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Chemodex
Salidroside
Product Details | |
---|---|
Synonyms | Rhodioloside; 2-(4-Hydroxyphenyl)ethyl β-D-glucopyranoside; p-Hydroxyphenethyl glucopyranoside |
Product Type | Chemical |
Properties | |
Formula | C14H20O7 |
MW | 300.30 |
CAS | 10338-51-9 |
Source/Host Chemicals | Synthetic. |
Purity Chemicals | ≥98% (HPLC) |
Appearance | White to off-white powder. |
Solubility | Soluble in DMSO (60mg/ml), water (60mg/ml) or ethanol (4mg/ml). |
Identity | Determined by NMR. |
Declaration | Manufactured by Chemodex. |
Other Product Data |
Click here for Original Manufacturer Product Datasheet |
InChi Key | ILRCGYURZSFMEG-RKQHYHRCSA-N |
Smiles | OC[C@H]1O[C@@H](OCCC2=CC=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O |
Shipping and Handling | |
Shipping | AMBIENT |
Short Term Storage | +20°C |
Long Term Storage | +4°C |
Handling Advice |
Keep cool and dry. Protect from light and moisture. |
Use/Stability | Stable for at least 2 years after receipt when stored at +4°C. |
Documents | |
MSDS | Download PDF |
Product Specification Sheet | |
Datasheet | Download PDF |
Glycoside isolated from plants, most commonly from members of the genus Rhodiola, with many biological activities. Shown to have neuroprotective, antioxidant, antiviral, antidepressant, cardioprotective, anti-inflammatory and anticancer activity. Ameliorates insulin resistance.
(1) P. Yu, et al.; Chem. Biodivers. 4, 508 (2007) | (2) H. Wang, et al.; Phytomedicine 16, 146 (2009) | (3) X. Hu, et al.; BBRC 398, 62 (2010) | (4) L. Zhang, et al.; Neurochem. Int. 57, 547 (2010) | (5) Y. Guo, et al.; Chem. Pharm. Bull. 58, 1327 (2010) | (6) Y. Tang, et al.; Br. J. Pharmacol. 171, 2440 (2014) | (7) S.J. Yang, et al.; Pharmacol. Biochem. Behav. 124, 451 (2014) | (8) T. Zheng, et al.; Br. J. Pharmacol. 172, 3284 (2015) | (9) G. Zhao, et al.; Oncol. Rep. 33, 2553 (2015) | (10) S.S. Xing, et al.; Vascul. Pharmacol. 72, 141 (2015) | (11) L. Zhu, et al.; Apoptosis 20, 1433 (2015)