MedKoo Cat#: 461710 | Name: Sakurasosaponin

Description:

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

Sakurasosaponin is a compound isolated from the plant J. flammea and has been identified to have antifungal effects.

Chemical Structure

Sakurasosaponin
Sakurasosaponin
CAS#59527-84-3

Theoretical Analysis

MedKoo Cat#: 461710

Name: Sakurasosaponin

CAS#: 59527-84-3

Chemical Formula: C60H98O27

Exact Mass: 1250.6295

Molecular Weight: 1251.41

Elemental Analysis: C, 57.59; H, 7.89; O, 34.52

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 #
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Synonym
Sakurasosaponin;
IUPAC/Chemical Name
(2S,3S,4S,5R,6R)-3-(((2S,3R,4S,5R,6R)-3-(((2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4-hydroxy-6-(((3S,6aR,6bS,8R,12bS,14bR)-8-hydroxy-4,4,6a,6b,11,11,14b-heptamethyloctadecahydro-1H,9H-12b,8a-(epoxymethano)picen-3-yl)oxy)-5-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-carboxylic acid
InChi Key
XHQPPRZQWSUZJV-MEXQKDRRSA-N
InChi Code
InChI=1S/C60H98O27/c1-23-32(64)36(68)40(72)49(78-23)84-44-38(70)33(65)24(2)79-51(44)86-45-39(71)35(67)26(21-62)81-52(45)83-43-42(74)46(85-50-41(73)37(69)34(66)25(20-61)80-50)53(87-47(43)48(75)76)82-31-12-13-56(7)27(55(31,5)6)10-14-57(8)28(56)11-15-60-29-18-54(3,4)16-17-59(29,22-77-60)30(63)19-58(57,60)9/h23-47,49-53,61-74H,10-22H2,1-9H3,(H,75,76)/t23-,24-,25+,26+,27?,28?,29?,30+,31-,32-,33-,34+,35-,36+,37-,38+,39-,40+,41+,42-,43-,44+,45+,46+,47-,49-,50-,51-,52-,53+,56-,57+,58-,59?,60-/m0/s1
SMILES Code
C[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O[C@@H]2[C@H](O)[C@@H](O)[C@H](C)O[C@H]2O[C@@H]3[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]3O[C@H]4[C@H](O)[C@@H](O[C@H]5[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O5)[C@H](O[C@H]6CC[C@]7(C)C8CC[C@@]9%10C%11CC(C)(C)CCC%11([C@H](O)C[C@@]%10(C)[C@]8(C)CCC7C6(C)C)CO9)O[C@@H]4C(O)=O)O1
Appearance
Solid powder
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
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 1,251.41 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: Vinh LB, Nguyet NTM, Yang SY, Kim JH, Thanh NV, Cuong NX, Nam NH, Minh CV, Hwang I, Kim YH. Cytotoxic triterpene saponins from the mangrove Aegiceras corniculatum. Nat Prod Res. 2017 Nov 16:1-7. doi: 10.1080/14786419.2017.1402320. [Epub ahead of print] PubMed PMID: 29143535. 2: García-Sosa K, Sánchez-Medina A, Álvarez SL, Zacchino S, Veitch NC, Simá-Polanco P, Peña-Rodriguez LM. Antifungal activity of sakurasosaponin from the root extract of Jacquinia flammea. Nat Prod Res. 2011 Jul;25(12):1185-9. doi: 10.1080/14786419.2010.511215. PubMed PMID: 21740284. 3: Sánchez-Medina A, Peña-Rodríguez LM, May-Pat F, Karagianis G, Waterman PG, Mallet AI, Habtemariam S. Identification of sakurasosaponin as a cytotoxic principle from Jacquinia flammea. Nat Prod Commun. 2010 Mar;5(3):365-8. PubMed PMID: 20420308.