(3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane

Modify Date: 2024-01-10 11:28:03

(3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane structure	Common Name	(3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane
	CAS Number	1180504-64-6	Molecular Weight	256.29644
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₁₆H₁₆O₃	Melting Point	N/A
	MSDS	N/A	Flash Point	N/A

Use of (3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane

(3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane is a homoisoflavonoid. (3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane increases the level of alkaline phosphatase (ALP) activity. (3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane promotes mesenchymal stem cells (MSCs) osteogenesis, but cannot enhance MSCs proliferation. (3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane can be used for osteoporosis research[1].

Name	7-Hydroxy-3-(4-hydroxybenzyl)chroman

Description	(3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane is a homoisoflavonoid. (3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane increases the level of alkaline phosphatase (ALP) activity. (3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane promotes mesenchymal stem cells (MSCs) osteogenesis, but cannot enhance MSCs proliferation. (3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane can be used for osteoporosis research[1].
Related Catalog	Signaling Pathways >> Metabolic Enzyme/Protease >> Phosphatase Research Areas >> Metabolic Disease
Target	Alkaline phosphatase (ALP)[1]
In Vitro	(3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane (10 μM) 通过增加碱性磷酸酶 (ALP) 活性水平显著促进 MSCs 成骨分化。与对照组相比，早期成骨细胞分化率为162.0±1.4[1]。
References	[1]. Xu X, et al. Isolation and chatacterization of homoisoflavonoids from Dracaena cochinchinensis and their osteogenic activities in mouse mesenchymal stem cells. J Pharm Biomed Anal. 2016 Sep 10;129:466-472.

Molecular Formula	C₁₆H₁₆O₃
Molecular Weight	256.29644

(3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane

Use of (3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane

Names

Biological Activity

Chemical & Physical Properties