土荆皮甲酸

更新时间：2025-08-21 13:09:50

土荆皮甲酸结构式	常用名	土荆皮甲酸	英文名	Pseudolaric Acid A
	CAS号	82508-32-5	分子量	388.454
	密度	1.23	沸点	571.5±50.0 °C at 760 mmHg
	分子式	C₂₂H₂₈O₆	熔点	206-207 ºC
	MSDS	N/A	闪点	196.6±23.6 °C

土荆皮甲酸用途

Pseudolaric Acid A 是一种从 Pseudolarix kaempferi 分离的二萜酸,具有抗真菌,细胞毒性,抗受精活性。

中文名	土槿皮甲酸
英文名	Pseudolaric Acid A
中文别名	土荆皮甲酸
英文别名	更多

描述	Pseudolaric Acid A 是一种从 Pseudolarix kaempferi 分离的二萜酸,具有抗真菌,细胞毒性,抗受精活性。
相关类别	研究领域 >> 感染信号通路 >> 抗感染 >> 真菌
参考文献	[1]. Zhang J, et al,. Antifungal activity of compounds extracted from Cortex Pseudolaricis against Colletotrichum gloeosporioides. J Agric Food Chem. 2014 May 28;62(21):4905-10. [2]. Pan DJ, et al. The cytotoxic principles of Pseudolarix kaempferi: pseudolaric acid-A and -B and related derivatives. Planta Med. 1990 Aug;56(4):383-5. [3]. Wang WC, et al. [Endocrine activity of pseudolaric acids A and B and their effects on sex hormones, prostaglandins, uteri, and fetuses]. Zhongguo Yao Li Xue Bao. 1991 Mar;12(2):187-90.

描述

Pseudolaric Acid A 是一种从 Pseudolarix kaempferi 分离的二萜酸,具有抗真菌,细胞毒性,抗受精活性。

相关类别

研究领域 >> 感染

信号通路 >> 抗感染 >> 真菌

参考文献

[1]. Zhang J, et al,. Antifungal activity of compounds extracted from Cortex Pseudolaricis against Colletotrichum gloeosporioides. J Agric Food Chem. 2014 May 28;62(21):4905-10.

[2]. Pan DJ, et al. The cytotoxic principles of Pseudolarix kaempferi: pseudolaric acid-A and -B and related derivatives. Planta Med. 1990 Aug;56(4):383-5.

[3]. Wang WC, et al. [Endocrine activity of pseudolaric acids A and B and their effects on sex hormones, prostaglandins, uteri, and fetuses]. Zhongguo Yao Li Xue Bao. 1991 Mar;12(2):187-90.

密度	1.23
沸点	571.5±50.0 °C at 760 mmHg
熔点	206-207 ºC
分子式	C₂₂H₂₈O₆
分子量	388.454
闪点	196.6±23.6 °C
精确质量	388.188599
PSA	89.90000
LogP	3.49
InChIKey	GOHMRMDXUXWCDQ-ADDXWAJHSA-N
SMILES	CC(=O)OC12CCC(C)=CCC13CCC2C(C)(C=CC=C(C)C(=O)O)OC3=O
蒸汽压	0.0±3.4 mmHg at 25°C
折射率	1.563
储存条件	2-8C

土荆皮甲酸毒性英文版

实验名称：Antiproliferative activity against HMEC1 cells by SRB assay
来源：ChEMBL
靶标：N/A
External Id：CHEMBL927442

实验名称：Antiproliferative activity against human HL60 cells by SRB assay
来源：ChEMBL
靶标：HL-60
External Id：CHEMBL927443

实验名称：Antiproliferative activity against human A459 cells by SRB assay
来源：ChEMBL
靶标：NON-PROTEIN TARGET
External Id：CHEMBL927444

实验名称：Cytotoxicity against human HL60 cells after 48 hrs by MTT assay
来源：ChEMBL
靶标：HL-60
External Id：CHEMBL914002

实验名称：Cytotoxicity against human Bel7402 cells after 48 hrs by MTT assay
来源：ChEMBL
靶标：N/A
External Id：CHEMBL912949

实验名称：Cytotoxicity against human BGC823 cells after 48 hrs by MTT assay
来源：ChEMBL
靶标：N/A
External Id：CHEMBL914005

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(2E,4E)-5-[(1R,7S,8S,9R)-7-Acetoxy-4,9-dimethyl-11-oxo-10-oxatricyclo[6.3.2.0]tridec-3-en-9-yl]-2-methyl-2,4-pentadienoic acid

(2E,4E)-5-[(1R,7S,8S,9R)-7-Acetoxy-4,9-dimethyl-11-oxo-10-oxatricyclo[6.3.2.0]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid

(2E,4E)-5-[(1R,7R,8S,9S)-7-Acetoxy-4,9-dimethyl-11-oxo-10-oxatricyclo[6.3.2.0]tridec-3-en-9-yl]-2-methyl-2,4-pentadienoic acid

(2E,4E)-5-[(3R,4S,4aS,9aR)-4a-(acetyloxy)-3,7-dimethyl-1-oxo-3,4,4a,5,6,9-hexahydro-4,9a-ethanocyclohepta[c]pyran-3(1H)-yl]-2-methylpenta-2,4-dienoic acid

pseudolaric acid A

PseudolaricAcid A