SHIN1

CAS No. 2146095-85-2

SHIN1( RZ-2994 )

Catalog No. M26439 CAS No. 2146095-85-2

SHIN1 is an inhibitor of human serine hydroxymethyltransferse 1(SHMT1) with IC50 of 5 nM and human serine hydroxymethyltransferse 2 (SHMT2) with an IC50 of 13 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 151 In Stock
5MG 139 In Stock
10MG 207 In Stock
25MG 376 In Stock
50MG 573 In Stock
100MG 882 In Stock
200MG 1209 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    SHIN1
  • Note
    Research use only, not for human use.
  • Brief Description
    SHIN1 is an inhibitor of human serine hydroxymethyltransferse 1(SHMT1) with IC50 of 5 nM and human serine hydroxymethyltransferse 2 (SHMT2) with an IC50 of 13 nM.
  • Description
    SHIN1 is an inhibitor of human serine hydroxymethyltransferse 1(SHMT1) with IC50 of 5 nM and human serine hydroxymethyltransferse 2 (SHMT2) with an IC50 of 13 nM.(In Vitro):SHIN1 inhibits the growth of SHMT2 deletion HCT-116 cells (IC50 = 10 nM). SHIN1 inhibits SHMT1/2 in HCT-116 cells. SHIN1 blocks cell growth through a progressive depletion of purines, leading to loss of nucleotide triphosphates. SHIN1 is particularly active against B-cell malignancies.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    RZ-2994
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    HMG-CoA reductase
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2146095-85-2
  • Formula Weight
    400.482
  • Molecular Formula
    C24H24N4O2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 66.67 mg/mL (166.48 mM)
  • SMILES
    CC(C)C1(c2c(C)n[nH]c2OC(N)=C1C#N)c1cc(CO)cc(c1)-c1ccccc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Morikawa S, et al. Relative induction of mRNA for HMG CoA reductase and LDL receptor by five different HMG-CoA reductase inhibitors in cultured human cells. J Atheroscler Thromb. 2000;7(3):138-44.
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