(-)-Ampelopsin HCAS# N/A |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | N/A | SDF | Download SDF |
| PubChem ID | 21606291 | Appearance | Powder |
| Formula | C56H42O12 | M.Wt | 906.94 |
| Type of Compound | Phenols | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | (1R,4R,5R,11R,12R,15R,16R,22R)-4,15-bis(3,5-dihydroxyphenyl)-5,11,16,22-tetrakis(4-hydroxyphenyl)-6,17-dioxahexacyclo[10.10.0.02,10.03,7.013,21.014,18]docosa-2(10),3(7),8,13(21),14(18),19-hexaene-9,20-diol | ||
| SMILES | C1=CC(=CC=C1C2C3C(C(C4=C(C=C5C(=C34)C(C(O5)C6=CC=C(C=C6)O)C7=CC(=CC(=C7)O)O)O)C8=CC=C(C=C8)O)C9=C1C(C(OC1=CC(=C29)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O | ||
| Standard InChIKey | HEIKOEZNFLUAEJ-OAPWRRNMSA-N | ||
| Standard InChI | InChI=1S/C56H42O12/c57-31-9-1-25(2-10-31)43-47-39(65)23-41-49(45(29-17-35(61)21-36(62)18-29)55(67-41)27-5-13-33(59)14-6-27)53(47)52-44(26-3-11-32(58)12-4-26)48-40(66)24-42-50(54(48)51(43)52)46(30-19-37(63)22-38(64)20-30)56(68-42)28-7-15-34(60)16-8-28/h1-24,43-46,51-52,55-66H/t43-,44-,45-,46-,51+,52+,55+,56+/m1/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 | Ampelopsin H has antioxidant activity, it shows that activity as radical hydroxyl scavenger an IC 50 4840.0 ug/mL. |
| Targets | ROS |
| In vitro | BALANOCARPOL AND AMPELOPSIN H, TWO OLIGORESVERATROLS FROM STEM BARK OF Hopea odorata (DIPTEROCARPACEAE)[Reference: WebLink]Indonesian Journal of Chemistry, 2010, 6(3).Two oligoresveratrol, namely balanocarpol (2) and ampelopsin H (3) had been isolated from the steam bark of Hopea odorata (Dipterocarpaceae). |
(-)-Ampelopsin H Dilution Calculator
(-)-Ampelopsin H Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 1.1026 mL | 5.513 mL | 11.0261 mL | 22.0522 mL | 27.5652 mL |
| 5 mM | 0.2205 mL | 1.1026 mL | 2.2052 mL | 4.4104 mL | 5.513 mL |
| 10 mM | 0.1103 mL | 0.5513 mL | 1.1026 mL | 2.2052 mL | 2.7565 mL |
| 50 mM | 0.0221 mL | 0.1103 mL | 0.2205 mL | 0.441 mL | 0.5513 mL |
| 100 mM | 0.011 mL | 0.0551 mL | 0.1103 mL | 0.2205 mL | 0.2757 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
- Zingerone
Catalog No.:BCN1192
CAS No.:122-48-5
- Glycerine trioleate
Catalog No.:BCN2287
CAS No.:122-32-7
- Tetraethoxypropane
Catalog No.:BCN2221
CAS No.:122-31-6
- Sulfadimethoxine
Catalog No.:BCC5159
CAS No.:122-11-2
- (±)-Anatoxin A fumarate
Catalog No.:BCC6796
CAS No.:1219922-30-1
- PF 4778574
Catalog No.:BCC6322
CAS No.:1219633-99-4
- 4,5-Diepipsidial A
Catalog No.:BCN3920
CAS No.:1219603-97-0
- PKA inhibitor fragment (6-22) amide
Catalog No.:BCC1042
CAS No.:121932-06-7
- Dihydrodaidzin
Catalog No.:BCN2879
CAS No.:121927-96-6
- Sophoraflavanone C
Catalog No.:BCN3543
CAS No.:121927-91-1
- Aurothioglucose
Catalog No.:BCC5446
CAS No.:12192-57-3
- CCT 031374 hydrobromide
Catalog No.:BCC6258
CAS No.:1219184-91-4
- Cinnamyl cinnamate
Catalog No.:BCN4722
CAS No.:122-69-0
- Phenylacetaldehyde
Catalog No.:BCN3819
CAS No.:122-78-1
- 3-Phenyl-1-propanol
Catalog No.:BCC8102
CAS No.:122-97-4
- Sulfamonomethoxine
Catalog No.:BCC9156
CAS No.:1220-83-3
- Niazirin
Catalog No.:BCN7300
CAS No.:122001-32-5
- Cyhalofop
Catalog No.:BCC5474
CAS No.:122008-78-0
- PLP (139-151)
Catalog No.:BCC5920
CAS No.:122018-58-0
- Monomethyl lithospermate B
Catalog No.:BCN2533
CAS No.:122021-74-3
- Khayalenoid E
Catalog No.:BCN6111
CAS No.:1220508-29-1
- [bAla8]-Neurokinin A(4-10)
Catalog No.:BCC7137
CAS No.:122063-01-8
- 2'-O-Acetylsprengerinin C
Catalog No.:BCN6655
CAS No.:1220707-33-4
- Charantadiol A
Catalog No.:BCN3483
CAS No.:1220890-23-2
BALANOCARPOL AND AMPELOPSIN H, TWO OLIGORESVERATROLS FROM STEM BARK OF Hopea odorata (DIPTEROCARPACEAE)
Indonesian Journal of Chemistry, 2010, 6(3).
Two oligoresveratrol, namely balanocarpol (2) and ampelopsin H (3) had been isolated from the steam bark of Hopea odorata (Dipterocarpaceae). The structures of these compounds were elucidated based on physical and spectroscopic data (MS, 1 H and 13 C NMR 1D and 2D). The activity of these compounds was evaluated against the 2-deoxyribose degradation induced by the hydroxyl radical generated via a Fenton-type reaction. The result showed that activity each compounds as radical hydroxyl scavenger of balanocarpol, and ampelopsin H with an IC 50 1802.3 and 4840.0 ug/mL. respectively. Each compound showed low activity. Vitamin C (IC 50 83.9 ug/mL) and butylated hydroxyl toluene (1328.0 ug/mL) were used as positif controls. These results suggest that oligoresveratrols from stem bark of H. odorata may be useful as potential sources of natural antioxidants.
