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Results for "

2’-Chloro-2’-deoxyadenosine

" in MedChemExpress (MCE) Product Catalog:
Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-13599
    Cladribine
    3 Publications Verification

    2-Chloro-2′-deoxyadenosine; CldAdo; 2CdA

    		 Adenosine Deaminase Apoptosis Cardiovascular Disease Cancer
    Cladribine (2-Chloro-2′-deoxyadenosine), a purine nucleoside analog, is an orally active adenosine deaminase inhibitor. Cladribine functions as an inhibitor of DNA synthesis to block the repair of the damaged DNA. Cladribine can inhibit DNA methylation. Cladribine has anti-lymphoma activity. Cladribine can be used for the research of several hematologic malignancies and multiple sclerosis .
    Cladribine
  • HY-152334
    2’-Chloro-2’-deoxyadenosine

    		Nucleoside Antimetabolite/Analog Others
    2’-Chloro-2’-deoxyadenosine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .
    2’-<em>Chloro-2</em>’-<em>deoxyadenosine</em>
  • HY-134291
    8-Chloro-2'-deoxyadenosine

    		Nucleoside Antimetabolite/Analog Cancer
    8-Chloro-2'-deoxyadenosine is an adenosine analog. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. Its popular products are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277) .
    8-<em>Chloro-2</em>'-<em>deoxyadenosine</em>
  • HY-154123
    N6-Benzoyl-2’-chloro-2’-deoxyadenosine

    		Nucleoside Antimetabolite/Analog Cancer
    N6-Benzoyl-2’-chloro-2’-deoxyadenosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .
    N6-Benzoyl-2’-<em>chloro-2</em>’-<em>deoxyadenosine</em>

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