A-317567 (Synonyms: 6-{2-[2-methyl-1-(propan-2-yl)-1，2，3，4-tetrahydroisoquinolin-7-yl]cyclopropyl}naphthalene-2-carboximidamide) |
カタログ番号GF17169
One-Click Copy Product Info
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Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 371217-32-2
Sample solution is provided at 25 µL, 10mM.
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In acutely dissociated adult rat dorsal root ganglion (DRG) neurons, A-317567 produces concentration-dependent inhibition of all pH 4.5-evoked ASIC currents with an IC50 ranging between 2 and 30 渭M. A-317567 equipotently blocks the sustained phase of ASIC3-like current, a biphasic current akin to cloned ASIC3, which is predominant in DRG[2].
A-317567 (1-100 渭mol/kg; i.p; once) is fully analgesic effects in the CFA model (ED50 of 17 渭mol/kg). There is no significant effect of A-317567 on the withdrawal latency of the contralateral paw under these conditions[2].
[1]. Kuduk SD, et al. Synthesis, structure-activity relationship, and pharmacological profile of analogs of the ASIC-3 inhibitor A-317567. ACS Chem Neurosci. 2010 Jan 20;1(1):19-24.
[2]. Dub茅 GR, et al. Electrophysiological and in vivo characterization of A-317567, a novel blocker of acid sensing ion channels. Pain. 2005 Sep;117(1-2):88-96.
| Cas No. | 371217-32-2 | SDF | |
| 同義語 | 6-{2-[2-methyl-1-(propan-2-yl)-1，2，3，4-tetrahydroisoquinolin-7-yl]cyclopropyl}naphthalene-2-carboximidamide | ||
| Formula | C27H31N3 | M.Wt | 397.56 |
| 溶解度 | DMSO : 50 mg/mL (125.77 mM; ultrasonic and warming and heat to 60°C ) | Storage | 2-8°C， sealed storage，away from moisture |
| General tips | Please select the appropriate solvent to prepare the stock solution according to the
solubility of the product in different solvents; once the solution is prepared, please store it in
separate packages to avoid product failure caused by repeated freezing and thawing.Storage method
and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored
at -20°C, please use it within 1 month. To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time. |
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| Shipping Condition | Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request. | ||
| Prepare stock solution | |||
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1 mg | 5 mg | 10 mg |
| 1 mM | 2.5153 mL | 12.5767 mL | 25.1534 mL |
| 5 mM | 503.1 μL | 2.5153 mL | 5.0307 mL |
| 10 mM | 251.5 μL | 1.2577 mL | 2.5153 mL |
Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
g
μL
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 saline, 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.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.
3. All of the above co-solvents are available for purchase on the GlpBio website.
Quality Control & SDS
- View current batch:
- Purity: >98.00% Appearance: A solid
- COA (Certificate of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Average Rating: 5 (Based on Reviews and 30 reference(s) in Google Scholar.)