Non-Antibody Products — page 2 of 31,394



Non-Antibody Products
Page 2 of 31,394
  • Records 51 - 100 of 1,569,681
Name Description Size Catalog # Supplier
A-966492 MW: 324.35. 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 PARP2 wi… 5 mg, 1ml/10mM (In DMSO), 10 mg, 25 mg, 50 mg MBS578914 MYBIOSOURCE INC.
MYBIOSOURCE INC.
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A 769662 MW: 360.4. A 769662 is a potent and reversible activator of AMP-activated… 5 mg, 25 mg abx076760 ABBEXA
ABBEXA
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A-803467 MW: 357.79. A selective blocker of Nav1.8 channels. A-803467 potently redu… 10 mg, 50 mg abx076576 ABBEXA
ABBEXA
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A83 01 MW: 421.5. A83-01 is a selective inhibitor of TGF-β type I receptor A… 5 mg, 25 mg abx076740 ABBEXA
ABBEXA
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A-967079 MW: 207.3. A-967079 is a TRPA1 antagonist (1) and cell permeable. It has b… 10 mg, 50 mg abx076611 ABBEXA
ABBEXA
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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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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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A-196 A selective inhibitor of SUV420H1 and SUV420H2 (IC50s = 25 and 144 nM, res… 500 µg 18317-500 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-205804 A potent inhibitor of E-selectin and ICAM-1 expression in HUVECs stimulate… 1 mg 21252-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-205804 A potent inhibitor of E-selectin and ICAM-1 expression in HUVECs stimulate… 10 mg 21252-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-205804 A potent inhibitor of E-selectin and ICAM-1 expression in HUVECs stimulate… 5 mg 21252-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-205804 A potent inhibitor of E-selectin and ICAM-1 expression in HUVECs stimulate… 50 mg 21252-50 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A23187 A divalent cation ionophore, commonly used to facilitate the movement of C… 1 mg 11016-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A23187 A divalent cation ionophore, commonly used to facilitate the movement of C… 10 mg 11016-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A23187 A divalent cation ionophore, commonly used to facilitate the movement of C… 25 mg 11016-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A23187 A divalent cation ionophore, commonly used to facilitate the movement of C… 5 mg 11016-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-317491 A P2X3 and P2X2 / 3 receptor antagonist (Kis = 22-92 nM in a calcium influ… 1 mg 19256-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-317491 A P2X3 and P2X2 / 3 receptor antagonist (Kis = 22-92 nM in a calcium influ… 10 mg 19256-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-317491 A P2X3 and P2X2 / 3 receptor antagonist (Kis = 22-92 nM in a calcium influ… 25 mg 19256-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-317491 A P2X3 and P2X2 / 3 receptor antagonist (Kis = 22-92 nM in a calcium influ… 5 mg 19256-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-366 A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… 10 mg 16081-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-366 A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… 5 mg 16081-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-366 A potent, peptide-competitive inhibitor of the lysine methyltransferase G9… 50 mg 16081-50 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-419259 An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… 1 mg 25605-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-419259 An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… 10 mg 25605-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-419259 An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… 5 mg 25605-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-419259 An inhibitor of Src family kinases, including Src, LCK, Lyn, and Hck (IC50… 500 µg 25605-500 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-443654 A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… 1 mg 16499-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-443654 A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… 5 mg 16499-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-443654 A pan Akt inhibitor (Ki = 160 pmol / L for all three isoforms) that interf… 500 µg 16499-500 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-61603 A selective α1A-adrenergic receptor agonist that is at least 35-fold… 1 mg 17358-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-61603 A selective α1A-adrenergic receptor agonist that is at least 35-fold… 10 mg 17358-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-61603 A selective α1A-adrenergic receptor agonist that is at least 35-fold… 5 mg 17358-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-66 A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… 1 mg 17382-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-66 A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… 10 mg 17382-10 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-66 A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… 25 mg 17382-25 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-66 A potent, selective inhibitor of the PI3K isoform p110α (IC50 = 32 n… 5 mg 17382-5 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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A-674563 An orally available, reversible inhibitor of Akt (Ki = 11 nM for Akt1); al… 1 mg 18715-1 CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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