Glisoprenin A
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Category | Enzyme inhibitors |
Catalog number | BBF-01253 |
CAS | 144376-62-5 |
Molecular Weight | 703.14 |
Molecular Formula | C45H82O5 |
Purity | 95% |
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Description
It is produced by the strain of Gliocladium sp. FO-1513. It is a cholesterol acyltransferase (ACAT) inhibitor, and it can inhibit the formation of Appressorium on the hydrophobic surface of Magnaporthegrisea.
Specification
Synonyms | (+)-GlisopreninA; FO 1513A; 2,6,10,14,34-Hexatriacontapentaene-1,19,23,27,31-pentol,3,7,11,15,19,23,27,31,35-nonamethyl- |
IUPAC Name | (2E,6E,10E,14E)-3,7,11,15,19,23,27,31,35-nonamethylhexatriaconta-2,6,10,14,34-pentaene-1,19,23,27,31-pentol |
Canonical SMILES | CC(=CCCC(C)(CCCC(C)(CCCC(C)(CCCC(C)(CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)O)O)O)O)C |
InChI | InChI=1S/C45H82O5/c1-37(2)19-14-28-42(7,47)30-16-32-44(9,49)34-18-35-45(10,50)33-17-31-43(8,48)29-15-26-40(5)24-12-22-38(3)20-11-21-39(4)23-13-25-41(6)27-36-46/h19-20,23-24,27,46-50H,11-18,21-22,25-26,28-36H2,1-10H3/b38-20+,39-23+,40-24+,41-27+ |
InChI Key | DVYSZUSSOIXHOF-VNEVDCACSA-N |
Properties
Appearance | Colorless Oily Matter |
Antibiotic Activity Spectrum | Fungi |
Boiling Point | 779.1 °C at 760 mmHg |
Density | 0.968 g/cm3 |
Solubility | Soluble in Methanol, Chloroform |
Reference Reading
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Bio Calculators
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2