SIBA

CAS No. 35899-54-8

SIBA( 5'-Isobutylthioadenosine | 5'-Deoxy-5'-isobutylthioadenosine )

Catalog No. M24314 CAS No. 35899-54-8

SIBA is a synthetic analogue of SAH, acts as an inhibitor of S-adenosylmethionine-mediated transmethylation. SIBA can interfere with a variety of enzymatic activities in vitro, such as SAH hydrolase, methylthioadenosine phosphorylase and cAMP phosphodiesterase.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 101 In Stock
5MG 90 In Stock
10MG 113 In Stock
25MG 219 In Stock
50MG 322 In Stock
100MG 458 In Stock
200MG 639 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    SIBA
  • Note
    Research use only, not for human use.
  • Brief Description
    SIBA is a synthetic analogue of SAH, acts as an inhibitor of S-adenosylmethionine-mediated transmethylation. SIBA can interfere with a variety of enzymatic activities in vitro, such as SAH hydrolase, methylthioadenosine phosphorylase and cAMP phosphodiesterase.
  • Description
    SIBA is a synthetic analogue of SAH, acts as an inhibitor of S-adenosylmethionine-mediated transmethylation. SIBA can interfere with a variety of enzymatic activities in vitro, such as SAH hydrolase, methylthioadenosine phosphorylase and cAMP phosphodiesterase. SIBA reversibly blocks the multiplication of herpes simplex type 1 virus (HSV) .
  • In Vitro
    SIBA (0.5 mM; 24-96 h) shows strong anti-proliferative activity against 3LL and RMS-J1 tumour cells.SIBA (1 mM; 12, 24 h) reversibly inhibits HSV production in HEp2 cells (infected by HSV-1).SIBA inhibits protein synthesis by 98% after 10 h infection of HEp2 cells (infected by HSV-1).SIBA (1 mM; 8.5 h) inhibits protein synthesis and RNA methylation in HEp2 cells (infected by HSV-1).SIBA (0.5, 1.0 mM; 24, 48 h) inhibits the conversion of putrescine into spermidine and/or spermine and that this inhibition is a reversible one (interferes with polyamine biosynthesis, probably by blocking aminopropyltransferase). Cell Proliferation Assay Cell Line:3 LL and RMS-J1 cells Concentration:0.5 mM Incubation Time:24-96 h Result:Inhibited 3LL and RMS-J1 tumor cell growth potently by 96% and 88%, respectively.Cell Viability Assay Cell Line:HEp2 cells (infected by HSV-1) Concentration:1 mM Incubation Time:12, 24 h Result:Decreased virus production by 88.4 and 98.2% when at 12 and 24 h, respectively.Cell Viability Assay Cell Line:HEp2 cells (infected by HSV-1) Concentration:1 mM Incubation Time:8.5 h Result:Reduced protein synthesis by 41.3% in normal medium and by 63.5% in medium poor in methionine.Inhibited RNA methylation by 65.4%.Cell Viability AssayCell Line:chick embryo fibroblastsConcentration:0.5, 1.0 mMIncubation Time:24, 48 h Result:Inhibited the uptake of the radioactive diamine and that the inhibition was dose-dependent.Markedly inhibited the formation of [14C]spermidine and [14C]spermine from [14C]putrescine.Inhibited the growth of chick embryo fibroblasts mainly after exposure for 48 h.
  • In Vivo
    SIBA (150 mg/kg; i.p.; twice weekly for 3 weeks) inhibits tumor growth in vivo.SIBA (15 mg/kg; i.p.; thrice weekly for 4 weeks) inhibits metastatic spread of RMS-J1 cells in vivo. Animal Model:C57BL/6 female mice (4-8 weeks old).Dosage:150 mg/kg Administration:Intraperitoneal injection; twice weekly for 3 weeks.Result:Significantly reduced the median number of lung metastases.Animal Model:Adult syngeneic Wistar AG rats (8-week-old; subcutaneously grafted with RMS-J1 cells).Dosage:15 mg/kg Administration:Intraperitoneal injection; thrice weekly for 4 weeks.Result:Inhibited in vivo metastatic spread of RMS-J1 cells, and showed median numbers of lung metastatic nodules was 26.
  • Synonyms
    5'-Isobutylthioadenosine | 5'-Deoxy-5'-isobutylthioadenosine
  • Pathway
    Microbiology/Virology
  • Target
    HSV
  • Recptor
    HSV|Nucleoside Antimetabolite/Analog
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    35899-54-8
  • Formula Weight
    339.41
  • Molecular Formula
    C14H21N5O3S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:90 mg/mL (265.17 mM)
  • SMILES
    CC(C)CSC[C@H]([C@H]([C@H]1O)O)O[C@H]1n1c2ncnc(N)c2nc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Carteni-Farina M, et al. Studies on the metabolism of 5'-isobutylthioadenosine (SIBA): phosphorolytic cleavage by methylthioadenosinephosphorylase. FEBS Lett. 1979 Aug 15;104(2):266-270.
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