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BioViotica
Palmarumycin C3
155
CHF
CHF 155.00
In stock
BVT-0078-M0011 mgCHF 155.00
BVT-0078-M0055 mgCHF 470.00
| Product Details | |
|---|---|
| Synonyms | (1a'R,7a'S)-3',6'-Dihydroxy-1a'H-spiro[naphtho[1,8-de][1,3]dioxine-2,2'-naphtho[2,3-b]oxiren]-7'(7a'H)-one |
| Product Type | Chemical |
| Properties | |
| Formula |
C20H12O6 |
| MW | 348.3 |
| CAS | 159934-11-9 |
| Source/Host Chemicals | Isolated from Sphaeropsidales sp. |
| Purity Chemicals | ≥97% (HPLC) |
| Appearance | Yellow to green solid. |
| Solubility | Soluble in DMSO, dichloromethane, acetone or methanol. |
| Identity | Determined by 1H-NMR. |
| Declaration | Manufactured by BioViotica. |
| InChi Key | BDXBHYOFNNANPN-RTBURBONSA-N |
| Smiles | OC1=CC=C(O)C2=C1C(=O)[C@H]1O[C@H]1C21OC2=CC=CC3=C2C(O1)=CC=C3 |
| Shipping and Handling | |
| Shipping | AMBIENT |
| Short Term Storage | +4°C |
| Long Term Storage | -20°C |
| Use/Stability |
Stable for at least 1 year after receipt when stored at -20°C. After reconstitution protect from light at -20°C. |
| Documents | |
| MSDS |
 Download PDF |
| Product Specification Sheet | |
| Datasheet |
Download PDF |
Description
- Rasfarnesyltransferase inhibitor.
- Antifungal, antibacterial and herbicidal.
- Structurally unique natural products. The basic structure of palmarumycin C1 can be modified by a number of hydroxylation, oxygenation, dehydrogenation and chlorination steps.
- Antioxidant.
Product References
- Biologically Active Metabolites from Fungi, 4. Palmarumycins CP1-CP4 from Coniothyrium palmarum: Isolation, structure elucidation, and biological activity: K. Krohn, et al.; Liebigs Ann. Chem. 1994, 1093 (1994)
- Biologically Active Metabolites from Fungi, 5. Palmarumycins C1-C16 from Coniothyrium sp.: Isolation, structure elucidation, and biological activity: K. Krohn, et al.; Liebigs Ann. Chem. 1994, 1099 (1994)
- Secondary metabolites by chemical screening, 42 Cladospirones B to I from Sphaeropsidales sp. F-24'707 by variation of culture conditions: H.B. Bode, et al.; Eur. J. Org. Chem. 2000, 3185-3193 (2000)
- Unified route to the palmarumycin and preussomerin natural products. Enantioselective synthesis of (-)-preussomerin G: A.G. Barrett, et al.; J. Org. Chem. 67, 2735-2750 (2002)
- Natural products derived from naphthalenoid precursors by oxidative dimerization: K. Krohn; Prog. Chem. Org. Nat. Prod. 85, 1-49 (2003) (Review)
- Antimicrobial and Antioxidant Activities and Effect of 1-Hexadecene Addition on Palmarumycin C2 and C3 Yields in Liquid Culture of Endophytic Fungus Berkleasmium sp. Dzf12: Y. Mou, et al.; Molecules 18, 15587 (2013)
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