IUPAC/Chemical Name
1,2-Benzenediol, 4-((2R,3R)-2,3-dihydro-3-(hydroxymethyl)-6-((1E)-3-hydroxy-1-propenyl)-1,4-benzodioxin-2-yl)-, rel-
InChi Key
NKYXNCKZTCGVJJ-ZHEVZCJESA-N
InChi Code
InChI=1S/C18H18O6/c19-7-1-2-11-3-6-15-16(8-11)23-17(10-20)18(24-15)12-4-5-13(21)14(22)9-12/h1-6,8-9,17-22H,7,10H2/b2-1+/t17-,18-/m1/s1
SMILES Code
OC1=CC=C([C@H]2OC3=CC=C(/C=C/CO)C=C3O[C@@H]2CO)C=C1O
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
2934.99.03.00
Preparing Stock Solutions
The following data is based on the
product
molecular weight
330.34
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: Fukuyama Y, Hasegawa T, Toda M, Kodama M, Okazaki H. Structures of americanol A and isoamericanol A having a neurotrophic property from the seeds of Phytolacca americana. Chem Pharm Bull (Tokyo). 1992 Jan;40(1):252-4. PubMed PMID: 1576680.
2: Galarraga Montes E, Amaro-Luis JM. Icosandrin, a novel peltogynoid from the fruits of Phytolacca icosandra (Phytolaccaceae). Nat Prod Res. 2016;30(1):89-94. doi: 10.1080/14786419.2015.1038537. Epub 2015 May 5. PubMed PMID: 25942389.
3: Waibel R, Benirschke G, Benirschke M, Achenbach H. Sesquineolignans and other constituents from the seeds of Joannesia princeps. Phytochemistry. 2003 Mar;62(5):805-11. PubMed PMID: 12620334.
4: Li X, Li L, Wang J, Wang T, Wang L. Two new lignans with antioxidative activities from Jatropha curcas. Nat Prod Res. 2014;28(22):1985-91. doi: 10.1080/14786419.2014.919284. Epub 2014 May 28. PubMed PMID: 24870973.
5: Etoh H, Murakami K, Yogoh T, Ishikawa H, Fukuyama Y, Tanaka H. Anti-oxidative compounds in barley tea. Biosci Biotechnol Biochem. 2004 Dec;68(12):2616-8. PubMed PMID: 15618635.
6: Kim KH, Moon E, Kim SY, Lee KR. Lignans from the tuber-barks of Colocasia antiquorum var. esculenta and their antimelanogenic Activity. J Agric Food Chem. 2010 Apr 28;58(8):4779-85. doi: 10.1021/jf100323q. PubMed PMID: 20359228.
7: Kamiya K, Tanaka Y, Endang H, Umar M, Satake T. Chemical constituents of Morinda citrifolia fruits inhibit copper-induced low-density lipoprotein oxidation. J Agric Food Chem. 2004 Sep 22;52(19):5843-8. PubMed PMID: 15366830.