1. Anti-infection
  2. HIV CMV
  3. PMEDAP

PMEDAP is a potent inhibitor of human immunodeficiency virus (HIV) replication. PMEDAP has anti-murine cytomegalovirus (MCMV) activity. PMEDAP is a very potent inhibitor of Moloney murine sarcoma virus (MSV)-induced tumor formation and associated mortality.

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

PMEDAP Chemical Structure

PMEDAP Chemical Structure

CAS No. : 113852-41-8

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Description

PMEDAP is a potent inhibitor of human immunodeficiency virus (HIV) replication. PMEDAP has anti-murine cytomegalovirus (MCMV) activity. PMEDAP is a very potent inhibitor of Moloney murine sarcoma virus (MSV)-induced tumor formation and associated mortality[1][2].

Cellular Effect
Cell Line Type Value Description References
CCRF-HSB-2 CC50
> 56 μM
Compound: PME-DAP
Cytotoxicity against human HSB2 cell after 4 hrs by MTS assay
Cytotoxicity against human HSB2 cell after 4 hrs by MTS assay
[PMID: 18852272]
Daudi CC50
> 50 μM
Compound: PME-DAP
Cytotoxicity against human Daudi cell after 4 hrs by MTS assay
Cytotoxicity against human Daudi cell after 4 hrs by MTS assay
[PMID: 18852272]
HEL 299 EC50
> 173 μM
Compound: 3b, PMEDAP
Antiviral activity against Camelpox virus CML1 infected in HEL299 cells assessed as inhibition of virus-induced cytopathic effect after 6 days by Giemsa staining
Antiviral activity against Camelpox virus CML1 infected in HEL299 cells assessed as inhibition of virus-induced cytopathic effect after 6 days by Giemsa staining
[PMID: 17893157]
HEL 299 EC50
> 173 μM
Compound: 3b, PMEDAP
Antiviral activity against Camelpox virus CML14 infected in HEL299 cells assessed as inhibition of virus-induced cytopathic effect after 6 days by Giemsa staining
Antiviral activity against Camelpox virus CML14 infected in HEL299 cells assessed as inhibition of virus-induced cytopathic effect after 6 days by Giemsa staining
[PMID: 17893157]
HEL 299 CC50
100 μM
Compound: 3b, PMEDAP
Cytotoxicity against HEL299 cells after 4 days by Z1 Coulter counting analysis
Cytotoxicity against HEL299 cells after 4 days by Z1 Coulter counting analysis
[PMID: 17893157]
HFF EC50
> 10 μM
Compound: PME-DAP
Antiviral activity against herpes simplex virus 1 E-377 infected in HFF cells by plaque reduction assay
Antiviral activity against herpes simplex virus 1 E-377 infected in HFF cells by plaque reduction assay
[PMID: 18852272]
HFF EC50
> 10 μM
Compound: PME-DAP
Antiviral activity against herpes simplex virus 2 MS infected in HFF cells by plaque reduction assay
Antiviral activity against herpes simplex virus 2 MS infected in HFF cells by plaque reduction assay
[PMID: 18852272]
HFF CC50
> 100 μM
Compound: PME-DAP
Cytotoxicity against human HFF cells after 7 days by neutral red dye method
Cytotoxicity against human HFF cells after 7 days by neutral red dye method
[PMID: 18852272]
HFF EC50
0.2 μM
Compound: PME-DAP
Antiviral activity against Murine cytomegalovirus Smith infected in HFF cells by plaque reduction assay
Antiviral activity against Murine cytomegalovirus Smith infected in HFF cells by plaque reduction assay
[PMID: 18852272]
HFF EC50
13 μM
Compound: PME-DAP
Antiviral activity against Human cytomegalovirus AD169 infected in HFF cells by plaque reduction assay
Antiviral activity against Human cytomegalovirus AD169 infected in HFF cells by plaque reduction assay
[PMID: 18852272]
HFF EC50
2.9 μM
Compound: PME-DAP
Antiviral activity against Varicella zoster virus Ellen infected in HFF cells by plaque reduction assay
Antiviral activity against Varicella zoster virus Ellen infected in HFF cells by plaque reduction assay
[PMID: 18852272]
MOLT-3 CC50
39 μM
Compound: PME-DAP
Cytotoxicity against human MOLT3 cell after 4 hrs by MTS assay
Cytotoxicity against human MOLT3 cell after 4 hrs by MTS assay
[PMID: 18852272]
In Vivo

PMEDAP (0.25-5 mg/kg; IP; daily; starting on the day of MSV-infected and continuing for an additional four days) causes a dose-dependent suppression of tumor formation and mortality in newborn mice inoculated with MSV[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Three-week-old male NMRI mice[1]
Dosage: 0.25 mg/kg, 1 mg/kg, 5 mg/kg
Administration: IP; daily; starting on the day of infection and continuing for an additional four days
Result: Effected a significant delay in tumor appearance and an enhancement of the survival rate of tumor-bearing mice.
Molecular Weight

288.20

Formula

C8H13N6O4P

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

O=P(O)(COCCN1C=NC2=C1N=C(N)N=C2N)O

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

Solvent & Solubility
In Vitro: 

0.1 M NaOH : 14.29 mg/mL (49.58 mM; ultrasonic and adjust pH to 12 with NaOH)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 3.4698 mL 17.3491 mL 34.6981 mL
5 mM 0.6940 mL 3.4698 mL 6.9396 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

  • Molarity Calculator

  • Dilution Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration: mg/mL
Purity & Documentation
References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
0.1 M NaOH 1 mM 3.4698 mL 17.3491 mL 34.6981 mL 86.7453 mL
5 mM 0.6940 mL 3.4698 mL 6.9396 mL 17.3491 mL
10 mM 0.3470 mL 1.7349 mL 3.4698 mL 8.6745 mL
15 mM 0.2313 mL 1.1566 mL 2.3132 mL 5.7830 mL
20 mM 0.1735 mL 0.8675 mL 1.7349 mL 4.3373 mL
25 mM 0.1388 mL 0.6940 mL 1.3879 mL 3.4698 mL
30 mM 0.1157 mL 0.5783 mL 1.1566 mL 2.8915 mL
40 mM 0.0867 mL 0.4337 mL 0.8675 mL 2.1686 mL
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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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PMEDAP
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