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Zopfiellamide A
Zopfiellamide A
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Product Name Zopfiellamide A
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CAS No.: 478945-64-1
Catalog No.: CFN00145
Molecular Formula: C25H35NO6
Molecular Weight: 445.55 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Cryst.
Source: From the fermentations of the facultative marine fungus Zopfiella latipes CBS 611.97.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison (Web)  (SDF)
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Biological Activity
Description: Zopfiellamide A and Zopfiellamide B are antimicrobial metabolites.
Targets: Antifection
Zopfiellamide A Description
Source: From the fermentations of the facultative marine fungus Zopfiella latipes CBS 611.97.
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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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 2.2444 mL 11.2221 mL 22.4442 mL 44.8883 mL 56.1104 mL
5 mM 0.4489 mL 2.2444 mL 4.4888 mL 8.9777 mL 11.2221 mL
10 mM 0.2244 mL 1.1222 mL 2.2444 mL 4.4888 mL 5.611 mL
50 mM 0.0449 mL 0.2244 mL 0.4489 mL 0.8978 mL 1.1222 mL
100 mM 0.0224 mL 0.1122 mL 0.2244 mL 0.4489 mL 0.5611 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:
Tetrahedron , 2002, 58(39): 7781-4.
Zopfiellamides A and B, antimicrobial pyrrolidinone derivatives from the marine fungus Zopfiella latipes[Reference: WebLink]

METHODS AND RESULTS:
Two new antimicrobial metabolites, Zopfiellamide A (1) and zopfiellamide B (2) were isolated from fermentations of the facultative marine fungus Zopfiella latipes CBS 611.97. Their structures were elucidated by spectroscopic techniques, and they are pyrrolidinone derivatives.
CFN00105Antibiotic 2158182320-34-9519.72C33H45NO4
CFN00106Antibiotic AB 4015B162857-79-6413.6C26H39NO3
CFN00107Antibiotic AB 4063B160041-33-8413.6C26H39NO3
CFN00108Antibiotic PF 1052147317-15-5429.60C26H39NO4
CFN00113Delaminomycin A149779-38-4501.66C29H43NO6
CFN00115Equisetin57749-43-6373.49C22H31NO4
CFN00129Oteromycin170591-45-4487.68C32H41NO3
CFN00130Antibiotic ZG 1494alpha182320-33-8505.70C32H43NO4
CFN00143Vermisporin122301-98-8415.57C25H37NO4
CFN00145Zopfiellamide A478945-64-1445.55C25H35NO6
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