Structure Info
- Chemspace ID
- CSCS06256078517 (Synthesis)
- IUPAC Name
- (3aS,6R,6aR)-6-hexyl-3-methylidene-hexahydrofuro[3,4-b]furan-2,4-dione
- Mol formula
- C13H18O4
- Mol weight
- 238 Da
- Catalog Number(s)
- 29323, AA007FND, AD262211, AD46773, HY-N8499, TN7789
- Copy structure to query editor
- SMILES
- INCHI
- INCHI key
- MOL
Properties
- LogP
- 2.96
- Heavy atoms count
- 17
- Rotatable bond count
- 5
- Number of rings
- 2
- Carbon bond saturation, Fsp3
- 0.69230769230769
- Polar surface area (Å)
- 53
- Hydrogen bond acceptors count
- 2
- Hydrogen bond donors count
- 0
- Zoom the structure
- CSCS06256078517
Items Overall 5 items from 4 suppliers
Supplier | Lead time | Ships from | Purity | Pack | Price, $ | Qty |
---|---|---|---|---|---|---|
Advanced ChemBlock Inc | 30 days | United States To: | 97 | 1 mg | 335 | |
Advanced ChemBlock Inc | 30 days | United States To: | 97 | 5 mg | 1,175 | |
Description: Sporothriolide; CAS: 154799-92-5 | ||||||
MedChemExpress | TBD | United States To: | 90 | 1 mg | POA | |
Description: Names: Sporothriolide; Product Description: Sporothriolide is a metabolite produced by Nodulisporium sp. A21 . Sporothriolide has potently antifungal against R. solani and S. sclerotiorum , with EC 50 values of 11.6 μM and 10.7 μM, respectively. Sporothriolide inhibits conidium germination of Magnaporthe oryzae in vitro and in vivo .; Target: Fungal; CAS: 154799-92-5 | ||||||
MedChemExpress EU | TBD | Sweden To: | 90 | 1 mg | POA | |
Description: Names: Sporothriolide; Product Description: Sporothriolide is a metabolite produced by Nodulisporium sp. A21. Sporothriolide has potently antifungal against R. solani and S. sclerotiorum, with EC50 values of 11.6 μM and 10.7 μM, respectively. Sporothriolide inhibits conidium germination of Magnaporthe oryzae in vitro and in vivo; Target: Fungal; CAS: 154799-92-5 | ||||||
Targetmol Chemicals Inc | TBD | United States To: | 90 | 1 mg | POA | |
Description: Sporothriolide, a metabolite produced by Nodulisporium sp. A21, demonstrates potent antifungal activity against R. solani and S. sclerotiorum, with EC50 values of 11.6 μM and 10.7 μM, respectively. It also inhibits conidium germination of Magnaporthe oryzae in vitro and in vivo [1].; CAS: 154799-92-5 |
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