6-Ketoestradiol
Modify Date: 2026-07-04 11:57:00
6-Ketoestradiol structure
|
Common Name | 6-Ketoestradiol | ||
|---|---|---|---|---|
| CAS Number | 571-92-6 | Molecular Weight | 286.366 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 478.9±45.0 °C at 760 mmHg | |
| Molecular Formula | C18H22O3 | Melting Point | 281-283ºC | |
| MSDS | USA | Flash Point | 257.5±25.2 °C | |
Use of 6-Ketoestradiol6-Ketoestradiol can be used to synthesize re-containing 7α-substituted estradiol complexes[1]. |
| Name | 6-Keto 17β-Estradiol |
|---|---|
| Synonym | More Synonyms |
| Description | 6-Ketoestradiol can be used to synthesize re-containing 7α-substituted estradiol complexes[1]. |
|---|---|
| Related Catalog | |
| References |
| Density | 1.3±0.1 g/cm3 |
|---|---|
| Boiling Point | 478.9±45.0 °C at 760 mmHg |
| Melting Point | 281-283ºC |
| Molecular Formula | C18H22O3 |
| Molecular Weight | 286.366 |
| Flash Point | 257.5±25.2 °C |
| Exact Mass | 286.156891 |
| PSA | 57.53000 |
| LogP | 3.30 |
| Vapour Pressure | 0.0±1.3 mmHg at 25°C |
| Index of Refraction | 1.612 |
| InChIKey | ZHTDDOWJIRXOMA-YVEZLPLXSA-N |
| SMILES | CC12CCC3c4ccc(O)cc4C(=O)CC3C1CCC2O |
| Precursor 7 | |
|---|---|
| DownStream 4 | |
![[(8S,9S,13S,14S,17S)-3-acetyloxy-13-methyl-6-oxo-8,9,11,12,14,15,16,17-octahydro-7H-cyclopenta[a]phenanthren-17-yl] acetate Structure](https://image.chemsrc.com/caspic/092/3434-45-5.png)
CAS#:3434-45-5
CAS#:147802-61-7![(8R,9S,13S,14S,17S)-13-methyl-8,9,12,13,14,15,16,17-octahydro-11H-cyclopenta[a]phenanthrene-3,6,17-triyl triacetate Structure](https://image.chemsrc.com/caspic/157/78149-51-6.png)
CAS#:78149-51-6![(17β)-3,17-Bis[(tetrahydro-2H-pyran-2-yl)oxy]-estra-1,3,5(10)-trien-6-one Structure](https://image.chemsrc.com/caspic/106/53573-82-3.png)
CAS#:53573-82-3
CAS#:2243-06-3
CAS#:1971-65-9
CAS#:78149-47-0
CAS#:35048-47-6
CAS#:38002-18-5
CAS#:3583-03-7
CAS#:1476-34-2|
C6-(N,N-butyl-methyl-heptanamide) derivatives of estrone and estradiol as inhibitors of type 1 17beta-hydroxysteroid dehydrogenase: Chemical synthesis and biological evaluation.
Bioorg. Med. Chem. 15 , 714-26, (2007) A series of estrone and estradiol derivatives having an N-butyl,methyl heptanamide side chain at C6-position were synthesized, tested as inhibitors of type 1 17beta-HSD and assessed for their possible... |
|
|
An efficient stereoselective synthesis of 6-alpha-aminoestradiol: preparation of estradiol fluorescent probes.
Steroids 62 , 462, (1997) 6-Oxoestradiol (2) was protected as its bis[(2-trimethylsilylethoxy)methyl] ether (4) and converted to the corresponding oxime (4). The oxime (4) on reduction with zinc in ethanol afforded the bis-SEM... |
|
|
RP-HPLC analysis of phenolic acids of selected Central European Carex L. (Cyperaceae) species and its implication for taxonomy.
J. AOAC Int. 94 , 9-16, (2011) Eighteen species belonging to the Carex genus were checked for the presence and the amount of eight phenolic acids (p-hydroxybenzoic, vanillic, caffeic, syringic, protocatechuic, p-coumaric, sinapic, ... |
|
Name: Primary cell-based high-throughput screening assay for identification of compounds th...
Source: Johns Hopkins Ion Channel Center
Target: regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id: JHICC_RGS_Act_HTS
|
|
Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
|
|
Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
|
|
Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
|
|
Name: uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
Source: Burnham Center for Chemical Genomics
Target: N/A
External Id: BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
|
|
Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
|
|
Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
|
|
Name: Flow Cytometric HTS Screen for inhibitors of the ABC transporter ABCB6 for Validation...
Source: NMMLSC
Target: ATP-binding cassette sub-family B member 6, mitochondrial [Homo sapiens]
External Id: UNMCMD_ABCB6_1o_ValidationSet
|
|
Name: Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
Source: Broad Institute
Target: N/A
External Id: 7124-01_Inhibitor_SinglePoint_HTS_Activity
|
|
Name: Fluorescence-based cell-based primary high throughput screening assay to identify pos...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
|
Total 123, Current Page 1 of 13
1
2
3
4
5
| 6-ketoestradiol |
| (17β)-3,17-Dihydroxyestra-1,3,5(10)-trien-6-one |