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Chemical Structure| 328104-79-6 Chemical Structure| 328104-79-6

Structure of DNMDP
CAS No.: 328104-79-6

Chemical Structure| 328104-79-6

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DNMDP is a PDE3A inhibitor and a highly efficient, selective cytotoxic molecule for tumor cells. DNMDP promotes the interaction between PDE3A and Schlafen 12 (SLFN12). DNMDP possesses significant cell-selective cytotoxicity.

Synonyms: DNMDP

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Product Details of DNMDP

CAS No. :328104-79-6
Formula : C15H20N4O3
M.W : 304.34
SMILES Code : O=C1CC(C)C(C2=CC=C(N(CC)CC)C([N+]([O-])=O)=C2)=NN1
Synonyms :
DNMDP
MDL No. :MFCD01829240

Safety of DNMDP

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
HeLa 10-100 nM 48 hours To test the cell-selective cytotoxicity of DNMDP Nat Chem Biol. 2016 Feb;12(2):102-8
HeLa cells 10 µM 8 h To assess DNMDP-induced PDE3A-SLFN12 complex formation Nat Commun. 2021 Jul 16;12(1):4375
HeLa cells 1 μM 20 or 30 hours To assess DNMDP cytotoxicity in HeLa cells, finding that PDE3A overexpression increased sensitivity to DNMDP. Biosci Rep. 2017 Aug 31;37(4):BSR20170975
GB1 glioblastoma cells 100 nM 5 days To identify DNMDP resistance mutations by deep mutational scanning Nat Commun. 2021 Jul 16;12(1):4375
SK-MEL-3 cells 1 nM to 10 μM 3 days Evaluating the cytotoxicity of DNMDP analogs, DNMDP had an EC50 of 12 nM ACS Med Chem Lett. 2019 Oct 18;10(11):1537-1542
HeLa cells 1 nM to 10 μM 3 days Evaluating the cytotoxicity of DNMDP analogs, DNMDP had an EC50 of 6.9 nM ACS Med Chem Lett. 2019 Oct 18;10(11):1537-1542
A549 10 µM 48 hours To identify anti-cancer compounds with cell-selective cytotoxic activity Nat Chem Biol. 2016 Feb;12(2):102-8
NCI-H1734 10 µM 48 hours To identify anti-cancer compounds with cell-selective cytotoxic activity Nat Chem Biol. 2016 Feb;12(2):102-8

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.29mL

0.66mL

0.33mL

16.43mL

3.29mL

1.64mL

32.86mL

6.57mL

3.29mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
 

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