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经验公式(希尔记法):
C18H23NO4S
化学文摘社编号:
分子量:
349.44
UNSPSC Code:
12352202
NACRES:
NA.77
MDL number:
SMILES string
[S](=O)(=O)(N)Oc1cc2c(cc1)[C@@H]3[C@H]([C@H]4[C@](CC3)(C(=O)CC4)C)CC2
InChI
1S/C18H23NO4S/c1-18-9-8-14-13-5-3-12(23-24(19,21)22)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16H,2,4,6-9H2,1H3,(H2,19,21,22)/t14-,15-,16+,18+/m1/s1
InChI key
RVKFQAJIXCZXQY-CBZIJGRNSA-N
biological source
synthetic (organic)
assay
≥98%
form
powder
storage temp.
−20°C
Quality Level
Application
Lead compound for design of steroid sulfatase inhibitors.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
A Purohit et al.
Biochemistry, 34(36), 11508-11514 (1995-09-12)
Steroid sulfatases are responsible for the hydrolysis of 3beta-hydroxy steroid sulfates, such as cholesterol and pregnenolone sulfate, and have an important role in regulating the synthesis of estrogenic steroids, from estrone sulfate and dehydroepiandrosterone sulfate, in endocrine-dependent tumors. Although little
Active site directed inhibition of estrone sulfatase by nonsteroidal coumarin sulfamates.
L W Woo et al.
Journal of medicinal chemistry, 39(7), 1349-1351 (1996-03-29)
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