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Home >> Signaling Pathways >> Cardiovascular >> Acute Phase Reactants

Acute Phase Reactants

Products for  Acute Phase Reactants

  1. Cat.No. Product Name Information
  2. GC49118 10-hydroxy Warfarin A metabolite of (R)-warfarin 10-hydroxy Warfarin Chemical Structure
  3. GC18219 6-hydroxy Warfarin 6-hydroxy Warfarin is a metabolite of (+)-warfarin , which is a weaker vitamin K antagonist than (-)-warfarin . 6-hydroxy Warfarin Chemical Structure
  4. GC40529 7-hydroxy Warfarin 7-hydroxy Warfarin is a metabolite of (-)-warfarin, which is a more potent vitamin K antagonist than (+)-warfarin. 7-hydroxy Warfarin Chemical Structure
  5. GC52359 ATX-100 An ionizable cationic lipid ATX-100 Chemical Structure
  6. GC49784 AZD 2716 An sPLA2 inhibitor AZD 2716 Chemical Structure
  7. GC90993 CL4F8-6

    An ionizable cationic lipid

     CL4F8-6 Chemical Structure
  8. GC49266 Compstatin (trifluoroacetate salt)

    ICVVQDWGHHRCT

     A peptide inhibitor of complement activation Compstatin (trifluoroacetate salt) Chemical Structure
  9. GC49131 Dehydro Warfarin

    NSC 289346

     A metabolite of (±)-warfarin Dehydro Warfarin Chemical Structure
  10. GC52193 Eptifibatide Eptifibatide is a cyclic heptapeptide, acts as a competitive antagonist for the activated platelet glycoprotein IIb/IIIa receptor, with anti-platelet activity. Eptifibatide Chemical Structure
  11. GC90684 Lipid 2,2(8,8) 4C CH3

    An ionizable cationic lipid

     Lipid 2,2(8,8) 4C CH3 Chemical Structure
  12. GC90490 PMX-53 (trifluoroacetate salt)

    A C5a receptor antagonist

     PMX-53 (trifluoroacetate salt) Chemical Structure
  13. GC49107 Rosuvastatin lactone

    (+)-Rosuvastatin lactone, Rosuvastatin-5S-lactone, RSTL

     The lactone form of rosuvastatin Rosuvastatin lactone Chemical Structure
  14. GC48060 Rosuvastatin-d6 (sodium salt) An internal standard for the quantification of rosuvastatin Rosuvastatin-d6 (sodium salt) Chemical Structure
  15. GC72527 S-(-)-Warfarin S-(-)-Warfarin Chemical Structure
  16. GC52084 YSK05 YSK05 is a pH-sensitive cationic lipid. YSK05 improves the intracellular trafficking of non-viral vectors. YSK05-MEND shows significantly good gene silencing activity and hemolytic activity. YSK05 overcomes the suppression of endosomal escape by PEGylation. YSK05 effectively enhances siRNA delivery both in vitro and in vivo. YSK05 Chemical Structure

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