1. Cell Cycle/DNA Damage
  2. Nucleoside Antimetabolite/Analog
  3. 4-Amino-5-iodo-7-(2-β-C-methyl-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine

4-Amino-5-iodo-7-(2-β-C-methyl-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine 

Cat. No.: HY-152819
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4-Amino-5-iodo-7-(2-β-C-methyl-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine 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.

For research use only. We do not sell to patients.

4-Amino-5-iodo-7-(2-β-C-methyl-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine Chemical Structure

4-Amino-5-iodo-7-(2-β-C-methyl-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine Chemical Structure

CAS No. : 847551-49-9

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Description

4-Amino-5-iodo-7-(2-β-C-methyl-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine 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[1].

Cellular Effect
Cell Line Type Value Description References
CCRF-CEM IC50
4.38 μM
Compound: 6
Cytotoxicity against human CCRF-CEM cells incubated for 3 days by XTT assay
Cytotoxicity against human CCRF-CEM cells incubated for 3 days by XTT assay
[PMID: 22877872]
DU-145 GI50
3.38 μM
Compound: 6
Cytostatic activity against human DU145 cells incubated for 3 days by SRB assay
Cytostatic activity against human DU145 cells incubated for 3 days by SRB assay
[PMID: 22877872]
HCT-116 GI50
6.65 μM
Compound: 6
Cytostatic activity against human HCT116 cells incubated for 3 days by SRB assay
Cytostatic activity against human HCT116 cells incubated for 3 days by SRB assay
[PMID: 22877872]
HeLa S3 IC50
7.5 μM
Compound: 6
Cytotoxicity against human HeLaS3 cells incubated for 3 days by XTT assay
Cytotoxicity against human HeLaS3 cells incubated for 3 days by XTT assay
[PMID: 22877872]
HL-60 IC50
> 10 μM
Compound: 6
Cytotoxicity against human HL60 cells incubated for 3 days by XTT assay
Cytotoxicity against human HL60 cells incubated for 3 days by XTT assay
[PMID: 22877872]
Huh-7 EC50
0.37 μM
Compound: 6
Antiviral activity against Hepatitis C virus subtype 1a replicons infected in human HuH7 cells assessed as reduction in viral RNA levels by Rt-PCR
Antiviral activity against Hepatitis C virus subtype 1a replicons infected in human HuH7 cells assessed as reduction in viral RNA levels by Rt-PCR
[PMID: 22877872]
Huh-7 EC50
0.38 μM
Compound: 6
Antiviral activity against Hepatitis C virus subtype 1b replicons infected in human HuH7 cells assessed as reduction in viral RNA levels by Rt-PCR
Antiviral activity against Hepatitis C virus subtype 1b replicons infected in human HuH7 cells assessed as reduction in viral RNA levels by Rt-PCR
[PMID: 22877872]
Huh-7 CC50
19.75 μM
Compound: 6
Toxicity against human HuH7 cells incubated for 3 days by CellTiter 96 AQueous One Solution cell proliferation assay
Toxicity against human HuH7 cells incubated for 3 days by CellTiter 96 AQueous One Solution cell proliferation assay
[PMID: 22877872]
NCI-H23 GI50
0.79 μM
Compound: 6
Cytostatic activity against human NCI-H23 cells incubated for 3 days by SRB assay
Cytostatic activity against human NCI-H23 cells incubated for 3 days by SRB assay
[PMID: 22877872]
Molecular Weight

406.18

Formula

C12H15IN4O4

CAS No.
SMILES

OC[C@@H]1[C@@H](O)[C@](O)(C)[C@H](N2C=C(I)C3=C2N=CN=C3N)O1

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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4-Amino-5-iodo-7-(2-β-C-methyl-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine Related Classifications

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
4-Amino-5-iodo-7-(2-β-C-methyl-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine
Cat. No.:
HY-152819
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