8-(1,1-Dimethylallyl)genisteinCAS# 651750-08-2 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
| Cas No. | 651750-08-2 | SDF | Download SDF |
| PubChem ID | N/A | Appearance | Powder |
| Formula | C20H18O5 | M.Wt | 338.4 |
| Type of Compound | Flavonoids | Storage | Desiccate at -20°C |
| Synonyms | 5,7,4'-Trihydroxy-8-(1,1-dimethylprop-2-enyl)isoflavone | ||
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| 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. | ||
8-(1,1-Dimethylallyl)genistein Dilution Calculator
8-(1,1-Dimethylallyl)genistein Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 2.9551 mL | 14.7754 mL | 29.5508 mL | 59.1017 mL | 73.8771 mL |
| 5 mM | 0.591 mL | 2.9551 mL | 5.9102 mL | 11.8203 mL | 14.7754 mL |
| 10 mM | 0.2955 mL | 1.4775 mL | 2.9551 mL | 5.9102 mL | 7.3877 mL |
| 50 mM | 0.0591 mL | 0.2955 mL | 0.591 mL | 1.182 mL | 1.4775 mL |
| 100 mM | 0.0296 mL | 0.1478 mL | 0.2955 mL | 0.591 mL | 0.7388 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
- (19S,23R)-5β,19-Epoxy-19,23-dimethoxycucurbita-6,24-dien-3β-ol
Catalog No.:BCN0565
CAS No.:1474062-47-9
- Glaucocalyxin A diacetate
Catalog No.:BCN0564
CAS No.:79498-37-6
- Lespedezaflavanone H
Catalog No.:BCN0563
CAS No.:138822-59-0
- 2,3-Dihydroxybenzeneacetonitrile
Catalog No.:BCN0562
CAS No.:1513469-96-9
- Philippin A
Catalog No.:BCN0561
CAS No.:1848254-99-8
- Sachaconitine
Catalog No.:BCN0560
CAS No.:1361-02-0
- 14-O-Acetylsachaconitine
Catalog No.:BCN0559
CAS No.:102719-98-2
- Falconeridine
Catalog No.:BCN0558
CAS No.:121880-22-6
- Haplamide
Catalog No.:BCN0557
CAS No.:31991-78-3
- Velutinam
Catalog No.:BCN0556
CAS No.:146428-62-8
- (19S,23E)-5β,19-Epoxy-19-methoxycucurbita-6,23,25-trien-3β-ol
Catalog No.:BCN0555
CAS No.:874287-87-3
- Glochidiolide
Catalog No.:BCN0554
CAS No.:213528-23-5
- 5-Hydroxyoxindole
Catalog No.:BCN0567
CAS No.:3416-18-0
- 7,4'-Di-O-methylvitexin 2''-O-rhamnoside
Catalog No.:BCN0568
CAS No.:1236226-98-4
- (19R,23S)-5β,19-Epoxy-19,23-dimethoxycucurbita-6,24-dien-3β-ol
Catalog No.:BCN0569
CAS No.:2281872-79-3
- 3β-(4-Hydroxybenzoyloxy)-21β,29-dihydroxyserrat-14-en-24-oic acid
Catalog No.:BCN0570
CAS No.:1217268-13-7
- 3β-Vanilloyloxy-21β,29-dihydroxyserrat-14-en-24-oic acid
Catalog No.:BCN0571
CAS No.:1217268-14-8
- 16α-Hydroxy-19,20-epoxy-20β-methoxy-ent-kaurane
Catalog No.:BCN0572
CAS No.:197369-57-6
- Lycernuic ketone B
Catalog No.:BCN0573
CAS No.:448260-79-5
- Inundoside E
Catalog No.:BCN0574
CAS No.:80244-83-3
- Flemichin D
Catalog No.:BCN0575
CAS No.:57096-07-8
- Neochlorogenin 6-O-α-L-rhamnopyranosyl-(1→3)-β-D-quinovopyranoside
Catalog No.:BCN0576
CAS No.:184686-01-9
- Karaviloside X
Catalog No.:BCN0577
CAS No.:934739-34-1
- Neochlorogenin 6-O-β-D-xylopyranosyl-(1→3)-β-D-quinovopyranoside
Catalog No.:BCN0578
CAS No.:184686-02-0
Estrogenic and antiestrogenic activities of the roots of Moghania philippinensis and their constituents.[Pubmed:15056864]
Biol Pharm Bull. 2004 Apr;27(4):548-53.
In the course of our search for natural estrogenic compounds from medicinal plants, we found that the methanolic extract from the roots of Moghania philippinensis (Fabaceae) showed significant effects on the proliferation of MCF-7 cells (human breast cancer) and induction of beta-galactosidase activity in a yeast two-hybrid assay. Through estrogenic activity-guided fractionation, we isolated several active flavonoids including prenylated ones. The CHCl(3) fraction and its new constituent, 8-(1,1-Dimethylallyl)genistein (9), appreciably increased the uterine weight in ovariectomized rats when administered orally for 14 consecutive days, in which compound 9 showed stronger estrogenic activity than genistein. Antiestrogenic activities were also examined based on the inhibition of MCF-7 cell proliferation and beta-galactosidase activity in the yeast two-hybrid assay, mediated by 17beta-estradiol. 5,7,3',4'-Tetrahydroxy-6,8-diprenylisoflavone (6) showed the strongest antiestrogenic activity.
Prenylated flavonoids from Moghania philippinensis.[Pubmed:14630004]
Phytochemistry. 2003 Dec;64(8):1389-94.
Five prenylated flavonoids, 8-(1,1-Dimethylallyl)genistein (1), 5,7,3',4'-tetrahydroxy-2',5'-di(3-methylbut-2-enyl)isoflavone (2), 5,7,3'-trihydroxy-2'-(3-methylbut-2-enyl)-4',5'-(3,3-dimethylpyrano)isoflavone (3), (2R)-5,2',4'-trihydroxy-8,5'-di(3-methylbut-2-enyl)-6,7-(3,3-dimethylpyrano)flava none (4a) and (2S)-5, 2', 4'-trihydroxy-8,5'-di(3-methylbut-2-enyl)-6,7-(3,3-dimethylpyrano)flavanone (4b), were isolated from the roots of Moghania philippinensis. The structures of these compounds were determined on the basis of spectroscopic and chemical means.
