Cimicifugoside H2CAS# 161097-77-4 |
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
| Cas No. | 161097-77-4 | SDF | Download SDF |
| PubChem ID | 10100589 | Appearance | Powder |
| Formula | C35H54O10 | M.Wt | 634.8 |
| Type of Compound | Triterpenoids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| SMILES | CC(CC(=O)C(C(C)(C)O)O)C1C(=O)CC2(C1(CC(C34C2=CCC5C3(C4)CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)O)C)C | ||
| Standard InChIKey | SUNYLGIAMKNXMN-GLWILYKISA-N | ||
| Standard InChI | InChI=1S/C35H54O10/c1-17(12-18(36)28(42)31(4,5)43)25-19(37)13-32(6)22-9-8-21-30(2,3)24(45-29-27(41)26(40)20(38)15-44-29)10-11-34(21)16-35(22,34)23(39)14-33(25,32)7/h9,17,20-21,23-29,38-43H,8,10-16H2,1-7H3/t17-,20-,21+,23+,24+,25+,26+,27-,28+,29+,32+,33-,34-,35+/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 | Cimicifugoside H2 is a natural product from Cimicifuga foetida. |
| Structure Identification | Zhongguo Zhong Yao Za Zhi. 2009 Aug;34(15):1930-4.Cycloartane triterpenoid of Cimicifuga foetida.[Pubmed: 19894537]To study cycloartane triterpenoid of Cimicifuga foetida and their osteoclast inhibition activity. |
Cimicifugoside H2 Dilution Calculator
Cimicifugoside H2 Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 1.5753 mL | 7.8765 mL | 15.753 mL | 31.506 mL | 39.3825 mL |
| 5 mM | 0.3151 mL | 1.5753 mL | 3.1506 mL | 6.3012 mL | 7.8765 mL |
| 10 mM | 0.1575 mL | 0.7876 mL | 1.5753 mL | 3.1506 mL | 3.9382 mL |
| 50 mM | 0.0315 mL | 0.1575 mL | 0.3151 mL | 0.6301 mL | 0.7876 mL |
| 100 mM | 0.0158 mL | 0.0788 mL | 0.1575 mL | 0.3151 mL | 0.3938 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
- Formyl-DL-Trp-OH
Catalog No.:BCC3120
CAS No.:16108-03-5
- Epimedokoreanin C
Catalog No.:BCN8080
CAS No.:161068-54-8
- Epimedokoreanin B
Catalog No.:BCN6483
CAS No.:161068-53-7
- VT-464
Catalog No.:BCC5398
CAS No.:1610537-15-9
- Hosenkoside M
Catalog No.:BCN4518
CAS No.:161016-51-9
- Dihydroperaksine
Catalog No.:BCN1713
CAS No.:16100-84-8
- TH588
Catalog No.:BCC6397
CAS No.:1609960-31-7
- TH287
Catalog No.:BCC6400
CAS No.:1609960-30-6
- Silodosin
Catalog No.:BCN2164
CAS No.:160970-54-7
- 2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethyl methanesulfonate
Catalog No.:BCN1546
CAS No.:160969-03-9
- 2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethyl bromide
Catalog No.:BCN1547
CAS No.:160969-00-6
- Mps1-IN-3
Catalog No.:BCC5496
CAS No.:1609584-72-6
- Bidwillol A
Catalog No.:BCN4858
CAS No.:161099-42-9
- H-Asp(OEt)-OEt.HCl
Catalog No.:BCC2888
CAS No.:16115-68-7
- Cimicidanol 3-O-alpha-L-arabinoside
Catalog No.:BCN6528
CAS No.:161207-05-2
- H-Orn(Z)-OtBu.HCl
Catalog No.:BCC2677
CAS No.:161234-80-6
- SR-9243
Catalog No.:BCC3983
CAS No.:1613028-81-1
- 1-O-Acetyl-6-O-isobutyrylbritannilactone
Catalog No.:BCN7795
CAS No.:1613152-34-3
- Fmoc-Chg-OH
Catalog No.:BCC3164
CAS No.:161321-36-4
- SGC-CBP30
Catalog No.:BCC2419
CAS No.:1613695-14-9
- HTH-01-015
Catalog No.:BCC4010
CAS No.:1613724-42-7
- ABT
Catalog No.:BCC7998
CAS No.:1614-12-6
- SIN-1 chloride
Catalog No.:BCC5670
CAS No.:16142-27-1
- 7-NINA
Catalog No.:BCC5674
CAS No.:161467-34-1
[Cycloartane triterpenoid of Cimicifuga foetida].[Pubmed:19894537]
Zhongguo Zhong Yao Za Zhi. 2009 Aug;34(15):1930-4.
OBJECTIVE: To study cycloartane triterpenoid of Cimicifuga foetida and their osteoclast inhibition activity. METHOD: The compounds were isolated and purified by normal and reversed phase column chromatographic methods. Structures were identified by spectroscopic analyses. Their osteoclast inhibition activity was then studied. RESULT: Thirteen cycloartane triterpenoids were isolated from the rhizomes of C. foetida and were characterized as 25-O-acetyl-cimigenol (1), cimigenol (2), cimicidanol (3), 26-deoxyactein (4), asiaticoside A (5), 23-epi-26-deoxyactein (6), actein (7), 12beta-hydroxycimigenol (8), cimiside E (9), (23R, 24S) 25-O-acetyl-cimigenol-3-O-beta-D-xylopyranoside (10), (23R, 24S) cimigenol-3-O-beta-D-xylopyranoside (11), cimicifugoside H-1 (12) and cimicifugoside H-2 (13). CONCLUSION: Compound 5 was isolated from this genus for the first time, compound 7 was isolated firstly from the plant and compound 2, 7, 10 and 11 exhibit osteoclast inhibition activity.
