Icariside D2

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Icariside D2 

Icariside D2 可从Annona glabra 中分离得到,可抑制血管紧张素转换酶。Icariside 对HL-60 细胞的IC50 值为9.0 ± 1.0 μM。Icariside D2 可诱导凋亡。

Icariside D2

Icariside D2 Chemical Structure

CAS No. : 38954-02-8

规格 是否有货
5 mg 询价
10 mg 询价
25 mg 询价

* Please select Quantity before adding items.

生物活性

Icariside D2, isolated from Annona glabra fruit, inhibits angiotensin-converting enzyme. Icariside D2 shows significant cytotoxic activity on the HL-60 cell line with the IC50 value of 9.0 ± 1.0 μM. Icariside D2 induces apoptosis [1][2].

体外研究
(In Vitro)

Icariside D2 3 induces apoptosis via alteration of expression of apoptosis-related proteins and decreases phosphorylation of AKT in HL-60 cells[1].
Icariside D2 exhibits anti-inflammatory and anti-HIV activity[3].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

300.30

Formula

C14H20O7

CAS 号

38954-02-8

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]. Nguyen Thi Thu Hien, et al. Chemical Constituents of the Annona Glabra Fruit and Their Cytotoxic Activity. Pharm Biol. 2015;53(11):1602-7.

    [2]. Xue Liu, et al. Metabolic Engineering Escherichia coli for Efficient Production of Icariside D2. Biotechnol Biofuels. 2019 Nov 6;12:261.

    [3]. Jin-YuLi, et al. Three new acylated prenylflavonol glycosides from Epimedium koreanum. Phytochemistry Letters Volume 17, September 2016, Pages 206-212.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Icariside D2

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Icariside D2 

Icariside D2 可从Annona glabra 中分离得到,可抑制血管紧张素转换酶。Icariside 对HL-60 细胞的IC50 值为9.0 ± 1.0 μM。Icariside D2 可诱导凋亡。

Icariside D2

Icariside D2 Chemical Structure

CAS No. : 38954-02-8

规格 是否有货
5 mg 询价
10 mg 询价
25 mg 询价

* Please select Quantity before adding items.

生物活性

Icariside D2, isolated from Annona glabra fruit, inhibits angiotensin-converting enzyme. Icariside D2 shows significant cytotoxic activity on the HL-60 cell line with the IC50 value of 9.0 ± 1.0 μM. Icariside D2 induces apoptosis [1][2].

体外研究
(In Vitro)

Icariside D2 3 induces apoptosis via alteration of expression of apoptosis-related proteins and decreases phosphorylation of AKT in HL-60 cells[1].
Icariside D2 exhibits anti-inflammatory and anti-HIV activity[3].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

300.30

Formula

C14H20O7

CAS 号

38954-02-8

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]. Nguyen Thi Thu Hien, et al. Chemical Constituents of the Annona Glabra Fruit and Their Cytotoxic Activity. Pharm Biol. 2015;53(11):1602-7.

    [2]. Xue Liu, et al. Metabolic Engineering Escherichia coli for Efficient Production of Icariside D2. Biotechnol Biofuels. 2019 Nov 6;12:261.

    [3]. Jin-YuLi, et al. Three new acylated prenylflavonol glycosides from Epimedium koreanum. Phytochemistry Letters Volume 17, September 2016, Pages 206-212.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Icariside D2

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Icariside D2 

Icariside D2 可从Annona glabra 中分离得到,可抑制血管紧张素转换酶。Icariside 对HL-60 细胞的IC50 值为9.0 ± 1.0 μM。Icariside D2 可诱导凋亡。

Icariside D2

Icariside D2 Chemical Structure

CAS No. : 38954-02-8

规格 是否有货
5 mg 询价
10 mg 询价
25 mg 询价

* Please select Quantity before adding items.

生物活性

Icariside D2, isolated from Annona glabra fruit, inhibits angiotensin-converting enzyme. Icariside D2 shows significant cytotoxic activity on the HL-60 cell line with the IC50 value of 9.0 ± 1.0 μM. Icariside D2 induces apoptosis [1][2].

体外研究
(In Vitro)

Icariside D2 3 induces apoptosis via alteration of expression of apoptosis-related proteins and decreases phosphorylation of AKT in HL-60 cells[1].
Icariside D2 exhibits anti-inflammatory and anti-HIV activity[3].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

300.30

Formula

C14H20O7

CAS 号

38954-02-8

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]. Nguyen Thi Thu Hien, et al. Chemical Constituents of the Annona Glabra Fruit and Their Cytotoxic Activity. Pharm Biol. 2015;53(11):1602-7.

    [2]. Xue Liu, et al. Metabolic Engineering Escherichia coli for Efficient Production of Icariside D2. Biotechnol Biofuels. 2019 Nov 6;12:261.

    [3]. Jin-YuLi, et al. Three new acylated prenylflavonol glycosides from Epimedium koreanum. Phytochemistry Letters Volume 17, September 2016, Pages 206-212.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Icariside B1(Synonyms: 淫羊藿次甙B1;淫羊藿次甙 B1;淫羊藿次苷B1)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Icariside B1 (Synonyms: 淫羊藿次甙B1;淫羊藿次甙 B1;淫羊藿次苷B1)

Icariside B1 是一种从 Petasites tricholobus Franch 分离出来的降碳倍半萜类化合物,具有抗癌作用。

Icariside B1(Synonyms: 淫羊藿次甙B1;淫羊藿次甙 B1;淫羊藿次苷B1)

Icariside B1 Chemical Structure

CAS No. : 109062-00-2

规格 是否有货
5 mg 询价
10 mg 询价
25 mg 询价

* Please select Quantity before adding items.

生物活性

Icariside B1 is a megastigmane glycoside compound isolated from Petasites tricholobus Franch, with an anticancer effect[1][2].

分子量

386.44

Formula

C19H30O8

CAS 号

109062-00-2

中文名称

淫羊藿次甙B1;淫羊藿次甙 B1;淫羊藿次苷B1

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]. Yong Zhang, et al. Two new sulfated sesquiterpenoids from Petasites tricholobus. Yao Xue Xue Bao. 2014 Oct;49(10):1433-7.

    [2]. Nguyen Thi Thu Hien, et al. Chemical constituents of the Annona glabra fruit and their cytotoxic activity. Pharm Biol. 2015;53(11):1602-7.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Icariside B1(Synonyms: 淫羊藿次甙B1;淫羊藿次甙 B1;淫羊藿次苷B1)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Icariside B1 (Synonyms: 淫羊藿次甙B1;淫羊藿次甙 B1;淫羊藿次苷B1)

Icariside B1 是一种从 Petasites tricholobus Franch 分离出来的降碳倍半萜类化合物,具有抗癌作用。

Icariside B1(Synonyms: 淫羊藿次甙B1;淫羊藿次甙 B1;淫羊藿次苷B1)

Icariside B1 Chemical Structure

CAS No. : 109062-00-2

规格 是否有货
5 mg 询价
10 mg 询价
25 mg 询价

* Please select Quantity before adding items.

生物活性

Icariside B1 is a megastigmane glycoside compound isolated from Petasites tricholobus Franch, with an anticancer effect[1][2].

分子量

386.44

Formula

C19H30O8

CAS 号

109062-00-2

中文名称

淫羊藿次甙B1;淫羊藿次甙 B1;淫羊藿次苷B1

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]. Yong Zhang, et al. Two new sulfated sesquiterpenoids from Petasites tricholobus. Yao Xue Xue Bao. 2014 Oct;49(10):1433-7.

    [2]. Nguyen Thi Thu Hien, et al. Chemical constituents of the Annona glabra fruit and their cytotoxic activity. Pharm Biol. 2015;53(11):1602-7.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Icariside B1(Synonyms: 淫羊藿次甙B1;淫羊藿次甙 B1;淫羊藿次苷B1)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Icariside B1 (Synonyms: 淫羊藿次甙B1;淫羊藿次甙 B1;淫羊藿次苷B1)

Icariside B1 是一种从 Petasites tricholobus Franch 分离出来的降碳倍半萜类化合物,具有抗癌作用。

Icariside B1(Synonyms: 淫羊藿次甙B1;淫羊藿次甙 B1;淫羊藿次苷B1)

Icariside B1 Chemical Structure

CAS No. : 109062-00-2

规格 是否有货
5 mg 询价
10 mg 询价
25 mg 询价

* Please select Quantity before adding items.

生物活性

Icariside B1 is a megastigmane glycoside compound isolated from Petasites tricholobus Franch, with an anticancer effect[1][2].

分子量

386.44

Formula

C19H30O8

CAS 号

109062-00-2

中文名称

淫羊藿次甙B1;淫羊藿次甙 B1;淫羊藿次苷B1

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]. Yong Zhang, et al. Two new sulfated sesquiterpenoids from Petasites tricholobus. Yao Xue Xue Bao. 2014 Oct;49(10):1433-7.

    [2]. Nguyen Thi Thu Hien, et al. Chemical constituents of the Annona glabra fruit and their cytotoxic activity. Pharm Biol. 2015;53(11):1602-7.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Icariside I hydrate对照品

Icariside I hydrate对照品

  【编号】:SPR03205

  【产品名称】:Icariside I hydrate对照品

  【规格】:10mg

  【用途】:

  Icariside I hydrate对照品

  编号:SPR03205
  英文名称:Icariside I hydrate
  CAS No.:128988-55-6
  分 子 式:C27H32O12
  分 子 量:548.541
  类别:上海金畔生物科技有限公司,天然提取物
  作为标准品,对照品或者供研究用,不能直接用于人体。