Size | Price | |
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500mg | ||
1g | ||
Other Sizes |
Targets |
p38α 0.5 nM (Ki) p38β 3.6 nM (Ki) p38δ 2600 nM (Ki) p38γ 4100 nM (Ki) dog p38α 5.0 nM (Ki) JNK1 11480 nM (Ki) JNK2 39 nM (Ki) JNK3 61 nM (Ki) CK1
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ln Vitro |
AMG-548 hydrochloride demonstrates >1000 fold selectivity towards p38γ (Ki = 2600 nM) and p38δ (ki = 4100 nM." The selectivity of AMG-548 hydrochloride against JNK2 (ki=39 nM) and JNK3 (ki=61 nM) is moderate. Additionally, whole blood LPS stimulated TNFa (IC50=3 nM) and IL1b (IC50=7 nM), as well as TNFa-induced IL-8 (IC50=0.7 nM) and IL-1b-induced IL-6 (IC5050=1.3 nM), are all highly inhibited by AMG-548 hydrochloride[1]. Ten micrograms of AMG-548 hydrochloride suppresses the hDvl2 shift[2].
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ln Vivo |
Rat F of AMG-548 hydrochloride is 62%, while dog F is 47%. In rats, the t1/2 is 4.6 hours, whereas in dogs, it is 7.3 hours[1].
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References |
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CAS # |
2437438-16-7
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Related CAS # |
AMG-548 dihydrochloride;2518299-32-4;AMG-548;864249-60-5
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Appearance |
Typically exists as solid at room temperature
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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) |
May dissolve in DMSO (in most cases), if not, try other solvents such as H2O, Ethanol, or DMF with a minute amount of products to avoid loss of samples
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Solubility (In Vivo) |
Note: Listed below are some common formulations that may be used to formulate products with low water solubility (e.g. < 1 mg/mL), you may test these formulations using a minute amount of products to avoid loss of samples.
Injection Formulations
Injection Formulation 1: DMSO : Tween 80: Saline = 10 : 5 : 85 (i.e. 100 μL DMSO stock solution → 50 μL Tween 80 → 850 μL Saline)(e.g. IP/IV/IM/SC) *Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH ₂ O to obtain a clear solution. Injection Formulation 2: DMSO : PEG300 :Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL DMSO → 400 μLPEG300 → 50 μL Tween 80 → 450 μL Saline) Injection Formulation 3: DMSO : Corn oil = 10 : 90 (i.e. 100 μL DMSO → 900 μL Corn oil) Example: Take the Injection Formulation 3 (DMSO : Corn oil = 10 : 90) as an example, if 1 mL of 2.5 mg/mL working solution is to be prepared, you can take 100 μL 25 mg/mL DMSO stock solution and add to 900 μL corn oil, mix well to obtain a clear or suspension solution (2.5 mg/mL, ready for use in animals). View More
Injection Formulation 4: DMSO : 20% SBE-β-CD in saline = 10 : 90 [i.e. 100 μL DMSO → 900 μL (20% SBE-β-CD in saline)] Oral Formulations
Oral Formulation 1: Suspend in 0.5% CMC Na (carboxymethylcellulose sodium) Oral Formulation 2: Suspend in 0.5% Carboxymethyl cellulose Example: Take the Oral Formulation 1 (Suspend in 0.5% CMC Na) as an example, if 100 mL of 2.5 mg/mL working solution is to be prepared, you can first prepare 0.5% CMC Na solution by measuring 0.5 g CMC Na and dissolve it in 100 mL ddH2O to obtain a clear solution; then add 250 mg of the product to 100 mL 0.5% CMC Na solution, to make the suspension solution (2.5 mg/mL, ready for use in animals). View More
Oral Formulation 3: Dissolved in PEG400  (Please use freshly prepared in vivo formulations for optimal results.) |
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.