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Chemical Structure| 58131-57-0 Chemical Structure| 58131-57-0

Structure of NSC-207895
CAS No.: 58131-57-0

Chemical Structure| 58131-57-0

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NSC-207895 (XI-006), a DNA damaging agent, is an anticancer agent and p53 activator.

Synonyms: XI-006; NSC 179940; NSC-207895, NSC207895, NSC 207895, NSC179940, NSC-179940, NSC 179940, XI-006, XI 006, XI006

4.5 *For Research Use Only !

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Product Details of NSC-207895

CAS No. :58131-57-0
Formula : C11H13N5O4
M.W : 279.25
SMILES Code : O=[N+](C1=CC=C(N2CCN(C)CC2)C3=[N+]([O-])ON=C31)[O-]
Synonyms :
XI-006; NSC 179940; NSC-207895, NSC207895, NSC 207895, NSC179940, NSC-179940, NSC 179940, XI-006, XI 006, XI006
MDL No. :MFCD01660065

Safety of NSC-207895

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H315-H319-H228
Precautionary Statements:P240-P210-P241-P264-P280-P302+P352-P370+P378-P337+P313-P305+P351+P338-P362+P364-P332+P313
Class:4.1
UN#:1325
Packing Group:

Isoform Comparison

Biological Activity

Description
NSC-207895 (XI-006), a DNA damaging agent, serves as an anticancer agent and p53 activator[1][2][3].

In Vitro:

Cell Line
Concentration Treated Time Description References
HT1080 cells 5 µM 24 h Inhibited MDMX expression Mol Cancer Ther. 2011 Jan;10(1):69-79.
MCF-7 cells 5 µM 16 h Activated p53 and induced pro-apoptotic gene expression Mol Cancer Ther. 2011 Jan;10(1):69-79.
B6-2 7.29 μM 48 h NSC207895 showed significant cytotoxic and antiproliferative effects in B6-2 cells Sci Rep. 2021 Feb 3;11(1):2967.
HepT1 1.47 μM 48 h NSC207895 showed significant cytotoxic and antiproliferative effects in HepT1 cells Sci Rep. 2021 Feb 3;11(1):2967.
Huh-6 3.03 μM 48 h NSC207895 showed significant cytotoxic and antiproliferative effects in Huh-6 cells Sci Rep. 2021 Feb 3;11(1):2967.
HepG2 0.95 μM 48 h NSC207895 showed significant cytotoxic and antiproliferative effects in HepG2 cells Sci Rep. 2021 Feb 3;11(1):2967.
Osteosarcoma cell lines 2.14–5.41 μM 48 h XI-006 induced cell cycle arrest rather than apoptosis in osteosarcoma cell lines. Sci Rep. 2015 Jun 22;5:11465.
Ewing sarcoma cell lines 0.099–1.61 μM 48 h XI-006 induced potent p53-independent apoptosis in Ewing sarcoma cell lines, independent of MDM4 mRNA/protein levels or TP53 status. Sci Rep. 2015 Jun 22;5:11465.
mouse primary chondrocytes 0.5 μM 6 h NSC-207895 activates p53 and reverses the inhibitory effect of miR-325-3p on mechanical overloading-induced chondrocyte senescence. Arthritis Res Ther. 2023 Apr 4;25(1):54.

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Mice HepT1 orthotopic xenograft model Intraperitoneal injection 5 mg/kg Every other day for three weeks NSC207895 significantly decreased tumor weight and increased apoptosis in the treatment group Sci Rep. 2021 Feb 3;11(1):2967.

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.58mL

0.72mL

0.36mL

17.91mL

3.58mL

1.79mL

35.81mL

7.16mL

3.58mL

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
Protocol 2

References

 

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