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Tropine nonanoate
Tropine nonanoate
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Tropine nonanoate
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CAS No.: 146018-90-8
Catalog No.: CFN00209
Molecular Formula: C17H31NO2
Molecular Weight: 281.44 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Oil
Source: The herbs of Atropa belladonna L.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF
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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Product Use Citation
Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
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Related Libraries
Biological Activity
Description: Tropine nonanoate displays antimuscarinic action.
In vitro:
Journal of Medicinal and Aromatic Plant Sciences, 2003: 25(1): 118-133
Present status of research in Australian cork wood tree Duboisia myoporoides and its related species[Reference: WebLink]

METHODS AND RESULTS:
Hyoscine and atropine are found to possess mydriatic, antispasmodic and anticholinergic properties while Tropine nonanoate displayed antimuscarinic action. Ursolic acid showed promising antifeedant action against Spilosoma obliqua and Spodoptera litura.
Tropine nonanoate Description
Source: The herbs of Atropa belladonna L.
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
More...

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 3.5532 mL 17.7658 mL 35.5316 mL 71.0631 mL 88.8289 mL
5 mM 0.7106 mL 3.5532 mL 7.1063 mL 14.2126 mL 17.7658 mL
10 mM 0.3553 mL 1.7766 mL 3.5532 mL 7.1063 mL 8.8829 mL
50 mM 0.0711 mL 0.3553 mL 0.7106 mL 1.4213 mL 1.7766 mL
100 mM 0.0355 mL 0.1777 mL 0.3553 mL 0.7106 mL 0.8883 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:
International Journal of Pharmacognosy,1995,33(1):78-80.
Synthesis and Antimuscarinic Activity of Tropine Nonanoate[Reference: WebLink]

METHODS AND RESULTS:
The recently isolated Tropine nonanoate from Duboisia myoporoides R. Brown (Solanaceae) was synthesized, and the sulfate and hydrochloride salts were prepared. In addition, the 1H- and 13C-NMR spectral data is reported. Finally, the antimuscarinic potency of the synthesized sulfate of Tropine nonanoate was compared to atropine sulfate in a radioligand binding assay.
CFN00217Pseudotropine135-97-7141.21C8H15NO
CFN002183-Acetoxytropane3423-26-5183.25C10H17NO2
CFN00220Tropinone532-24-1139.19C8H13NO
CFN004776-Hydroxytropinone5932-53-6155.2C8H13NO2
CFN00221Physoperuvine60723-27-5141.21C8H15NO
CFN00226Scopine498-45-3155.20C8H13NO2
CFN00205Tropine120-29-6141.21C8H15NO
CFN00206Tropine acetate3423-27-6183.25C10H17NO2
CFN00207Tropine isobutyrate495-80-7211.30C12H21NO2
CFN00209Tropine nonanoate146018-90-8281.44C17H31NO2
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