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Stachybotrylactam
Stachybotrylactam
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Stachybotrylactam
Price:
CAS No.: 163391-76-2
Catalog No.: CFN96659
Molecular Formula: C23H31NO4
Molecular Weight: 385.50 g/mol
Purity: >=98%
Type of Compound: Sesquiterpenoids
Physical Desc.: Powder
Source: The mycelia and culture broth of Stachybotrys sp. MF347.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison (Web)  (SDF)
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Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
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Biological Activity
Description: Stachybotrylactam has toxicity.
In vitro:
Indoor & Built Environment, 2010, 19(19):668-675.
A study of the toxicity of moulds isolated from dwellings.[Reference: WebLink]

METHODS AND RESULTS:
An analysis of the toxicity of moulds isolated from 34 dwellings with mould-affected walls was performed. During the analysis 74 moulds strains were isolated, 17.5% of them were toxic. Detailed analysis by high performance liquid chromatography/tandem mass spectrometry of six toxic strains proved their ability to grow on building materials and produce mycotoxins. It was confirmed that the toxins Stachybotrylactam, sterigmatocystin and roquefortin were produced on gypsum board and concrete by Stachybotrys chartarum, Aspergillus versicolor and Penicillium chrysogenum, respectively. This is also the first report on the production of aflatoxin B1 and G1 by A. flavus on building materials. Extracts from A. versicolor, A. flavus, P. chrysogenum growing on building materials were found to have cytotoxic potential.
CONCLUSIONS:
It was found that some mycotoxin production may be reduced or may even vanish, when moulds grow on building materials. However, taking into consideration the appreciable amounts of some mycotoxins that were still produced on the building materials investigated, the study indicated a toxic risk in the mould-affected buildings analysed.
Stachybotrylactam Description
Source: The mycelia and culture broth of Stachybotrys sp. MF347.
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.

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

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IF=13.903(2019)

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Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.594 mL 12.9702 mL 25.9403 mL 51.8807 mL 64.8508 mL
5 mM 0.5188 mL 2.594 mL 5.1881 mL 10.3761 mL 12.9702 mL
10 mM 0.2594 mL 1.297 mL 2.594 mL 5.1881 mL 6.4851 mL
50 mM 0.0519 mL 0.2594 mL 0.5188 mL 1.0376 mL 1.297 mL
100 mM 0.0259 mL 0.1297 mL 0.2594 mL 0.5188 mL 0.6485 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:
Mar Drugs. 2014 Apr 1;12(4):1924-38.
Spirocyclic drimanes from the marine fungus Stachybotrys sp. strain MF347.[Pubmed: 24694571 ]

METHODS AND RESULTS:
A novel spirocyclic drimane coupled by two drimane fragment building blocks 2 and a new drimane 1 were identified in mycelia and culture broth of Stachybotrys sp. MF347. Their structures were established by spectroscopic means. This is the first example of spirocyclic drimane coupled by a spirodihydrobenzofuranlactam unit and a spirodihydroisobenzofuran unit; and the connecting position being N-C instead of an N and N connecting unit. Strain MF347 produced also the known spirocyclic drimanes stachybocin A (12) and stachybocin B (11) featured by two sesquiterpene-spirobenzofuran structural units connected by a lysine residue; the known spirocyclic drimanes chartarlactam O (5); chartarlactam K (6); F1839A (7); Stachybotrylactam (8); stachybotramide (9); and 2α-acetoxyStachybotrylactam acetate (10); as well as ilicicolin B (13), a known sesquiterpene. The relative configuration of two known spirobenzofuranlactams (3 and 4) was determined.
CONCLUSIONS:
All compounds were subjected to biological activity tests. The spirocyclic drimane 2, 11, and 12, as well as the sesquiterpene 13, exhibited antibacterial activity against the clinically relevant methicillin-resistant Staphylococcus aureus (MRSA).
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