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Rebaudioside G Sale

(Synonyms: 甜菊糖G苷) 目录号 : GC37077

Rebaudioside G 是从甜叶菊叶中分离出的次要成分,用于甜味剂研究。

Rebaudioside G Chemical Structure

Cas No.:127345-21-5

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1mg
¥780.00
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5mg
¥2,800.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

Rebaudioside G is the minor constituent isolated from the leaves of Stevia rebaudiana Bertoni, used for sweeteners research[1].

[1]. Ibrahim MA, et al. Rebaudiosides R and S, Minor Diterpene Glycosides from the Leaves of Stevia rebaudiana. J Nat Prod. 2016 May 27;79(5):1468-72.

Chemical Properties

Cas No. 127345-21-5 SDF
别名 甜菊糖G苷
Canonical SMILES C[C@]([C@]1([H])CC2)(CCC[C@@]1(C)C(O[C@@H]([C@@H]([C@@H](O)[C@@H]3O)O)O[C@@H]3CO)=O)[C@@]4([H])[C@]2(CC5=C)C[C@@]5(O[C@@](O[C@H](CO)[C@@H](O)[C@@H]6O[C@]([C@@H]([C@@H](O)[C@@H]7O)O)([H])O[C@@H]7CO)([H])[C@@H]6O)CC4
分子式 C38H60O18 分子量 804.87
溶解度 Soluble in DMSO 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 1.2424 mL 6.2122 mL 12.4244 mL
5 mM 0.2485 mL 1.2424 mL 2.4849 mL
10 mM 0.1242 mL 0.6212 mL 1.2424 mL
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Research Update

Rebaudiosides R and S, Minor Diterpene Glycosides from the Leaves of Stevia rebaudiana

J Nat Prod 2016 May 27;79(5):1468-72.PMID:27119206DOI:10.1021/acs.jnatprod.6b00048.

Two new diterpene glycosides have been isolated from a commercial extract of the leaves of Stevia rebaudiana. Compound 1 was shown to be 13-[(2-O-β-d-glucopyranosyl-3-O-β-d-glucopyranosyl-β-d-xylopyranosyl)oxy]ent-kaur-16-en-19-oic acid β-d-glucopyranosyl ester (rebaudioside R), while compound 2 was determined to be 13-[(2-O-α-d-glucopyranosyl-β-d-glucopyranosyl)oxy]ent-kaur-16-en-19-oic acid 2-O-α-l-rhamnopyranosyl-β-d-glucopyranosyl ester (rebaudioside S). Six additional known compounds were identified, dulcoside B, 13-[(2-O-β-d-xylopyranosyl-β-d-glucopyranosyl)oxy]ent-kaur-16-en-19-oic acid β-d-glucopyranosyl ester, eugenol diglucoside, Rebaudioside G, 13-[(2-O-6-deoxy-β-d-glucopyranosyl-3-O-β-d-glucopyranosyl-β-d-glucopyranosyl)oxy]ent-kaur-16-en-19-oic acid β-d-glucopyranosyl ester, and rebaudioside D (3), respectively. The structures of 1 and 2 were determined based on comprehensive 1D and 2D NMR (COSY, HSQC, and HMBC) studies. A high-quality crystal of compound 3 allowed confirmation of its structure by X-ray diffraction.