Structure of Rofecoxib
CAS No.: 162011-90-7
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Rofecoxib is a potent inhibitor of the COX2-dependent production of PGE2 in human osteosarcoma cells with IC50 of 26±10 nM and Chinese hamster ovary cells expressing human COX-2 with IC50 of 18±7 nM.
Synonyms: MK 966; MK-0966; Ceoxx
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Wegner, Scott A ; Kim, Hahn ; Avalos, José L ;
Abstract: Lactate transport plays a crucial role in the metabolism, microenvironment, and survival of cancer cells. However, current drugs targeting either MCT1 or MCT4, which traditionally mediate lactate import or efflux respectively, show limited efficacy beyond in vitro models. This limitation partly arises from the existence of both isoforms in certain tumors, however existing high-affinity MCT1/4 inhibitors are years away from human testing. Therefore, we conducted an optogenetic drug screen in Saccharomyces cerevisiae on a subset of the FDA-approved drug library to identify existing scaffolds that could be repurposed as monocarboxylate transporter (MCT) inhibitors. Our findings show that several existing drug classes inhibit MCT1 activity, including non-steroidal estrogens, non-steroidal anti-inflammatory drugs (NSAIDs), and natural products (in total representing approximately 1% of the total library, 78 out of 6400), with a moderate affinity (IC50 1.8–21 μM). Given the well-tolerated nature of NSAIDs, and their known anticancer properties associated with COX inhibition, we chose to further investigate their MCT1 inhibition profile. The majority of NSAIDs in our screen cluster into a single large structural grouping. Moreover, this group is predominantly comprised of FDA-approved NSAIDs, with seven exhibiting moderate MCT1 inhibition. Since these molecules form a distinct structural cluster with known NSAID MCT4 inhibitors, such as diclofenac, ketoprofen, and indomethacin, we hypothesize that these newly identified inhibitors may also inhibit both transporters. Consequently, NSAIDs as a class, and piroxicam specifically (IC50 4.4 μM), demonstrate MCT1 inhibition at theoretically relevant human dosages, suggesting immediate potential for standalone MCT inhibition or combined anticancer therapy.
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Purchased from AmBeed: 61-68-7 ; 22071-15-4 ; 1448671-31-5 ; 169590-42-5 ; 71125-38-7 ; 29679-58-1 ; 42924-53-8 ; 162011-90-7 ; 500-38-9
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CAS No. : | 162011-90-7 |
Formula : | C17H14O4S |
M.W : | 314.36 |
SMILES Code : | O=C1OCC(C2=CC=C(S(=O)(C)=O)C=C2)=C1C3=CC=CC=C3 |
Synonyms : |
MK 966; MK-0966; Ceoxx
|
MDL No. : | MFCD00935806 |
InChI Key : | RZJQGNCSTQAWON-UHFFFAOYSA-N |
Pubchem ID : | 5090 |
GHS Pictogram: |
![]() |
Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
Target |
|
In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
Murine hepatic S-9 fraction | 1 μM | 2 h | Rofecoxib increased the production of 20-HETE in a time- and dose-dependent manner. | PMC2947894 |
Rat platelets | 10^-9 to 10^-5 M | 3 min | 20-HETE significantly increased ADP-induced platelet aggregation, while rofecoxib had no such effect. | PMC2947894 |
adult rat cardiac myocytes | 0.1, 0.3, 1, 3, 10 µM | 60 min | To assess the effect of rofecoxib on cell viability after simulated ischemia/reperfusion injury. Results showed rofecoxib significantly increased cell survival at concentrations of 0.1, 0.3, 1, and 3 µM. | PMC7140447 |
Murine hepatic S-9 fraction | 1 μM | 2 hours | Investigate the effect of Valdecoxib on 20-HETE production; Valdecoxib significantly increased 20-HETE production | PMC2947894 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
C57BL/6 mice | Oral administration of rofecoxib for 3 months | Oral | 50 mg/L,in drinking water | 3 months | Rofecoxib significantly shortened tail bleeding time and dramatically increased plasma levels of 20-HETE. | PMC2947894 |
Rats | Male Sprague-Dawley rats | Intravenous, intraperitoneal, and oral | 0.5, 5.95, 10 mg/kg | Single dose | To evaluate the pharmacokinetic characteristics of rofecoxib in rats and the impact of enterohepatic recirculation (EHC). Results showed that EHC increased systemic exposure to rofecoxib by 15% and prolonged the inhibition of PGE2 and the duration of anti-inflammatory effects (24 hours). | PMC2267282 |
New Zealand White rabbits | Cholesterol-fed atherosclerosis model | Oral | 25 mg/kg | Twice daily for 12 weeks | To evaluate the antagonistic effect of rofecoxib on the antithrombotic and anti-atherosclerotic actions of aspirin. Results showed that rofecoxib alone had no significant effect on atherosclerotic plaque formation, but when combined with aspirin, it significantly attenuated the antithrombotic and anti-atherosclerotic effects of aspirin. | PMC3188910 |
Male CD-1 mice | PTZ-induced acute seizures and kindling model | Oral | 30 mg/kg | Once daily for 5 days | To evaluate the effect of rofecoxib on PTZ-induced acute seizures and kindling model. Results showed that rofecoxib did not attenuate the severity of acute PTZ-induced seizures and failed to alter kindling development or maintenance. | PMC4445939 |
Wistar rats | Quinolinic acid-induced neurotoxicity model | Oral | 10 mg/kg | Once daily for 21 days | Rofecoxib significantly attenuated QA-induced behavioral alterations and restored the redox status in striatum. | PMC5552501 |
Male Wistar rats | Ischemia/reperfusion injury model | Oral gavage | 5.12 mg/kg | Once daily for four weeks | To evaluate the cardiotoxicity of rofecoxib under ischemia/reperfusion conditions. Results showed rofecoxib increased arrhythmia incidence, prolonged action potential duration, and increased acute mortality. | PMC7140447 |
Rat | Wistar rats | Intragastric administration | 5 mg/kg | Once daily for four weeks | To evaluate the effect of long-term selective inhibition of COX-2 on gastrointestinal mucosal integrity and the composition of small intestinal microbiota. Results showed that rofecoxib did not cause significant gastrointestinal mucosal damage or small intestinal dysbiosis. | PMC6468807 |
Mice (C57BL/6) | Chronic administration model | Oral | 50 mg/L (in drinking water) | 3 months | Evaluate the cardiovascular risk of Valdecoxib; chronic administration led to significantly shorter tail bleeding time and elevated plasma 20-HETE levels | PMC2947894 |
Clinical Trial:
NCT Number | Conditions | Phases | Recruitment | Completion Date | Locations |
NCT00026819 | Pain | PHASE2 | COMPLETED | 2025-11-03 | National Institute of Dental A... More >>nd Craniofacial Research (NIDCR), Bethesda, Maryland, 20892, United States Less << |
NCT00263094 | Headache | COMPLETED | 2025-11-04 | Sheba Medical Center, Tel Hash... More >>omer, Israel Less << |
Bio Calculators | ||||
Preparing Stock Solutions | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
3.18mL 0.64mL 0.32mL |
15.91mL 3.18mL 1.59mL |
31.81mL 6.36mL 3.18mL |
Tags: Rofecoxib | MK 966 | MK966 | MK-966 | COX | Cyclooxygenase | COX-2 inhibitor | prostaglandin synthesis | prostaglandin inhibition | selective NSAID | inflammation relief | 162011-90-7
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