IUPAC/Chemical Name
1-Benzopyrylium, 3,5-bis(beta-D-glucopyranosyloxy)-7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-, chloride
InChi Key
NLSMPWTZYGSAEU-CYUNEVMDSA-N
InChi Code
InChI=1S/C28H32O16.ClH/c1-39-16-4-10(2-3-13(16)32)26-17(42-28-25(38)23(36)21(34)19(9-30)44-28)7-12-14(40-26)5-11(31)6-15(12)41-27-24(37)22(35)20(33)18(8-29)43-27;/h2-7,18-25,27-30,33-38H,8-9H2,1H3,(H-,31,32);1H/t18-,19-,20-,21-,22+,23+,24-,25-,27-,28-;/m1./s1
SMILES Code
COC1=CC(C2=C(O[C@H]3[C@@H]([C@H]([C@@H]([C@@H](CO)O3)O)O)O)C=C4C(C=C(O)C=C4O[C@H]5[C@@H]([C@H]([C@@H]([C@@H](CO)O5)O)O)O)=[O+]2)=CC=C1O.[Cl-]
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
Preparing Stock Solutions
The following data is based on the
product
molecular weight
661.01
Batch specific molecular weights may vary
from batch to batch
due to the degree of hydration, which will
affect the solvent
volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass |
1 mg |
5 mg |
10 mg |
1 mM |
1.15 mL |
5.76 mL |
11.51 mL |
5 mM |
0.23 mL |
1.15 mL |
2.3 mL |
10 mM |
0.12 mL |
0.58 mL |
1.15 mL |
50 mM |
0.02 mL |
0.12 mL |
0.23 mL |
1: Xiao J, Chen B, Wang Q, Yang L, Guo H. Paeonin extracted from potatoes protects gastric epithelial cells from H(2)O(2)-induced oxidative damage in vitro by PI3K/Akt-mediated Nrf2 signaling pathway. Sci Rep. 2018 Jul 18;8(1):10865. doi: 10.1038/s41598-018-28772-5. PubMed PMID: 30022028; PubMed Central PMCID: PMC6052145.
2: Li P, Zhang ZM, Li T, Zhang YB, Sze SC, Wang GC, Li YL, Ye WC. Monoterpene derivatives from the roots of Paeonia lactiflora and their anti-proliferative activity. Fitoterapia. 2014 Oct;98:124-9. doi: 10.1016/j.fitote.2014.07.017. Epub 2014 Jul 25. PubMed PMID: 25068201.
3: Zou L, Hu LF, Guo YD, Song Y, Fu Q. Lipoxygenase-inhibiting phenolic glycosides and monoterpene glycosides from Paeonia lactiflora. J Asian Nat Prod Res. 2015;17(8):808-12. doi: 10.1080/10286020.2015.1007960. Epub 2015 Mar 23. PubMed PMID: 25798791.
4: Wu CF. [A review on the pharmacology of Paeonia lactiflora and its chemical components]. Zhong Yao Tong Bao. 1985 Jun;10(6):43-5. Review. Chinese. PubMed PMID: 2934174.
5: Riaz N, Malik A, Rehman AU, Ahmed Z, Muhammad P, Nawaz SA, Siddiqui J, Choudhary MI. Lipoxygenase inhibiting and antioxidant oligostilbene and monoterpene galactoside from Paeonia emodi. Phytochemistry. 2004 Apr;65(8):1129-35. PubMed PMID: 15110694.
6: Riaz N, Anis I, Malik A, Ahmed Z, Aziz-ur-rehman, Muhammad P, Nawaz SA, Choudhary MI. Paeonins A and B, lipoxygenase inhibiting monoterpene galactosides from Paeonia emodi. Chem Pharm Bull (Tokyo). 2003 Mar;51(3):252-4. PubMed PMID: 12612406.