19870-30-5
Chemical Structure
Tuliposide A
- CAS No.: 19870-30-5
- Formula:C11H18O8
- Molecular Weight:278.26
IUPAC Name: (2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl 4-hydroxy-2-methylenebutanoate
InChIKey: SQRUWMQAWMLKPR-DZEUPHNYSA-N
SMILES: O(C(C(CCO)=C)=O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Biological Activity: Tuliposide A is a glycoside precursor compound derived from Tulipa gesneriana L. Tuliposide A exists in two spontaneously interconvertible isomers, and can release glucose via hydrolysis or enzymatic decomposition to generate the active intermediate Tulipaline A. Tuliposide A produces hydrolysates that suppress infection and expansion of Fusarium oxysporum, trigger cutaneous contact irritation, and lower the viability of in vitro plant calli. Tuliposide A can be used in studies related to fungal infections and dermatitis[1][2].
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Tuliposide A | Tuliposide A is a glycoside precursor compound derived from Tulipa gesneriana L. Tuliposide A exists in two spontaneously interconvertible isomers, and can release glucose via hydrolysis or enzymatic decomposition to generate the active intermediate Tulipaline A. Tuliposide A produces hydrolysates that suppress infection and expansion of Fusarium oxysporum, trigger cutaneous contact irritation, and lower the viability of in vitro plant calli. Tuliposide A can be used in studies related to fungal infections and dermatitis. | |||||||||||||||||||||
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- [1]. Hausen BM, et al. The sensitizing capacity of Alstroemeria cultivars in man and guinea pig: Remarks on the occurrence, quantity and irritant and sensitizing potency of their constituents tuliposide A and tulipalin A (α-methylene-γ-butyrolactone). Contact Dermatitis. 1983;9(1):33-42.
- [2]. Ueno H, et al. Effect of simultaneous testing of two mice in the tail suspension test and forced swim test. Scientific Reports. 2022;12:9224.
Keywords
