InChI=1S/C21H26O2/c1- 4- 21(22) 12- 10- 19- 18- 7- 5- 14- 13- 15(23- 3) 6- 8- 16(14) 17(18) 9- 11- 20(19,21) 2/h1,6,8,13,17- 19,22H,5,7,9- 12H2,2- 3H3/t17- ,18- ,19+,20+,21+/m1/s1 |
IMSSROKUHAOUJS-MJCUULBUSA-N |
[H][C@]12CC[C@@]3(C)[C@@]([H])(CC[C@@]3(O)C#C)[C@]1([H])CCc1cc(OC)ccc21 |
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xenoestrogen
A synthetic or semi-synthetic compound that has oestrogenic activity.
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prodrug
A compound that, on administration, must undergo chemical conversion by metabolic processes before becoming the pharmacologically active drug for which it is a prodrug.
xenoestrogen
A synthetic or semi-synthetic compound that has oestrogenic activity.
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View more via ChEBI Ontology
17-ethynyl-3-methoxyestra-1(10),2,4-trien-17β-ol
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mestranol
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KEGG DRUG
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mestranolum
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ChemIDplus
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(+)-17α-Ethynyl-17β-hydroxy-3-methoxy-1,3,5(10)-estratriene
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NIST Chemistry WebBook
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(+)-17α-Ethynyl-17β-hydroxy-3-methoxy-1,3,5(10)-oestratriene
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NIST Chemistry WebBook
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17-ethynyl-3-methoxyoestra-1(10),2,4-trien-17β-ol
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ChEBI
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3-Methoxy-17α-ethynylestradiol
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NIST Chemistry WebBook
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3-Methoxy-19-norpregna-1,3,5(10)-trien-20-yn-17β-ol
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NIST Chemistry WebBook
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Ethynylestradiol 3-methyl ether
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NIST Chemistry WebBook
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Mestranol
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KEGG COMPOUND
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2625905
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Reaxys Registry Number
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Reaxys
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72-33-3
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CAS Registry Number
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KEGG COMPOUND
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72-33-3
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CAS Registry Number
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ChemIDplus
|
12139060
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PubMed citation
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Europe PMC
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16414683
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PubMed citation
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Europe PMC
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