Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C19H26O2 |
| Molecular Weight | 286.4085 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@]3([H])C4=C(CC[C@@]23[H])C(C)=C(O)C=C4
InChI
InChIKey=CSHOYPMKTGTOLM-SMYFESCOSA-N
InChI=1S/C19H26O2/c1-11-12-3-4-15-14(13(12)5-7-17(11)20)9-10-19(2)16(15)6-8-18(19)21/h5,7,14-16,18,20-21H,3-4,6,8-10H2,1-2H3/t14-,15-,16+,18+,19+/m1/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Pharmacological effects of 2- and 4-methyloestradiol as a probe to test the biological importance of 2- and 4-hydroxylation of oestrogens (catecholoestrogen-formation). | 1983 Jan |
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| Interactions of methylestrogens with cytoplasmic and nuclear estrogen receptors in rat pituitary gland, hypothalamus and uterus. | 1984 Mar 5 |
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| Biphasic modulation of pituitary sensitivity to GnRH by oestrogens: the effects of A- and D-ring substitution on LH release in cultured pituitary cells. | 1984 Nov |
Patents
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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6171-48-8
Created by
admin on Sat Dec 16 06:42:42 GMT 2023 , Edited by admin on Sat Dec 16 06:42:42 GMT 2023
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94DM04YP7A
Created by
admin on Sat Dec 16 06:42:42 GMT 2023 , Edited by admin on Sat Dec 16 06:42:42 GMT 2023
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66437
Created by
admin on Sat Dec 16 06:42:42 GMT 2023 , Edited by admin on Sat Dec 16 06:42:42 GMT 2023
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DTXSID20872685
Created by
admin on Sat Dec 16 06:42:42 GMT 2023 , Edited by admin on Sat Dec 16 06:42:42 GMT 2023
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PRIMARY |
SUBSTANCE RECORD
