Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C20H24O3 |
| Molecular Weight | 312.4028 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)OC1=CC2=C(C=C1)[C@H]3CC[C@@]4(C)[C@@H](CCC4=O)[C@@H]3CC2
InChI
InChIKey=KDPQTPZDVJHMET-XSYGEPLQSA-N
InChI=1S/C20H24O3/c1-12(21)23-14-4-6-15-13(11-14)3-5-17-16(15)9-10-20(2)18(17)7-8-19(20)22/h4,6,11,16-18H,3,5,7-10H2,1-2H3/t16-,17-,18+,20+/m1/s1
| Molecular Formula | C20H24O3 |
| Molecular Weight | 312.4028 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/1021287
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1021287
Estrone acetate is a synthetic steroid hormone, which is used in biochemical research.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| [Estrone Reference Standard (Control 021) of National Institute of Health Sciences]. | 2003 |
|
| Production of 16beta-(acetoxy)acetoxy derivatives by reaction of 17-keto steroid enol acetates with lead (IV) acetate. | 2001-10 |
|
| Surface changes and hormone production in pituitary cells during tumorigenesis. | 1999-12 |
|
| Color reaction of estrone with the antimony trichloride reagent. | 1976-06 |
| Substance Class |
Chemical
Created
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admin
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Edited
Mon Mar 31 18:38:36 GMT 2025
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Mon Mar 31 18:38:36 GMT 2025
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| Record UNII |
4L6USG266B
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Validated (UNII)
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m5033
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Estrone acetate
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300000053357
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4L6USG266B
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