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5-Geranoxy-7-methoxycoumarin 7380-39-4

5-Geranoxy-7-methoxycoumarin 7380-39-4

CAS No.: 7380-39-4

5-Geranoxy-7-methoxycoumarin is a coumarin with anticancer, antifungal, and anti-bacterial effect. 5-Geranoxy-7-methoxyc
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5-Geranoxy-7-methoxycoumarin is a coumarin with anticancer, antifungal, and anti-bacterial effect. 5-Geranoxy-7-methoxycoumarin causes apoptosis.

Physicochemical Properties


Molecular Formula C20H24O4
Molecular Weight 328.40
Exact Mass 328.167
CAS # 7380-39-4
PubChem CID 6441377
Appearance Typically exists as solid at room temperature
Density 1.092g/cm3
Boiling Point 487.1ºC at 760 mmHg
Melting Point 86-88ºC
Flash Point 213.2ºC
Index of Refraction 1.542
LogP 4.873
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 7
Heavy Atom Count 24
Complexity 514
Defined Atom Stereocenter Count 0
SMILES

CC(=CCCC(=CCOC1=CC(=CC2=C1C=CC(=O)O2)OC)C)C

InChi Key WXUOSNJWDJOHGW-XNTDXEJSSA-N
InChi Code

InChI=1S/C20H24O4/c1-14(2)6-5-7-15(3)10-11-23-18-12-16(22-4)13-19-17(18)8-9-20(21)24-19/h6,8-10,12-13H,5,7,11H2,1-4H3/b15-10+
Chemical Name

5-[(2E)-3,7-dimethylocta-2,6-dienoxy]-7-methoxychromen-2-one
HS Tariff Code 2934.99.9001
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)

Biological Activity


ln Vitro In SW480 cells, 5-geranoxy-7-methoxycoumarin (12.5-200 µM; 24-72 hours) significantly inhibits cell proliferation in a time-dependent fashion[1]. 5-Geranoxy-7-methoxycoumarin (50 µM; 48 hours) inhibits the p38 MAPK signaling pathway in SW480 cells, which leads to DNA fragmentation and apoptosis[1]. After 48 hours of incubation, the percentage of cells in the sub G1/G0 phase rises from 5.3% (in control cells) to 18% when 5-geranoxy-7-methoxycoumarin (50 µM) is added[1].
Cell Assay Cell Proliferation Assay [1]
Cell Types: SW480
Tested Concentrations: 0-20 μM
Incubation Duration: 24, 48 and 72 hrs (hours)
Experimental Results: Inhibited cell growth by 67% at 72 hrs (hours).

Apoptosis Analysis[1]
Cell Types: SW480 cells
Tested Concentrations: 50 μM
Incubation Duration: 48 hrs (hours)
Experimental Results: Induced cell apoptosis.

Cell Cycle Analysis[1]
Cell Types: SW480 cells
Tested Concentrations: 50 μM
Incubation Duration: 48 hrs (hours)
Experimental Results: Inhibited cell cycle progression in vitro.
References

[1]. 5-Geranyloxy-7-methoxycoumarin inhibits colon cancer (SW480) cells growth by inducing apoptosis. Planta Med. 2013 Mar;79(3-4):219-26.

[2]. Synergism of coumarins from the Chinese drug Zanthoxylum nitidum with antibacterial agents against methicillin-resistant Staphylococcus aureus (MRSA). Phytomedicine.

Additional Infomation 5-Geranyloxy-7-methoxycoumarin is a terpene lactone.

Solubility Data


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
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
(e.g. IP/IV/IM/SC)
Injection Formulation 1: DMSO : Tween 80: Saline = 10 : 5 : 85 (i.e. 100 μL DMSO stock solution 50 μL Tween 80 850 μL Saline)
*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).
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)]
*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.
Injection Formulation 5: 2-Hydroxypropyl-β-cyclodextrin : Saline = 50 : 50 (i.e. 500 μL 2-Hydroxypropyl-β-cyclodextrin 500 μL Saline)
Injection Formulation 6: DMSO : PEG300 : castor oil : Saline = 5 : 10 : 20 : 65 (i.e. 50 μL DMSO 100 μLPEG300 200 μL castor oil 650 μL Saline)
Injection Formulation 7: Ethanol : Cremophor : Saline = 10: 10 : 80 (i.e. 100 μL Ethanol 100 μL Cremophor 800 μL Saline)
Injection Formulation 8: Dissolve in Cremophor/Ethanol (50 : 50), then diluted by Saline
Injection Formulation 9: EtOH : Corn oil = 10 : 90 (i.e. 100 μL EtOH 900 μL Corn oil)
Injection Formulation 10: EtOH : PEG300:Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL EtOH 400 μLPEG300 50 μL Tween 80 450 μL 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).
Oral Formulation 3: Dissolved in PEG400
Oral Formulation 4: Suspend in 0.2% Carboxymethyl cellulose
Oral Formulation 5: Dissolve in 0.25% Tween 80 and 0.5% Carboxymethyl cellulose
Oral Formulation 6: Mixing with food powders

Note: Please be aware that the above formulations are for reference only. InvivoChem strongly recommends customers to read literature methods/protocols carefully before determining which formulation you should use for in vivo studies, as different compounds have different solubility properties and have to be formulated differently.

 (Please use freshly prepared in vivo formulations for optimal results.)
Preparing Stock Solutions 1 mg 5 mg 10 mg
1 mM 3.0451 mL 15.2253 mL 30.4507 mL
5 mM 0.6090 mL 3.0451 mL 6.0901 mL
10 mM 0.3045 mL 1.5225 mL 3.0451 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.