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8-Hydroxy-9,10-diisobutyryloxythymol
8-Hydroxy-9,10-diisobutyryloxythymol
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name 8-Hydroxy-9,10-diisobutyryloxythymol
Price:
CAS No.: 22518-08-7
Catalog No.: CFN89511
Molecular Formula: C18H26O6
Molecular Weight: 338.39 g/mol
Purity: >=98%
Type of Compound: Terpenoids
Physical Desc.: Powder
Source: The flowers of Inula helianthus-aquatica.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison (Web)  (SDF)
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Biological Activity
Description: 8-Hydroxy-9,10-diisobutyryloxythymol shows cytotoxicity on six cancer cell lines (K562, HT-29, SGC-7901, DU145, MDA-MB-231, U251). 8-Hydroxy-9,10-diisobutyryloxythymol may have antibacterial activity.
Targets: Antifection
In vitro:
Acta Botanica Yunnanica, 2009, 31(2):190-192.
New Cytotoxic Thymol Derivatives from Inula helianthus-aquatica (Compositae).[Reference: WebLink]

METHODS AND RESULTS:
A new thymol derivative, 8-hydroxy-9,10-dioxyisopropylidenethymol (1), together with three known thymol derivatives 10-hydroxy-8, 9-dioxyisopropylidenethymol (2), 8-Hydroxy-9,10-diisobutyryloxythymol (3) and 8, 10-dihydroxy-9-isobutyryloxy-thymol (4), was isolated from 95% EtOH extract of the flowers of Inula helianthus-aquatica. Their structures were elucidated on the basis of detailed spectroscopic analysis.
CONCLUSIONS:
These compounds showed cytotoxicities on six cancer cell lines (K562, HT-29, SGC-7901, DU145, MDA-MB-231, U251), and compound 2 is the strongest one with IC50s of 4.20-33.12 μmol/L. This is the first time that the cytotoxic thymol derivatives were isolated from this titled plant.
8-Hydroxy-9,10-diisobutyryloxythymol Description
Source: The flowers of Inula helianthus-aquatica.
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.

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

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 2.9552 mL 14.7759 mL 29.5517 mL 59.1034 mL 73.8793 mL
5 mM 0.591 mL 2.9552 mL 5.9103 mL 11.8207 mL 14.7759 mL
10 mM 0.2955 mL 1.4776 mL 2.9552 mL 5.9103 mL 7.3879 mL
50 mM 0.0591 mL 0.2955 mL 0.591 mL 1.1821 mL 1.4776 mL
100 mM 0.0296 mL 0.1478 mL 0.2955 mL 0.591 mL 0.7388 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:
Molecules. 2007 Jan 27;12(8):1606-13.
Antibacterial thymol derivatives isolated from Centipeda minima.[Pubmed: 17960076]

METHODS AND RESULTS:
Two new monoterpenoids, 8,10-dihydroxy-9(2)-methylbutyryloxythymol (1) and 10-hydroxy-8,9-dioxyisopropylidene-thymol (2), together with five known thymol derivatives: 8,9,10-trihydroxythymol (3), thymol-beta-glucopyranoside (4), 9-hydroxythymol (5), 8,10-dihydroxy-9-isobutyryloxythymol (6), and 8-Hydroxy-9,10-diisobutyryloxythymol (7), were isolated from Centipeda minima. Their structures were identified by means of spectroscopic analyses. Interestingly, compound 2 is not an extraction artifact according to a close HPLC examination of material after extraction by analytical MeOH at ambient temperature.
CONCLUSIONS:
The antibacterial activities of compounds 1-7 were evaluated against eight microbial strains by the agar dilution method.
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