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

MedKoo CAT#: 461710

CAS#: 59527-84-3

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

Chemical Structure

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 not in stock, which may be available by custom synthesis. For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge). Quote less than 1g will not be provided. To request quote, please email to sales or click below button.
Note: Price will be listed if it is available in the future.

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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 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

Preparing Stock Solutions

The following data is based on the product molecular weight 1251.41 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

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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.