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  1. N-cadherin antagonist

    Exherin is a small, cyclic pentapeptide vascular-targeting agent with potential antineoplastic and antiangiogenic activities.
  2. GR antagonist

    AL082D06 is a nonsteroidal glucocorticoid receptor antagonist.
  3. GPIIb/IIIa antagonist

    Tirofiban, Hydrochloride Hydrate is a specific nonpeptide platelet fibrinogen receptor (GPIIb/IIIa) antagonist.
  4. NRP1 antagonist

    EG01377 TFA salt is a selective neuropilin-1 (NRP1) antagonist. CAS: 2227996-00-9 (Free base)
  5. fibrinogen receptor antagonist

    SC-52012 is an orally active fibrinogen receptor antagonist, with antiplatelet activities.

  6. VKOR antagonist

    Tecarfarin sodium (ATI-5923 sodium) is a novel orally active non-competitive vitamin K epoxide reductase (VKOR) antagonist, impairs the activation of the vitamin K-dependent clotting factors II, VII, IX and X.
  7. NGF antagonist

    PD 90780 is a non peptide antagonist of nerve growth factor (NGF) binding to the P75 NGF receptor, inhibits NGF-p75 NTR interaction with IC50s values of 23.1 ?M and 1.8 ?M in PC12 cells and PC12 nnr5 cells, respectively .
  8. RBP4 antagonist

    A 1120, a nonretinoid retinol-binding protein 4 (RBP4) antagonist, has a high affinity with the Ki value of 8.3 nM, which disrupts the interaction between RBP4 and its binding partner transthyretin.
  9. R18

    14.3.3 proteins Antagonist

    R18, antagonist of 14.3.3 proteins (KD ??? 80 nM). Competitively inhibits 14.3.3-ligand interactions without requiring phosphorylation.
  10. 20-HETE antagonist

    20-HEDE (WIT 002) is an antagonist of 20-hydroxyeicosatetraenoic acid (20-HETE).
  11. MC4 antagonist

    SNT207858 is a 22 nM MC4 antagonist with a 170-fold selectivity vs. MC3 and a 40-fold selectivity versus MC5.
  12. cytoplasmic dynein antagonist

    Ciliobrevin D is the first specific small molecule antagonist of cytoplasmic dynein
  13. MC4-Receptor Antagonist

    SNT-207707 is an oral MC4-Receptor Antagonist
  14. pan-selectin antagonist

    Bimosiamose is a pan-selectin antagonist, inhibits E-, P-, and L-selectin with IC50s of 88 μM, 20 μM, and 86 μM, respectively, and can be used in the research of inflammatory disease.
  15. antagonist of melanopsin-mediated phototransduction

    AA41612 is an antagonist of melanopsin-mediated phototransduction.

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