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MedKoo Cat#: 145965 | Name: Actinidioionoside

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Actinidioionoside is a plant growth regulator primarily used to enhance growth and improve stress tolerance in crops. It works by modulating plant hormone levels, particularly auxins, which are involved in processes like root development and cell elongation. This regulation helps to improve nutrient absorption, support stronger plant structures, and increase resilience to environmental stresses such as drought or disease. Actinidioionoside is commonly applied in agriculture to optimize the growth of various crops, leading to higher yields and improved quality.

Chemical Structure

Actinidioionoside
Actinidioionoside
CAS#540528-05-0

Theoretical Analysis

MedKoo Cat#: 145965

Name: Actinidioionoside

CAS#: 540528-05-0

Chemical Formula: C19H34O9

Exact Mass: 406.2200

Molecular Weight: 406.47

Elemental Analysis: C, 56.14; H, 8.43; O, 35.42

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
Actinidioionoside;
IUPAC/Chemical Name
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-(((R,E)-4-((1R,2R,4S)-1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)but-3-en-2-yl)oxy)tetrahydro-2H-pyran-3,4,5-triol
InChi Key
XZRJEYQBLXDNNU-UWAGUHGBSA-N
InChi Code
1S/C19H34O9/c1-10(27-16-15(24)14(23)13(22)12(9-20)28-16)5-6-19(26)17(2,3)7-11(21)8-18(19,4)25/h5-6,10-16,20-26H,7-9H2,1-4H3/b6-5+/t10-,11+,12-,13-,14+,15-,16-,18-,19-/m1/s1
SMILES Code
C[C@@H](O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)\C=C\[C@@]2(O)C(C)(C)C[C@H](O)C[C@@]2(C)O
Appearance
To be determined
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
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
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
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 406.47 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.

Recalculate based on batch purity %
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: Samy MN, Sugimoto S, Matsunami K, Otsuka H, Kamel MS. Taxiphyllin 6'-O-gallate, actinidioionoside 6'-O-gallate and myricetrin 2″-O-sulfate from the leaves of Syzygium samarangense and their biological activities. Chem Pharm Bull (Tokyo). 2014;62(10):1013-8. doi: 10.1248/cpb.c14-00352. Erratum in: Chem Pharm Bull (Tokyo). 2014;62(11):1151. Mamdouh, Nabil Samy [corrected to Samy, Mamdouh Nabil]. PMID: 25273060. 2: Otsuka H, Hirata E, Shinzato T, Takeda Y. Stereochemistry of megastigmane glucosides from Glochidion zeylanicum and Alangium premnifolium. Phytochemistry. 2003 Mar;62(5):763-8. doi: 10.1016/s0031-9422(02)00614-3. PMID: 12620329. 3: Samy MN, Hamed AN, Sugimoto S, Otsuka H, Kamel MS, Matsunami K. Officinalioside, a new lignan glucoside from Borago officinalis L. Nat Prod Res. 2016;30(8):967-72. doi: 10.1080/14786419.2015.1088540. Epub 2015 Sep 18. PMID: 26382913. 4: Liu Y, Liu S, Xu ZP, Wang SY, Jiang YK, Guan W, Pan J, Kuang HX, Yang BY. Terpenoid compounds from the fruits of Solanum virginianum. Z Naturforsch C J Biosci. 2023 Sep 27;78(11-12):415-420. doi: 10.1515/znc-2023-0028. PMID: 37748096. 5: Schwindl S, Kraus B, Heilmann J. Phytochemical study of Juglans regia L. leaves. Phytochemistry. 2017 Dec;144:58-70. doi: 10.1016/j.phytochem.2017.08.012. Epub 2017 Sep 8. PMID: 28888783.