Halymecin C

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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It is commonly abbreviated as: C1V1 = C2V2

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Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
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