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Key Documents

SMB01055

Sigma-Aldrich

Colladin

≥90% (LC/MS-ELSD)

Synonyme(s) :

Coladin

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About This Item

Formule empirique (notation de Hill):
C26H32O5
Numéro CAS:
Poids moléculaire :
424.53
Code UNSPSC :
12352205
Nomenclature NACRES :
NA.25

Source biologique

plant

Pureté

≥90% (LC/MS-ELSD)

Forme

solid

Poids mol.

424.53

Solubilité

water: slightly soluble

Application(s)

metabolomics
vitamins, nutraceuticals, and natural products

Température de stockage

−20°C

Description générale

Colladin, a sesquiterpenoid coumarin, is a natural product commonly available from Ferula Sp. (F. arrigonii, F. vesceritensis, F. campestris and F. sinaica) plants. Existing research suggests that this plant-derived metabolite exerts various biological activities, including anticancer, neuroprotective, and antiglaucoma properties.

Application

It is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.

Actions biochimiques/physiologiques

According to the existing research, Coladin exhibited notable anti-cancer properties by substantially reducing cell proliferation and mitochondrial dehydrogenase activity in mouse B16F1 melanoma cells. These effects induced apoptosis through mechanisms involving decreased mitochondrial membrane potential and mitochondrial respiratory rate, underscoring its potential as a natural anti-cancer agent. Isolated from the roots of Ferulago campestris, coladin, along with other compounds such as umbelliprenin and epielmanticine, displayed inhibitory activity against Acetylcholinesterase (AChE) with an IC50 of 0.1 mM, suggesting its potential application in the treatment of neurological disorders like Alzheimer′s disease. Coladin, identified as one of the constituents in Heptaptera triquetra fruit, exhibited remarkable inhibitory activity against acetylcholinesterase (AChE), human carbonic anhydrase isoenzyme (hCA) I, and hCA II, with IC50 values of 8.25 nM, 28.90 nM, and 43.31 nM, respectively. This highlights its potential in the development of phytotherapeutics for conditions like Alzheimer′s disease (AD) and glaucoma.

Caractéristiques et avantages

  • High quality compound suitable for multiple research applications
  • Compatible with HPLC and mass spectrometry techniques

Autres remarques

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Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Phytochemical content and enzyme inhibitory effect of Heptaptera triquetra (Vent.) Tutin fruit against acetylcholinesterase and carbonic anhydrase I and II isoenzymes
Kaya AC, et al.
Chemical Papers, 77, 5829?5837-5829?5837 (2023)
Identification of non-alkaloid acetylcholinesterase inhibitors from Ferulago campestris (Besser) Grecescu (Apiaceae)
Dall'Acqua S, et al.
Fitoterapia, 81, 1208-1212 (2010)
Sesquiterpene esters and sesquiterpene coumarin ethers from Ferula linkii-TF
Gonzalez A G, et al.
Phytochemistry, 33(4), 863-866 (1993)
Cytotoxicity of sesquiterpenes ferulenol and coladin on liver FAO and B16F1 melanoma cells
Boulmeltout M, et al.
Pharmacognosy magazine, 14, 333-337 (2018)

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