Regaloside D(Synonyms: 王百合苷D)

天然产物 糖类和糖苷 Saccharides and Glycosides

Regaloside D;(Synonyms: 王百合苷D)

Regaloside D 是一种苯丙素,分离于Lilium Longiflorum

Regaloside D(Synonyms: 王百合苷D)

Regaloside D Chemical Structure

CAS No. : 120601-66-3

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生物活性

Regaloside D is a phenylpropanoid isolated from Lilium Longiflorum[1].

分子量

400.38

Formula

C18H24O10

CAS 号

120601-66-3

中文名称

王百合苷D

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Kim BR, et al. Purification of Phenylpropanoids from the Scaly Bulbs of Lilium Longiflorum by CPC and Determination of Their DPP-IV Inhibitory Potentials. ACS Omega. 2020;5(8):4050-4057. Published 2020 Feb 20.

Regaloside B(Synonyms: 王百合苷 B)

天然产物 糖类和糖苷 Saccharides and Glycosides

Regaloside B;(Synonyms: 王百合苷 B)

Regaloside B 是一种从 Lilium longiflorum 中分离出来的苯丙烷。Regaloside B 可以抑制 iNOSCOX-2 的表达,具有抗炎活性。

Regaloside B(Synonyms: 王百合苷 B)

Regaloside B Chemical Structure

CAS No. : 114420-67-6

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生物活性

Regaloside B is a phenylpropanoid isolated from Lilium longiflorum. Regaloside B can inhibit the expression of iNOS and COX-2. Regaloside B has anti-inflammatory activity[1][2].

分子量

442.41

Formula

C20H26O11

CAS 号

114420-67-6

中文名称

王百合苷 B

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Thi NN, et, al. Phenylpropanoids from Lilium Asiatic hybrid flowers and their anti-inflammatory activities. Applied Biological Chemistry. 2017; 60: 527–533.

    [2]. Kim BR, et, al. Purification of Phenylpropanoids from the Scaly Bulbs of Lilium Longiflorum by CPC and Determination of Their DPP-IV Inhibitory Potentials. ACS Omega. 2020 Feb 20; 5(8): 4050-4057.

Regaloside H(Synonyms: 王百合苷H)

天然产物 糖类和糖苷 Saccharides and Glycosides

Regaloside H;(Synonyms: 王百合苷H)

Regaloside H 是一种苯丙酸甘油糖苷,是糖异生抑制剂。Regaloside H 可减少大鼠肝癌细胞中葡萄糖的生成。

Regaloside H(Synonyms: 王百合苷H)

Regaloside H Chemical Structure

CAS No. : 126239-77-8

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生物活性

Regaloside H, a phenylpropanoid glycerol glucoside, is a gluconeogenesis inhibitor. Regaloside H can reduce glucose production in Hepatocytes[1].

体外研究
(In Vitro)

Regaloside H (10 μM) suppresses the glucose production by 36.8% in H4IIE rat hepatoma cells[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

400.38

Formula

C18H24O10

CAS 号

126239-77-8

中文名称

王百合苷H

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Murray AF, et, al. Phenylpropanoid Glycerol Glucosides Attenuate Glucose Production in Hepatocytes. ACS Omega. 2019 Jun 19;4(6):10670-10676.

Regaloside A(Synonyms: 王百合苷A)

天然产物 糖类和糖苷 Saccharides and Glycosides

Regaloside A;(Synonyms: 王百合苷A)

Regaloside A 是一种苯丙烷,在 160 ppm 时显示出 58.0% 的显着 DPPH 自由基清除活性。Regaloside A 具有抗炎活性。

Regaloside A(Synonyms: 王百合苷A)

Regaloside A Chemical Structure

CAS No. : 114420-66-5

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生物活性

Regaloside A, a phenylpropanoid, shows significant DPPH radical scavenging activity of 58.0% at 160 ppm. Regaloside A has anti-inflammatory activity[1].

IC50 Target[1]

p65

;

体外研究
(In Vitro)

Regaloside A (50 μg/mL; 2 hours) inhibits the expression of iNOS to 70.3 decreasing COX-2 expression to 131.6 in Raw 264.7 cells treated with LPS (1 μg/ml; pretreatment for 15 min). Regaloside A decreases the ratio of p-p65/p-65 to 40.7[1].
Regaloside A (50 μg/mL; pretreatment for 2 hours) decreases the expression of VCAM-1 to 48.6 in HASMCs with TNF-a (10 ng/ml; for 12 h)[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

400.38

Formula

C18H24O10

CAS 号

114420-66-5

中文名称

王百合苷A;岷江百合苷A

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Nhan Nguyen Thi, et al. Phenylpropanoids from Lilium Asiatic hybrid flowers and their anti-inflammatory activities. Appl Biol Chem (2017) 60(5):527–533.