Isariin B

Isariin B

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Category Antibiotics
Catalog number BBF-01506
CAS 80111-95-1
Molecular Weight 595.77
Molecular Formula C30H53N5O7

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Description

Isariin B is originally isolated from Isaria felina.

Specification

Synonyms 19-hexyl-6-methyl-9-(2-methylpropyl)-3,12-di(propan-2-yl)-1-oxa-4,7,10,13,16-pentaazacyclononadecane-2,5,8,11,14,17-hexone
IUPAC Name (3S,6S,9R,12R,19R)-19-hexyl-6-methyl-9-(2-methylpropyl)-3,12-di(propan-2-yl)-1-oxa-4,7,10,13,16-pentazacyclononadecane-2,5,8,11,14,17-hexone
Canonical SMILES CCCCCCC1CC(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)O1)C(C)C)C)CC(C)C)C(C)C
InChI InChI=1S/C30H53N5O7/c1-9-10-11-12-13-21-15-23(36)31-16-24(37)34-25(18(4)5)29(40)33-22(14-17(2)3)28(39)32-20(8)27(38)35-26(19(6)7)30(41)42-21/h17-22,25-26H,9-16H2,1-8H3,(H,31,36)(H,32,39)(H,33,40)(H,34,37)(H,35,38)/t20-,21+,22+,25+,26-/m0/s1
InChI Key QWBKHPNGPXORRV-KJWQPKDSSA-N

Properties

Boiling Point 935.7°C at 760 mmHg
Melting Point 268°C
Density 1.016 g/cm3

Reference Reading

1. Genomics-driven discovery of a new cyclodepsipeptide from the guanophilic fungus Amphichorda guana
Min Liang, Hai-Ning Lyu, Zi-Ying Ma, Er-Wei Li, Lei Cai, Wen-Bing Yin Org Biomol Chem. 2021 Mar 11;19(9):1960-1964. doi: 10.1039/d1ob00100k.
Two potential non-ribosomal peptide synthetases (NRPSs) were identified in the genome of a guanophilic fungus Amphichorda guana by bioinformatics analysis and gene knockout experiments. Liquid chromatography coupled with mass spectrometry (LC-MS) guided isolation led to the discovery of a new cyclodepsipeptide isaridin H (1) and seven known analogs, desmethylisaridin E (2), isaridin E (3), isariin A (4), iso-isariin B (5), iso-isariin D (6), isariin E (7), and nodupetide (8). The absolute configuration of isaridin H (1) was achieved by Marfey's method. Isaridin H (1) showed significant antifungal activity against Botrytis cinerea and Alternaria solani.
2. Insecticidal cyclodepsipeptides from Beauveria felina
Aude Langenfeld, Alain Blond, Sabelle Gueye, Patrick Herson, Bastien Nay, Joëlle Dupont, Soizic Prado J Nat Prod. 2011 Apr 25;74(4):825-30. doi: 10.1021/np100890n. Epub 2011 Mar 25.
A novel cyclodepsipeptide, iso-isariin B (1), and the known isaridin E (2) were isolated from the entomopathogenic fungus Beauveria felina. Their structures were elucidated using MS/MS fragmentation and extensive 2D-heteronuclear NMR. The X-ray structure of isaridin E was obtained, showing two potent intramolecular H bonds and a type-VI turn with the HyLeu(1)-Pro(2) amide bond in a cis conformation. Iso-isariin B (1) was active against the pest-insect Sitophilus spp. with an LD(50) value of 10 μg/mL. This observation also gives some clues for ecological interpretation of cyclodepsipeptide production by B. felina.
3. Cyclodepsipeptides and other O-containing heterocyclic metabolites from Beauveria felina EN-135, a marine-derived entomopathogenic fungus
Feng-Yu Du, Xiao-Ming Li, Peng Zhang, Chun-Shun Li, Bin-Gui Wang Mar Drugs. 2014 May 13;12(5):2816-26. doi: 10.3390/md12052816.
Bioassay-guided fractionation of a culture extract of Beauveria felina EN-135, an entomopathogenic fungus isolated from a marine bryozoan, led to the isolation of a new cyclodepsipeptide, iso-isariin D (1); two new O-containing heterocyclic compounds that we have named felinones A and B (2 and 3); and four known cyclodepsipeptides (4-7). The structures were elucidated via spectroscopic analysis, and the absolute configurations of 1 and 2 were determined using single-crystal X-ray diffraction and CD, respectively. All isolated compounds were evaluated for antimicrobial activity and brine-shrimp (Artemia salina) lethality.

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