Pyrenophorol
| Code | Size | Price |
|---|
| BVT-0289-C500 | 500 ug | £150.00 |
Quantity:
| BVT-0289-M001 | 1 mg | £245.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
20°C
Storage:
-20°C
Documents
Further Information
Alternate Names/Synonyms:
Helmidiol; (-)-Pyrenophorol; (3E,5S,8R,11E,13S,16R)-5,13-Dihydroxy-8,16-dimethyl-1,9-dioxacyclohexadeca-3,11-diene-2,10-dione
Appearance:
White to off-white solid.
CAS:
155326-45-7 and 22248-41-5
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.Protect from light when in solution.
Hazards:
H302, H312, H319, H332
InChi:
InChI=1S/C16H24O6/c1-11-3-5-13(17)8-10-16(20)22-12(2)4-6-14(18)7-9-15(19)21-11/h7-14,17-18H,3-6H2,1-2H3/b9-7+,10-8+/t11-,12-,13+,14+/m1/s1
InChiKey:
RBQNDQOKFICJGL-UTBFYLPBSA-N
Long Description:
Chemical. CAS: 155326-45-7 and 22248-41-5. Formula: C16H24O6. MW: 312.4. Isolated from Phoma sp. Phytotoxic, antifungal and anthelmintic. Prolyl endopeptidase inhibitor.
MDL:
MFCD18379612
Molecular Formula:
C16H24O6
Molecular Weight:
312.4
Package Type:
Plastic Vial
Precautions:
P261, P270, P280, P301, P312, P302, P352, P312
Product Description:
Phytotoxic, antifungal and anthelmintic. Prolyl endopeptidase inhibitor.
Purity:
>98% (HPLC)
Signal word:
Warning
SMILES:
C[C@@H]1CC[C@H](O)C=CC(=O)O[C@H](C)CC[C@H](O)C=CC(=O)O1
Solubility Chemicals:
Soluble in DMSO (5 mg/ml), methanol (5 mg/ml) or dichloromethane.
Source / Host:
Isolated from Phoma sp.
Transportation:
Non-hazardous
UNSPSC Category:
Natural Products/Extracts
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 1 year after receipt when stored at -20°C. After reconstitution protect from light at -20°C.
References
Secondary Metabolites by Chemical Screening. 30.1 Helmidiol, a New Macrodiolide from Alternaria alternata.: R. Kind, et al.; J. Nat. Prod. 59, 539 (1996) | Albocycline- and carbomycin-type macrolides, inhibitors of human prolylendopeptidases.: C. Christner, et al.; J. Antibiot. 51, 368 (1998) | Bioactivity of the fungal metabolite (8R,16R)-(-)-pyrenophorin on graminaceous plants.: M.A. Kastanias, et al.; J. Agric. Food Chem. 53, 5943 (2005) | Diversity of antimicrobial pyrenophorol derivatives from an endophytic fungus, Phoma sp.: W. Zang, et al.; Eur. J. Org. Chem. 2008, 4320 (2008)