(+)-Aphidicolin

(+)-Aphidicolin

Catalog Number:
A004364324APE
Mfr. No.:
APE-B7832
Price:
$252
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      • Overview
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          Background

          Aphidicolin, a tetracyclic diterpenoid, is an antibiotic with novel structure produced by the mold Cephalosporium aphidicola. Aphidicolin is an inhibitor of DNA polymerase-α [1].DNA polymerase-α is an enzyme complex involved in initiation of DNA replication and during synthesis of Okazaki fragments on the lagging strand. The DNA polymerase-α complex consists of 4 subunits: POLA1, POLA2, PRIM1, and PRIM2. POLA1 is the catalytic subunit. POLA2 is the regulatory subunit. PRIM1 and PRIM2 are the small and the large primase subunits [2].Aphidicolin selectively inhibited the activity of DNA polymerase-α without activity for DNA polymerase-β and mitochondrial DNA polymerase. Aphidicolin prevented cell division in sea urchin embryos [1]. Aphidicolin was a potent inhibitor of cellular deoxyribonucleic acid synthesis. Aphidicolin strongly inhibited the growth of herpes simplex virus both in tissue culture and in the rabbit eye. Aphidicolin was active against iododeoxyuridine-resistant herpes virus [3]. Aphidicolin showed antiviral activity and inhibited the incorporation of thymidine into DNA of cultured human embryonic lung cells. Aphidicolin (15 μg/ml) reduced the activity of crude and partially purified DNA polymerases from the cytosol [4].

          [1] Ikegami S, TAGUCHI T, OHASHI M, et al. Aphidicolin prevents mitotic cell division by interfering with the activity of DNA polymerase-α[J]. Nature, 1978, 275(5679): 458-460.
          [2] Lehman I R, Kaguni L S, Krause K H, et al. DNA polymerase alpha[J]. J. Biol. Chem, 1989, 264.
          [3] Bucknall R A, Moores H, Simms R, et al. Antiviral effects of aphidicolin, a new antibiotic produced by Cephalosporium aphidicola[J]. Antimicrobial agents and chemotherapy, 1973, 4(3): 294-298.
          [4] Ohashi M, Taguchi T, Ikegami S. Aphidicolin: a specific inhibitor of DNA polymerases in the cytosol of rat liver[J]. Biochemical and biophysical research communications, 1978, 82(4): 1084-1090.

      • Properties
        • Categories
          tetracyclic diterpene antibiotic
          Alternative Name
          (3R,4R,4aR,6aS,8R,9R,11aS,11bS)-4,9-bis(hydroxymethyl)-4,11b-dimethyltetradecahydro-8,11a-methanocyclohepta[a]naphthalene-3,9-diol
          CAS Number
          38966-21-1
          Molecular Formula
          C20H34O4
          Molecular Weight
          338.48
          Appearance
          A white to off-white solid
          Purity
          98.00%
          Solubility
          ≥33.33 mg/mL in DMSO; insoluble in EtOH; insoluble in H2O
          Storage
          Store at -20°C
          SMILES
          O[[email protected]@]1(CC[[email protected]@]23[[email protected]@]([H])(CC[[email protected]]4([[email protected]@](C)([[email protected]@H](CC[[email protected]@]43C)O)CO)[H])C[[email protected]@H]1C2)CO

          * For Research Use Only

      • Reference
        • 1. Viola Ellison, George K. Annor, et al. "Frame-shift mediated reduction of gain-of-function p53 R273H and deletion of the R273H C-terminus in breast cancer cells result in replication-stress sensitivity." Oncotarget. 2021 Jun 8;12(12):1128-1146. PMID:34136083

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