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YS-49 monohydrate

产品号 Y1521 公司名称 Sigma Aldrich
CAS号 132836-42-1(anhydrous) 公司网站 http://www.sigmaaldrich.com
分子式 C20H22BrNO3 电 话 1-800-521-8956
分子量 404.29758 传 真
纯 度 ≥98% (HPLC) 电子邮件
保 存 Chembase数据库ID: 154662

产品价格信息

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产品别名

标题
YS-49 monohydrate
IUPAC标准名
1-(naphthalen-1-ylmethyl)-1,2,3,4-tetrahydroisoquinoline-6,7-diol hydrate hydrobromide
IUPAC传统名
1-(naphthalen-1-ylmethyl)-1,2,3,4-tetrahydroisoquinoline-6,7-diol hydrate hydrobromide
别名
1,2,3,4-Tetrahydro-1-(1-naphthalenylmethyl)-6,7-Isoquinolinediol hydrobromide monohydrate

产品登记号

CAS号 132836-42-1(anhydrous)
MDL号 MFCD16875442

产品性质

Empirical Formula (Hill Notation) C20H19NO2 · HBr · H2O
纯度 ≥98% (HPLC)
外观 solid
溶解度 H2O: >10 mg/mL
GHS危险品标识 GHS07
GHS警示词 Warning
GHS危险声明 H302
欧盟危险性物质标志 有害性(Harmful) 有害性(Harmful) (Xn)
欧盟危险性物质标志 环境危害性(Nature polluting) 环境危害性(Nature polluting) (N)
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危险公开号 22-50
安全公开号 61
保存温度 2-8°C
德国WGK号 3

产品详细信息

详细说明 (English)
Biochem/physiol Actions
YS-49 protects cells from oxidant injury; anti-inflammatory agent; activator of PI3K/Akt signaling. YS-49, an analog of higenamine, induces heme oxygenase (HO-1) in endothelial cells and protects cells from oxidant injury. The compound was reported to inhibit Ang II-stimulated VSMC proliferation through HO-1 production, which inhibits both the JNK pathway and ROS production. A study (JPET) reported that CKD712 (S-YS-49) confer cardiac protection and anti-inflammatory via activation of the PI3K signal pathway. These effects were antagonized by a PI3K inhibitor, wortmannin.
详细说明 (简体中文)
Biochem/physiol Actions
YS-49 protects cells from oxidant injury; anti-inflammatory agent; activator of PI3K/Akt signaling. YS-49, an analog of higenamine, induces heme oxygenase (HO-1) in endothelial cells and protects cells from oxidant injury. The compound was reported to inhibit Ang II-stimulated VSMC proliferation through HO-1 production, which inhibits both the JNK pathway and ROS production. A study (JPET) reported that CKD712 (S-YS-49) confer cardiac protection and anti-inflammatory via activation of the PI3K signal pathway. These effects were antagonized by a PI3K inhibitor, wortmannin.

参考文献