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Harzianic acid
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Product Name Harzianic acid
Price:
CAS No.: 157148-06-6
Catalog No.: CFN00118
Molecular Formula: C19H27NO6
Molecular Weight: 365.42 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The branches of Broussonetia papyrifera
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF    Manual
Similar structural: Comparison (Web)  (SDF)
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Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: Harzianic acid is a Trichoderma secondary metabolite, it shows plant growth promotion activity. Harzianic acid has antifungal activity and antibiotic activity against Pythium irregulare, Sclerotinia sclerotiorum, and Rhizoctonia solani.
Targets: Antifection
In vitro:
J Nat Prod. 2009 Nov;72(11):2032-5.
Harzianic acid, an antifungal and plant growth promoting metabolite from Trichoderma harzianum.[Pubmed: 19894739]
A Trichoderma harzianum strain, isolated from composted hardwood bark in Western Australia, was found to produce a metabolite with antifungal and plant growth promoting activity.
METHODS AND RESULTS:
The structure and absolute configuration of the fungal compound, Harzianic acid (1), were determined by X-ray diffraction studies. Harzianic acid showed antibiotic activity against Pythium irregulare, Sclerotinia sclerotiorum, and Rhizoctonia solani. A plant growth promotion effect was observed at low concentrations of 1.
FEMS Microbiol Lett. 2013 Oct;347(2):123-9.
Harzianic acid: a novel siderophore from Trichoderma harzianum.[Pubmed: 23909277]

METHODS AND RESULTS:
Agriculture-relevant microorganisms are considered to produce secondary metabolites during processes of competition with other micro- and macro-organisms, symbiosis, parasitism or pathogenesis. Many different strains of the genus Trichoderma, in addition to a direct activity against phytopathogens, are well-known producers of secondary metabolites and compounds that substantially affect the metabolism of the host plant. Harzianic acid is a Trichoderma secondary metabolite, showing antifungal and plant growth promotion activities.
CONCLUSIONS:
This report demonstrates the ability of this tetramic acid to bind with a good affinity essential metals such as Fe(3+) , which may represent a mechanism of iron solubilisation that significantly alters nutrient availability in the soil environment for other microorganisms and the host plant.
Molecules. 2014 Jul 8;19(7):9760-72.
A novel fungal metabolite with beneficial properties for agricultural applications.[Pubmed: 25006784]
Harzianic acid (HA) is a T. harzianum metabolite able to promote plant growth and strongly bind iron.
METHODS AND RESULTS:
In this work, we isolated from the culture filtrate of a T. harzianum strain a new metabolite, named isoHarzianic acid (iso-HA), a stereoisomer of Harzianic acid. The structure and absolute configuration of this compound has been determined by spectroscopic methods, including UV-Vis, MS, 1D and 2D NMR analyses. In vitro applications of iso-Harzianic acid inhibited the mycelium radial growth of Sclerotinia sclerotiorum and Rhizoctonia solani. Moreover, iso Harzianic acid improved the germination of tomato seeds and induced disease resistance.
CONCLUSIONS:
HPLC-DAD experiments showed that the production of Harzianic acid and iso Harzianic acid was affected by the presence of plant tissue in the liquid medium. In particular, tomato tissue elicited the production of Harzianic acid but negatively modulated the biosynthesis of its analogue iso-Harzianic acid, suggesting that different forms of the same Trichoderma secondary metabolite have specific roles in the molecular mechanism regulating the Trichoderma plant interaction.
Harzianic acid Description
Source: The branches of Broussonetia papyrifera
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.7366 mL 13.6829 mL 27.3658 mL 54.7315 mL 68.4144 mL
5 mM 0.5473 mL 2.7366 mL 5.4732 mL 10.9463 mL 13.6829 mL
10 mM 0.2737 mL 1.3683 mL 2.7366 mL 5.4732 mL 6.8414 mL
50 mM 0.0547 mL 0.2737 mL 0.5473 mL 1.0946 mL 1.3683 mL
100 mM 0.0274 mL 0.1368 mL 0.2737 mL 0.5473 mL 0.6841 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Structure Identification:
Org Lett. 2015 Feb 6;17(3):692-5.
Total synthesis and biological evaluation of the tetramic acid based natural product harzianic acid and its stereoisomers.[Pubmed: 25629709]

METHODS AND RESULTS:
The bioactive natural product Harzianic acid was prepared for the first time in just six steps (longest linear sequence) with an overall yield of 22%. The identification of conditions to telescope amide bond formation and a Lacey-Dieckmann reaction into one pot proved important. The three stereoisomers of Harzianic acid were also prepared, providing material for comparison of their biological activity.
CONCLUSIONS:
While all of the isomers promoted root growth, improved antifungal activity was unexpectedly associated with isomers in the enantiomeric series opposite that of Harzianic acid.
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