research use only
Cat.No.S1734
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In vitro |
DMSO
: 30 mg/mL
(85.37 mM)
Water : Insoluble Ethanol : Insoluble |
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In vivo |
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Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
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| Molecular Weight | 351.4 | Formula | C14H13N3O4S2 |
Storage (From the date of receipt) | |
|---|---|---|---|---|---|
| CAS No. | 71125-38-7 | Download SDF | Storage of Stock Solutions |
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| Synonyms | N/A | Smiles | CC1=CN=C(S1)NC(=O)C2=C(C3=CC=CC=C3S(=O)(=O)N2C)O | ||
| Targets/IC50/Ki |
COX
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|---|---|
| In vitro |
Meloxicam significantly reduces HCA-7 and Moser-S colony size. This compound significantly inhibits HCA-7 colony and tumor growth but has no effect on the growth of the COX-2 negative HCT-116 cells. It inhibits PGE(2) production, proliferation and invasiveness especially in MG-63 cells, which express relatively high levels of COX-2. This chemical causes apoptosis and upregulates Bax mRNA and protein in MG-63 cell culture.
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| In vivo |
Meloxicam suppresses LM-8 tumor growth and lung metastasis in vivo mouse model. This compound causes a significant reduction in lameness at post injection hour (PIH) 8 and 24 and tends to reduce effusion in horse. It significantly suppresses synovial fluid (SF) prostaglandin E2 and substance P release at PIH 8 and bradykinin at PIH 24 compared to placebo treatment in horse. This agent reduces general MMP activity at PIH 8 and 24 in horse. This compound- or flunixin-treated horses has improved postoperative pain scores and clinical variables, compared with SS-treated horses. It results in high numbers of neutrophils in ischemia-injured tissue of horse. Its administration significantly suppresses PGE2 concentrations in blood and synovial fluid at days 7 and 21, but has no effect on concentrations of TXB2 in blood or PGE2 in gastric mucosa in dogs.
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References |
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(data from https://clinicaltrials.gov, updated on 2024-05-22)
| NCT Number | Recruitment | Conditions | Sponsor/Collaborators | Start Date | Phases |
|---|---|---|---|---|---|
| NCT05702827 | Recruiting | Stress Urinary Incontinence|Surgical Incision|Pain Vulva |
TriHealth Inc. |
January 23 2023 | Phase 3 |
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