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4-Chloro-7-(2-deoxy-3,5-bis-O-(p-toluoyl)-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine

CAT:
804-HY-152977
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  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
4-Chloro-7-(2-deoxy-3,5-bis-O-(p-toluoyl)-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine - image 1

4-Chloro-7-(2-deoxy-3,5-bis-O-(p-toluoyl)-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine

  • UNSPSC Description:

    4-Chloro-7-(2-deoxy-3,5-bis-O-(p-toluoyl)-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine is a pyrimidine nucleoside analog. Pyrimidine nucleoside analogs have a wide range of biochemical and anticancer activities. These include DNA synthesis inhibition, RNA synthesis inhibition, antiviral effects, and immunomodulatory effects[1].

  • Target Antigen:

    Nucleoside Antimetabolite/Analog

  • Type:

    Oligonucleotides

  • Related Pathways:

    Cell Cycle/DNA Damage

  • Field of Research:

    Others

  • Assay Protocol:

    https://www.medchemexpress.com/4-chloro-7-2-deoxy-3-5-bis-o-p-toluoyl-β-d-ribofuranosyl-7h-pyrrolo-2-3-d-pyrimidine.html

  • Solubility:

    10 mM in DMSO

  • Smiles:

    ClC1=NC=NC2=C1C=CN2[C@@H]3O[C@H](COC(C4=CC=C(C)C=C4)=O)[C@@H](OC(C5=CC=C(C)C=C5)=O)C3

  • Molecular Weight:

    505.95

  • References & Citations:

    [1]Galmarini CM, et al. Pyrimidine nucleoside analogs in cancer treatment. Expert Rev Anticancer Ther. 2003 Oct;3(5):717-28.

  • Shipping Conditions:

    Room temperature

  • Clinical Information:

    No Development Reported

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