(5S,6R)-METHYL 5,6,7-TRIHYDROXYHEPTANOATE

(5S,6R)-METHYL 5,6,7-TRIHYDROXYHEPTANOATE

中文名称(5S,6R)-METHYL 5,6,7-TRIHYDROXYHEPTANOATE
中文同义词化合物 T22526;BML-111,脂蛋白A4激动剂
英文名称5(S),6(R),7-TRIHYDROXYHEPTANOIC ACID, METHYL ESTER
英文同义词BML-111;5(S),6(R),7-TRIHYDROXYHEPTANOIC ACID, METHYL ESTER;6(R)-7-trihydroxymethyl Heptanoate;Heptanoic acid, 5,6,7-trihydroxy-, methyl ester, (5S,6R)-;(5S,6R)-METHYL 5,6,7-TRIHYDROXYHEPTANOATE;1,3-Benzodioxole-9-sulfonylchloride;5(S),6(R)-trihydroxy-7-heptanoic acid, methyl ester;BML111,BML 111
CAS号78606-80-1
分子式C8H16O5
分子量192.21
EINECS号
相关类别
Mol文件Mol File
结构式(5S,6R)-METHYL 5,6,7-TRIHYDROXYHEPTANOATE 结构式

(5S,6R)-METHYL 5,6,7-TRIHYDROXYHEPTANOATE 性质

沸点360.8±42.0 °C(Predicted)
密度1?+-.0.06 g/cm3(Predicted)
储存条件-20°C
溶解度H2O:≥20mg/mL
酸度系数(pKa)13.74±0.20(Predicted)
形态粉末
颜色白色至米色
稳定性自购买之日起,稳定期为 1 年。 其DMSO 或乙醇溶液可在 -20°C 下保存长达 3 个月。

(5S,6R)-METHYL 5,6,7-TRIHYDROXYHEPTANOATE 用途与合成方法

BML-111 一种脂蛋白 A4 类似物,是一种脂蛋白 A4 (lipoxin A4) 受体激动剂。BML-111 可抑制血管紧张素转化酶 (ACE) 的活性,并增加血管紧张素转化酶 2 (ACE2) 的活性。BML-111 具有抗血管生成,抗肿瘤和抗炎的特性。

Lipoxin A4 receptor
Angiotensin converting enzyme (ACE)

In H22 cells, BML-111 inhibits the production of vascular endothelial growth factor and reduces hypoxia-inducible factor-1α level.
BML-111 inhibits leukotriene B4-induced cellular migration with an IC 50 of 5 nM.

BML-111 (1 mg/kg; intraperitoneal injection; for 15 days; male Imprinting Control Region mice) treatment suppresses tumor-related angiogenesis and tumor growth in vivo. BML-111 also enhances the in situ apoptosis while inhibiting macrophage infiltration in tumor tissue.
BML-111 protects LPS-induced acute lung injury and LPS/D-GalN-induced acute liver injury. BML-111 represses the activity of ACE, but increases the activity of ACE2. BML-111 decreases the expression levels of ACE, AngII, and AngII type 1 receptor (AT1R), meanwhile increases the levels of ACE2, angiotensin-(1-7) (Ang-1-7), and Mas.

Animal Model: Male Imprinting Control Region mice (5-6-week-old,18-22 g) injected with H22 cells
Dosage: 1 mg/kg
Administration: Intraperitoneal injection; injected 5 minutes before and 4 hours after H22 cell inoculation, then every 12 hours for 2 consecutive days, then daily in an additional 3 days and every other day for the last 10 days
Result: Suppressed tumor-related angiogenesis and tumor growth in vivo.

安全信息

WGK Germany3

MSDS信息

更新日期产品编号产品名称CAS号包装价格
2024/04/30HY-100450BML-1111 mg2020元
2024/04/30HY-100450(5S,6R)-METHYL 5,6,7-TRIHYDROXYHEPTANOATE
BML-111
78606-80-15mg5050元

(5S,6R)-METHYL 5,6,7-TRIHYDROXYHEPTANOATE 上下游产品信息

上游原料
"(5S,6R)-METHYL 5,6,7-TRIHYDROXYHEPTANOATE"相关产品信息
扎鲁司特 6-异丙氧基-9-氧代氧杂蒽-2-羧酸 植物鞘氨醇 银杏内酯B
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