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Supelco

Bacoside A3

analytical standard

Sinonimo/i:

(3β,16β,23R)-16,23:16,30-Diepoxy-20-hydroxydammar-24-en-3-yl O-α-L-arabinofuranosyl-(1→2)-O-[β-D-glucopyranosyl-(1→3)]-β-D-glucopyranoside, Jujubogenin 3-O-[α-L-arabinofuranosyl-(1→2)-O-[β-D-glucopyranosyl-(1→3)]-β-D-glucopyranoside]

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About This Item

Formula empirica (notazione di Hill):
C47H76O18
Numero CAS:
157408-08-7
Peso molecolare:
929.10
Numero MDL:
MFCD07779137
Codice UNSPSC:
85151701
ID PubChem:
329758014
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Saggio

≥95% (HPLC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

food and beverages

Formato

neat

Stringa SMILE

C\C(C)=C\[C@H]1C[C@](C)(O)[C@@H]2[C@H]3CC[C@@H]4[C@@]5(C)CC[C@H](O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O[C@@H]7O[C@H](CO)[C@@H](O)[C@H](O)[C@H]7O)[C@H]6O[C@@H]8O[C@@H](CO)[C@H](O)[C@H]8O)C(C)(C)[C@@H]5CC[C@@]4(C)[C@@]39CO[C@@]2(C9)O1

InChI

1S/C47H76O18/c1-21(2)14-22-15-45(7,57)38-23-8-9-28-43(5)12-11-29(42(3,4)27(43)10-13-44(28,6)46(23)19-47(38,65-22)58-20-46)62-41-37(64-39-34(55)31(52)25(17-49)60-39)36(32(53)26(18-50)61-41)63-40-35(56)33(54)30(51)24(16-48)59-40/h14,22-41,48-57H,8-13,15-20H2,1-7H3/t22-,23+,24+,25-,26+,27-,28+,29-,30+,31-,32+,33-,34+,35+,36-,37+,38-,39-,40-,41-,43-,44+,45-,46-,47-/m0/s1
CDEVGTJBRPBOPH-INTDMYAHSA-N

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Descrizione generale

Bacoside A3 is a triterpenoid saponin and an important constituent of bacosides, a saponin mixture of Bacopa monniera.

Applicazioni

Bacoside A3 may be used as a reference standard in the determination of bacoside A3 in Bacopa monnieri (L.) Wettst. extract using reversed-phase high performance liquid chromatography (RP-HPLC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Certificati d'analisi (COA)

Lot/Batch Number
WXBF4533V
BCCK7697
BCCG2103
BCCD2192
BCCD1186

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Charinrat Tothiam et al.
Phytochemical analysis : PCA, 22(5), 385-391 (2011-03-18)
In Ayurvedic medicines, Bacopa monnieri (L.) Wettst. (brahmi) is known as a medicinal plant used for memory enhancement. Its active compounds are classified as pseudojujubogenin and jujubogenin glycosides. Owing to the lack of chromophore in the saponin glycoside structures, HPLC-UV-vis
Khalid Rauf et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 18(10), 836-842 (2011-03-08)
Opioids are extensively used for the management of both chronic malignant and non malignant pains. One major serious limitation associated with chronic use of opioids is the development of tolerance to its analgesic effect. The effect of Bacopa monnieri, a
S Rastogi et al.
Phytochemistry, 36(1), 133-137 (1994-05-01)
A new triterpenoid saponin, bacoside A3, a constituent of bacosides the saponin mixture of Bacopa monniera, was isolated and characterized. Its structure was established as 3-beta-[O-beta-D-glucopyranosyl(1-->3)-O- [alpha-L-arabinofuranosyl(1-->2) ]O-beta-D-glucopyranosyl)oxy]jujubogenin by chemical and spectral analyses. The cis-isomer of ebelin lactone was also
Sukanya Majumdar et al.
Plant cell reports, 31(10), 1899-1909 (2012-06-27)
Genetic transformation of the Indian medicinal plant, Bacopa monnieri, using a gene encoding cryptogein, a proteinaceous elicitor, via Ri and Ti plasmids, were established and induced bioproduction of bacopa saponins in crypt-transgenic plants were obtained. Transformed roots obtained with A.
R Pawar et al.
Planta medica, 67(8), 752-754 (2001-12-04)
The hydroalcoholic extract of the whole plant of Bacopa monniera Wettst. (Scrophulariaceae), exhibited an inhibitory effect on superoxide released from polymorphonuclear (PMN) cells in the nitroblue tetrazolium (NBT) assay. The major saponin bacoside A(3) was found to be responsible for
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