Schisanlactone ECAS# 136040-43-2 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 136040-43-2 | SDF | Download SDF |
| PubChem ID | 14844611 | Appearance | Cryst. |
| Formula | C30H44O4 | M.Wt | 468.67 |
| Type of Compound | Triterpenoids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| SMILES | CC1=CCC(OC1=O)C(C)C2CCC3(C2(CCC45C3CCC(C4(C5)CCC(=O)O)C(=C)C)C)C | ||
| Standard InChIKey | RRSQKAFYPICCAZ-PTWMZBRVSA-N | ||
| Standard InChI | InChI=1S/C30H44O4/c1-18(2)21-8-10-24-28(6)13-11-22(20(4)23-9-7-19(3)26(33)34-23)27(28,5)15-16-30(24)17-29(21,30)14-12-25(31)32/h7,20-24H,1,8-17H2,2-6H3,(H,31,32)/t20-,21-,22+,23+,24-,27+,28-,29+,30-/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 | 1. Schisanlactone E may show moderate cytotoxic activity against the human tumor cell lines Bel-7402, BGC-823, MCF-7 and HL-60. |
| Targets | NO |
Schisanlactone E Dilution Calculator
Schisanlactone E Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 2.1337 mL | 10.6685 mL | 21.337 mL | 42.6739 mL | 53.3424 mL |
| 5 mM | 0.4267 mL | 2.1337 mL | 4.2674 mL | 8.5348 mL | 10.6685 mL |
| 10 mM | 0.2134 mL | 1.0668 mL | 2.1337 mL | 4.2674 mL | 5.3342 mL |
| 50 mM | 0.0427 mL | 0.2134 mL | 0.4267 mL | 0.8535 mL | 1.0668 mL |
| 100 mM | 0.0213 mL | 0.1067 mL | 0.2134 mL | 0.4267 mL | 0.5334 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
- Fmoc-Tic-OH
Catalog No.:BCC3341
CAS No.:136030-33-6
- (1R,2S)-1-Amino-2-indanol
Catalog No.:BCC8381
CAS No.:136030-00-7
- Angiotensin III (human, mouse)
Catalog No.:BCC1031
CAS No.:13602-53-4
- AVL-292 benzenesulfonate
Catalog No.:BCC1386
CAS No.:1360053-81-1
- Ranaconitine
Catalog No.:BCN3870
CAS No.:1360-76-5
- Tetracaine HCl
Catalog No.:BCC4399
CAS No.:136-47-0
- Phenazopyridine HCl
Catalog No.:BCC4698
CAS No.:136-40-3
- Caulophylline B
Catalog No.:BCN7499
CAS No.:1359978-55-4
- SR 2211
Catalog No.:BCC6310
CAS No.:1359164-11-6
- RP 67580
Catalog No.:BCC7134
CAS No.:135911-02-3
- Lupinol C
Catalog No.:BCN4809
CAS No.:135905-53-2
- H-D-Asp(OtBu)-OtBu.HCl
Catalog No.:BCC2898
CAS No.:135904-71-1
- Fmoc-Cys(pMeBzl)-OH
Catalog No.:BCC3476
CAS No.:136050-67-4
- Justiciresinol
Catalog No.:BCN3419
CAS No.:136051-41-7
- [D-Lys3]-GHRP-6
Catalog No.:BCC5850
CAS No.:136054-22-3
- Desrhamnosylmartynoside
Catalog No.:BCN7648
CAS No.:136055-64-6
- 9-Dehydroxyeurotinone
Catalog No.:BCN7397
CAS No.:1360606-85-4
- Necrosulfonamide
Catalog No.:BCC7992
CAS No.:1360614-48-7
- 5-Methoxyisolariciresinol
Catalog No.:BCN7016
CAS No.:136082-41-2
- Onjixanthone II
Catalog No.:BCN7559
CAS No.:136083-93-7
- Lobetyolin
Catalog No.:BCN5894
CAS No.:136085-37-5
- Isomucronulatol 7-O-beta-glucoside
Catalog No.:BCN8088
CAS No.:136087-29-1
- 14-Dehydrodelcosine
Catalog No.:BCN8119
CAS No.:1361-18-8
- LDC1267
Catalog No.:BCC5577
CAS No.:1361030-48-9
Bioactive metabolites of Schisanlactone E transformed by Cunninghamella blakesleana AS 3.970.[Pubmed:25451796]
Fitoterapia. 2014 Dec;99:352-61.
Schisanlactone E (SE) is a major triterpene obtained from the plants of genus Kadsura. The aim of this research was to investigate the transformed metabolites of SE by fungi and evaluate the bioactivities of these products. After screening 10 strains of filamentous fungi, Cunninghamella blakesleana AS 3.970 was chosen as a potent organism to be used for the biotransformation of SE. 13 metabolites were obtained and determined to be new compounds through the use of spectroscopic data, including UV, 1D-, 2D-NMR, and HR-ESIMS. Furthermore, in an in vitro bioassay, metabolites 7 and 9 showed moderate inhibitory effects on the nitric oxide production in LPS-induced macrophages with IC50 values of 16.73, 5.91 muM, respectively; 9 could inhibit the proliferation of acetaldehyde-induced HSC-T6 cells, with the IC50 value of 21.4 muM. Preliminary findings on the structure-activity relationships for these metabolites were also discussed.
New triterpenoids from Kadsura heteroclita and their cytotoxic activity.[Pubmed:16557460]
Planta Med. 2006 Apr;72(5):450-7.
Phytochemical investigations of the stem of Kadsura heteroclita (Roxb) Craib (Schizandraceae) resulted in the isolation and structure elucidation of six new triterpenoidal compounds named heteroclitalactones A-E (1-5) as well as heteroclic acid (6) and heteroclitalactone F (7), which was isolated for the first time from a natural source, and the six known compounds Schisanlactone E (8), cycloartenone (9), schisandronic acid (10), nigranoic acid (11), changnanic acid (12) and schisanlactone B (13), respectively. The structures of these compounds were characterized by extensive 1D and 2D NMR spectral analyses. The majority of these triterpenoids showed moderate cytotoxic activity against the human tumor cell lines Bel-7402, BGC-823, MCF-7 and HL-60. Among the compounds tested, heteroclitalactone D (4) showed the strongest cytotoxic activity against the HL-60 cells with an IC50 of 6.76 microM.
