1955-26-6
Chemical Structure
UDP-rhamnose
- CAS No.: 1955-26-6
- Formula:C15H24N2O16P2
- Molecular Weight:550.30
IUPAC Name: 4-(3-(3-(2-(5-fluoro-1H-indol-3-yl)thiazol-4-yl)-1H-pyrrolo[2,3-b]pyridin-1-yl)propyl)morpholine
InChIKey: DRDCJEIZVLVWNC-SLBWPEPYSA-N
SMILES: O[C@H]1[C@@](N2C(NC(C=C2)=O)=O)([H])O[C@@H]([C@H]1O)COP(OP(O[C@@H]3[C@@H]([C@@H]([C@H]([C@@H](O3)C)O)O)O)(O)=O)(O)=O
Biological Activity: UDP-rhamnose, the activated form of Rhamnose (HY-N1420) in fungi, is a key precursor for fungi to synthesize rhamnose-containing glycans. UDP-rhamnose can be used in the research on the treatment of fungal diseases[1][2].
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UDP-rhamnose | 96.47% | UDP-rhamnose, the activated form of Rhamnose (HY-N1420) in fungi, is a key precursor for fungi to synthesize rhamnose-containing glycans. UDP-rhamnose can be used in the research on the treatment of fungal diseases. | ||||||||||||||||||||
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- [1]. Martinez V, et al. Biosynthesis of UDP-4-keto-6-deoxyglucose and UDP-rhamnose in pathogenic fungi Magnaporthe grisea and Botryotinia fuckeliana. J Biol Chem. 2012 Jan 6;287(2):879-92. [Content Brief]
- [2]. Jianjun Pei, et al., Construction of a novel UDP-rhamnose regeneration system by a two-enzyme reaction system and application in glycosylation of flavonoid, Biochemical Engineering Journal, Volume 139, 2018, Pages 33-42, ISSN 1369-703X.
Keywords
