SMB01382
2-Methoxyestrone
≥95% (HPLC), from synthetic, solid
别名:
2,3-Dihydroxy-1,3,5(10)-estratrien-17-one 2-methyl ether, 2-Hydroxyestrone 2-methyl ether, 3-Hydroxy-2-methoxy-1,3,5(10)-estratrien-17-one
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关于此项目
经验公式（希尔记法）:
C19H24O3
化学文摘社编号:
分子量:
300.39
UNSPSC Code:
12352211
NACRES:
NA.79
MDL number:
InChI
1S/C19H24O3/c1-19-8-7-12-13(15(19)5-6-18(19)21)4-3-11-9-16(20)17(22-2)10-14(11)12/h9-10,12-13,15,20H,3-8H2,1-2H3/t12-,13+,15-,19-/m0/s1
InChI key
WHEUWNKSCXYKBU-QPWUGHHJSA-N
SMILES string
C[C@@]12[C@](CCC2=O)([H])[C@]3([H])CCC4=CC(O)=C(OC)C=C4[C@@]3([H])CC1
biological source
synthetic
assay
≥95% (HPLC)
form
solid
mp
187-190 °C
storage temp.
2-8°C
Quality Level
相关类别
General description
2-Methoxyestrone is an endogenous, naturally occurring methoxylated catechol estrogen and an estrone metabolite formed by catechol O-methyltransferase via the intermediate 2-hydroxyestrone. Unlike estrone but similarly to 2-hydroxyestrone and 2-methoxyestradiol, 2-methoxyestrone has very low affinity for the estrogen receptor and lacks significant estrogenic activity
Preparation Note
Heat sensitive
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
涉药品监管产品
此项目有
Urinary estrogen metabolites and gastric cancer risk among postmenopausal women.
Camargo MC, et al.
Cancer reports (Hoboken, N.J.), 5, e1574-e1574 (2022)
Reproducibility of fifteen urinary estrogens and estrogen metabolites over a 2- to 3-year period in premenopausal women.
Eliassen AH, et al.
Cancer Epidemiology, Biomarkers & Prevention, 18, 2860-2868 (2009)
Individual and cyclic estrogenic profile in women: Structure and variability of the data.
Bozzolino C, et al.
Steroids, 150, 108432-108432 (2019)
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