Propargyl-PEG12-acid

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。

Propargyl-PEG12-acid 

Propargyl-PEG12-acid 是一种 PROTAC linker,属于 PEG 类。可用于合成 PROTAC 分子。

Propargyl-PEG12-acid

Propargyl-PEG12-acid Chemical Structure

规格 是否有货
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生物活性

Propargyl-PEG12-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].

IC50 & Target

PEGs

 

体外研究
(In Vitro)

PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins[1].

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

分子量

612.70

Formula

C28H52O14

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]. Nalawansha DA, et al. PROTACs: An Emerging Therapeutic Modality in Precision Medicine. Cell Chem Biol. 2020;27(8):998-1003.

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Propargyl-PEG11-acid

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。

Propargyl-PEG11-acid 

Propargyl-PEG11-acid 是一种 PROTAC linker,属于 PEG 类。可用于合成 PROTAC 分子。

Propargyl-PEG11-acid

Propargyl-PEG11-acid Chemical Structure

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

生物活性

Propargyl-PEG11-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].

IC50 & Target

PEGs

 

体外研究
(In Vitro)

PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins[1].

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

分子量

568.65

Formula

C26H48O13

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]. Nalawansha DA, et al. PROTACs: An Emerging Therapeutic Modality in Precision Medicine. Cell Chem Biol. 2020;27(8):998-1002.

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

Propargyl-PEG11-acid

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。

Propargyl-PEG11-acid 

Propargyl-PEG11-acid 是一种 PROTAC linker,属于 PEG 类。可用于合成 PROTAC 分子。

Propargyl-PEG11-acid

Propargyl-PEG11-acid Chemical Structure

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

生物活性

Propargyl-PEG11-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].

IC50 & Target

PEGs

 

体外研究
(In Vitro)

PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins[1].

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

568.65

Formula

C26H48O13

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]. Nalawansha DA, et al. PROTACs: An Emerging Therapeutic Modality in Precision Medicine. Cell Chem Biol. 2020;27(8):998-1002.

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

Propargyl-PEG12-acid

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。

Propargyl-PEG12-acid 

Propargyl-PEG12-acid 是一种 PROTAC linker,属于 PEG 类。可用于合成 PROTAC 分子。

Propargyl-PEG12-acid

Propargyl-PEG12-acid Chemical Structure

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

生物活性

Propargyl-PEG12-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].

IC50 & Target

PEGs

 

体外研究
(In Vitro)

PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins[1].

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

分子量

612.70

Formula

C28H52O14

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]. Nalawansha DA, et al. PROTACs: An Emerging Therapeutic Modality in Precision Medicine. Cell Chem Biol. 2020;27(8):998-1003.

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

Propargyl-PEG12-acid

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。

Propargyl-PEG12-acid 

Propargyl-PEG12-acid 是一种 PROTAC linker,属于 PEG 类。可用于合成 PROTAC 分子。

Propargyl-PEG12-acid

Propargyl-PEG12-acid Chemical Structure

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

生物活性

Propargyl-PEG12-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].

IC50 & Target

PEGs

 

体外研究
(In Vitro)

PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins[1].

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

612.70

Formula

C28H52O14

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]. Nalawansha DA, et al. PROTACs: An Emerging Therapeutic Modality in Precision Medicine. Cell Chem Biol. 2020;27(8):998-1003.

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

Pygenic acid A(Synonyms: 脓毒酸A)

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。

Pygenic acid A (Synonyms: 脓毒酸A)

Pygenic acid A 是一种天然化合物,存在 Prunella vulgaris 中。Pygenic acid A 能诱导转移性乳腺癌细胞凋亡 (apoptosis)。Pygenic acid A 可用于糖尿病、炎症和癌症的研究。

Pygenic acid A(Synonyms: 脓毒酸A)

Pygenic acid A Chemical Structure

CAS No. : 52213-27-1

规格 是否有货
5 mg 询价
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25 mg 询价

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生物活性

Pygenic acid A is a natural compound that can be found in Prunella vulgaris. Pygenic acid A induces apoptosis in metastatic breast cancer cells. Pygenic acid A can be used for the research of diabetes, inflammatory diseases, and cancers[1].

体外研究
(In Vitro)

Pygenic acid A sensitizes metastatic breast cancer cells to anoikis via multiple pathways, such as inhibition of pro-survival pathways and activation of ER stress and autophagy, leading to the inhibition of metastasis[1].

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

分子量

472.70

Formula

C30H48O4

CAS 号

52213-27-1

中文名称

脓毒酸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]. Ga-Eun Lim, et al. Pygenic Acid A (PA) Sensitizes Metastatic Breast Cancer Cells to Anoikis and Inhibits Metastasis In Vivo. Int J Mol Sci. 2020 Nov; 21(22): 8444.

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

Pygenic acid A(Synonyms: 脓毒酸A)

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。

Pygenic acid A (Synonyms: 脓毒酸A)

Pygenic acid A 是一种天然化合物,存在 Prunella vulgaris 中。Pygenic acid A 能诱导转移性乳腺癌细胞凋亡 (apoptosis)。Pygenic acid A 可用于糖尿病、炎症和癌症的研究。

Pygenic acid A(Synonyms: 脓毒酸A)

Pygenic acid A Chemical Structure

CAS No. : 52213-27-1

规格 是否有货
5 mg 询价
10 mg 询价
25 mg 询价

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生物活性

Pygenic acid A is a natural compound that can be found in Prunella vulgaris. Pygenic acid A induces apoptosis in metastatic breast cancer cells. Pygenic acid A can be used for the research of diabetes, inflammatory diseases, and cancers[1].

体外研究
(In Vitro)

Pygenic acid A sensitizes metastatic breast cancer cells to anoikis via multiple pathways, such as inhibition of pro-survival pathways and activation of ER stress and autophagy, leading to the inhibition of metastasis[1].

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

分子量

472.70

Formula

C30H48O4

CAS 号

52213-27-1

中文名称

脓毒酸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]. Ga-Eun Lim, et al. Pygenic Acid A (PA) Sensitizes Metastatic Breast Cancer Cells to Anoikis and Inhibits Metastasis In Vivo. Int J Mol Sci. 2020 Nov; 21(22): 8444.

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

Pygenic acid A(Synonyms: 脓毒酸A)

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。

Pygenic acid A (Synonyms: 脓毒酸A)

Pygenic acid A 是一种天然化合物,存在 Prunella vulgaris 中。Pygenic acid A 能诱导转移性乳腺癌细胞凋亡 (apoptosis)。Pygenic acid A 可用于糖尿病、炎症和癌症的研究。

Pygenic acid A(Synonyms: 脓毒酸A)

Pygenic acid A Chemical Structure

CAS No. : 52213-27-1

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

Pygenic acid A is a natural compound that can be found in Prunella vulgaris. Pygenic acid A induces apoptosis in metastatic breast cancer cells. Pygenic acid A can be used for the research of diabetes, inflammatory diseases, and cancers[1].

体外研究
(In Vitro)

Pygenic acid A sensitizes metastatic breast cancer cells to anoikis via multiple pathways, such as inhibition of pro-survival pathways and activation of ER stress and autophagy, leading to the inhibition of metastasis[1].

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

472.70

Formula

C30H48O4

CAS 号

52213-27-1

中文名称

脓毒酸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]. Ga-Eun Lim, et al. Pygenic Acid A (PA) Sensitizes Metastatic Breast Cancer Cells to Anoikis and Inhibits Metastasis In Vivo. Int J Mol Sci. 2020 Nov; 21(22): 8444.

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

3-Epidehydropachymic acid

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。

3-Epidehydropachymic acid 

3-Epidehydropachymic acid,一种羊毛甾烷三萜,对人急性单核细胞白血病细胞系 THP-1 具有毒性作用 (IC50=52.51 μM)。

3-Epidehydropachymic acid

3-Epidehydropachymic acid Chemical Structure

CAS No. : 168293-15-0

规格 是否有货
5 mg 询价
10 mg 询价
25 mg 询价

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生物活性

3-Epidehydropachymic acid, a lanostane triterpenoid, shows totoxicity effect against human acute monocytic leukemia cell line THP-1 (IC50=52.51 μM)[1].

分子量

526.75

Formula

C33H50O5

CAS 号

168293-15-0

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]. Tohtahon Z, et al. Cytotoxic lanostane triterpenoids from the fruiting bodies of Piptoporus betulinus. Phytochemistry. 2017;143:98-103

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5-Feruloylquinic acid

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。

5-Feruloylquinic acid  纯度: ≥99.0%

5-Feruloylquinic acid (5-FQA) 具有抗氧化作用和酪氨酸酶抑制活性。

5-Feruloylquinic acid

5-Feruloylquinic acid Chemical Structure

CAS No. : 40242-06-6

规格 价格 是否有货 数量
1 mg ¥2000 In-stock
5 mg ¥4500 In-stock
10 mg ¥7200 In-stock
50 mg   询价  
100 mg   询价  

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5-Feruloylquinic acid 相关产品

相关化合物库:

  • Natural Product Library Plus
  • Bioactive Compound Library Plus
  • Metabolism/Protease Compound Library
  • Natural Product Library
  • Anti-Cancer Compound Library
  • Phenols Library

生物活性

5-Feruloylquinic acid (5-FQA) possesses antioxidative effects and tyrosinase inhibitory activities[1].

分子量

368.34

Formula

C17H20O9

CAS 号

40242-06-6

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20°C, sealed storage, away from moisture and light

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)

参考文献
  • [1]. Kazuya Iwai, et al. In vitro antioxidative effects and tyrosinase inhibitory activities of seven hydroxycinnamoyl derivatives in green coffee beans. J Agric Food Chem. 2004 Jul 28;52(15):4893-8.

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

5-O-Caffeoylshikimic acid

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。

5-O-Caffeoylshikimic acid 

5-O-Caffeoylshikimic acid 可用于非小细胞肺癌的研究。

5-O-Caffeoylshikimic acid

5-O-Caffeoylshikimic acid Chemical Structure

CAS No. : 73263-62-4

规格 是否有货
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生物活性

5-O-Caffeoylshikimic acid can be used in the study for NSCLC[1][2].

体外研究
(In Vitro)

5-O-cafeoylshikimic acid likely to be a key player to modulate NSCLC drug resistance in the near future[2].

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

分子量

336.29

Formula

C16H16O8

CAS 号

73263-62-4

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]. Oleksandr Shulha, et al. Lignans and sesquiterpene lactones from Hypochaeris radicata subsp. neapolitana (Asteraceae, Cichorieae). Phytochemistry. 2019 Sep;165:112047.

    [2]. https://pubmed.ncbi.nlm.nih.gov/31203102

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Ganoderenic acid B(Synonyms: 灵芝烯酸 B)

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。

Ganoderenic acid B (Synonyms: 灵芝烯酸 B)

Ganoderenic acid B 是从 Ganoderma lucidum 中分离的一种三萜类化合物。Ganoderenic acid B 可有效逆转 ABCB1 介导的HepG2/ADM 细胞对 Doxorubicin 的耐药性。

Ganoderenic acid B(Synonyms: 灵芝烯酸 B)

Ganoderenic acid B Chemical Structure

CAS No. : 100665-41-6

规格 是否有货
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生物活性

Ganoderenic acid B is a lanostane-type triterpene isolated from Ganoderma lucidum. Ganoderenic acid B exhibits potent reversal effect on ABCB1-mediated multidrug resistance of HepG2/ADM cells to Doxorubicin[1].

分子量

514.65

Formula

C30H42O7

CAS 号

100665-41-6

中文名称

灵芝烯酸 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]. Liu DL, et al. Ganoderma lucidum derived ganoderenic acid B reverses ABCB1-mediated multidrug resistance in HepG2/ADM cells. Int J Oncol. 2015 May;46(5):2029-38.

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

3-Epidehydropachymic acid

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。

3-Epidehydropachymic acid 

3-Epidehydropachymic acid,一种羊毛甾烷三萜,对人急性单核细胞白血病细胞系 THP-1 具有毒性作用 (IC50=52.51 μM)。

3-Epidehydropachymic acid

3-Epidehydropachymic acid Chemical Structure

CAS No. : 168293-15-0

规格 是否有货
5 mg 询价
10 mg 询价
25 mg 询价

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生物活性

3-Epidehydropachymic acid, a lanostane triterpenoid, shows totoxicity effect against human acute monocytic leukemia cell line THP-1 (IC50=52.51 μM)[1].

分子量

526.75

Formula

C33H50O5

CAS 号

168293-15-0

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]. Tohtahon Z, et al. Cytotoxic lanostane triterpenoids from the fruiting bodies of Piptoporus betulinus. Phytochemistry. 2017;143:98-103

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

3-Epidehydropachymic acid

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。

3-Epidehydropachymic acid 

3-Epidehydropachymic acid,一种羊毛甾烷三萜,对人急性单核细胞白血病细胞系 THP-1 具有毒性作用 (IC50=52.51 μM)。

3-Epidehydropachymic acid

3-Epidehydropachymic acid Chemical Structure

CAS No. : 168293-15-0

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

3-Epidehydropachymic acid, a lanostane triterpenoid, shows totoxicity effect against human acute monocytic leukemia cell line THP-1 (IC50=52.51 μM)[1].

分子量

526.75

Formula

C33H50O5

CAS 号

168293-15-0

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]. Tohtahon Z, et al. Cytotoxic lanostane triterpenoids from the fruiting bodies of Piptoporus betulinus. Phytochemistry. 2017;143:98-103

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5-Feruloylquinic acid

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。

5-Feruloylquinic acid  纯度: ≥99.0%

5-Feruloylquinic acid (5-FQA) 具有抗氧化作用和酪氨酸酶抑制活性。

5-Feruloylquinic acid

5-Feruloylquinic acid Chemical Structure

CAS No. : 40242-06-6

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5 mg ¥4500 In-stock
10 mg ¥7200 In-stock
50 mg   询价  
100 mg   询价  

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5-Feruloylquinic acid 相关产品

相关化合物库:

  • Natural Product Library Plus
  • Bioactive Compound Library Plus
  • Metabolism/Protease Compound Library
  • Natural Product Library
  • Anti-Cancer Compound Library
  • Phenols Library

生物活性

5-Feruloylquinic acid (5-FQA) possesses antioxidative effects and tyrosinase inhibitory activities[1].

分子量

368.34

Formula

C17H20O9

CAS 号

40242-06-6

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20°C, sealed storage, away from moisture and light

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)

参考文献
  • [1]. Kazuya Iwai, et al. In vitro antioxidative effects and tyrosinase inhibitory activities of seven hydroxycinnamoyl derivatives in green coffee beans. J Agric Food Chem. 2004 Jul 28;52(15):4893-8.

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5-O-Caffeoylshikimic acid

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。

5-O-Caffeoylshikimic acid 

5-O-Caffeoylshikimic acid 可用于非小细胞肺癌的研究。

5-O-Caffeoylshikimic acid

5-O-Caffeoylshikimic acid Chemical Structure

CAS No. : 73263-62-4

规格 是否有货
5 mg 询价
10 mg 询价
25 mg 询价

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生物活性

5-O-Caffeoylshikimic acid can be used in the study for NSCLC[1][2].

体外研究
(In Vitro)

5-O-cafeoylshikimic acid likely to be a key player to modulate NSCLC drug resistance in the near future[2].

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

分子量

336.29

Formula

C16H16O8

CAS 号

73263-62-4

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]. Oleksandr Shulha, et al. Lignans and sesquiterpene lactones from Hypochaeris radicata subsp. neapolitana (Asteraceae, Cichorieae). Phytochemistry. 2019 Sep;165:112047.

    [2]. https://pubmed.ncbi.nlm.nih.gov/31203102

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

5-Feruloylquinic acid

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。

5-Feruloylquinic acid  纯度: ≥99.0%

5-Feruloylquinic acid (5-FQA) 具有抗氧化作用和酪氨酸酶抑制活性。

5-Feruloylquinic acid

5-Feruloylquinic acid Chemical Structure

CAS No. : 40242-06-6

规格 价格 是否有货 数量
1 mg ¥2000 In-stock
5 mg ¥4500 In-stock
10 mg ¥7200 In-stock
50 mg   询价  
100 mg   询价  

* Please select Quantity before adding items.

5-Feruloylquinic acid 相关产品

相关化合物库:

  • Natural Product Library Plus
  • Bioactive Compound Library Plus
  • Metabolism/Protease Compound Library
  • Natural Product Library
  • Anti-Cancer Compound Library
  • Phenols Library

生物活性

5-Feruloylquinic acid (5-FQA) possesses antioxidative effects and tyrosinase inhibitory activities[1].

分子量

368.34

Formula

C17H20O9

CAS 号

40242-06-6

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20°C, sealed storage, away from moisture and light

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)

参考文献
  • [1]. Kazuya Iwai, et al. In vitro antioxidative effects and tyrosinase inhibitory activities of seven hydroxycinnamoyl derivatives in green coffee beans. J Agric Food Chem. 2004 Jul 28;52(15):4893-8.

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

5-O-Caffeoylshikimic acid

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。

5-O-Caffeoylshikimic acid 

5-O-Caffeoylshikimic acid 可用于非小细胞肺癌的研究。

5-O-Caffeoylshikimic acid

5-O-Caffeoylshikimic acid Chemical Structure

CAS No. : 73263-62-4

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

5-O-Caffeoylshikimic acid can be used in the study for NSCLC[1][2].

体外研究
(In Vitro)

5-O-cafeoylshikimic acid likely to be a key player to modulate NSCLC drug resistance in the near future[2].

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

336.29

Formula

C16H16O8

CAS 号

73263-62-4

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]. Oleksandr Shulha, et al. Lignans and sesquiterpene lactones from Hypochaeris radicata subsp. neapolitana (Asteraceae, Cichorieae). Phytochemistry. 2019 Sep;165:112047.

    [2]. https://pubmed.ncbi.nlm.nih.gov/31203102

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

Ganoderenic acid B(Synonyms: 灵芝烯酸 B)

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。

Ganoderenic acid B (Synonyms: 灵芝烯酸 B)

Ganoderenic acid B 是从 Ganoderma lucidum 中分离的一种三萜类化合物。Ganoderenic acid B 可有效逆转 ABCB1 介导的HepG2/ADM 细胞对 Doxorubicin 的耐药性。

Ganoderenic acid B(Synonyms: 灵芝烯酸 B)

Ganoderenic acid B Chemical Structure

CAS No. : 100665-41-6

规格 是否有货
5 mg 询价
10 mg 询价
25 mg 询价

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生物活性

Ganoderenic acid B is a lanostane-type triterpene isolated from Ganoderma lucidum. Ganoderenic acid B exhibits potent reversal effect on ABCB1-mediated multidrug resistance of HepG2/ADM cells to Doxorubicin[1].

分子量

514.65

Formula

C30H42O7

CAS 号

100665-41-6

中文名称

灵芝烯酸 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]. Liu DL, et al. Ganoderma lucidum derived ganoderenic acid B reverses ABCB1-mediated multidrug resistance in HepG2/ADM cells. Int J Oncol. 2015 May;46(5):2029-38.

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

Ganoderenic acid B(Synonyms: 灵芝烯酸 B)

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。

Ganoderenic acid B (Synonyms: 灵芝烯酸 B)

Ganoderenic acid B 是从 Ganoderma lucidum 中分离的一种三萜类化合物。Ganoderenic acid B 可有效逆转 ABCB1 介导的HepG2/ADM 细胞对 Doxorubicin 的耐药性。

Ganoderenic acid B(Synonyms: 灵芝烯酸 B)

Ganoderenic acid B Chemical Structure

CAS No. : 100665-41-6

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

Ganoderenic acid B is a lanostane-type triterpene isolated from Ganoderma lucidum. Ganoderenic acid B exhibits potent reversal effect on ABCB1-mediated multidrug resistance of HepG2/ADM cells to Doxorubicin[1].

分子量

514.65

Formula

C30H42O7

CAS 号

100665-41-6

中文名称

灵芝烯酸 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]. Liu DL, et al. Ganoderma lucidum derived ganoderenic acid B reverses ABCB1-mediated multidrug resistance in HepG2/ADM cells. Int J Oncol. 2015 May;46(5):2029-38.

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