Daclatasvir dihydrochloride

CAS No. 1009119-65-6

Daclatasvir dihydrochloride( BMS-790052 dihydrochloride | BMS790052 dihydrochloride | BMS 790052 dihydrochloride )

Catalog No. M10060 CAS No. 1009119-65-6

A potent HCV NS5A inhibitor with EC50 of <50 pM against genotype 1 replicons.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 42 In Stock
5MG 33 In Stock
10MG 41 In Stock
25MG 52 In Stock
50MG 60 In Stock
100MG 69 In Stock
200MG Get Quote In Stock
500MG 161 In Stock
1G 238 In Stock

Biological Information

  • Product Name
    Daclatasvir dihydrochloride
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent HCV NS5A inhibitor with EC50 of <50 pM against genotype 1 replicons.
  • Description
    A potent HCV NS5A inhibitor with EC50 of <50 pM against genotype 1 replicons; exhibits picomolar EC(50) towards replicons expressing a broad range of HCV genotypes and the JFH-1 genotype 2a infectious virus in cell culture.HCV Infection Approved(In Vitro):Daclatasvir (BMS-790052) demonstrates potent inhibitory activity towards all genotypes tested, with EC50 values ranging from 9 pM to 146 pM. Daclatasvir inhibits HCV replicon genotype 1a, 1b, 2a, 3a, 4a and 5a with EC50 values of 50 pM, 9 pM, 71 pM, 146 pM, 12 pM and 33 pM, respectively. Daclatasvir is a potent inhibitor of the JFH-1 genotype 2a infectious virus that replicates in cell culture (EC50=28 pM). Daclatasvir (BMS-790052) binds tightly to NS5A33-202 and NS5A26-202 with Kds of 8 nM and 210 nM, respectively.(In Vivo):Daclatasvir (BMS-790052; 30 mg/kg; oral administration; daily; for 27 days) treatment reduces serum HCV RNA titers very rapidly by ~1.5 log10 at day 3.
  • In Vitro
    Daclatasvir (BMS-790052) demonstrates potent inhibitory activity towards all genotypes tested, with EC50 values ranging from 9 pM to 146?pM. Daclatasvir inhibits HCV replicon genotype 1a, 1b, 2a, 3a, 4a and 5a with EC50 values of 50 pM, 9?pM, 71 pM, 146 pM, 12 pM and 33 pM, respectively. Daclatasvir is a potent inhibitor of the JFH-1 genotype 2a infectious virus that replicates in cell culture (EC50=28 pM).Daclatasvir (BMS-790052) binds tightly to NS5A33-202 and NS5A26-202 with Kds of 8 nM and 210 nM, respectively.
  • In Vivo
    Daclatasvir (BMS-790052; 30?mg/kg; oral administration; daily; for 27 days) treatment reduces serum HCV RNA titers very rapidly by ~1.5 log10 at day 3. Animal Model:NOD/SCID male mice (5 weeks of age, 18-20?g) bearing HCV RNA-transfected cellsDosage:30?mg/kg Administration:Oral administration; daily; for 27 days Result:Reduced serum HCV RNA titers very rapidly by ~1.5 log10 at day 3.
  • Synonyms
    BMS-790052 dihydrochloride | BMS790052 dihydrochloride | BMS 790052 dihydrochloride
  • Pathway
    Microbiology/Virology
  • Target
    HCV
  • Recptor
    HCVNS5A
  • Research Area
    Infection
  • Indication
    HCV Infection

Chemical Information

  • CAS Number
    1009119-65-6
  • Formula Weight
    811.7969
  • Molecular Formula
    C40H52Cl2N8O6
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: ≥ 56 mg/mL
  • SMILES
    CC(C)[C@@H](C(=O)N1CCC[C@H]1C2=NC=C(N2)C3=CC=C(C=C3)C4=CC=C(C=C4)C5=CN=C(N5)[C@@H]6CCCN6C(=O)[C@H](C(C)C)NC(=O)OC)NC(=O)OC.Cl.Cl
  • Chemical Name
    Carbamic acid, N,N'-[[1,1'-biphenyl]-4,4'-diylbis[1H-imidazole-5,2-diyl-(2S)-2,1-pyrrolidinediyl[(1S)-1-(1-methylethyl)-2-oxo-2,1-ethanediyl]]]bis-, C,C'-dimethyl ester, hydrochloride (1:2)

Shipping & Storage Information

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

Reference

1. Gao M, et al. Nature. 2010 May 6;465(7294):96-100. 2. Lemm JA, et al. Antimicrob Agents Chemother. 2011 Aug;55(8):3795-802. 3. Fridell RA, et al. Antimicrob Agents Chemother. 2010 Sep;54(9):3641-50. 4. Fridell RA, et al. J Virol. 2011 Jul;85(14):7312-20.
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