Albamycinsodium

CAS No. 1476-53-5

Albamycinsodium( NSC 2382 )

Catalog No. M12036 CAS No. 1476-53-5

Novobiocin Sodium is an antibiotic compound derived from Streptomyces niveus.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG 38 In Stock
50MG 53 In Stock
100MG 78 In Stock
200MG Get Quote In Stock
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Biological Information

  • Product Name
    Albamycinsodium
  • Note
    Research use only, not for human use.
  • Brief Description
    Novobiocin Sodium is an antibiotic compound derived from Streptomyces niveus.
  • Description
    Novobiocin Sodium is an antibiotic compound derived from Streptomyces niveus.(In Vitro):Bosentan (BOS) competitively and specifically antagonizes binding of 125I-labelled ET-1 to ETA receptors on human smooth muscle cells (SMC) and ETB receptors on human placenta cells. The in vitro binding affinity of Bosentan to ETA receptors on human SMC is 4.7 nM and to ETB receptors on human SMC or placenta cells is 41 or 95 nM. Bosentan has 67-fold greater selectivity for ETA than ETB receptors (mean IC50=7.1 vs 474.8 nM) in an in vitro 125I-labeling assay.(In Vivo):Single-dose Bosentan 62.5 mg significantly (p<0.01 vs baseline) plasma ET-1 levels by 2-fold in 7 pts with WHO class II or III idiopathic or CTD-associated PAH, with peak levels achieved at 8 h. In hypertensive rats, Macitentan 30 mg/kg further decreases mean arterial blood pressure (MAP) by 19 mm Hg when given on top of Bosentan 100 mg/kg. Conversely, Bosentan given on top of Macitentan fails to induce an additional MAP decrease. In pulmonary hypertensive rats, Macitentan 30 mg/kg further decreases mean pulmonary artery pressure (MPAP) by 4 mm Hg on top of Bosentan, whereas a maximal effective dose of Bosentan given on top of Macitentan does not cause any additional MPAP decrease.
  • In Vitro
    Novobiocin sodium (1 mM) competitively inhibits ATP binding to gyrase B to interfere with nucleotide binding and interferes with the association of the co-chaperones Hsc70 and p23 with Hsp90.Novobiocin sodium (200 μM; 24 h) inhibits the rate of repair of both cis-DDP and BCNU induced DNA interstrand cross-links and with a corresponding decrease in the clonogenic survival of the human glioblastoma multiforme cells.Novobiocin sodium (0.3 mM; 48 hours) induces a caspase-3/7 enzyme–dependent apoptosis assays with an induction of approximately three- to fivefold of apoptotic cells in K562, HL60, Mutz-2. Western Blot Analysis Cell Line:K562, HL60, Mutz-2 cells Concentration: 0.3 mM Incubation Time:48 hours Result:Decreased caspase-3/7 activity in K562, HL60, Mutz-2 cells.
  • In Vivo
    Novobiocin sodium (25, 50, 100, 200 mg/kg; s.c.; 4 times at 1, 5, 24 and 48 h after infection) shows anti-infection activity in mice infected with amoxicillin-resistant Streptococcus pneumoniae. Animal Model:30 g adult female Swiss mice (sepsis induced by the penicillin-susceptible strain (AR33118))Dosage:25, 50, 100, 200 mg/kg Administration:S.c.; given at 1, 5, 24 and 48 h after infection Result:Showed anti-infection activity in mice infected with amoxicillin-resistant S. pneumoniae.
  • Synonyms
    NSC 2382
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    ABC
  • Recptor
    ABCG2| DNA gyrase| Bile salt export pump| Topo I
  • Research Area
    Infection
  • Indication
    ——

Chemical Information

  • CAS Number
    1476-53-5
  • Formula Weight
    634.61
  • Molecular Formula
    C31H35N2NaO11
  • Purity
    >98% (HPLC)
  • Solubility
    Ethanol: 127 mg/mL (200.12 mM); Water: 127 mg/mL (200.12 mM); DMSO: 127 mg/mL (200.12 mM)
  • SMILES
    [Na+].CO[C@@H]1[C@@H](OC(=O)N)[C@@H](O)[C@H](Oc2ccc3C(=C(NC(=O)c4ccc(O)c(CC=C(C)C)c4)C(=O)Oc3c2C)[O-])OC1(C)C
  • Chemical Name
    sodium 7-(((2R,3R,4S,5R)-4-(carbamoyloxy)-3-hydroxy-5-methoxy-6,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-3-(4-hydroxy-3-(3-methylbut-2-en-1-yl)benzamido)-8-methyl-2-oxo-2H-chromen-4-olate

Shipping & Storage Information

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

Reference

1.Gormley NA, et al. Biochemistry. 1996 Apr 16;35(15):5083-92.
molnova catalog
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