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Pandamarilactonine A
Pandamarilactonine A
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Pandamarilactonine A
Price:
CAS No.: 303008-80-2
Catalog No.: CFN98380
Molecular Formula: C18H23NO4
Molecular Weight: 317.4 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The barks of Pandanus amaryllifolius
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF    Manual
Similar structural: Comparison (Web)  (SDF)
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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
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: Pandamarilactonine A has antimicrobial activity, it is active with an MIC of 15.6 ug/mL and MBC of 31.25 ug/mL against Pseudomonas aeruginosa.
Targets: Antifection
In vitro:
J. Appl. Pharm.Sci.,2015,5(10):151-3.
Antimicrobial alkaloids from the leaves of Pandanus amaryllifolius[Reference: WebLink]

METHODS AND RESULTS:
Chemical investigation on the crude base of the Pandanus amaryllifolius leaves led to the isolation and identification of pandamarilactone-1 (1), pandamarilactone-32 (2), Pandamarilactonine A (3), and pandamarilactonine B (4). Their structures were elucidated based on 1H and 13C NMR and in comparison with the literature data. Compound 3 was found to be the most active among the four isolates with an MIC of 15.6 ug/mL and MBC of 31.25 ug/mL against Pseudomonas aeruginosa.
CONCLUSIONS:
This is the first report on the antimicrobial activity of the isolated alkaloids from the genus Pandanus.
Pandamarilactonine A Description
Source: The barks of Pandanus amaryllifolius
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 3.1506 mL 15.753 mL 31.506 mL 63.012 mL 78.765 mL
5 mM 0.6301 mL 3.1506 mL 6.3012 mL 12.6024 mL 15.753 mL
10 mM 0.3151 mL 1.5753 mL 3.1506 mL 6.3012 mL 7.8765 mL
50 mM 0.063 mL 0.3151 mL 0.6301 mL 1.2602 mL 1.5753 mL
100 mM 0.0315 mL 0.1575 mL 0.3151 mL 0.6301 mL 0.7876 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:
Chem Pharm Bull (Tokyo). 2002 Sep;50(9):1303-4.
Isolation and structure elucidation of two new alkaloids, pandamarilactonine-C and -D, from Pandanus amaryllifolius and revision of relative stereochemistry of pandamarilactonine-A and -B by total synthesis.[Pubmed: 12237561]

METHODS AND RESULTS:
Two new pyrrolidine alkaloids, pandamarilactonine-C and -D, were isolated from Pandanus amaryllifolius.
CONCLUSIONS:
Based on the total synthesis of pandamarilactonine-C and its related alkaloid, Pandamarilactonine A, the relative stereochemistry of Pandamarilactonine A and -B, which was previously proposed by spectroscopic analysis, was revised.
Arch Pharm (Weinheim). 2008 Sep;341(9):578-83.
Diastereoselective synthesis of N-Boc-norpandamarilactonine-B and pandamarilactonine-A.[Pubmed: 18763717]

METHODS AND RESULTS:
Optically pure N-Boc-norpandamarilactonine-B was diastereoselectively synthesized starting from L-serine by employing a double ring closing metathesis (RCM) of a tetraene derivative as a key reaction. N-Boc-norpandamarilactonine-B obtained was further converted to Pandamarilactonine A.
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