Albatrelin A

CAS# 1417805-15-2

Albatrelin A

2D Structure

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Albatrelin A: 5mg $1116 In Stock
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Quality Control of Albatrelin A

3D structure

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Albatrelin A

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Chemical Properties of Albatrelin A

Cas No. 1417805-15-2 SDF Download SDF
PubChem ID 71524348 Appearance Powder
Formula C24H34O4 M.Wt 386.52
Type of Compound Phenols Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name methyl 4,6-dihydroxy-2-methyl-3-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]benzoate
SMILES CC1=C(C(=CC(=C1CC=C(C)CCC=C(C)CCC=C(C)C)O)O)C(=O)OC
Standard InChIKey XISGBSYLXCXJCJ-OUBUNXTGSA-N
Standard InChI InChI=1S/C24H34O4/c1-16(2)9-7-10-17(3)11-8-12-18(4)13-14-20-19(5)23(24(27)28-6)22(26)15-21(20)25/h9,11,13,15,25-26H,7-8,10,12,14H2,1-6H3/b17-11+,18-13+
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 A

The fruiting bodies of Albatrellus ovinus.

Biological Activity of Albatrelin A

DescriptionAlbatrelin A is a natural product from Albatrellus ovinus.

Protocol of Albatrelin A

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 A Dilution Calculator

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Albatrelin A Molarity Calculator

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Preparing Stock Solutions of Albatrelin A

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.5872 mL 12.9359 mL 25.8719 mL 51.7438 mL 64.6797 mL
5 mM 0.5174 mL 2.5872 mL 5.1744 mL 10.3488 mL 12.9359 mL
10 mM 0.2587 mL 1.2936 mL 2.5872 mL 5.1744 mL 6.468 mL
50 mM 0.0517 mL 0.2587 mL 0.5174 mL 1.0349 mL 1.2936 mL
100 mM 0.0259 mL 0.1294 mL 0.2587 mL 0.5174 mL 0.6468 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 A

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

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

Eight grifolin derivatives, involving three new monomers, albatrelins A-C (1-3), three novel dimers (meroterpenoid pigments), albatrelins D-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. 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.

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