Enpp/Carbonic anhydrase-IN-1

CAS No. 2883495-35-8

Enpp/Carbonic anhydrase-IN-1( —— )

Catalog No. M35976 CAS No. 2883495-35-8

Enpp/Carbonic anhydrase-IN-1 (compound 1e) is a potent inhibitor of Enpp and carbonic anhydrase, exhibiting IC50s of 1.36, 1.35, 3.00, 0.88, and 1.02 μM for NPP1, NPP2, NPP3, CA-II, and CA-IX respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 36 Get Quote
10MG 55 Get Quote
25MG 109 Get Quote
50MG 181 Get Quote
100MG 291 Get Quote
200MG 410 Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Enpp/Carbonic anhydrase-IN-1
  • Note
    Research use only, not for human use.
  • Brief Description
    Enpp/Carbonic anhydrase-IN-1 (compound 1e) is a potent inhibitor of Enpp and carbonic anhydrase, exhibiting IC50s of 1.36, 1.35, 3.00, 0.88, and 1.02 μM for NPP1, NPP2, NPP3, CA-II, and CA-IX respectively.
  • Description
    Enpp/Carbonic anhydrase-IN-1 (compound 1e) is a potent Enpp and carbonic anhydrase inhibitor with IC50s of 1.36, 1.35, 3.00, 0.88, 1.02 μM for NPP1, NPP2, NPP3, CA-II, CA-IX respectively. Enpp/Carbonic anhydrase-IN-1 shows antiproliferative activity for cancer cells and low cytotoxic against normal cells. Enpp/Carbonic anhydrase-IN-1 induces Apoptosis.
  • In Vitro
    Enpp/Carbonic anhydrase-IN-1 (compound 1e) (0-100 μM; ) inhibits some cancer cells growth with IC50s of 0.32, 0.40, 0.58, 0.87, 0.40, 0.96 μM for K-562, RPMI-8226, SR, COLO 205, HT-29, SF-539 cells, respectively.Enpp/Carbonic anhydrase-IN-1 (0-2 μM) shows low cytotoxic against normal breast epithelial cells (HME1) and normal skin fibroblast cells (F180) with IC50s of > 50 μM.Enpp/Carbonic anhydrase-IN-1 (0.32, 0.64 μM) induces apoptosis in a dose-dependent manner at K-562 cells.Cell Proliferation Assay Cell Line:K-562, RPMI-8226, SR, COLO 205, HT-29, SF-539 cells Concentration:0-100 μM Incubation Time:Result:Inhibited the cell growth with IC50s of 0.32, 0.40, 0.58, 0.87, 0.40, 0.96 μM for K-562, RPMI-8226, SR, COLO 205, HT-29, SF-539 cells, respectively.Apoptosis Analysis Cell Line:K-562 cells Concentration:0.32, 0.64 μM Incubation Time:Result:Induced apoptosis in a dose-dependent manner.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    Carbonic Anhydrase
  • Recptor
    Carbonic Anhydrase | PDE
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2883495-35-8
  • Formula Weight
    411.51
  • Molecular Formula
    C23H25NO4S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (243.01 mM; Ultrasonic (<50°C)
  • SMILES
    O=C(Nc1ccc(OS(=O)(=O)c2ccccc2)cc1)C12CC3CC(CC(C3)C1)C2
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Afnan I.Shahin, et al. Design and synthesis of new adamantyl derivatives as promising antiproliferative agents. European Journal of Medicinal Chemistry, 2022.
molnova catalog
related products
  • Girentuximab

    Girentuximab (G250) is a potent anti-carbonic anhydrase IX (CAIX) monoclonal antibody with anticancer activity for the study of uroepithelial carcinoma PET (ZiPUP).

  • hCAII-IN-9

    hCAII-IN-9 is a potent carbonic anhydrase inhibitor with IC50 values of 1.18 μM for hCA II, 0.17 μM for hCA IX, and 2.99 μM for hCA XII. It is not blood-brain barrier permeable.

  • 1,3-Diphenylurea

    1, 3-Diphenylurea is involved with Epoxide hydrolase activity.