biological source
synthetic
Quality Level
assay
≥95% (HPLC)
form
solid
mp
187-190 °C
storage temp.
2-8°C
SMILES string
C[C@@]12[C@](CCC2=O)([H])[C@]3([H])CCC4=CC(O)=C(OC)C=C4[C@@]3([H])CC1
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
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)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| SMB01382-50MG | 04065269395805 |
| SMB01382-10MG | 04065269395799 |

