Puromycin dihydrochloride

CAS No. 58-58-2

Puromycin dihydrochloride( CL 13,900 | CL 16,536 | NSC 3055 | PDH )

Catalog No. M15154 CAS No. 58-58-2

Puromycin 2hydrochloride is an aminonucleoside antibiotic, which acts as a protein synthesis inhibitor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
10MG 37 In Stock
25MG 67 In Stock
50MG 113 In Stock
100MG 183 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Puromycin dihydrochloride
  • Note
    Research use only, not for human use.
  • Brief Description
    Puromycin 2hydrochloride is an aminonucleoside antibiotic, which acts as a protein synthesis inhibitor.
  • Description
    Puromycin 2hydrochloride is an aminonucleoside antibiotic, which acts as a protein synthesis inhibitor.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    CL 13,900 | CL 16,536 | NSC 3055 | PDH
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    DNA/RNA Synthesis
  • Recptor
    DNA synthesis| 60S ribosome
  • Research Area
    Other Indications
  • Indication
    ——

Chemical Information

  • CAS Number
    58-58-2
  • Formula Weight
    544.44
  • Molecular Formula
    C22H31Cl2N7O5
  • Purity
    >98% (HPLC)
  • Solubility
    Water: 100 mg/mL warmed (183.67 mM); DMSO: 100 mg/mL warmed (183.67 mM)
  • SMILES
    O=C(N[C@@H]1[C@@H](CO)O[C@@H](N2C=NC3=C(N(C)C)N=CN=C23)[C@@H]1O)[C@@H](N)CC4=CC=C(OC)C=C4.[H]Cl.[H]Cl
  • Chemical Name
    (2S)-2-Amino-N-[(2S,3S,4R,5R)-5-[6-(dimethylamino)purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]-3-(4-methoxyphenyl)propanamide dihydrochloride

Shipping & Storage Information

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

Reference

1.Shibouta Y, et al. Kidney Int. 1991 May;39(5):920-9.
molnova catalog
related products
  • DTP3 TFA

    DTP3 TFA is a potent and selective GADD45β/MKK7 (growth arrest and DNA-damage-inducible β/mitogen-activated protein kinase kinase 7) inhibitor. DTP3 (10 μM; 1-21 days) causes the potent and tumor-selective induction of JNK activation and apoptosis.

  • Dmt-2fluoro-da(bz) a...

    Dmt-2'fluoro-da(bz) amidite is a 2'-deoxy-2'-fluoro-phosphorothioate oligonucleotide with high affinity and specificity for RNA targets and serves as an intermediate in the synthesis of 5'-DMT-3'-phosphoramidite, an antisense compound resistant to nuclease.

  • ART812

    ART812 is an orally active inhibitor of DNA polymerase Polθ, possessing an IC50 value of 7.6 nM. Additionally, ART812 exhibits a cell-based microhomology-mediated end joining (MMEJ) IC50 value of 240 nM.