21796-15-6
21796-15-6
Chemical Structure
Thalifoline
- CAS. Nr.: 21796-15-6
- Formula:C11H13NO3
- Molecular Weight:207.23
IUPAC Name: 7-hydroxy-6-methoxy-2-methyl-3,4-dihydroisoquinolin-1(2H)-one
InChIKey: WPKMGEQXTYQXGI-UHFFFAOYSA-N
SMILES: O=C1N(C)CCC2=C1C=C(O)C(OC)=C2
Biological Activity: Thalifoline is an isoquinoline alkaloid. Thalifoline exerts cytotoxic effects on cancer cells. Thalifoline inhibits the growth of Fusarium oxysporum f. sp. lycopersici. Thalifoline can be used in research related to lung adenocarcinoma, colon cancer, oral epidermoid carcinoma, and fungal infections[1][2][3].
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
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Thalifoline | 99.19% | Thalifoline is an isoquinoline alkaloid. Thalifoline exerts cytotoxic effects on cancer cells. Thalifoline inhibits the growth of Fusarium oxysporum f. sp. lycopersici. Thalifoline can be used in research related to lung adenocarcinoma, colon cancer, oral epidermoid carcinoma, and fungal infections. | ||||||||||||||||||||
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References
- [1]. Chen IS, et al. New aporphine alkaloids and cytotoxic constituents of Hernandia nymphaeifolia. Planta Med. 1997;63(2):154-157. [Content Brief]
- [2]. Oscar J. Patin˜o, et al. Monophyllidin, a new alkaloid L-proline derivative from Zanthoxylum monophyllum. Phytochemistry Letters Volume 4, Issue 1, 15 March 2011, Pages 22-25.
- [3]. Nan ZD, et al. Nitrogenous chemical constituents and their antitumor activities evaluation in vitro from the aerial parts of Corydalis impatiens (pall.) Fisch. Nat Prod Res. 2025 Mar;39(5):1027-1038. [Content Brief]
