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Darlingine
Darlingine
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Darlingine
Price:
CAS No.: 58471-10-6
Catalog No.: CFN00188
Molecular Formula: C13H17NO2
Molecular Weight: 219.28 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Needles
Source: The leaves of triunia erythrocarpa.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF
Similar structural: Comparison (Web)  (SDF)
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Description: Reference standards.
Darlingine Description
Source: The leaves of triunia erythrocarpa.
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 4.5604 mL 22.8019 mL 45.6038 mL 91.2076 mL 114.0095 mL
5 mM 0.9121 mL 4.5604 mL 9.1208 mL 18.2415 mL 22.8019 mL
10 mM 0.456 mL 2.2802 mL 4.5604 mL 9.1208 mL 11.4009 mL
50 mM 0.0912 mL 0.456 mL 0.9121 mL 1.8242 mL 2.2802 mL
100 mM 0.0456 mL 0.228 mL 0.456 mL 0.9121 mL 1.1401 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:
J Nat Prod. 2000 May;63(5):688-9.
10-Hydroxydarlingine, a new tropane alkaloid from the Australian proteaceous plant triunia erythrocarpa.[Pubmed: 10843590]

METHODS AND RESULTS:
Triunia erythrocarpa was identified as containing alkaloids during chemical screening of Queensland Proteaceae using Dragendorff's reagent. A new tropane, 10-hydroxyDarlingine (1), and the known tropane, Darlingine (2), were isolated from the leaves of T. erythrocarpa.
CONCLUSIONS:
The absolute stereochemistry of 10-hydroxyDarlingine (1) was assigned using the advanced Mosher method. T. erythrocarpa is only the seventh member of the Proteaceae to have been shown to produce alkaloids.
Phytochemistry,1999,52(3):529–531.
Tropane alkaloids from Darlingia darlingiana[Reference: WebLink]

METHODS AND RESULTS:
A new γ-pyranotropane, Darlingine N-oxide, was isolated from the bark and leaves of Darlingia darlingiana, along with the known compound, Darlingine. 1D-NOESY NMR experiments indicated that the N-methyl groups of both alkaloids were orientated towards the pyran ring.
Australian Journal of Chemistry , 1979 , 32 (8) :1827-1840
Alkaloids of Bellendena montana[Reference: WebLink]
Fourteen alkaloids have been isolated from Bellendena montana, a monotypic proteaceous plant endemic in Tasmania.
METHODS AND RESULTS:
The structures of ten of these, bellendine (1), isobellendine (2), Darlingine (3),5,11-dihydroisobellendine (5), 2,3-dihydrobellendine (6), 2,3-epidihydrobellendine (7), 2,3-dihydroDarlingine(8), 3α-acetoxy-6β-isobutoxytropane (9), 6β-acetoxy-3α-isobutoxytropane (10) and 3α-acetoxy-6β-hydroxytropane (11), have been established.
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