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313367-92-9 分子结构
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4-[5-(4-methoxyphenyl)-1,3-oxazol-2-yl]-9H-fluoren-9-one

ChemBase编号:134081
分子式:C23H15NO3
平均质量:353.3701
单一同位素质量:353.10519335
SMILES和InChIs

SMILES:
COc1ccc(cc1)c1cnc(o1)c1cccc2c1c1ccccc1C2=O
Canonical SMILES:
COc1ccc(cc1)c1cnc(o1)c1cccc2c1c1ccccc1C2=O
InChI:
InChI=1S/C23H15NO3/c1-26-15-11-9-14(10-12-15)20-13-24-23(27-20)19-8-4-7-18-21(19)16-5-2-3-6-17(16)22(18)25/h2-13H,1H3
InChIKey:
SVICLWPFAQYZLX-UHFFFAOYSA-N

引用这个纪录

CBID:134081 http://www.chembase.cn/molecule-134081.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
4-[5-(4-methoxyphenyl)-1,3-oxazol-2-yl]-9H-fluoren-9-one
IUPAC传统名
4-[5-(4-methoxyphenyl)-1,3-oxazol-2-yl]fluoren-9-one
别名
4-[5-(4-Methoxyphenyl)-2-oxazolyl]-9H-Fluoren-9-one
UA62784
CAS号
313367-92-9
MDL号
MFCD00489199
PubChem SID
162228358
PubChem CID
3383533

数据来源

数据来源

所有数据来源 商品来源 非商品来源
数据来源 数据ID 价格
Sigma Aldrich
D9688 external link 加入购物车 请登录
U3385 external link 加入购物车 请登录
数据来源 数据ID
PubChem 3383533 external link

理论计算性质

理论计算性质

JChem
质子受体 质子供体
LogD (pH = 5.5) 4.4827905  LogD (pH = 7.4) 4.4827952 
Log P 4.4827952  摩尔折射率 112.9996 cm3
极化性 42.452343 Å3 极化表面积 52.33 Å2
可自由旋转的化学键 里宾斯基五规则 true 

分子性质

分子性质

理化性质 安全信息 药理学性质 产品相关信息 生物活性(PubChem)
溶解度
DMSO: >2 mg/mL expand 查看数据来源
外观
lyophilized powder expand 查看数据来源
yellow powder expand 查看数据来源
欧盟危险性物质标志
有害性(Harmful) 有害性(Harmful) (Xn) expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
危险公开号
22 expand 查看数据来源
GHS危险品标识
GHS07 expand 查看数据来源
GHS警示词
Warning expand 查看数据来源
GHS危险声明
H302 expand 查看数据来源
保存温度
-20°C expand 查看数据来源
2-8°C expand 查看数据来源
相关基因信息
human ... TNFRSF10C(8794) expand 查看数据来源
纯度
≥95% (SDS-PAGE) expand 查看数据来源
≥98% (HPLC) expand 查看数据来源
适用性
cell culture tested expand 查看数据来源
杂质
endotoxin, tested expand 查看数据来源
基因表达载体
expressed in NSO cells expand 查看数据来源
Mol. Weight
glycosylated form mol wt 75-90 kDa by SDS-PAGE (reducing) expand 查看数据来源
Empirical Formula (Hill Notation)
C23H15NO3 expand 查看数据来源

详细说明

详细说明

Sigma Aldrich Sigma Aldrich
Sigma Aldrich -  D9688 external link
Analysis Note
Activity is measured by its ability to inhibit apoptosis of mouse L929 cells treated with 20 ng/mL recombinant human TRAIL or 12 ng/mL cross-linked recombinant human TRAIL.
Biochem/physiol Actions
Glycosyl-phosphatidylinositol-linked membrane protein that is a member of the TNF receptor family. Acts as a decoy receptor that inhibits TRAIL signaling.
UA62784 is a specific inhibitor of centromere protein E (CENPE) kinesin-like protein; mitotic inhibitor. CENP-E is a kinesin-like motor protein that localizes to the kinetochore during mitosis and is essential for bipolar spindle formation. UA62784 is a novel specific inhibitor of CENP-E, which likely binds within the motor domain of CENP-E. UA62784 causes reversible cell cycle arrest in mitosis before metaphase, which leads to apoptosis. The compound is not interacting with microtubules directly.
Physical form
Lyophilized from a 0.2 μm filtered solution in phosphate buffered saline containing 5.0 mg bovine serum albumin.
Sigma Aldrich -  U3385 external link
Biochem/physiol Actions
UA62784 is a specific inhibitor of centromere protein E (CENPE) kinesin-like protein; mitotic inhibitor. CENP-E is a kinesin-like motor protein that localizes to the kinetochore during mitosis and is essential for bipolar spindle formation. UA62784 is a novel specific inhibitor of CENP-E, which likely binds within the motor domain of CENP-E. UA62784 causes reversible cell cycle arrest in mitosis before metaphase, which leads to apoptosis. The compound is not interacting with microtubules directly.

参考文献

参考文献

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专利

专利

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