Methylophiopogonone BCAS# 74805-89-3 |
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
| Cas No. | 74805-89-3 | SDF | Download SDF |
| PubChem ID | 23259413 | Appearance | Powder |
| Formula | C19H18O5 | M.Wt | 326.34 |
| Type of Compound | Flavonoids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | 5,7-dihydroxy-3-[(4-methoxyphenyl)methyl]-6,8-dimethylchromen-4-one | ||
| SMILES | CC1=C(C2=C(C(=C1O)C)OC=C(C2=O)CC3=CC=C(C=C3)OC)O | ||
| Standard InChIKey | BUTFXZVBLOLETI-UHFFFAOYSA-N | ||
| Standard InChI | InChI=1S/C19H18O5/c1-10-16(20)11(2)19-15(17(10)21)18(22)13(9-24-19)8-12-4-6-14(23-3)7-5-12/h4-7,9,20-21H,8H2,1-3H3 | ||
| 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. | ||
| Description | Methylophiopogonone B is a natural product from Ophiopogon japonicus. |
| Structure Identification | Zhongguo yao xue za zhi,2005,40(5):337-341.Studies on the liposoluble components from tuber of Ophiopogon japonicus.[Reference: WebLink]
|
Methylophiopogonone B Dilution Calculator
Methylophiopogonone B Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 3.0643 mL | 15.3214 mL | 30.6429 mL | 61.2858 mL | 76.6072 mL |
| 5 mM | 0.6129 mL | 3.0643 mL | 6.1286 mL | 12.2572 mL | 15.3214 mL |
| 10 mM | 0.3064 mL | 1.5321 mL | 3.0643 mL | 6.1286 mL | 7.6607 mL |
| 50 mM | 0.0613 mL | 0.3064 mL | 0.6129 mL | 1.2257 mL | 1.5321 mL |
| 100 mM | 0.0306 mL | 0.1532 mL | 0.3064 mL | 0.6129 mL | 0.7661 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. | |||||
Calcutta University
University of Minnesota
University of Maryland School of Medicine
University of Illinois at Chicago
The Ohio State University
University of Zurich
Harvard University
Colorado State University
Auburn University
Yale University
Worcester Polytechnic Institute
Washington State University
Stanford University
University of Leipzig
Universidade da Beira Interior
The Institute of Cancer Research
Heidelberg University
University of Amsterdam
University of Auckland
TsingHua University
The University of Michigan
Miami University
DRURY University
Jilin University
Fudan University
Wuhan University
Sun Yat-sen University
Universite de Paris
Deemed University
Auckland University
The University of Tokyo
Korea University
- Ciglitazone
Catalog No.:BCC7014
CAS No.:74772-77-3
- VER-50589
Catalog No.:BCC5296
CAS No.:747413-08-7
- AUY922 (NVP-AUY922)
Catalog No.:BCC2123
CAS No.:747412-49-3
- Pterolactone A
Catalog No.:BCN6513
CAS No.:74730-10-2
- Secoxyloganin methyl ester
Catalog No.:BCN4299
CAS No.:74713-15-8
- Zaltoprofen
Catalog No.:BCC4442
CAS No.:74711-43-6
- 5-Hydroxyxanthotoxin
Catalog No.:BCC8107
CAS No.:7471-73-0
- Hydroxychloroquine Sulfate
Catalog No.:BCC5560
CAS No.:747-36-4
- Vibsanin C
Catalog No.:BCN4590
CAS No.:74690-89-4
- 1-Methoxycarbonyl-beta-carboline-N-oxide
Catalog No.:BCN8205
CAS No.:74690-74-7
- 4-hydroxy-1-methoxycarbonyl-beta-carboline
Catalog No.:BCN7909
CAS No.:74690-72-5
- 3-Methoxy-4,5-methylenedioxycinnamaldehyde
Catalog No.:BCN1364
CAS No.:74683-19-5
- Methylophiopogonone A
Catalog No.:BCN2841
CAS No.:74805-90-6
- Methylophiopogonanone B
Catalog No.:BCN5418
CAS No.:74805-91-7
- Methylophiopogonanone A
Catalog No.:BCN5417
CAS No.:74805-92-8
- Zalcitabine
Catalog No.:BCC5026
CAS No.:7481-89-2
- 3',5'-Anhydrothymidine
Catalog No.:BCC8596
CAS No.:7481-90-5
- GRP (porcine)
Catalog No.:BCC5809
CAS No.:74815-57-9
- Boc-Hyp-Ome
Catalog No.:BCC3252
CAS No.:74844-91-0
- Argatroban
Catalog No.:BCC3723
CAS No.:74863-84-6
- alpha-Carotene
Catalog No.:BCN3880
CAS No.:7488-99-5
- Vernakalant Hydrochloride
Catalog No.:BCC2037
CAS No.:748810-28-8
- 5-Carboxamidotryptamine maleate
Catalog No.:BCC6652
CAS No.:74885-72-6
- 5-Acetoxymatairesinol dimethyl ether
Catalog No.:BCN4300
CAS No.:74892-45-8
Studies on the liposoluble components from tuber of Ophiopogon japonicus.
Zhongguo yao xue za zhi,2005,40(5):337-341.
The compounds were isolated by column chromatography with silica gel and Sephadex LH-20 and the structures were elucidated by spectras' analysis. Sixteen compounds were obtained as 7 homoisoflavones, 2 anthraquinones, 3 phenolic acids, 2 terpenes and 2 fatty acids. Their structures were identified as methylophiopogonanone A(I), methylophiopogonanone B(II), methylophiopogonone A(III), Methylophiopogonone B(IV), 2'-hydroxy-methylophiopogonone A(V), 6-aldehycto-isoophiopogo-nanone A(VI), 5,7-dihyelroxy-8-methoxy-6-methyl-3-(2'-hydroxy-4'-methoxybenzyl) chroman-4-one(VII), chrysophenol(VIII), emodin(IX), vanillic acid(X), P-hydroxy benzaldenhyde (XI), P-trans-coumarinic acid(XII), l-borneol-#beta#-D-glucopyranoside (XIII), oleanolia acid(XIV), azelaic acid (XV) and n-tricosanoic acid(XVI). The compound IV, VIII--XII and XIV--XVI were isolated from O. japonicus and the genus Ophiopogon for the first time, respectively. The types of anthraquinone, phenolic acid and triterpene were firstly obtained from the genus.
