1. Cell Cycle/DNA Damage Anti-infection
  2. DNA/RNA Synthesis HSV
  3. North-methanocarbathymidine

North-methanocarbathymidine (N-MCT) is a potent antiviral agent. North-methanocarbathymidine inhibits DNA synthesis. North-methanocarbathymidine demonstrates potent antiviral activity against HSV-1, HSV-2 and KSHV. North-methanocarbathymidine exhibits anticancer activity against colon adenocarcinoma expressing HSV-tk.

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

North-methanocarbathymidine

North-methanocarbathymidine Chemical Structure

CAS No. : 156126-12-4

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Description

North-methanocarbathymidine (N-MCT) is a potent antiviral agent. North-methanocarbathymidine inhibits DNA synthesis. North-methanocarbathymidine demonstrates potent antiviral activity against HSV-1, HSV-2 and KSHV. North-methanocarbathymidine exhibits anticancer activity against colon adenocarcinoma expressing HSV-tk[1].

IC50 & Target[1]

HSV-1

 

HSV-2

 

Cellular Effect
Cell Line Type Value Description References
HFF CC50
> 396 μM
Compound: 1a
Cytotoxic concentration for 50% inhibition of cell growth of HSV-1 infected HFF cells determined by CPE assay
Cytotoxic concentration for 50% inhibition of cell growth of HSV-1 infected HFF cells determined by CPE assay
[PMID: 14584954]
HFF CC50
> 396 μM
Compound: 1a
Cytotoxic concentration for 50% inhibition of cell growth of HSV-2 infected HFF cells determined by CPE assay
Cytotoxic concentration for 50% inhibition of cell growth of HSV-2 infected HFF cells determined by CPE assay
[PMID: 14584954]
HFF CC50
> 79 μM
Compound: 1a
Cytotoxic concentration for 50% inhibition of cell growth of HSV-1 infected HFF cells determined by VPR assay
Cytotoxic concentration for 50% inhibition of cell growth of HSV-1 infected HFF cells determined by VPR assay
[PMID: 14584954]
HFF CC50
> 79 μM
Compound: 1a
Cytotoxic concentration for 50% inhibition of cell growth of HSV-2 infected HFF cells determined by VPR assay
Cytotoxic concentration for 50% inhibition of cell growth of HSV-2 infected HFF cells determined by VPR assay
[PMID: 14584954]
HFF EC50
0.04 μM
Compound: 1a
Inhibitory concentration for HSV-1 plaque reduction (VPR) by 50% in HFF cells
Inhibitory concentration for HSV-1 plaque reduction (VPR) by 50% in HFF cells
[PMID: 14584954]
HFF EC50
0.12 μM
Compound: 1a
Inhibitory concentration required to reduce HSV-1 induced cytopathogenic effect (CPE) by 50 % in HFF cells
Inhibitory concentration required to reduce HSV-1 induced cytopathogenic effect (CPE) by 50 % in HFF cells
[PMID: 14584954]
HFF EC50
0.35 μM
Compound: 1a
Inhibitory concentration required to reduce HSV-2 induced cytopathogenic effect (CPE) by 50 % in HFF cells
Inhibitory concentration required to reduce HSV-2 induced cytopathogenic effect (CPE) by 50 % in HFF cells
[PMID: 14584954]
HFF EC50
0.47 μM
Compound: 1a
Inhibitory concentration for HSV-2 plaque reduction (VPR) by 50% in HFF cells
Inhibitory concentration for HSV-2 plaque reduction (VPR) by 50% in HFF cells
[PMID: 14584954]
Molecular Weight

252.27

Formula

C12H16N2O4

CAS No.
SMILES

O=C1NC(C(C)=CN1[C@@H]2[C@@]3([H])C[C@@]3(CO)[C@@H](O)C2)=O

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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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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North-methanocarbathymidine
Cat. No.:
HY-104083
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