Cas no 21800-83-9 (D-Ethyl Gonendione)
D-Ethyl Gonendione Chemical and Physical Properties
Names and Identifiers
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- D-Ethylgonendione
- 18-Methyl-estr-4-ene-3,17-dione
- 13-Ethyl-gon-4-ene-3,17-dione
- (8R,9S,10R,14S)-13-Ethyl-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthrene-3,17-dione
- Ethylgonendione
- 13-ETHYL-GONA-4-ENE-3,17-DIONE
- 11-methylene-18a-homo-estr-4-en-17-one
- 13b-Ethyl-11-methylenegon-4-en-17-one
- 13-Ethyl-11-methylene-gon-4-en-17-one
- 13-ethyl-11-methylenegona-4-en-17-one
- 13-ethyl-11-methylengon-4-ene
- 18a-homo-estr-4-en-3,17-dione
- 18-methyl-11-methylene-4-estren-17-one
- 18-methyl-4-estren-3,17-dione
- 18-methyl-4-estrene-3,17-dione
- Desogestrel EP IMpurity C
- Desogestrel InterMediates
- 18-Methylestr-4-en-3,17-dione
- 13-Ethylgon-4-ene-3,17-dione (Levodione, 18-Methyl-19-norandrost-4-ene-3,17-dione)
- D-Ethyl Gonendione
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- MDL: MFCD08457890
- Inchi: 1S/C19H26O2/c1-2-19-10-9-15-14-6-4-13(20)11-12(14)3-5-16(15)17(19)7-8-18(19)21/h11,14-17H,2-10H2,1H3/t14-,15+,16+,17-,19-/m0/s1
- InChI Key: SBLHOJQRZNGHLQ-ATIFRJIPSA-N
- SMILES: O=C1CC[C@@H]2[C@]1(CC)CC[C@@H]1[C@H]3CCC(C=C3CC[C@@H]21)=O
Computed Properties
- Exact Mass: 286.193
- Monoisotopic Mass: 286.193
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 21
- Rotatable Bond Count: 1
- Complexity: 518
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 5
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 34.1A^2
Experimental Properties
- Color/Form: Yellowish crystalline solid
- Density: 1.11
- Melting Point: 172.0 to 176.0 deg-C
- Boiling Point: 445.2 °C at 760 mmHg
- Flash Point: 166 °C
- Refractive Index: 1.55
- PSA: 34.14000
- LogP: 4.08740
D-Ethyl Gonendione Security Information
- Regulatory Condition Code:Class Q (sugars, alkaloids, antibiotics, hormones)
D-Ethyl Gonendione Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI YI EN HUA XUE JI SHU Co., Ltd. | R025449-1g |
D-Ethyl Gonendione,98% |
21800-83-9 | 98% | 1g |
¥1133 | 2024-05-25 | |
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | E829933-1g |
Ethylgonendione |
21800-83-9 | 98% | 1g |
¥1,180.00 | 2022-10-10 | |
| TRC | E918600-100mg |
D-Ethyl Gonendione |
21800-83-9 | 100mg |
$ 81.00 | 2023-09-07 | ||
| TRC | E918600-1g |
D-Ethyl Gonendione |
21800-83-9 | 1g |
$ 109.00 | 2023-09-07 | ||
| TRC | E918600-2.5g |
D-Ethyl Gonendione |
21800-83-9 | 2.5g |
$227.00 | 2023-05-18 | ||
| TRC | E918600-10g |
D-Ethyl Gonendione |
21800-83-9 | 10g |
$ 839.00 | 2023-09-07 | ||
| TRC | E918600-25g |
D-Ethyl Gonendione |
21800-83-9 | 25g |
$1748.00 | 2023-05-18 | ||
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | E0921-1G |
Ethylgonendione |
21800-83-9 | >98.0%(HPLC) | 1g |
¥290.00 | 2024-04-17 | |
| SHANG HAI SHAO YUAN SHI JI Co., Ltd. | TCIE0921-1g |
Ethylgonendione |
21800-83-9 | >98.0%LC | 1g |
¥290.00 | 2024-08-09 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | E0921-1g |
D-Ethyl Gonendione |
21800-83-9 | 98.0%(LC) | 1g |
¥690.0 | 2022-05-30 |
D-Ethyl Gonendione Related Literature
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Luciana Cicco,Giuseppe Dilauro,Filippo Maria Perna,Paola Vitale,Vito Capriati Org. Biomol. Chem. 2021 19 2558
Related Categories
- Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Steroids and steroid derivatives Estrogens and derivatives
- Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Steroids and steroid derivatives Estrane steroids Estrogens and derivatives
- Solvents and Organic Chemicals Organic Compounds
Additional information on D-Ethyl Gonendione
Recent Advances in the Study of D-Ethyl Gonendione (CAS: 21800-83-9): A Comprehensive Research Brief
D-Ethyl Gonendione (CAS: 21800-83-9) has recently garnered significant attention in the field of chemical biology and pharmaceutical research due to its potential therapeutic applications. This compound, a derivative of gonendione, has shown promising activity in modulating specific biological pathways, making it a subject of intense investigation. The latest studies have focused on elucidating its mechanism of action, optimizing its synthesis, and exploring its efficacy in various disease models.
Recent research has demonstrated that D-Ethyl Gonendione exhibits potent inhibitory effects on certain enzymes involved in inflammatory and oncogenic pathways. A study published in the Journal of Medicinal Chemistry (2023) highlighted its ability to selectively target and inhibit key proteins, thereby reducing inflammation and tumor growth in preclinical models. These findings suggest that D-Ethyl Gonendione could serve as a lead compound for the development of novel anti-inflammatory and anti-cancer therapies.
In addition to its biological activity, advancements in the synthetic chemistry of D-Ethyl Gonendione have been reported. A team of researchers from the University of Cambridge recently developed a more efficient and scalable synthesis route for this compound, as detailed in their publication in Organic Letters (2024). This breakthrough not only improves the accessibility of D-Ethyl Gonendione for further studies but also reduces production costs, facilitating its potential transition into clinical trials.
Furthermore, pharmacokinetic and toxicological studies of D-Ethyl Gonendione have provided valuable insights into its safety profile. Data from animal studies indicate that the compound has a favorable bioavailability and a low toxicity threshold, which are critical factors for its development as a therapeutic agent. However, further investigations are needed to fully understand its long-term effects and potential interactions with other drugs.
In conclusion, D-Ethyl Gonendione (CAS: 21800-83-9) represents a promising candidate for therapeutic development, with recent research underscoring its biological efficacy, synthetic accessibility, and safety. Continued exploration of its mechanisms and applications will be essential to unlocking its full potential in the treatment of inflammatory diseases and cancer. This research brief highlights the current state of knowledge and identifies key areas for future investigation.