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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
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Inaccessible (Haz class 6.1), International USD 150+
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Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 53164-05-9 Chemical Structure| 53164-05-9

Structure of Acemetacin
CAS No.: 53164-05-9

Chemical Structure| 53164-05-9

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Acemetacin is a non-steroidal anti-inflammatory drug and a glycolic acid ester of indometacin that is a cyclooxygenase inhibitor.

Synonyms: TVX 1322

4.5 *For Research Use Only !

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Product Details of Acemetacin

CAS No. :53164-05-9
Formula : C21H18ClNO6
M.W : 415.82
SMILES Code : O=C(OCC(O)=O)CC1=C(C)N(C(C2=CC=C(Cl)C=C2)=O)C3=C1C=C(OC)C=C3
Synonyms :
TVX 1322
MDL No. :MFCD00151473
InChI Key :FSQKKOOTNAMONP-UHFFFAOYSA-N
Pubchem ID :1981

Safety of Acemetacin

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H300-H310-H330
Precautionary Statements:P260-P264-P280-P284-P301+P310-P302+P350
Class:6.1
UN#:2811
Packing Group:

Isoform Comparison

Biological Activity

Target
  • COX

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Rats Gastric and intestinal damage model Oral 8, 28 or 56 µM/kg Single dose, evaluated after 3 hours To evaluate the damaging effects of Acemetacin and Indomethacin on the stomach and intestine. Results showed that Acemetacin caused significantly less gastric and intestinal damage than Indomethacin at the same doses. Br J Pharmacol. 2008 Nov;155(6):857-64
Rats Zymosan airpouch model Oral or direct injection into the pouch 2.7–83.8 µM/kg Single dose, exudate collected 6 hours later To evaluate the anti-inflammatory effects of Acemetacin and Indomethacin in an acute inflammation model and their impact on prostaglandin and thromboxane synthesis. Results showed that Acemetacin and Indomethacin had similar effects in reducing leukocyte infiltration and PGE2 and TXB2 synthesis, but Acemetacin caused less gastric damage. Br J Pharmacol. 2007 Nov;152(6):930-8
New Zealand White rabbits Acute vascular inflammation model Oral 3 mg/kg Single dose, 24 hours duration To evaluate the anti-inflammatory effects of Cu(II)ACM on acute vascular inflammation, showing an 88% reduction in endothelial VCAM-1 expression but no significant effect on ICAM-1 expression. Cell Biosci. 2016 Feb 6;6:9

Clinical Trial:

NCT Number Conditions Phases Recruitment Completion Date Locations
NCT01759355 - Active, not recruiting May 2019 United States, North Carolina ... More >> University of North Carolina-Chapel Hill Chapel Hill, North Carolina, United States, 27599 Less <<

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.40mL

0.48mL

0.24mL

12.02mL

2.40mL

1.20mL

24.05mL

4.81mL

2.40mL

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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