(•)-Drimenol (Synonyms: NSC 169775) |
رقم الكتالوجGC46000 |
A sesquiterpene alcohol
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 468-68-8
Sample solution is provided at 25 µL, 10mM.
(-)-Drimenol is a sesquiterpene alcohol originally isolated from B. trilobata that has antimicrobial and anticancer activities.1,2,3 It is active against the bacteria S. aureus, B. cereus, A. baumanii, E. coli, and P. aeruginosa (MICs = 667, 667, 583, 1,333, and 667 μg/ml, respectively), as well as the fungi C. cucumerinum and S. tritici (IC50s = 6.6 and 80.1 μg/ml, respectively).1,2 (-)-Drimenol decreases the proliferation of A2058 and A375 melanoma cell lines with IC50 values of 33.5 and 31.25 μg/ml, respectively.3
|1. Santos, T.G., Dognnini, J., Begnini, I.M., et al. Chemical characterization of essential oils from Drimys angustifolia miers (winteraceae) and antibacterial activity of their major compounds. J. Braz. Chem. Soc. 24(1), 164-170 (2013).|2. Scher, J.M., Speakman, J.B., Zapp, J., et al. Bioactivity guided isolation of antifungal compounds from the liverwort Bazzania trilobata (L.) S.F. Gray. Phytochemistry 65(18), 2583-2588 (2004).|3. Russo, A., Cardile, V., Graziano, A.C.E., et al. Antigrowth activity and induction of apoptosis in human melanoma cells by Drymis winteri forst extract and its active components. Chem. Biol. Interact. 305, 79-85 (2019).
Cas No. | 468-68-8 | SDF | |
المرادفات | NSC 169775 | ||
Canonical SMILES | CC1=CC[C@@]2([H])C(C)(C)CCC[C@]2(C)[C@H]1CO | ||
Formula | C15H26O | M.Wt | 222.4 |
الذوبان | DMF: Soluble,DMSO: Soluble,Ethanol: Soluble,Methanol: Soluble | 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 | 4.4964 mL | 22.482 mL | 44.964 mL |
5 mM | 0.8993 mL | 4.4964 mL | 8.9928 mL |
10 mM | 0.4496 mL | 2.2482 mL | 4.4964 mL |
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.
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: >95.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Average Rating: 5
(Based on Reviews and 10 reference(s) in Google Scholar.)GLPBIO products are for RESEARCH USE ONLY. Please make sure your review or question is research based.
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