(+)-PteryxinCAS# 13161-75-6 |
- Peucedanocoumarin II
Catalog No.:BCN3435
CAS No.:130464-56-1
- Peucedanocoumarin III
Catalog No.:BCN3471
CAS No.:130464-57-2
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 13161-75-6 | SDF | Download SDF |
| PubChem ID | 5281425 | Appearance | White powder |
| Formula | C21H22O7 | M.Wt | 386.4 |
| Type of Compound | Coumarins | Storage | Desiccate at -20°C |
| Solubility | >17.1mg/mL in DMSO | ||
| Chemical Name | [(9R,10R)-9-acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] (Z)-2-methylbut-2-enoate | ||
| SMILES | CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C | ||
| Standard InChIKey | LYUZYPKZQDYMEE-YRCPKEQFSA-N | ||
| Standard InChI | InChI=1S/C21H22O7/c1-6-11(2)20(24)27-18-16-14(28-21(4,5)19(18)25-12(3)22)9-7-13-8-10-15(23)26-17(13)16/h6-10,18-19H,1-5H3/b11-6-/t18-,19-/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 | (+)-Pteryxin has muscle-relaxant props, it also shows hepatoprotective and nitric oxide prodn. inhibitory activity. |
| Targets | NO |
| Structure Identification | Chemistry of Natural Compounds.2008 Sep;44(5):578-581.Plant Coumarins. 3. (+)-PTeryxin from Peucedanum terebinthaceum.[Reference: WebLink]The potentially medically valuable pyranocoumarin (+)-Pteryxin was isolated for the first time from Peucedanum terebinthaceum Fischer et Turcz. |
(+)-Pteryxin Dilution Calculator
(+)-Pteryxin Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 2.588 mL | 12.94 mL | 25.8799 mL | 51.7598 mL | 64.6998 mL |
| 5 mM | 0.5176 mL | 2.588 mL | 5.176 mL | 10.352 mL | 12.94 mL |
| 10 mM | 0.2588 mL | 1.294 mL | 2.588 mL | 5.176 mL | 6.47 mL |
| 50 mM | 0.0518 mL | 0.2588 mL | 0.5176 mL | 1.0352 mL | 1.294 mL |
| 100 mM | 0.0259 mL | 0.1294 mL | 0.2588 mL | 0.5176 mL | 0.647 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
- Amyloid Beta-peptide (25-35) (human)
Catalog No.:BCC1027
CAS No.:131602-53-4
- Betulinaldehyde
Catalog No.:BCN1249
CAS No.:13159-28-9
- Calystegine A3
Catalog No.:BCN1884
CAS No.:131580-36-4
- Camelliaside B
Catalog No.:BCN3872
CAS No.:131573-90-5
- Triumbelletin
Catalog No.:BCN6779
CAS No.:131559-54-1
- VU 591 hydrochloride
Catalog No.:BCC6126
CAS No.:1315380-70-1
- NPEC-caged-(1S,3R)-ACPD
Catalog No.:BCC7653
CAS No.:1315379-60-2
- Rac1 Inhibitor F56, control peptide
Catalog No.:BCC5887
CAS No.:1315378-77-8
- pep2-SVKE
Catalog No.:BCC5785
CAS No.:1315378-76-7
- MNI caged kainic acid
Catalog No.:BCC7297
CAS No.:1315378-75-6
- Bax inhibitor peptide, negative control
Catalog No.:BCC2395
CAS No.:1315378-74-5
- PDZ1 Domain inhibitor peptide
Catalog No.:BCC5883
CAS No.:1315378-73-4
- Rocilinostat (ACY-1215)
Catalog No.:BCC2144
CAS No.:1316214-52-4
- ACY-241
Catalog No.:BCC6460
CAS No.:1316215-12-9
- OPC 21268
Catalog No.:BCC7812
CAS No.:131631-89-5
- Chalepensin
Catalog No.:BCN7334
CAS No.:13164-03-9
- Turmeronol A
Catalog No.:BCN6777
CAS No.:131651-37-1
- 8-(1-Chloro-2-hydroxy-3-methylbut-3-enyl)-7-methoxycoumarin
Catalog No.:BCN7058
CAS No.:131652-35-2
- Parsonsianine
Catalog No.:BCN2110
CAS No.:131683-36-8
- (R)-(-)-4-Benzyl-3-propionyl-2-oxazolidinone
Catalog No.:BCC8392
CAS No.:131685-53-5
- Arbidol HCl
Catalog No.:BCC3722
CAS No.:131707-23-8
- Urolignoside
Catalog No.:BCN6758
CAS No.:131723-83-6
- Flavopiridol hydrochloride
Catalog No.:BCC3925
CAS No.:131740-09-5
- DAU 5884 hydrochloride
Catalog No.:BCC7263
CAS No.:131780-48-8
Coumarins and antiplatelet aggregation constituents from Formosan Peucedanum japonicum.[Pubmed:8821432]
Phytochemistry. 1996 Feb;41(2):525-30.
Four new khellactone esters, (-)-trans-3'-acetyl-4'-senecioylkhellactone, (+-)-cis-3'-acetyl-4'-tigloylkhellactone, (+-)-cis-4-tigloylkhellactone, (+)-trans-4'-tigloylkhellactone, together with 14 known coumarins, isoimperatorin, psoralen, bergapten, xanthotoxol, cnidilin, (-)-selinidin, (-)-deltoin, (+)-Pteryxin, (+)-peucedanocoumarin III, xanthotoxin, imperatorin, (+)-marmesin, (+)-oxypeucedanin hydrate, (+)-peucedanol and three chromones, eugenin, (-)-hamaudol, (+)-visamminol, have been isolated from the root of Formosan Peucedanum japonicum. The structures of the new compounds were elucidated by spectral data. The identities of (+)-trans-3'-tigloyl-4'-acetylkhellactone, formerly reported as a new compound, and (+)-cis-3'-angeloyl-4'-acetyl-khellactone, with the known (+)-peucedanocoumarin III and (+)-Pteryxin, respectively, are discussed. Among the isolates, seven compounds, eugenin, (-)-selinidin, (+)-Pteryxin, imperatorin, bergapten, cnidilin and (+)-visamminol, show strong antiplatelet aggregation activity in vitro.
