pCDPK1/TgCDPK1-IN-3

CAS No. 1092788-87-8

pCDPK1/TgCDPK1-IN-3( —— )

Catalog No. M36404 CAS No. 1092788-87-8

CpCDPK1/TgCDPK1-IN-3 is a dual inhibitor of CpCDPK1 and TgCDPK1 with an IC50 of 0.003 μM for CpCDPK1 and 0.0036 μM for TgCDPK1.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 128 Get Quote
5MG 178 Get Quote
10MG 265 Get Quote
25MG 438 Get Quote
50MG 641 Get Quote
100MG 893 Get Quote
500MG 1782 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    pCDPK1/TgCDPK1-IN-3
  • Note
    Research use only, not for human use.
  • Brief Description
    CpCDPK1/TgCDPK1-IN-3 is a dual inhibitor of CpCDPK1 and TgCDPK1 with an IC50 of 0.003 μM for CpCDPK1 and 0.0036 μM for TgCDPK1.
  • Description
    CpCDPK1/TgCDPK1-IN-3 (Compound 20) is a CpCDPK1 and TgCDPK1 inhibitor with IC50 values of 0.003 and 0.0036 μM, respectively. CpCDPK1/TgCDPK1-IN-3 can be used in the research of apicomplexan protozoa-related diseases, such as the research of T. gondii, C. parvum and C. hominus infection.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Microbiology/Virology
  • Target
    Parasite
  • Recptor
    Parasite
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1092788-87-8
  • Formula Weight
    306.36
  • Molecular Formula
    C17H18N6
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    NC1=C2C(=NN(C(C)C)C2=NC=N1)C=3C=C4C(=CC3)N(C)C=C4
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Wesley C. Van Voorhis, et al. Compositions And Methods For Treating Toxoplasmosis, Cryptosporidiosis, And Other Apicomplexan Protozoan Related Diseases. US20130018040A1.
molnova catalog
related products
  • Doramectin

    A derivative of ivermectin that approved for the treatment of parasites; a veterinary drug.

  • ELQ-300

    ELQ-300 is bioavailable antimalarial agent acts as an inhibitor of the reductive (Qi) site of the cytochrome bc1 complex (cyt bc1).

  • SpdSyn binder-1

    SpdSyn binder-1 is a weak binding agent that binds to the active site of Plasmodium falciparum spermidine synthase, offering partial inhibition of malaria and potential for malaria research.