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Results for "

2-chloro-2-

" in MedChemExpress (MCE) Product Catalog:

19

Inhibitors & Agonists

1

Biochemical Assay Reagents

1

Peptides

4

Isotope-Labeled Compounds

9

Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-150519S

    Isotope-Labeled Compounds Others
    2-Chloro-2-methylpropane-d9 is the deuterium labeled 2-Chloro-2-methylpropane .
    2-Chloro-2-methylpropane-d9
  • HY-13599
    Cladribine
    5+ Cited Publications

    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-101904

    Nucleoside Antimetabolite/Analog Others
    2-Chloro-2'-deoxycytidine is a cytidine nucleoside analog. Cytidine analogs have a mechanism of inhibiting DNA methyltransferases (such as Zebularine, HY-13420), and have potential anti-metabolic and anti-tumor activities .
    2-Chloro-2'-deoxycytidine
  • HY-154392

    Nucleoside Antimetabolite/Analog Cancer
    2-Chloro-2’-deoxy inosine 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 .
    2-Chloro-2’-deoxy inosine
  • HY-154395

    Nucleoside Antimetabolite/Analog Cancer
    2-Chloro-2′-deoxy-N,N-dimethyladenosine 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 .
    2-Chloro-2′-deoxy-N,N-dimethyladenosine
  • HY-152812

    Nucleoside Antimetabolite/Analog Others
    2-Chloro-2′-β-C-methyladenosine is an adenosine analogue. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. The popular products in this series are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277) .
    2-Chloro-2′-β-C-methyladenosine
  • HY-154393

    Nucleoside Antimetabolite/Analog Xanthine Oxidase Cancer
    2-Chloro-2'-deoxy-6-O-methylinosine is a hypoxanthine analog. Hypoxanthine is a kind of purine base mainly present in muscle tissue. And it is a metabolite produced by purine oxidase acting on xanthine. Hypoxanthine has typical anti-inflammatory effects and is a potential endogenous poly(ADP-ribose) polymerase (PARP) inhibitor. It is cytoprotective by inhibiting PAPR activity, inhibiting peroxynitrite-induced mitochondrial depolarization and secondary superoxide production. Hypoxanthine can also be used as an indicator of hypoxia .
    2-Chloro-2'-deoxy-6-O-methylinosine
  • HY-152711

    Nucleoside Antimetabolite/Analog Others
    2-Chloro-2’-β-C-methyl-6-N,N-dimethyladenosine 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-Chloro-2’-β-C-methyl-6-N,N-dimethyladenosine
  • HY-13599R

    2-chloro-2′-deoxyadenosine (Standard); CldAdo (Standard); 2CdA (Standard)

    Reference Standards Adenosine Deaminase Apoptosis Cardiovascular Disease Cancer
    Cladribine (Standard) is the analytical standard of Cladribine. This product is intended for research and analytical applications. 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 (Standard)
  • HY-13599S2

    2-chloro-2′-deoxyadenosine-15N; Cldado-15N; 2Cda-15N

    Isotope-Labeled Compounds Apoptosis Adenosine Deaminase Cardiovascular Disease Cancer
    Cladribine- 15N (2-Chloro-2′-deoxyadenosine- 15N) is 15N labeled Cladribine. 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-15N
  • HY-13599S

    2-chloro-2′-deoxyadenosine-d4; CldAdo-d4; 2CdA-d4

    Isotope-Labeled Compounds Cardiovascular Disease Cancer
    Cladribine-d4 (2-Chloro-2′-deoxyadenosine-d4) is deuterium labeled Cladribine. 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-d4
  • HY-13599S1

    2-chloro-2′-deoxyadenosine-13C5,15N2; CldAdo-13C5,15N2; 2CdA-13C5,15N2

    Isotope-Labeled Compounds Cardiovascular Disease Cancer
    Cladribine- 13C5, 15N2 (2-Chloro-2′-deoxyadenosine- 13C5, 15N2) is 13C and 15N labeled Cladribine. 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-13C5,15N2
  • HY-152334

    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’-Chloro-2’-deoxyadenosine
  • HY-W154172

    Nucleoside Antimetabolite/Analog Cancer
    2′-Chloro-2′-deoxyuridine 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 .
    2′-Chloro-2′-deoxyuridine
  • HY-154123

    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’-chloro-2’-deoxyadenosine
  • HY-77967R

    Reference Standards
    Ethyl 2-chloro-2-(2-(4-chlorophenyl)hydrazono)acetate (Standard) is the analytical standard of Ethyl 2-chloro-2-(2-(4-chlorophenyl)hydrazono)acetate. This product is intended for research and analytical applications.
    Apixaban impurity 4 (Standard)
  • HY-W883810R

    Reference Standards
    Ethyl (2Z)-2-chloro-2-[2-(4-methoxyphenyl)hydrazinylidene]acetate (Standard)
  • HY-W011331

    Biochemical Assay Reagents Others
    (Chloro(2-chlorophenyl)methylene)dibenzene is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    2-Chlorotrityl chloride
  • HY-P10579
    123B9
    1 Publications Verification

    Ephrin Receptor Cancer
    123B9, a tumor-homing agent, is a potent and selective EphA2 agonist with a Kd value of 4.0 μM. 123B9 selectively targets the EphA2 tyrosine kinase receptor ligand-binding domain. 123B9 does not appreciably inhibit the ligand binding domains of the most closely related EphA3 and EphA4 receptors .
    123B9

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