Home Cart Sign in  
Chemical Structure| 252017-04-2 Chemical Structure| 252017-04-2

Structure of AZD7545
CAS No.: 252017-04-2

Chemical Structure| 252017-04-2

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

AZD7545 is a selective inhibitor of PDHK2 (PDH kinase2) with IC50s of 36.8 nM and 6.4 nM for PDHK1 and PDHK2 respectively.

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of AZD7545

CAS No. :252017-04-2
Formula : C19H18ClF3N2O5S
M.W : 478.87
SMILES Code : O=C(N(C)C)C1=CC=C(S(=O)(C2=CC=C(NC([C@@](C)(O)C(F)(F)F)=O)C(Cl)=C2)=O)C=C1
MDL No. :MFCD25976792
InChI Key :DTDZLJHKVNTQGZ-GOSISDBHSA-N
Pubchem ID :16741245

Safety of AZD7545

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
A375 10 μM 90 h Inhibition of PDK1 leads to growth suppression of BRAFV600E mutant cells PMC5465587
PDK3 50 nM 30 min Determination of IC50 for AZD7545 on PDK3, resulting in 600 nM PMC2871385
PDK1 50 nM 30 min Determination of IC50 for AZD7545 on PDK1, resulting in 87 nM PMC2871385
SK-MEL-2 >100 μM 96 h AZD7545 did not significantly inhibit proliferation in SK-MEL-2 cells, IC50 >100 μM PMC8999016
SK-MEL-28 >100 μM 96 h AZD7545 did not significantly inhibit proliferation in SK-MEL-28 cells, IC50 >100 μM PMC8999016
MeWo 89.3 ±5.0 μM 96 h AZD7545 inhibited proliferation in MeWo cells with an IC50 of 89.3 ±5.0 μM PMC8999016
A375 35.0 ±4.1 μM 96 h AZD7545 inhibited proliferation in A375 cells with an IC50 of 35.0 ±4.1 μM PMC8999016
MelJuso 10 μM 120 h Inhibition of PDK1 leads to growth suppression of NRAS mutant cells PMC5465587
IPC298 10 μM 120 h Inhibition of PDK1 leads to growth suppression of NRAS mutant cells PMC5465587
SKMel30 10 μM 120 h Inhibition of PDK1 leads to growth suppression of NRAS mutant cells PMC5465587
501Mel 10 μM 90 h Inhibition of PDK1 leads to growth suppression of BRAFV600E mutant cells PMC5465587
IGR37 10 μM 90 h Inhibition of PDK1 leads to growth suppression of BRAFV600E mutant cells PMC5465587

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.09mL

0.42mL

0.21mL

10.44mL

2.09mL

1.04mL

20.88mL

4.18mL

2.09mL

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

 

Historical Records

Categories