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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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 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A66 Purity 97%+. MW: 393.53 2 mg, 5 mg, 1ml/10mM (in DMSO) MBS575616 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-674563 MW: 358.44 2 mg MBS8506244 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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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 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-674563 Purity ≥98%. MW: 358.445 100 mg, 500 mg MBS131746 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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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 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-769662 Purity ≥98% by HPLC. Background: Cell-permeable. A potent AMPK activato… 5 mg MBS842018 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-769662 Purity >98%. A-769662 is a new activator of AMP-activated protein kinase (… 5 mg, 10 mg, 1 mL (in DMSO) MBS384092 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A77 1726 Purity ≥98% by HPLC. Background: Physiologically active metabolite of t… 5 mg, 25 mg MBS842963 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A77-01 Purity ≥98%. MW: 286.33 2 mg, 5 mg, 1ml/10mM (in DMSO) MBS577536 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A77-01 Purity ≥98%. MW: 286.338 100 mg, 500 mg MBS130865 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-803467 Purity ≥98% (TLC). MW: 357.8 10 mg, 50 mg MBS565381 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-803467 Purity ≥98% by TLC. Background: A-803467 is a potent, selective inhibit… 5 mg, 25 mg MBS842200 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-803467 Purity ≥98%. MW: 357.79 100 mg, 500 mg MBS132100 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-803467 Purity ≥98%. MW: 357.79 1ml/10mM (in DMSO), 10 mg, 25 mg MBS575739 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-804598 Purity >98%. A-804598 is a P2X7 selective, competitive antagonist with the… 5 mg, 10 mg, 25 mg MBS384094 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A83-01 Purity >98% (TLC); NMR (Conforms). ALK inhibitor. Selective glycogen synth… 5 mg, 25 mg MBS515040 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-83-01 Purity 97%+. MW: 421.52 2 mg, 5 mg, 10 mg MBS575483 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-966492 A-966492 is a highly potent and efficacious poly(ADP-ribose) polymerase (P… 10 mg MBS8506196 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-966492 Purity ≥98%. A-966492 is a novel and potent inhibitor of PARP1 and PARP… 2 mg, 5 mg, 1ml/10mM (in DMSO) MBS578914 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-966492 Purity ≥98%. MW: 324.359 100 mg, 500 mg MBS132689 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A-966492 Purity >98%. A-966492 displayed high potency against the poly(ADP-ribose)… 5 mg, 1 mL (in DMSO), 10 mg MBS384096 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A 83-01 An inhibitor of ALK5, ALK4, and ALK7 (IC50s = 12, 45, and 7.5 nM, respecti… 1 mg 9001799-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A 83-01 An inhibitor of ALK5, ALK4, and ALK7 (IC50s = 12, 45, and 7.5 nM, respecti… 10 mg 9001799-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A 83-01 An inhibitor of ALK5, ALK4, and ALK7 (IC50s = 12, 45, and 7.5 nM, respecti… 25 mg 9001799-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A 83-01 An inhibitor of ALK5, ALK4, and ALK7 (IC50s = 12, 45, and 7.5 nM, respecti… 5 mg 9001799-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A01 A Smurf1 inhibitor (Kd = 3.67 nM); inhibits Smurf1-mediated ubiquitination… 10 mg 26137-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A01 A Smurf1 inhibitor (Kd = 3.67 nM); inhibits Smurf1-mediated ubiquitination… 25 mg 26137-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A01 A Smurf1 inhibitor (Kd = 3.67 nM); inhibits Smurf1-mediated ubiquitination… 5 mg 26137-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A01 A Smurf1 inhibitor (Kd = 3.67 nM); inhibits Smurf1-mediated ubiquitination… 50 mg 26137-50 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-1155463 A Bcl-xL inhibitor (Ki = is = 80 and 16 nM, respectively); inhibits the gr… 1 mg 27369-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-1155463 A Bcl-xL inhibitor (Ki = is = 80 and 16 nM, respectively); inhibits the gr… 10 mg 27369-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-1155463 A Bcl-xL inhibitor (Ki = is = 80 and 16 nM, respectively); inhibits the gr… 25 mg 27369-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-1155463 A Bcl-xL inhibitor (Ki = is = 80 and 16 nM, respectively); inhibits the gr… 5 mg 27369-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-1210477 A selective Mcl-1 inhibitor (Ki = 0.43 nM; IC50 = 26.2 nM); disrupts the i… 1 mg 21113-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-1210477 A selective Mcl-1 inhibitor (Ki = 0.43 nM; IC50 = 26.2 nM); disrupts the i… 10 mg 21113-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-1210477 A selective Mcl-1 inhibitor (Ki = 0.43 nM; IC50 = 26.2 nM); disrupts the i… 25 mg 21113-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-1210477 A selective Mcl-1 inhibitor (Ki = 0.43 nM; IC50 = 26.2 nM); disrupts the i… 5 mg 21113-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-1331852 An orally bioavailable Bcl-xL inhibitor; selectively binds Bcl-xL over Bcl… 1 mg 22963-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-1331852 An orally bioavailable Bcl-xL inhibitor; selectively binds Bcl-xL over Bcl… 10 mg 22963-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-1331852 An orally bioavailable Bcl-xL inhibitor; selectively binds Bcl-xL over Bcl… 5 mg 22963-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-196 A selective inhibitor of SUV420H1 and SUV420H2 (IC50s = 25 and 144 nM, res… 1 mg 18317-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-196 A selective inhibitor of SUV420H1 and SUV420H2 (IC50s = 25 and 144 nM, res… 5 mg 18317-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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