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Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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E126660-10mg | 10mg | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $64.90 | |
E126660-50mg | 50mg | In stock | $129.90 | |
E126660-250mg | 250mg | In stock | $585.90 | |
E126660-1g | 1g | In stock | $2,106.90 | |
E126660-5g | 5g | In stock | $9,477.90 |
Synonyms | MK-663 | MK-0663 | Etoricoxibe | F2173-0490 | SR-05000001486 | HY-15321 | Kingcox | 5-chloro-2-(6-methylpyridin-3-yl)-3-(4-(methylsulfonyl)phenyl)pyridine | HCC 150 | Nucoxia | CHLOROACETALDEHYDE [MI] | J-013140 | 2,3-Dihydroxybenzoate, IV | 5-Chloro-3-(4 |
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Specifications & Purity | Moligand™, ≥98% |
Biochemical and Physiological Mechanisms | Etoricoxib is a specific inhibitor of COX-2(Cyclooxygenase-2) |
Storage Temp | Store at 2-8°C,Argon charged |
Shipped In | Wet ice |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | Cyclooxygenase-2 inhibitor |
Note | 10mg售完停产,不再备货 |
Product Description | EtoricoxibEtoricoxib(MK-0663) selectively inhibited COX-2 in human whole blood assays in vitro, with an IC50 value of1.1 ± 0.1 μM for COX-2 (LPS-induced prostaglandin E2 synthesis), compared with an IC50 value of 116 ± 8 μM for COX-1 (serum thromboxane B2 generation after clotting of the blood). |
ALogP | 3.3 |
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IUPAC Name | 5-chloro-2-(6-methylpyridin-3-yl)-3-(4-methylsulfonylphenyl)pyridine |
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INCHI | InChI=1S/C18H15ClN2O2S/c1-12-3-4-14(10-20-12)18-17(9-15(19)11-21-18)13-5-7-16(8-6-13)24(2,22)23/h3-11H,1-2H3 |
InChi Key | MNJVRJDLRVPLFE-UHFFFAOYSA-N |
Canonical SMILES | CC1=NC=C(C=C1)C2=C(C=C(C=N2)Cl)C3=CC=C(C=C3)S(=O)(=O)C |
Isomeric SMILES | CC1=NC=C(C=C1)C2=C(C=C(C=N2)Cl)C3=CC=C(C=C3)S(=O)(=O)C |
WGK Germany | 3 |
PubChem CID | 123619 |
Molecular Weight | 358.84 |
Beilstein | 8073797 |
PubChem CID | 123619 |
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Wikipedia | Etoricoxib |
ChEMBL Ligand | CHEMBL416146 |
DrugBank Ligand | DB01628 |
CAS Registry No. | 202409-33-4 |
ChEBI | CHEBI:6339 |
RCSB PDB Ligand | 5CH |
PEP | etoricoxib |
DrugCentral Ligand | 1113 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
---|---|---|---|
J22111016 | Certificate of Analysis | Jul 16, 2024 | E126660 |
J22111017 | Certificate of Analysis | Jul 16, 2024 | E126660 |
J22111018 | Certificate of Analysis | Jul 16, 2024 | E126660 |
J22111019 | Certificate of Analysis | Jul 16, 2024 | E126660 |
K2129523 | Certificate of Analysis | Sep 21, 2023 | E126660 |
K2129631 | Certificate of Analysis | Sep 21, 2023 | E126660 |
H2004042 | Certificate of Analysis | Jun 14, 2022 | E126660 |
H2004041 | Certificate of Analysis | Jun 14, 2022 | E126660 |
H2004040 | Certificate of Analysis | Jun 14, 2022 | E126660 |
Solubility | Soluble in DMSO, and methanol |
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Pictogram(s) | GHS06 |
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Signal | Danger |
Hazard Statements | H302:Harmful if swallowed H310:Fatal in contact with skin |
Precautionary Statements | P280:Wear protective gloves/protective clothing/eye protection/face protection. P310:Immediately call a POISON CENTER or doctor/physician. P302+P350:IF ON SKIN: Gently wash with plenty of soap and water. |
WGK Germany | 3 |
1. Wang R. (2021) Etoricoxib may inhibit cytokine storm to treat COVID-19.. Med Hypotheses, 150 (3): (110557). [PMID:33730601] |