NeoliquiritinCAS# 5088-75-5 |
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
| Cas No. | 5088-75-5 | SDF | Download SDF |
| PubChem ID | 51666248 | Appearance | Powder |
| Formula | C21H22O9 | M.Wt | 418.4 |
| Type of Compound | Flavonoids | Storage | Desiccate at -20°C |
| Synonyms | 4',7-Dihydroxyflavanone 7-glucoside; Liquiritigenin 7-glucoside | ||
| Solubility | Soluble in methan | ||
| Chemical Name | (2S)-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one | ||
| SMILES | C1C(OC2=C(C1=O)C=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O | ||
| Standard InChIKey | HJBUYKZTEBZNSH-ZRWXNEIDSA-N | ||
| Standard InChI | InChI=1S/C21H22O9/c22-9-17-18(25)19(26)20(27)21(30-17)28-12-5-6-13-14(24)8-15(29-16(13)7-12)10-1-3-11(23)4-2-10/h1-7,15,17-23,25-27H,8-9H2/t15-,17+,18+,19-,20+,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. |
||
| 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 | Standard reference |
| In vitro | Assessment of genetic fidelity and composition: Mixed elicitors enhance triterpenoid and flavonoid biosynthesis of Glycyrrhiza uralensis Fisch. tissue cultures.[Pubmed: 26872048 ]Biotechnol Appl Biochem. 2017 Mar;64(2):211-217.Glycyrrhiza uralensis has acquired significant importance due to its medicinal properties and health function. In this study, the quality of G. uralensis adventitious roots was evaluated in terms of genetic stability, active compounds, and anti-inflammatory activity. |
Neoliquiritin Dilution Calculator
Neoliquiritin Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 2.3901 mL | 11.9503 mL | 23.9006 mL | 47.8011 mL | 59.7514 mL |
| 5 mM | 0.478 mL | 2.3901 mL | 4.7801 mL | 9.5602 mL | 11.9503 mL |
| 10 mM | 0.239 mL | 1.195 mL | 2.3901 mL | 4.7801 mL | 5.9751 mL |
| 50 mM | 0.0478 mL | 0.239 mL | 0.478 mL | 0.956 mL | 1.195 mL |
| 100 mM | 0.0239 mL | 0.1195 mL | 0.239 mL | 0.478 mL | 0.5975 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
- 1,5,6-Trihydroxy-3-methoxyxanthone
Catalog No.:BCN8121
CAS No.:50868-52-5
- Tetramisole HCl
Catalog No.:BCC4735
CAS No.:5086-74-8
- Friedelanol
Catalog No.:BCN5620
CAS No.:5085-72-3
- 1,3,5,6-Tetrahydroxyxanthone
Catalog No.:BCN3453
CAS No.:5084-31-1
- 14,15-Didehydroisoeburnamine
Catalog No.:BCN5619
CAS No.:50838-11-4
- Vortioxetine
Catalog No.:BCC2046
CAS No.:508233-74-7
- Ganoderic acid LM2
Catalog No.:BCN2442
CAS No.:508182-41-0
- Suchilactone
Catalog No.:BCN6752
CAS No.:50816-74-5
- Hastatoside
Catalog No.:BCN6898
CAS No.:50816-24-5
- Astrophylline
Catalog No.:BCN2151
CAS No.:5081-53-8
- Vasicinol
Catalog No.:BCN5812
CAS No.:5081-51-6
- Hellebrigenol
Catalog No.:BCN8238
CAS No.:508-79-2
- Liensinine diperchlorate
Catalog No.:BCN6336
CAS No.:5088-90-4
- 1,4-Bis(2-benzoxazolyl)naphthalene
Catalog No.:BCC8423
CAS No.:5089-22-5
- WY-14643 (Pirinixic Acid)
Catalog No.:BCC2265
CAS No.:50892-23-4
- 1-Acetyl-beta-carboline
Catalog No.:BCN3101
CAS No.:50892-83-6
- Gelsemine
Catalog No.:BCN5804
CAS No.:509-15-9
- Delsoline
Catalog No.:BCN5405
CAS No.:509-18-2
- Aconine
Catalog No.:BCN2394
CAS No.:509-20-6
- Napellonine
Catalog No.:BCN2536
CAS No.:509-24-0
- Strychnine phosphate
Catalog No.:BCC8257
CAS No.:509-42-2
- Mitraphylline
Catalog No.:BCC8213
CAS No.:509-80-8
- Arteannuin B
Catalog No.:BCN5623
CAS No.:50906-56-4
- Toxyloxanthone D
Catalog No.:BCN3070
CAS No.:50906-62-2
Assessment of genetic fidelity and composition: Mixed elicitors enhance triterpenoid and flavonoid biosynthesis of Glycyrrhiza uralensis Fisch. tissue cultures.[Pubmed:26872048]
Biotechnol Appl Biochem. 2017 Mar;64(2):211-217.
Glycyrrhiza uralensis has acquired significant importance due to its medicinal properties and health function. In this study, the quality of G. uralensis adventitious roots was evaluated in terms of genetic stability, active compounds, and anti-inflammatory activity. Monomorphic banding pattern obtained from the mother plant and tissue cultures of G. uralensis with randomly amplified polymorphic DNA markers confirmed the genetic stability of adventitious roots. Neoliquiritin (neoisoliquiritin), ononin, liquiritin, and glycyrrhizic acid were identified from G. uralensis adventitious roots on the basis of high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry analysis. This study also revealed that adventitious roots possessed a better anti-inflammatory effect than native roots. To increase the contents of G. uralensis active components, elicitors were used in the adventitious roots culture. The combination of methyl jasmonate and phenylalanine synergistically stimulated the accumulation of glycyrrhetinic acid (0.22 mg/g) and total flavonoid (5.43 mg/g) compared with single treatment. In conclusion, G. uralensis adventitious roots can be an exploitable system for the production of licorice.
