Albatrelin C

CAS# 1417805-17-4

Albatrelin C

Catalog No. BCN7591----Order now to get a substantial discount!

Product Name & Size Price Stock
Albatrelin C: 5mg $1098 In Stock
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Quality Control of Albatrelin C

Number of papers citing our products

Chemical structure

Albatrelin C

3D structure

Chemical Properties of Albatrelin C

Cas No. 1417805-17-4 SDF Download SDF
PubChem ID 102190844 Appearance Oil
Formula C22H30O2 M.Wt 326.48
Type of Compound Phenols Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 2-[(3E)-4,8-dimethylnona-3,7-dienyl]-2,5-dimethylchromen-7-ol
SMILES CC1=CC(=CC2=C1C=CC(O2)(C)CCC=C(C)CCC=C(C)C)O
Standard InChIKey QJCFVYYUAJZBKT-LICLKQGHSA-N
Standard InChI InChI=1S/C22H30O2/c1-16(2)8-6-9-17(3)10-7-12-22(5)13-11-20-18(4)14-19(23)15-21(20)24-22/h8,10-11,13-15,23H,6-7,9,12H2,1-5H3/b17-10+
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of Albatrelin C

The fruiting bodies of Albatrellus ovinus.

Biological Activity of Albatrelin C

DescriptionAlbatrelin C is a natural product from Albatrellus ovinus.

Protocol of Albatrelin C

Structure Identification
J Nat Prod. 2013 Jan 25;76(1):79-84.

Meroterpenoid pigments from the basidiomycete Albatrellus ovinus.[Pubmed: 23305465 ]


METHODS AND RESULTS:
Eight grifolin derivatives, involving three new monomers, Albatrelin A, albatrelin B, Albatrelin C (1-3), three novel dimers (meroterpenoid pigments), albatrelin D, albatrelin E, albatrelin F (4-6), and two known ones, 6a,7,8,9,10,10a-hexahydro-3,6,9-trimethyl-6-(4-methyl-3-penten-1-yl)-1,9-epoxy-6H-dibenzo[b,d]pyran (7) and confluentin (8), were isolated from Albatrellus ovinus. Their structures were established by extensive spectroscopic analysis. The absolute configurations of compounds 2-4 were determined as 9R by comparing their optical rotations with data reported in the literature.
CONCLUSIONS:
Albatrelin F (6) was isolated as a pair of C-2' tautomers with a ratio of 1.3:1. Confluentin (8) showed weak cytotoxicity against four human tumor cell lines, HL-60, SMMC-7712, A-549, and MCF-7, in vitro.

Albatrelin C Dilution Calculator

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Albatrelin C Molarity Calculator

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Preparing Stock Solutions of Albatrelin C

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.063 mL 15.3149 mL 30.6297 mL 61.2595 mL 76.5744 mL
5 mM 0.6126 mL 3.063 mL 6.1259 mL 12.2519 mL 15.3149 mL
10 mM 0.3063 mL 1.5315 mL 3.063 mL 6.1259 mL 7.6574 mL
50 mM 0.0613 mL 0.3063 mL 0.6126 mL 1.2252 mL 1.5315 mL
100 mM 0.0306 mL 0.1531 mL 0.3063 mL 0.6126 mL 0.7657 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on Albatrelin C

Nine new farnesylphenols from the basidiomycete albatrellus caeruleoporus.[Pubmed:24858140]

Nat Prod Bioprospect. 2014 Apr;4(2):119-28.

Nine previously-unreported farnesylphenols, involving eight neogrifolin derivatives (1-8) and one grifolin analogue (9), together with three known compounds, were isolated from the fruiting bodies of the mushroom Albatrellus caeruleoporus. Their structures were elucidated as (S)-17-hydroxy-18,20-ene-neogrifolin (1), (S)-18,19-dihydroxyneogrifolin (2), (S)-9-hydroxy-10,22-ene-neogrifolin (3), (9S,10R)-6,10-epoxy-9-hydroxyneo grifolin (4), (9S,10R)-6,9-epoxy-10-hydroxyneogrifolin (5), (-)-13,14-dihydroxyneogrifolin (6), albatrelin G (7), albatrelin H (8), and one grifolin analogue, (S)-10-hydroxygrifolin (9), grifolin (10), neogrifolin (11), and albatrellin (12) by extensive spectroscopic analyses and chemical methods. Compounds 7 and 8 showed weak cytotoxic activity to cell lines HL-60, SMMC-7721, A-549, and MCF-7, in vitro.

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