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Purity: ≥98%
JNJ0966 is a novel, potent and highly selective allosteric inhibitor of MMP-9 (matrix metalloproteinase-9) zymogen with an IC50 of 440 nM. JNJ0966 prevented the MMP-9 zymogen from activating and producing an enzyme that was catalytically active. JNJ0966 did not suppress activation of the closely related MMP-2 zymogen and had no effect on MMP-1, MMP-2, MMP-3, MMP-9, or MMP-14 catalytic activity. The molecular mechanism of this activity was identified as JNJ0966 interacting with a structural pocket, separate from the catalytic domain, close to the MMP-9 zymogen cleavage site near Arg-106. JNJ0966 effectively decreased the severity of the disease in an experimental autoimmune encephalomyelitis mouse model, indicating the feasibility of this treatment strategy.
| Targets |
MMP-9 (IC50 = 440 nM)
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|---|---|
| ln Vitro |
JNJ0966 is not a direct inhibitor of MMP-9 or MMP-3 enzymatic activity, but it does prevent the conversion of proMMP-9 to active MMP-9. JNJ0966 prevents the maturation of proMMP-9[1].
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| ln Vivo |
JNJ0966 administered orally dramatically reduces the clinical disease score in the mouse EAE model[1].
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| Cell Assay |
JNJ0966 is added to the upper chamber along with 13,000 HT1080 cells per well in 10 μL of serum-free medium. After adding 6% fetal bovine serum and JNJ0966 to serum-free medium, the bottom feeder tray is incubated for 24 hours at 37°C with 5% CO₂. To identify the cells that have moved to the bottom layer, calcein AM is added to the feeder layer. The fluorescence intensity of these cells is then measured. It computes the IC₅₀ values and mean percentage inhibition of invasion. On an inverted microscope, digital cameras are used to capture images of migrated cells[1].
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| Animal Protocol |
Female C57Bl/6 mice, aged 6 to 8 weeks, are used in encephalomyelitis (EAE) experiments. Mice are sorted into several groups at random. Animals treated with vehicles are given oral gavage containing 20% hydroxypropyl-β-cyclodextrin. Animals are given 10 or 30 mg of JNJ0966 per kg of body weight (mg/kg) via oral gavage after the drug is dissolved in 20% hydroxypropyl-β-cyclodextrin. Up until day 17 of the trial, all groups get two daily doses. At that time, the animals are sacrificed, and brain tissue and plasma are taken in order to use mass spectroscopy to determine the levels of JNJ0966 in the brain[1].
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| References |
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| Molecular Formula |
C16H16N4O2S2
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|---|---|
| Molecular Weight |
360.4538
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| Exact Mass |
360.07
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| Elemental Analysis |
C, 53.32; H, 4.47; N, 15.54; O, 8.88; S, 17.79
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| CAS # |
315705-75-0
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| Related CAS # |
315705-75-0
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| Appearance |
Solid powder
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| SMILES |
CC1=C(SC(=N1)NC(=O)C)C2=CSC(=N2)NC3=CC=CC=C3OC
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| InChi Key |
ZADCDCMLLGDCRM-UHFFFAOYSA-N
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| InChi Code |
InChI=1S/C16H16N4O2S2/c1-9-14(24-16(17-9)18-10(2)21)12-8-23-15(20-12)19-11-6-4-5-7-13(11)22-3/h4-8H,1-3H3,(H,19,20)(H,17,18,21)
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| Chemical Name |
N-[5-[2-(2-methoxyanilino)-1,3-thiazol-4-yl]-4-methyl-1,3-thiazol-2-yl]acetamide
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| Synonyms |
JNJ-0966; JNJ 0966; JNJ0966
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| HS Tariff Code |
2934.99.9001
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| Storage |
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
| Shipping Condition |
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
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| Solubility (In Vitro) |
DMSO: 72~100 mg/mL (199.8~277.4 mM)
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| Solubility (In Vivo) |
Solubility in Formulation 1: 2.5 mg/mL (6.94 mM) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (add these co-solvents sequentially from left to right, and one by one), suspension solution; with sonication.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of 20% SBE-β-CD physiological saline solution and mix evenly. Preparation of 20% SBE-β-CD in Saline (4°C，1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution. Solubility in Formulation 2: ≥ 2.5 mg/mL (6.94 mM) (saturation unknown) in 10% DMSO + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of corn oil and mix evenly. (Please use freshly prepared in vivo formulations for optimal results.) |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 2.7743 mL | 13.8715 mL | 27.7431 mL | |
| 5 mM | 0.5549 mL | 2.7743 mL | 5.5486 mL | |
| 10 mM | 0.2774 mL | 1.3872 mL | 2.7743 mL |
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.
Calculation results
Working concentration： mg/mL；
Method for preparing DMSO stock solution： mg drug pre-dissolved in μL DMSO (stock solution 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 stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O，mix and clarify.
(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
(2) Be sure to add the solvent(s) in order.
 JNJ0966 inhibited activation of proMMP-9 but exhibited no effect on catalytic activity or maturation of other MMPs.
JNJ0966 reduced motor symptoms in mouse EAE and penetrates into the brain. |
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 JNJ0966 reduced proMMP-9 maturation through intermediate states to active fully processed enzyme.J Biol Chem.2017 Oct 27;292(43):17963-17974. |
 Analysis of proMMP-9 maturation kinetics by gelatin zymography in the presence and absence of 10 μmJNJ0966.
Structural characterization of JNJ0966 and proMMP-9 complex. |
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