Hosenkoside GCAS# 160896-46-8 |
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
| Cas No. | 160896-46-8 | SDF | Download SDF |
| PubChem ID | 102004930 | Appearance | Powder |
| Formula | C47H80O19 | M.Wt | 949.2 |
| Type of Compound | Triterpenoids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | (2R,3R,4S,5S,6R)-2-[[(1R,2S,4aR,4bR,6aS,7R,8R,10aR,10bR,12aR)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-7-hydroxy-8-(hydroxymethyl)-8-[(Z)-5-hydroxy-4-methylpent-3-enyl]-1,4a,10a,10b-tetramethyl-3,4,4b,5,6,6a,7,9,10,11,12,12a-dodecahydro-2H-chrysen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol | ||
| SMILES | CC(=CCCC1(CCC2(C(C1O)CCC3C2(CCC4C3(CCC(C4(C)COC5C(C(C(C(O5)CO)O)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(CO7)O)O)O)C)C)C)CO)CO | ||
| Standard InChIKey | AJUACYVEKRAXEB-QXJSNOIISA-N | ||
| Standard InChI | InChI=1S/C47H80O19/c1-23(17-48)7-6-12-47(21-51)16-15-45(4)24(39(47)60)8-9-29-43(2)13-11-30(65-42-38(35(57)33(55)27(19-50)64-42)66-40-36(58)31(53)25(52)20-61-40)44(3,28(43)10-14-46(29,45)5)22-62-41-37(59)34(56)32(54)26(18-49)63-41/h7,24-42,48-60H,6,8-22H2,1-5H3/b23-7-/t24-,25-,26-,27-,28-,29-,30+,31+,32-,33-,34+,35+,36-,37-,38-,39-,40+,41-,42+,43+,44+,45-,46-,47-/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 | Hosenkoside G is a natural product from Impatiens balsamina L. |
| Structure Identification | Chem Pharm Bull (Tokyo). 1994 Jul;42(7):1422-6.Hosenkosides F, G, H, I, J, and K, novel baccharane glycosides from the seeds of Impatiens balsamina.[Pubmed: 7923465]From the seeds of Impatiens balsamina we have isolated six novel baccharane glycosides, hosenkosides F-K. |
Hosenkoside G Dilution Calculator
Hosenkoside G Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 1.0535 mL | 5.2676 mL | 10.5352 mL | 21.0704 mL | 26.338 mL |
| 5 mM | 0.2107 mL | 1.0535 mL | 2.107 mL | 4.2141 mL | 5.2676 mL |
| 10 mM | 0.1054 mL | 0.5268 mL | 1.0535 mL | 2.107 mL | 2.6338 mL |
| 50 mM | 0.0211 mL | 0.1054 mL | 0.2107 mL | 0.4214 mL | 0.5268 mL |
| 100 mM | 0.0105 mL | 0.0527 mL | 0.1054 mL | 0.2107 mL | 0.2634 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
- Hosenkoside F
Catalog No.:BCN2520
CAS No.:160896-45-7
- Fmoc-Valinol
Catalog No.:BCC2694
CAS No.:160885-98-3
- Chrysin 8-C-glucoside
Catalog No.:BCN7982
CAS No.:160880-89-7
- Ethyl 2-(3-cyano-4-isobutoxyphenyl)-4-methyl-5-thiazolecarboxylate
Catalog No.:BCC8967
CAS No.:160844-75-7
- H-Thr(Bzl)-ol
Catalog No.:BCC2577
CAS No.:160841-03-2
- AMG319
Catalog No.:BCC6510
CAS No.:1608125-21-8
- Indirubin-3'-oxime
Catalog No.:BCC7185
CAS No.:160807-49-8
- Ardisicrenoside B
Catalog No.:BCN8078
CAS No.:160791-12-8
- 2,3-Dihydro-3alpha-methoxynimbolide
Catalog No.:BCN7093
CAS No.:1607828-35-2
- 1,4,6-Trihydroxy-5-methoxy-7-prenylxanthone
Catalog No.:BCN1548
CAS No.:160623-47-2
- Villosin
Catalog No.:BCN1711
CAS No.:160598-92-5
- DMP 543
Catalog No.:BCC7331
CAS No.:160588-45-4
- Hosenkoside K
Catalog No.:BCN2577
CAS No.:160896-49-1
- Villosin C
Catalog No.:BCN1712
CAS No.:160927-81-1
- AZD3264
Catalog No.:BCC6514
CAS No.:1609281-86-8
- Mps1-IN-3
Catalog No.:BCC5496
CAS No.:1609584-72-6
- 2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethyl bromide
Catalog No.:BCN1547
CAS No.:160969-00-6
- 2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethyl methanesulfonate
Catalog No.:BCN1546
CAS No.:160969-03-9
- Silodosin
Catalog No.:BCN2164
CAS No.:160970-54-7
- TH287
Catalog No.:BCC6400
CAS No.:1609960-30-6
- TH588
Catalog No.:BCC6397
CAS No.:1609960-31-7
- Dihydroperaksine
Catalog No.:BCN1713
CAS No.:16100-84-8
- Hosenkoside M
Catalog No.:BCN4518
CAS No.:161016-51-9
- VT-464
Catalog No.:BCC5398
CAS No.:1610537-15-9
Hosenkosides F, G, H, I, J, and K, novel baccharane glycosides from the seeds of Impatiens balsamina.[Pubmed:7923465]
Chem Pharm Bull (Tokyo). 1994 Jul;42(7):1422-6.
From the seeds of Impatiens balsamina we have isolated six novel baccharane glycosides, hosenkosides F-K. The structures of all isolates were determined by the use of two dimensional (2D) NMR techniques (1H-1H correlation spectroscopy (COSY), heteronuclear multiple quantum coherence (HMQC), heteronuclear multiple-bond correlation (HMBC), rotating frame Overhauser enhancement spectroscopy (ROESY), total correlation spectroscopy (TOCSY)) and chemical derivatization. Hosenkosides F, H and I are hosenkol B 3-O-sambubiosido-26-O-glucoside, 3-O-sambubioside and 3,26-O-diglucoside, respectively. Hosenkoside G is hosenkol C 3-O-sambubiosido-28-O-glucoside. Hosenkosides J and K are hosenkol A 3-O-sophoroside and 3-O-sophorosido-26-O-glucosyl-28-O-glucoside, respectively.
