Aureothin

Chemical Information
Aureothin is a C-nitro compound that is (3Z)-3-[(2E)-2-methyl-3-(4-nitrophenyl)prop-2-en-1-ylidene]tetrahydrofuran which is substituted by a 6-methoxy-3,5-dimethyl-4-oxo-4H-pyran-2-yl group at position 5. It is isolated from the soil bacterium, Streptomyces thioluteus and exhibits antitumor, antifungal, and insecticidal activities. It has a role as an antibacterial agent, an antiparasitic agent, an antineoplastic agent, an antifungal agent, an EC 1.6.5.3 [NADH:ubiquinone reductase (H(+)-translocating)] inhibitor and a bacterial metabolite. It is a member of 4-pyranones, a ketene acetal, a member of oxolanes, a C-nitro compound and an olefinic compound. It is functionally related to a deoxyaureothin.
| CAS Number | 2825-00-5 |
| PubChem CID | 6569946 |
| IUPAC Name | 2-methoxy-3,5-dimethyl-6-[(2R,4Z)-4-[(E)-2-methyl-3-(4-nitrophenyl)prop-2-enylidene]oxolan-2-yl]pyran-4-one |
| Molecular Formula | C22H23NO6 |
| Molecular Weight | 397.4 |
| XLogP | 3.6 |
| Topological Polar Surface Area | 90.6 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 4 |
| Heavy Atom Count | 29 |
| Formal Charge | 0 |
| Complexity | 806 |
| Property | Value |
|---|---|
| Molecular Weight | 397.4 |
| XLogP3 | 3.6 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 4 |
| Exact Mass | 397.15253745 |
| Monoisotopic Mass | 397.15253745 |
| Topological Polar Surface Area | 90.6 Ų |
| Heavy Atom Count | 29 |
| Formal Charge | 0 |
| Complexity | 806 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 2 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
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