Drechslerine A

CAS# 405157-84-8

Drechslerine A

Catalog No. BCN7561----Order now to get a substantial discount!

Product Name & Size Price Stock
Drechslerine A:5mg Please Inquire In Stock
Drechslerine A:10mg Please Inquire In Stock
Drechslerine A:20mg Please Inquire In Stock
Drechslerine A:50mg Please Inquire In Stock

Quality Control of Drechslerine A

Number of papers citing our products

Chemical structure

Drechslerine A

3D structure

Chemical Properties of Drechslerine A

Cas No. 405157-84-8 SDF Download SDF
PubChem ID 10911204 Appearance Powder
Formula C14H24O2 M.Wt 224.34
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name [(1R,4R,5R,8S)-7-(hydroxymethyl)-1-methyl-4-propan-2-yl-8-bicyclo[3.2.1]oct-6-enyl]methanol
SMILES CC(C)C1CCC2(C(C1C=C2CO)CO)C
Standard InChIKey WCRQEYCIOPEQST-RFGFWPKPSA-N
Standard InChI InChI=1S/C14H24O2/c1-9(2)11-4-5-14(3)10(7-15)6-12(11)13(14)8-16/h6,9,11-13,15-16H,4-5,7-8H2,1-3H3/t11-,12+,13+,14+/m1/s1
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 Drechslerine A

The metabolites of the algicolous fungus Drechslera dematioidea.

Biological Activity of Drechslerine A

DescriptionDrechslerine A is a natural product from the metabolites of the algicolous fungus Drechslera dematioidea.

Protocol of Drechslerine A

Structure Identification
Tetrahedron, 2011, 67(22):4061-4068.

First total syntheses of bicyclic marine sesquiterpenoids drechslerines A and B.[Reference: WebLink]

The first total syntheses of the bicyclic sesquiterpenoids Drechslerine A (1) and drechslerine B (2), which were isolated from the algicolous fungus Drechslera dematioidea in the marine red alga Liagora viscida, has been accomplished starting from (S)-carvone (13) via three palladium-catalyzed reactions, namely, diastereoselective allylation, conjugate reduction, and carbon monoxide insertion, as the key reactions.

Drechslerine A Dilution Calculator

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Drechslerine A Molarity Calculator

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Preparing Stock Solutions of Drechslerine A

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.4575 mL 22.2876 mL 44.5752 mL 89.1504 mL 111.438 mL
5 mM 0.8915 mL 4.4575 mL 8.915 mL 17.8301 mL 22.2876 mL
10 mM 0.4458 mL 2.2288 mL 4.4575 mL 8.915 mL 11.1438 mL
50 mM 0.0892 mL 0.4458 mL 0.8915 mL 1.783 mL 2.2288 mL
100 mM 0.0446 mL 0.2229 mL 0.4458 mL 0.8915 mL 1.1144 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 Drechslerine A

First total syntheses of bicyclic marine sesquiterpenoids drechslerines A and B.

Tetrahedron, 2011, 67(22):4061-4068.

The first total syntheses of the bicyclic sesquiterpenoids Drechslerine A (1) and drechslerine B (2), which were isolated from the algicolous fungus Drechslera dematioidea in the marine red alga Liagora viscida, has been accomplished starting from (S)-carvone (13) via three palladium-catalyzed reactions, namely, diastereoselective allylation, conjugate reduction, and carbon monoxide insertion, as the key reactions.

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