2-Naphthalenecarboxylic acid, 4-(D-glucopyranosyloxy)-1-hydroxy-3-(3-hydroxy-3-methylbutyl)-, methyl ester Chemical Structure
CAS No. : 125906-48-1
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
2-Naphthalenecarboxylic acid, 4-(D-glucopyranosyloxy)-1-hydroxy-3-(3-hydroxy-3-methylbutyl)-, methyl ester (compound 3) is a natural product that can be isolated from the dried roots of Rubia cordifolia[1].
分子量
466.48
Formula
C23H30O10
CAS 号
125906-48-1
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]. Hideji Itokawa, et al. Anthraquinones and naphthohydroquinones from Rubia cordifolia. Phytochemistry, 1989. 28(12), 3465-3468.
16(R/S)-Hydroxy-3,13Z-kolavadien-15,16-olide-2-one (compound 9) 是从 Polyalthia longifolia var. pendula 的未成熟果实中分离出的二萜化合物。
16(R/S)-Hydroxy-3,13Z-kolavadien-15,16-olide-2-one Chemical Structure
CAS No. : 165459-53-0
规格
是否有货
100 mg
询价
250 mg
询价
500 mg
询价
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生物活性
16(R/S)-Hydroxy-3,13Z-kolavadien-15,16-olide-2-one (compound 9) is a diterpene compound isolated from the unripe fruits of Polyalthia longifolia var. pendula[1].
分子量
332.43
Formula
C20H28O4
CAS 号
165459-53-0
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]. Yu ZX, et al. New clerodane diterpenoids from the roots of Polyalthia laui. Fitoterapia. 2016;111:36-41.
5-Hydroxy-7-acetoxyflavone, an active natural flavone derivative found in various plant sources, modulates several biological activities[1].
分子量
296.27
Formula
C17H12O5
CAS 号
6674-40-4
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]. Apilak Worachartcheewan, et al. Probing the origins of anticancer activity of chrysin derivatives. Medicinal Chemistry Research. May 2015, 24(5):1884-1892.
5-Hydroxy-3-(4-hydroxybenzyl)-7-methoxychroman-4-one Chemical Structure
CAS No. : 108001-32-7
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-Hydroxy-3-(4-hydroxybenzyl)-7-methoxychroman-4-one (4a) is a natural compound[1].
分子量
300.31
Formula
C17H16O5
CAS 号
108001-32-7
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]. Tingjun Xu, et al. Virtual Screening for Reactive Natural Products and Their Probable Artifacts of Solvolysis and Oxidation. Biomolecules. 2020 Oct 27;10(11):1486.
2-Hydroxy-1-methoxyanthraquinone Chemical Structure
CAS No. : 6170-06-5
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
2-Hydroxy-1-methoxyanthraquinone could be isolated from the stem bark of Morinda lucida Benth. (Rubiaceae) and possesses antibacterial activity[1].
分子量
254.24
Formula
C15H10O4
CAS 号
6170-06-5
中文名称
茜素-1-甲醚
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]. Napoleon A. Mfonku, et al. Isolation and selective glycosylation of antisalmonellal anthraquinones from the stem bark of Morinda lucida Benth. (Rubiaceae). Phytochemistry Letters. Phytochemistry Letters 37 (2020) 80-84.
Isoferulic acid (3-Hydroxy-4-methoxycinnamic acid) is a cinnamic acid derivative that has antidiabetic activity. Isoferulic acid binds to and activates α1-adrenergic receptors (IC50=1.4 µM) to enhance secretion of β-endorphin (EC50=52.2 nM) and increase glucose use. Isoferulic acid also has anti-influenza virus activities.
分子量
194.18
Formula
C10H10O4
CAS 号
537-73-5
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Liu IM, et al. Mediation of beta-endorphin by isoferulic acid to lower plasma glucose in streptozotocin-induced diabetic rats. J Pharmacol Exp Ther. 2003 Dec;307(3):1196-204.
[2]. Sakai S, et al. Administration of isoferulic acid improved the survival rate of lethal influenza virus pneumonia in mice. Mediators Inflamm. 2001 Apr;10(2):93-6.