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Type HazMat fee for 500 gram (Estimated)
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Chemical Structure| 1431985-92-0 Chemical Structure| 1431985-92-0

Structure of K02288
CAS No.: 1431985-92-0

Chemical Structure| 1431985-92-0

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K02288 is an inhibitor of type I BMP receptor. It targeting ALK2, ALK1 and ALK6 with IC50 of 1.1, 1.8, 6.4 nM, respectively.

4.5 *For Research Use Only !

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

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Product Details of K02288

CAS No. :1431985-92-0
Formula : C20H20N2O4
M.W : 352.38
SMILES Code : OC1=CC=CC(C2=CC(C3=CC(OC)=C(OC)C(OC)=C3)=C(N)N=C2)=C1
MDL No. :MFCD26936347
InChI Key :CJLMANFTWLNAKC-UHFFFAOYSA-N
Pubchem ID :46173038

Safety of K02288

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H318
Precautionary Statements:P280-P301+P310-P305+P351+P338
Class:8(6.1)
UN#:2923
Packing Group:

Isoform Comparison

Biological Activity

Target
  • ALK1

    ALK1, IC50:1.8 nM

  • ALK2

    ALK2, IC50:1.1 nM

  • ALK6

    ALK6, IC50:6.4 nM

  • ALK3

    ALK3, IC50:34.4 nM

In Vitro:

Cell Line
Concentration Treated Time Description References
Huh7 cells 1 µM 24 hours suppressed the cell invasion/migration ability PMC8333780
MT cells 1 µM 24 hours suppressed the cell invasion/migration ability PMC8333780
Lgr5+ CSCs 6.4 nM 3, 5, 7 days K02288 attenuated the radiosensitizing effect of PD on Lgr5+ CSCs, indicating that PD regulates the radiosensitivity of CSCs through the BMP signaling pathway PMC6367551
Human Umbilical Vein Endothelial Cells (HUVECs) 1 µM 30 minutes K02288 inhibited BMP9-induced phosphorylation of SMAD1/5/8, reducing both the SMAD and Notch-dependent transcriptional responses. PMC4363482
abdominal preadipocytes 500 nM 30 minutes K02288 completely inhibited BMP2-induced SMAD1/5/8 phosphorylation PMC6892741
gluteal preadipocytes 500 nM 30 minutes K02288 completely inhibited BMP2-induced SMAD1/5/8 phosphorylation PMC6892741
C2C12 1 nM to 10 μM 30 minutes Measure inhibition of BMP6-induced transcriptional activity (BRE-Luciferase) PMC4191596
HEK293T 1 nM to 10 μM 30 minutes Measure inhibition of TGF-β1-induced transcriptional activity (CAGA-Luciferase) PMC4191596
Human Umbilical Vein Endothelial Cells (HUVECs) 1 µM 4 hours K02288 treatment significantly downregulated BMP9 and Notch-dependent target gene expression. PMC4363482
Huh7 cells 0.5 µM 48 hours suppressed the BMP9-induced upregulation of ID1 and EpCAM expression PMC8333780
Huh7 cells 0.25 µM 5 days suppressed not only ID1 and EpCAM expression PMC8333780
MT cells 0.25 µM 5 days suppressed not only ID1 and EpCAM expression PMC8333780
NGT16 50 µM 72 hours To evaluate the effect of ALK2 inhibitor K02288 on NGT16 cell line, showing approximately 30% reduction in cell viability. PMC6985080
VSMCs 10 μM K02288 treatment abrogated the effect of TXNIP suppression on osteodifferentiation PMC9829043

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Chicken Chick Embryo Chorioallantoic Membrane (CAM) Model Topical Administration 100 µL Single dose, lasting 4 days K02288 caused dysfunctional vessel formation, characterized by hypersprouting and low vessel density. PMC4363482

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.84mL

0.57mL

0.28mL

14.19mL

2.84mL

1.42mL

28.38mL

5.68mL

2.84mL

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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