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(-)-Phyllocladene
(-)-Phyllocladene
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Product Name (-)-Phyllocladene
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CAS No.: 20070-61-5
Catalog No.: CFN89383
Molecular Formula: C20H32
Molecular Weight: 272.46 g/mol
Purity: >=98%
Type of Compound: Diterpenoids
Physical Desc.: Oil
Source: The leaves essential oil of Callicarpa macrophylla.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison (Web)  (SDF)
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Product Use Citation
Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: (-)-Phyllocladene is a natural product from Callicarpa macrophylla.
(-)-Phyllocladene Description
Source: The leaves essential oil of Callicarpa macrophylla.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.6703 mL 18.3513 mL 36.7026 mL 73.4053 mL 91.7566 mL
5 mM 0.7341 mL 3.6703 mL 7.3405 mL 14.6811 mL 18.3513 mL
10 mM 0.367 mL 1.8351 mL 3.6703 mL 7.3405 mL 9.1757 mL
50 mM 0.0734 mL 0.367 mL 0.7341 mL 1.4681 mL 1.8351 mL
100 mM 0.0367 mL 0.1835 mL 0.367 mL 0.7341 mL 0.9176 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Structure Identification:
Synthetic Communications, 1983, 13(9):715-719.
Palladium(II)-Mediated Cycloalkenylation. A Simple Total Synthesis of (±)-Phyllocladene[Reference: WebLink]
An efficient and stereoselective synthesis of (+)-phyllocladene,(-)-Phyllocladene based on Pd(II)-mediated cycloalkenylation is described.
CFN9795412alpha-Hydroxygrandiflorenic acid63768-17-2316.4C20H28O3
CFN8949612alpha-Methoxygrandiflorenic acid135383-94-7330.46C21H30O3
CFN8934512-Oxograndiflorenic acid74284-42-7314.41C20H26O3
CFN96436Wedelobatin B1589488-35-6452.67C30H44O3
CFN96437Wedelobatin A1589488-34-5454.68C30H46O3
CFN97703Kaurenoic acid6730-83-2302.46C20H30O2
CFN97685Pterokaurene L377658-38-9318.46C20H30O3
CFN964813Alaph-Tigloyloxypterokaurene L31588516-87-3416.56C25H36O5
CFN96012Sventenic acid126778-79-8318.5C20H30O3
CFN97982Acetylsventenic acid126737-42-6360.5C22H32O4
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