Acetylisoeugenol | CAS:93-29-8 | Manufacturer ChemFaces

Acetylisoeugenol

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Size /Price /Stock	10 mM * 1 mL in DMSO / $8.9 / In-stock
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Description:

Acetylisoeugenol is a mild sensitizer in vivo, it shows good antifungal activities against R. solani and F. oxysporum.

Targets:

Antifection

In vitro:

Industrial Crops & Products, 2017, 97:388-394.

Structure-activity relationships of cinnamaldehyde and eugenol derivatives against plant pathogenic fungi.[Reference: WebLink]

METHODS AND RESULTS:
Cinnamon bark oil showed a lower activity than clove bud oil. The fungicidal activity of cinnamaldehyde (IC50 = 75.4 and 156.9 μg/mL, respectively) and eugenol (IC50 = 58.9 and 52.9 μg/mL, respectively) against R. solani and F. oxysporum was also evalutated. Comparisons of the antifungal activities of cinnamaldehyde and eugenol derivatives revealed that α-methylcinnamaldehyde, α-methylcinnamic acid, methyleugenol, acetyleugenol, isoeugenol, methylisoeugenol, and Acetylisoeugenol showed good antifungal activities against R. solani and F. oxysporum. In structure-activity relationships, the fungicidal activity of cinnamaldehyde derivatives could be related to conjugated double bond and the length of CH chain outside the ring. In addition, the presence of the lipophilicity may have a considerable influence on the toxicity of phenylpropenes.
CONCLUSIONS:
The present approach may help future work in the search for fungicidal compounds.

In vivo:

J Dermatol. 1985 Apr;12(2):153-60.

Factors influencing conjugation of phenolic compounds with the epsilon-amino group.[Reference: WebLink]

METHODS AND RESULTS:
Factors influencing the conjugation potency of eugenol (E), isoeugenol (IE), methyl isoeugenol (MIE), and Acetylisoeugenol (AIE) with [l-14C]07-aminocaproic acid are investigated. The conjugation reaction for IE is accelerated in the presence of H2O2-peroxidase and inhibited under anaerobic conditions by nitrogen gas flow. An oxidation reaction is found to be necessary for the conjugation of IE with 07-aminocaproic acid. Immediately after mixing the phenolic compounds with [1-14C]07-aminocaproic acid and H2O2-peroxidase, the main conjugates are 7.7% for IE, 2.1% for E, 0.7% for AIE, and 0.2% for MIE. IE, which is a potent sensitizer in vivo, produces the greatest amount of conjugates while MIE, which is negative in vivo, produces almost no conjugates.
CONCLUSIONS:
AIE and E, both mild sensitizers in vivo, produce less conjugates than IE.

Acetylisoeugenol Description

Source:	From Cinnamon bark oil.
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.

Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

More...

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

CAS No.	93-29-8	Price	$30 / 20mg
Catalog No.	CFN96771	Purity	>=98%
Molecular Weight	206.24	Type of Compound	Phenylpropanoids
Formula	C₁₂H₁₄O₃	Physical Description	Powder
Download	COA MSDS	Similar structural	Comparison (Web) (SDF)

Product Name	Acetylisoeugenol
CAS No.:	93-29-8
Catalog No.:	CFN96771
Molecular Formula:	C₁₂H₁₄O₃
Molecular Weight:	206.24 g/mol
Purity:	>=98%
Type of Compound:	Phenylpropanoids
Physical Desc.:	Powder
Targets:	Antifection
Source:	From Cinnamon bark oil.
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:	$30 / 20mg
Download:	COA MSDS
Similar structural:	Comparison (Web) (SDF)

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Antifungal Compound Library Sensitizers Compound Library Phenylpropanoids Compound Library Antifection Inhibitor Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	4.8487 mL	24.2436 mL	48.4872 mL	96.9744 mL	121.218 mL
5 mM	0.9697 mL	4.8487 mL	9.6974 mL	19.3949 mL	24.2436 mL
10 mM	0.4849 mL	2.4244 mL	4.8487 mL	9.6974 mL	12.1218 mL
50 mM	0.097 mL	0.4849 mL	0.9697 mL	1.9395 mL	2.4244 mL
100 mM	0.0485 mL	0.2424 mL	0.4849 mL	0.9697 mL	1.2122 mL

CFN98057	Cinnamyl acetate	21040-45-9	176.2	C₁₁H₁₂O₂
CFN99037	3-(4-Hydroxyphenyl)-1-propanol	10210-17-0	152.2	C₉H₁₂O₂
CFN96011	p-Coumaryl alcohol	3690-05-9	150.2	C₉H₁₀O₂
CFN89230	4-Methoxycinnamyl alcohol	53484-50-7	164.20	C₁₀H₁₂O₂
CFN92410	trans-3,4-Methylenedioxycinnamyl alcohol	58095-76-4	178.2	C₁₀H₁₀O₃
CFN97760	Coniferyl alcohol	32811-40-8	180.20	C₁₀H₁₂O₃
CFN96742	Dihydroconiferyl alcohol	2305-13-7	182.21	C₁₀H₁₄O₃
CFN96094	Gamma-Methoxyisoeugenol	63644-71-3	194.2	C₁₁H₁₄O₃
CFN96771	Acetylisoeugenol	93-29-8	206.24	C₁₂H₁₄O₃
CFN98088	beta-Hydroxypropiovanillone	2196-18-1	196.2	C₁₀H₁₂O₄