Halymecin C
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| Category | Others |
| Catalog number | BBF-01317 |
| CAS | 167173-82-2 |
| Molecular Weight | 618.79 |
| Molecular Formula | C32H58O11 |
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Description
It is produced by the strain of Fusarium sp. FE-71-1.
Specification
| Synonyms | Decanoic acid, 3-(acetyloxy)-5-[(3,5-dihydroxy-1-oxodecyl)oxy]-, 1-(3-carboxy-2-hydroxypropyl)hexyl ester, [3R-[1[R*(R*)],3R*,5R*(3R*,5R*)]]- |
| IUPAC Name | (3R,5R)-5-[(3R,5R)-3-acetyloxy-5-[(3R,5R)-3,5-dihydroxydecanoyl]oxydecanoyl]oxy-3-hydroxydecanoic acid |
| Canonical SMILES | CCCCCC(CC(CC(=O)OC(CCCCC)CC(CC(=O)OC(CCCCC)CC(CC(=O)O)O)OC(=O)C)O)O |
| InChI | InChI=1S/C32H58O11/c1-5-8-11-14-24(34)17-25(35)20-31(39)43-28(16-13-10-7-3)21-29(41-23(4)33)22-32(40)42-27(15-12-9-6-2)18-26(36)19-30(37)38/h24-29,34-36H,5-22H2,1-4H3,(H,37,38)/t24-,25-,26-,27-,28-,29-/m1/s1 |
| InChI Key | VKMYCUDYNRAXCY-PADYGVHUSA-N |
Properties
| Appearance | Colorless Oily Matter |
| Solubility | Soluble in Dichloromethane |
Reference Reading
1. Halymecins, new antimicroalgal substances produced by fungi isolated from marine algae
C Chen, N Imamura, M Nishijima, K Adachi, M Sakai, H Sano J Antibiot (Tokyo). 1996 Oct;49(10):998-1005. doi: 10.7164/antibiotics.49.998.
Novel antimicroalgal substances halymecins A (1), B (2) and C (3) were isolated from the fermentation broth of a Fusarium sp. and halymecins D (4) and E (5) from an Acremonium sp. The structures of these halymecins, Fig. 1, were determined based on extensive 2D NMR studies as well as mass spectral data. These chemical structures are conjugates of di- and trihydroxydecanoic acid. Halymecin A showed antimicroalgal activity against Skeletonema costatum.
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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
* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳
