Danshenol CCAS# 910856-25-6 |
- Danshenol A
Catalog No.:BCN3145
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- 15-Epi-Danshenol-A
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Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
Cas No. | 910856-25-6 | SDF | Download SDF |
PubChem ID | 11688609 | Appearance | Red powder |
Formula | C21H20O4 | M.Wt | 336.4 |
Type of Compound | Diterpenoids | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | (1R,10R)-10-hydroxy-1,6-dimethyl-10-(2-oxopropyl)-1,2-dihydronaphtho[1,2-g][1]benzofuran-11-one | ||
SMILES | CC1COC2=C1C(=O)C(C3=C2C=CC4=C3C=CC=C4C)(CC(=O)C)O | ||
Standard InChIKey | WQYKPUPMMFGHQW-LAJNKCICSA-N | ||
Standard InChI | InChI=1S/C21H20O4/c1-11-5-4-6-15-14(11)7-8-16-18(15)21(24,9-13(3)22)20(23)17-12(2)10-25-19(16)17/h4-8,12,24H,9-10H2,1-3H3/t12-,21+/m0/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. |
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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. |
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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. |
Description | Standard reference |
In vitro | Two new abietane diterpenoids from Salvia yunnanensis.[Reference: WebLink]Planta Med. 2006 Jan;72(1):84-6.
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Danshenol C Dilution Calculator
Danshenol C Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 2.9727 mL | 14.8633 mL | 29.7265 mL | 59.453 mL | 74.3163 mL |
5 mM | 0.5945 mL | 2.9727 mL | 5.9453 mL | 11.8906 mL | 14.8633 mL |
10 mM | 0.2973 mL | 1.4863 mL | 2.9727 mL | 5.9453 mL | 7.4316 mL |
50 mM | 0.0595 mL | 0.2973 mL | 0.5945 mL | 1.1891 mL | 1.4863 mL |
100 mM | 0.0297 mL | 0.1486 mL | 0.2973 mL | 0.5945 mL | 0.7432 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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[Chemical Constituents from Salvia przewalskii Root].[Pubmed:26762059]
Zhong Yao Cai. 2015 Jun;38(6):1197-201.
OBJECTIVE: To study the chemical constituents of the root of Salvia przewalakii. METHODS: The chemical constituents were isolated and purified by means of chromatographic techniques and their structures were elucidated by spectroscopic methods. RESULTS: 17 compounds were isolated and identified as danshenxinkun B (1), Danshenol C (2), isotanshinone (3), 1,2-dihydroisodihydrotanshinone-I (4), isotanshinone-II A (5), dihydrotanshinone-I (6), tanshinlactone (7), danshenol B (8), tanshinone-I (9), danshenspiroketallactone (10), ferrugino (11), epi-danshenspiroketallactone (12), danshenxinkun A (13), sapriolactone (14), 12-hydroxy-6,7-secoabieta-8,11,13-trien-6,7-diol (15), 6alpha-hydroxysugiol (16) and hypargenin B (17). CONCLUSION: Compounds 1 - 8 are isolated from this plant for the first time.
Two new abietane diterpenoids from Salvia yunnanensis.[Pubmed:16450305]
Planta Med. 2006 Jan;72(1):84-6.
Two new abietane diterpenoids, yunnannin A and Danshenol C, were isolated from Salvia yunnanensis together with ten known diterpenoids, danshenol A, przewalskin, tanshinone IIA, tanshinone I, crypotanshinone, 1,2-dihydrotanshinone, tanshinlactone, 5,6-dehydrosugiol, 12-hydroxy-6,7-seco-8,11,3-abietatriene-6,7-dial and phytol. Their structures were established based on spectroscopic data, chemical reactions and comparison with literature data. Compounds were tested for their antitumor activity in T-24, QGY, K562, Me180 and BIU87 cell lines. Compound showed inhibited growth of K562 (IC50=0.53 microg/mL), T-24 (IC50=7.94 microg/mL), QGY (IC50=4.65 microg/mL) and Me180 (IC50=6.89 microg/mL) cell lines while compound was inactive. Compound showed moderate inhibitory activity on QGY (IC50=16.75 microg/mL) and Me180 (IC50=5.84 microg/mL) cells.