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9-ING-41 is a glycogen synthase kinase-3 (GSK-3) inhibitor. 9-ING-41 leads to cell cycle arrest, autophagy and...
9-Me-BC is an analytical reference standard categorized as a nootropic. 9-Methyl-β-carboline improves spatial...
9-Methoxyellipticine is an alkaloid and a derivative of the DNA intercalating agent ellipticine that has been found...
9-PAHSA is a FAHFA (fatty acid ester of a hydroxy fatty acid) obtained by formal condensation of the carboxy group of...
9-Phenanthrol is an inhibitor of transient receptor potential melastatin 4 (TRPM4). It is selective for TRPM4 over...
9(Z),11(E)-Conjugated linoleic acid is an isomer of linoleic acid that has been found in beef and milk fat. It binds...
Potent glycogen synthase kinase-3 (GSK-3) inhibitor (Ki = 0.6 nM for GSK-3α and GSK-3β). Displays high selectivity (>...
A 1120 is a retinol-binding protein 4 (RBP4) antagonist (Ki = 8.3 nM) that can reduce serum RBP4 and retinol, and...
A-1155463 is a highly potent and selective BCL-XL inhibitor. A-1155463 is substantially more potent against...
A-1210477 is a potent and selective MCL-1 inhibitor. A-1210477 induces the hallmarks of intrinsic apoptosis and...
A 127722 is highly potent and a selective ETA endothelin receptor antagonist (IC50 values are 0.11 nM and 98 nM for...
A12B4C3 is a selective hPNKP phosphatase inhibitor.
A-1331852 is a potent BCL-XL-selective inhibitor. BCL-XL is the major antiapoptotic survival protein and may be a...
A1874 is a nutlin-based and BRD4-degrading PROTAC which induces BRD4 degradation in cells.
A1899 is a potent and selective TASK-1 and TASK-3 antagonist.
A-192621 is an endothelin-B antagonist. A-192621 markedly enhanced MAP, TPR, and mesenteric, and the renal...
A-196 is the first potent and selective chemical probe for SUV420H1 and SUV420H2. The in vitro activity of A-196...
A-205804 is a potent and selective inhibitor of E-selectin and ICAM-1 expression with IC50 of 20 nM and 25 nM...
CAS#: 22816-60-0 (HCl)
A22 is an inhibitor of MreB, an actin-like bacterial protein, and has been shown to act as an antiobiotic adjuvant....
A2-32-01 is a HsClpP antagonist.
A2793 is an inhibitor of TRESK (IC50 value of 6.8 μM for mTRESK). A2793 inhibited TWIK-related acid-sensitive K+...
A286982 is an inhibitor that blocks the integrin-ligand interaction between leukocyte function-associated antigen-1...
A2AR agonist-1 is an agonist of the adenosine A2A receptor and an inhibitor of equilibrative nucleoside transporter 1...
CAS#: Unknown (sodium)
A-317491 is a potent and selective non-nucleotide antagonist of P2X3 and P2X2/3 receptors. A-317491 transiently...
A 33 is a potent and selective PDE4B inhibitor.