1. Metabolic Enzyme/Protease
  2. Drug Metabolite
  3. cPrPMEDAP

cPrPMEDAP is an intermediate metabolite of GS-9219. cpr-PMEDAP functions as a proagent of the guanine nucleotide analog PMEG and has antiproliferative activity. cPrPMEDAP is negatively charged at physiologic pH and has poor permeability into the skin.

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

cPrPMEDAP Chemical Structure

cPrPMEDAP Chemical Structure

CAS No. : 182798-83-0

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5 mg USD 381 In-stock
10 mg USD 610 In-stock
25 mg USD 1220 In-stock
50 mg USD 1960 In-stock
100 mg USD 3130 In-stock
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Based on 1 publication(s) in Google Scholar

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Description

cPrPMEDAP is an intermediate metabolite of GS-9219. cpr-PMEDAP functions as a proagent of the guanine nucleotide analog PMEG and has antiproliferative activity. cPrPMEDAP is negatively charged at physiologic pH and has poor permeability into the skin[1][2].

Cellular Effect
Cell Line Type Value Description References
Ca-Ski EC50
1410 nM
Compound: cPrPMEDAP
Antiproliferative activity against HPV-transformed human CaSki cells after 7 days by SRB assay
Antiproliferative activity against HPV-transformed human CaSki cells after 7 days by SRB assay
[PMID: 19398642]
CCRF-HSB-2 CC50
3 μM
Compound: PME-cPrDAP
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
20 μM
Compound: PME-cPrDAP
Cytotoxicity against human Daudi cell after 4 hrs by MTS assay
Cytotoxicity against human Daudi cell after 4 hrs by MTS assay
[PMID: 18852272]
HeLa EC50
6930 nM
Compound: cPrPMEDAP
Antiproliferative activity against HPV-transformed human HeLa cells after 7 days by SRB assay
Antiproliferative activity against HPV-transformed human HeLa cells after 7 days by SRB assay
[PMID: 19398642]
HFF EC50
< 0.06 μM
Compound: PME-cPrDAP
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 CC50
> 100 μM
Compound: PME-cPrDAP
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
0.4 μM
Compound: PME-cPrDAP
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
0.8 μM
Compound: PME-cPrDAP
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]
HFF EC50
4 μM
Compound: PME-cPrDAP
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
7.9 μM
Compound: PME-cPrDAP
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]
HT-3 EC50
7040 nM
Compound: cPrPMEDAP
Antiproliferative activity against HPV-non-transformed human HT3 cells after 7 days by SRB assay
Antiproliferative activity against HPV-non-transformed human HT3 cells after 7 days by SRB assay
[PMID: 19398642]
ME-180 EC50
8320 nM
Compound: cPrPMEDAP
Antiproliferative activity against HPV-transformed human ME180 cells after 7 days by SRB assay
Antiproliferative activity against HPV-transformed human ME180 cells after 7 days by SRB assay
[PMID: 19398642]
MOLT-3 CC50
8.5 μM
Compound: PME-cPrDAP
Cytotoxicity against human MOLT3 cell after 4 hrs by MTS assay
Cytotoxicity against human MOLT3 cell after 4 hrs by MTS assay
[PMID: 18852272]
SCC-4 EC50
1430 nM
Compound: cPrPMEDAP
Antiproliferative activity against HPV-non-transformed human SCC4 cells after 7 days by SRB assay
Antiproliferative activity against HPV-non-transformed human SCC4 cells after 7 days by SRB assay
[PMID: 19398642]
SCC-9 EC50
10100 nM
Compound: cPrPMEDAP
Antiproliferative activity against HPV-non-transformed human SCC9 cells after 7 days by SRB assay
Antiproliferative activity against HPV-non-transformed human SCC9 cells after 7 days by SRB assay
[PMID: 19398642]
SiHa EC50
> 20000 nM
Compound: cPrPMEDAP
Inhibition of DNA synthesis in HPV-transformed human SiHa cells assessed as decrease in BrdU incorporation after 72 to 75 hrs by ELISA
Inhibition of DNA synthesis in HPV-transformed human SiHa cells assessed as decrease in BrdU incorporation after 72 to 75 hrs by ELISA
[PMID: 19398642]
SiHa EC50
1500 nM
Compound: cPrPMEDAP
Inhibition of DNA synthesis in HPV-transformed human SiHa cells assessed as decrease in BrdU incorporation after 6 to 9 hrs by ELISA
Inhibition of DNA synthesis in HPV-transformed human SiHa cells assessed as decrease in BrdU incorporation after 6 to 9 hrs by ELISA
[PMID: 19398642]
SiHa EC50
1860 nM
Compound: cPrPMEDAP
Inhibition of DNA synthesis in HPV-transformed human SiHa cells assessed as decrease in BrdU incorporation after 3 to 6 hrs by ELISA
Inhibition of DNA synthesis in HPV-transformed human SiHa cells assessed as decrease in BrdU incorporation after 3 to 6 hrs by ELISA
[PMID: 19398642]
SiHa EC50
2300 nM
Compound: cPrPMEDAP
Inhibition of DNA synthesis in HPV-transformed human SiHa cells assessed as decrease in BrdU incorporation after 24 to 27 hrs by ELISA
Inhibition of DNA synthesis in HPV-transformed human SiHa cells assessed as decrease in BrdU incorporation after 24 to 27 hrs by ELISA
[PMID: 19398642]
SiHa EC50
2650 nM
Compound: cPrPMEDAP
Inhibition of DNA synthesis in HPV-transformed human SiHa cells assessed as decrease in BrdU incorporation after 48 to 51 hrs by ELISA
Inhibition of DNA synthesis in HPV-transformed human SiHa cells assessed as decrease in BrdU incorporation after 48 to 51 hrs by ELISA
[PMID: 19398642]
SiHa EC50
290 nM
Compound: cPrPMEDAP
Antiproliferative activity against HPV-transformed human SiHa cells after 7 days by SRB assay
Antiproliferative activity against HPV-transformed human SiHa cells after 7 days by SRB assay
[PMID: 19398642]
SiHa EC50
8840 nM
Compound: cPrPMEDAP
Inhibition of DNA synthesis in HPV-transformed human SiHa cells assessed as decrease in BrdU incorporation after 3 hrs by ELISA
Inhibition of DNA synthesis in HPV-transformed human SiHa cells assessed as decrease in BrdU incorporation after 3 hrs by ELISA
[PMID: 19398642]
In Vitro

cPrPMEDAP shows antiproliferative activity in SiHa cells with an EC50 of 290 nM (SiHa cells: HPV-transformed cervical carcinoma cell lines)[1].
PMEG forms an active phosphorylated metabolite, PMEG diphosphate (PMEG-DP), in cells, which inhibits the growth of various transformed cell lines due to potent inhibition of the nuclear DNA polymerases α, δ and ɛ, resulting in inhibition of DNA synthesis and/or DNA repair. In animal models, PMEG has antiproliferative effects; the utility of PMEG as an antiproliferative agent is limited by its poor cellular permeability and toxicity. cPrPMEDAP has similar antiproliferative effects in vitro and reduced toxicity in vivo but, like PMEG, is negatively charged at physiologic pH and has poor permeability into the skin[1].

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

Molecular Weight

328.26

Formula

C11H17N6O4P

CAS No.
Appearance

Solid

Color

Off-white to light yellow

SMILES

NC1=NC(NC2CC2)=C3N=CN(CCOCP(O)(O)=O)C3=N1

Shipping

Room temperature in continental US; may vary elsewhere.

Storage
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Solvent & Solubility
In Vitro: 

DMSO : 10 mg/mL (30.46 mM; ultrasonic and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 3.0464 mL 15.2318 mL 30.4637 mL
5 mM 0.6093 mL 3.0464 mL 6.0927 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. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

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In Vivo Dissolution Calculator
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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. 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
DMSO 1 mM 3.0464 mL 15.2318 mL 30.4637 mL 76.1591 mL
5 mM 0.6093 mL 3.0464 mL 6.0927 mL 15.2318 mL
10 mM 0.3046 mL 1.5232 mL 3.0464 mL 7.6159 mL
15 mM 0.2031 mL 1.0155 mL 2.0309 mL 5.0773 mL
20 mM 0.1523 mL 0.7616 mL 1.5232 mL 3.8080 mL
25 mM 0.1219 mL 0.6093 mL 1.2185 mL 3.0464 mL
30 mM 0.1015 mL 0.5077 mL 1.0155 mL 2.5386 mL
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cPrPMEDAP Related Classifications

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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cPrPMEDAP
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HY-101677
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