Mogroside I A1;(Synonyms: 罗汉果苷 I A1;罗汉果甜苷 I A1;罗汉果甙 I A1;罗汉果甜甙 I A1) 纯度: 99.77%
Mogroside I A1 是一种三萜糖苷。Mogroside I A1 是一种非糖类甜味剂。Mogroside 比蔗糖更甜。Mogroside 具有抗氧化,抗糖尿病和抗癌活性。
Mogroside I A1 Chemical Structure
CAS No. : 88901-46-6
规格
价格
是否有货
数量
5 mg
¥5040
In-stock
10 mg
¥8570
In-stock
50 mg
;
询价
;
100 mg
;
询价
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Mogroside I A1 相关产品
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生物活性
Mogroside I A1 is a triterpenoid glycoside and a nonsugar sweetener. Mogrosides are sweeter than sucrose. Mogrosides exhibit antioxidant, antidiabetic and anticancer activities[1].
分子量
638.87
Formula
C36H62O9
CAS 号
88901-46-6
中文名称
罗汉果苷 I A1;罗汉果甜苷 I A1;罗汉果甙 I A1;罗汉果甜甙 I A1
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Itkin M, et al. The biosynthetic pathway of the nonsugar, high-intensity sweetener mogroside V from Siraitia grosvenorii.Proc Natl Acad Sci U S A. 2016 Nov 22;113(47):E7619-E7628.
Mogroside III 是一种三萜糖苷,是一种非糖类甜味剂。Mogroside 比蔗糖更甜。Mogroside 具有抗氧化,抗糖尿病和抗癌活性。
Mogroside III Chemical Structure
CAS No. : 130567-83-8
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价格
是否有货
数量
5 mg
¥2690
In-stock
10 mg
¥4570
In-stock
50 mg
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询价
;
100 mg
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;
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Mogroside III 相关产品
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生物活性
Mogroside III is a triterpenoid glycoside and a nonsugar sweetener. Mogrosides are sweeter than sucrose. Mogrosides exhibit antioxidant, antidiabetic and anticancer activities[1].
分子量
963.15
Formula
C48H82O19
CAS 号
130567-83-8
中文名称
罗汉果苷 III;罗汉果甜苷 III;罗汉果甙 III;罗汉果甜甙 III
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Itkin M, et al. The biosynthetic pathway of the nonsugar, high-intensity sweetener mogroside V from Siraitia grosvenorii.Proc Natl Acad Sci U S A. 2016 Nov 22;113(47):E7619-E7628.
Mogroside V 是一种三萜糖苷,是一种非糖类甜味剂。Mogroside V 比蔗糖甜近 300倍。Mogrosides 具有抗氧化,抗糖尿病和抗癌活性。
Mogroside V Chemical Structure
CAS No. : 88901-36-4
规格
价格
是否有货
数量
10;mM;*;1 mL in DMSO
¥1590
In-stock
5 mg
¥800
In-stock
10 mg
¥1120
In-stock
50 mg
¥3350
In-stock
100 mg
;
询价
;
200 mg
;
询价
;
* Please select Quantity before adding items.
Mogroside V 相关产品
bull;相关化合物库:
Natural Product Library Plus
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Traditional Chinese Medicine Monomer Library
生物活性
Mogroside V is a triterpenoid glycoside and a nonsugar sweetener. Mogroside V is nearly 300 times sweeter than sucrose. Mogrosides exhibit antioxidant, antidiabetic and anticancer activities. Mogrosides are sweeter than sucrose[1].
分子量
1287.43
Formula
C60H102O29
CAS 号
88901-36-4
中文名称
罗汉果苷 V;罗汉果甜苷 V;罗汉果甙 V;罗汉果甜甙 V
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Itkin M, et al. The biosynthetic pathway of the nonsugar, high-intensity sweetener mogroside V from Siraitia grosvenorii.Proc Natl Acad Sci U S A. 2016 Nov 22;113(47):E7619-E7628.
[1]. Itkin M, et al. The biosynthetic pathway of the nonsugar, high-intensity sweetener mogroside V from Siraitia grosvenorii.Proc Natl Acad Sci U S A. 2016 Nov 22;113(47):E7619-E7628.
Mogroside IV-A, a triterpenoid glycoside isolated from the extracts of Luo Han Guo, is a nonsugar sweetener. Mogrosides are sweeter than sucrose. Mogrosides exhibit antioxidant, antidiabetic and anticancer activities[1].
分子量
1125.29
Formula
C54H92O24
CAS 号
88901-41-1
中文名称
罗汉果苷 IV-A;罗汉果甜苷 IV-A;罗汉果甙 IV-A;罗汉果甜甙 IV-A
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Ukiya M, et al. Inhibitory effects of cucurbitane glycosides and other triterpenoids from the fruit of Momordica grosvenori on epstein-barr virus early antigen induced by tumor promoter 12-O-tetradecanoylphorbol-13-acetate. J Agric Food Chem. 2002 Nov 6;50(23):6710-5.
Mogroside IIA1 is a triterpenoid glycoside and a nonsugar sweetener. Mogrosides are sweeter than sucrose. Mogrosides exhibit antioxidant, antidiabetic and anticancer activities[1].
分子量
801.01
Formula
C42H72O14
CAS 号
88901-44-4
中文名称
罗汉果苷 IIA1;罗汉果甜苷 IIA1;罗汉果甙 IIA1;罗汉果甜甙 IIA1
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Itkin M, et al. The biosynthetic pathway of the nonsugar, high-intensity sweetener mogroside V from Siraitia grosvenorii.Proc Natl Acad Sci U S A. 2016 Nov 22;113(47):E7619-E7628.
Mogroside III-A1 is a triterpenoid glycoside and a nonsugar sweetener. Mogrosides are sweeter than sucrose. Mogrosides exhibit antioxidant, antidiabetic and anticancer activities[1].
分子量
963.15
Formula
C48H82O19
CAS 号
88901-42-2
中文名称
罗汉果苷 III-A1;罗汉果甜苷 III-A1;罗汉果甙 III-A1罗汉果甜甙 III-A1
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Itkin M, et al. The biosynthetic pathway of the nonsugar, high-intensity sweetener mogroside V from Siraitia grosvenorii.Proc Natl Acad Sci U S A. 2016 Nov 22;113(47):E7619-E7628.
Mogroside II-A2 is a triterpenoid glycoside and a nonsugar sweetener. Mogrosides are sweeter than sucrose. Mogrosides exhibit antioxidant, antidiabetic and anticancer activities[1].
分子量
801.01
Formula
C42H72O14
CAS 号
88901-45-5
中文名称
罗汉果苷 II-A2;罗汉果甜苷 II-A2;罗汉果甙 II-A2;罗汉果甜甙 II-A2
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Itkin M, et al. The biosynthetic pathway of the nonsugar, high-intensity sweetener mogroside V from Siraitia grosvenorii.Proc Natl Acad Sci U S A. 2016 Nov 22;113(47):E7619-E7628.
Siamenoside I is one of the mogrosides that has several kinds of bioactivities.
体内研究 (In Vivo)
In rat, the metabolic reactions of siamenoside I include deglycosylation, hydroxylation, dehydrogenation, deoxygenation, isomerization, and glycosylation. Siamenoside I and its metabolites are mainly distributed to the intestines, stomach, kidneys, and brain[1].
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
分子量
1125.29
Formula
C54H92O24
CAS 号
126105-12-2
中文名称
赛门苷 I;翅子罗汉果 I
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
-20deg;C, sealed storage, away from moisture and light
*In solvent : -80deg;C, 6 months; -20deg;C, 1 month (sealed storage, away from moisture and light)
溶解性数据
In Vitro:;
DMSO : 100 mg/mL (88.87 mM; Need ultrasonic)
配制储备液
浓度溶剂体积质量
1 mg
5 mg
10 mg
1 mM
0.8887 mL
4.4433 mL
8.8866 mL
5 mM
0.1777 mL
0.8887 mL
1.7773 mL
10 mM
0.0889 mL
0.4443 mL
0.8887 mL
*
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:
[1]. Yang XR, et al. Metabolites of Siamenoside I and Their Distributions in Rats. Molecules. 2016 Jan 30;21(2):176.
Animal Administration [1]
The animal experiment lasts six days. The whole urine and feces of days 1-2 are collected as blank urine and feces samples, respectively. On days 3-5, the rats of test group are orally administrated with siamenoside I [50 mg/kg body weight, in normal saline (NS) solution] at 9:00, and all 72-h urine and feces are collected as drug-containing urine and feces samples, respectively. The rats of blank group are orally administrated with the same volume of NS. On day 6 at 9:00, the test and the blank group are treated with siamenoside I and NS again, respectively. After 1 h, blood sample is collected into a vacuum tube with sodium citrate as anticoagulant from rat heart under anesthesia. Then, the organs (heart, liver, spleen, lung, kidneys, stomach, small intestine, brain) and skeletal muscles of rats are collected and washed with NS, separately. All samples are kept at −80°C before further pretreatment.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
参考文献
[1]. Yang XR, et al. Metabolites of Siamenoside I and Their Distributions in Rats. Molecules. 2016 Jan 30;21(2):176.