ITD-1

CAS No. 1099644-42-4

ITD-1( ITD-1 )

Catalog No. M10381 CAS No. 1099644-42-4

ITD-1 is a potent, selective TGF-β inhibitor that induces type II TGFβ receptor (TGFBR2) degradation with IC50 of 0.85 uM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 30 In Stock
5MG 47 In Stock
10MG 71 In Stock
25MG 113 In Stock
50MG 152 In Stock
100MG 235 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    ITD-1
  • Note
    Research use only, not for human use.
  • Brief Description
    ITD-1 is a potent, selective TGF-β inhibitor that induces type II TGFβ receptor (TGFBR2) degradation with IC50 of 0.85 uM.
  • Description
    ITD-1 is a potent, selective TGF-β inhibitor that induces type II TGFβ receptor (TGFBR2) degradation with IC50 of 0.85 uM, enhances proteasomal degradation of TGFBR2; effectively clears the receptor from the cell surface and selectively inhibits intracellular signaling; selectively enhances the differentiation of uncommitted mesoderm to cardiomyocytes, but not to vascular smooth muscle and endothelial cells.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ITD-1
  • Pathway
    TGF-beta/Smad
  • Target
    TGFBR
  • Recptor
    TGFβ
  • Research Area
    Cardiovascular Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    1099644-42-4
  • Formula Weight
    415.524
  • Molecular Formula
    C27H29NO3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: < 9 mg/mL
  • SMILES
    O=C(C1=C(C)NC2=C(C(CC(C)(C)C2)=O)C1C3=CC=C(C4=CC=CC=C4)C=C3)OCC
  • Chemical Name
    3-Quinolinecarboxylic acid, 4-[1,1'-biphenyl]-4-yl-1,4,5,6,7,8-hexahydro-2,7,7-trimethyl-5-oxo-, ethyl ester

Shipping & Storage Information

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

Reference

1. Willems E, et al. Cell Stem Cell. 2012 Aug 3;11(2):242-52. 2. Sun Z, et al. Dev Biol. 2017 Jan 15;421(2):149-160. 3. Mingyuan X, et al. Oncotarget. 2017 Dec 14;9(3):3188-3197.
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