Salidroside
| Code | Size | Price |
|---|
| CDX-S0092-M025 | 25 mg | £169.00 |
Quantity:
| CDX-S0092-M100 | 100 mg | £487.00 |
Quantity:
| CDX-S0092-M500 | 500 mg | £1,915.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
+20°C
Documents
Further Information
Alternate Names/Synonyms:
Rhodioloside; 2-(4-Hydroxyphenyl)ethyl beta-D-glucopyranoside; p-Hydroxyphenethyl glucopyranoside
Appearance:
White to off-white powder.
CAS:
10338-51-9
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H319
InChi:
InChI=1S/C14H20O7/c15-7-10-11(17)12(18)13(19)14(21-10)20-6-5-8-1-3-9(16)4-2-8/h1-4,10-19H,5-7H2/t10-,11-,12+,13-,14-/m1/s1
InChiKey:
ILRCGYURZSFMEG-RKQHYHRCSA-N
Long Description:
Chemical. CAS: 10338-51-9. Formula: C14H20O7. MW: 300.3. Synthetic. 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.
MDL:
MFCD00210553
Molecular Formula:
C14H20O7
Molecular Weight:
300.3
Package Type:
Vial
Precautions:
P305, P351, P338
Product Description:
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.
Purity:
>98% (HPLC)
Signal word:
Warning
SMILES:
OC[C@H]1O[C@@H](OCCC2=CC=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O
Solubility Chemicals:
Soluble in DMSO (60mg/ml), water (60mg/ml) or ethanol (4mg/ml).
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at +4°C.
References
(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)
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