research use only
Cat.No.S4835
| Related Targets | PD-1/PD-L1 CXCR STING AhR CD markers Interleukins Anti-infection Antioxidant COX Histamine Receptor |
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| Other Immunology & Inflammation related Inhibitors | Cl-amidine Bestatin (Ubenimex) Bindarit (AF 2838) Tranilast Tempol Sinomenine GI254023X (GI4023) ATP Geniposidic acid CORM-3 |
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In vitro |
DMSO
: 70 mg/mL
(197.63 mM)
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In vivo |
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Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
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.)
Calculation results:
Working concentration: mg/ml;
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 | 354.18 | Formula | C16H13Cl2NO4 |
Storage (From the date of receipt) | |
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| CAS No. | 89796-99-6 | -- | Storage of Stock Solutions |
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| Synonyms | Preservex, Airtal | Smiles | C1=CC=C(C(=C1)CC(=O)OCC(=O)O)NC2=C(C=CC=C2Cl)Cl | ||
| In vivo |
Long term oral administration of aceclofenac causes gastrointestinal (GI) ulcers and GI bleeding. Aceclofenac is well absorbed orally with hepatic first pass metabolism. It exhibits elimination half life of 4h, volume of distribution 25 L, 99 % of protein binding and 60-70% of bioavailability after oral administration.
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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 |
|---|---|---|---|---|---|
| NCT05558150 | Completed | Drug Interaction Potentiation |
Il-Yang Pharm. Co. Ltd. |
November 10 2022 | Phase 1 |
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