UR-144 N-(5-bromopentyl) analog |
カタログ番号GC45122
One-Click Copy Product Info
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UR-144は、周辺のCB2受容体（Ki = 1.8 nM）に中心的なCB1受容体（Ki = 150 nM）よりも選択的に結合する強力な合成カンナビノイド（CB）です。
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 1628690-26-5
Sample solution is provided at 25 µL, 10mM.
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UR-144 is a potent synthetic cannabinoid (CB) which preferentially binds the peripheral CB2 receptor (Ki = 1.8 nM) over the central CB1 receptor (Ki = 150 nM). UR-144 N-(5-bromopentyl) analog differs from UR-144 by having a bromine atom on the terminal carbon of the alkyl group. While similar modifications have little effect on the receptor affinities of analogs of tetrahydrocannabinol, the activity of this compound has not been examined. This product is intended for research and forensic applications.
| Cas No. | 1628690-26-5 | SDF | |
| Canonical SMILES | O=C(C1=CN(CCCCCBr)C2=C1C=CC=C2)C3C(C)(C)C3(C)C | ||
| Formula | C21H28BrNO | M.Wt | 390.4 |
| 溶解度 | DMF: 14 mg/ml,DMF:PBS(pH7.2) (1:2): 0.3 mg/ml,DMSO: 5 mg/ml,Ethanol: 5 mg/ml | Storage | Store at -20°C |
| 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 | 2.5615 mL | 12.8074 mL | 25.6148 mL |
| 5 mM | 512.3 μL | 2.5615 mL | 5.123 mL |
| 10 mM | 256.1 μL | 1.2807 mL | 2.5615 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 5 reference(s) in Google Scholar.)