(-)-Isodocarpin

CAS# 10391-08-9

(-)-Isodocarpin

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Product Name & Size Price Stock
(-)-Isodocarpin: 5mg $748 In Stock
(-)-Isodocarpin: 10mg Please Inquire In Stock
(-)-Isodocarpin: 20mg Please Inquire Please Inquire
(-)-Isodocarpin: 50mg Please Inquire Please Inquire
(-)-Isodocarpin: 100mg Please Inquire Please Inquire
(-)-Isodocarpin: 200mg Please Inquire Please Inquire
(-)-Isodocarpin: 500mg Please Inquire Please Inquire
(-)-Isodocarpin: 1000mg Please Inquire Please Inquire

Quality Control of (-)-Isodocarpin

Number of papers citing our products

Chemical structure

(-)-Isodocarpin

3D structure

Chemical Properties of (-)-Isodocarpin

Cas No. 10391-08-9 SDF Download SDF
PubChem ID 165869 Appearance Cryst.
Formula C20H26O5 M.Wt 346.4
Type of Compound Diterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
SMILES CC1(CCC2C3(C1C(OC3)O)C4CCC5CC4(C(=O)C5=C)C(=O)O2)C
Standard InChIKey QOAOBBJDPFYUKJ-UHFFFAOYSA-N
Standard InChI InChI=1S/C20H26O5/c1-10-11-4-5-12-19(8-11,15(10)21)17(23)25-13-6-7-18(2,3)14-16(22)24-9-20(12,13)14/h11-14,16,22H,1,4-9H2,2-3H3
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 (-)-Isodocarpin

The herbs of Isodon japonicus

Protocol of (-)-Isodocarpin

Structure Identification
Angewandte Chemie International Edition.

Divergent Total Syntheses of Enmein-Type Natural Products:(-)-Enmein, (-)-Isodocarpin and (-)-Sculponin R.[Reference: WebLink]


METHODS AND RESULTS:
Divergent total syntheses of enmein-type natural products, (–)-enmein, (-)-Isodocarpin and (–)-sculponin R, have been achieved in a concise fashion.
CONCLUSIONS:
Key features of the strategy include (a) an efficient early-stage cage formation to control succeeding diastereoselectivity, (b) an one-pot acylation/akylation/lactonization to construct the C-ring and C8 quarternary center, (c) a reductive alkenylation approach to construct enmain D/E rings and (d) a flexible route to allow divergent syntheses of three natural products.

(-)-Isodocarpin Dilution Calculator

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(-)-Isodocarpin Molarity Calculator

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Preparing Stock Solutions of (-)-Isodocarpin

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.8868 mL 14.4342 mL 28.8684 mL 57.7367 mL 72.1709 mL
5 mM 0.5774 mL 2.8868 mL 5.7737 mL 11.5473 mL 14.4342 mL
10 mM 0.2887 mL 1.4434 mL 2.8868 mL 5.7737 mL 7.2171 mL
50 mM 0.0577 mL 0.2887 mL 0.5774 mL 1.1547 mL 1.4434 mL
100 mM 0.0289 mL 0.1443 mL 0.2887 mL 0.5774 mL 0.7217 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 (-)-Isodocarpin

Divergent Total Syntheses of Enmein-Type Natural Products: (-)-Enmein, (-)-Isodocarpin, and (-)-Sculponin R.[Pubmed:29644802]

Angew Chem Int Ed Engl. 2018 May 22;57(21):6333-6336.

Divergent total syntheses of the enmein-type natural products (-)-enmein, (-)-Isodocarpin, and (-)-sculponin R have been achieved in a concise fashion. Key features of the strategy include 1) an efficient early-stage cage formation to control succeeding diastereoselectivity, 2) a one-pot acylation/akylation/lactonization to construct the C-ring and C8 quarternary center, 3) a reductive alkenylation approach to construct the enmain D/E rings and 4) a flexible route to allow divergent syntheses of three natural products.

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