582-17-2
582-17-2
Chemical Structure
2,7-Dihydroxynaphthalene
Synonym(s): 2,7-DHN; Naphthalene-2,7-diol
- CAS. Nr.: 582-17-2
- Formula:C10H8O2
- Molecular Weight:160.17
IUPAC Name: naphthalene-2,7-diol
InChIKey: DFQICHCWIIJABH-UHFFFAOYSA-N
SMILES: OC1=CC2=CC(O)=CC=C2C=C1
Biological Activity: 2,7-Dihydroxynaphthalene (2,7-DHN) is a substrate of a new group of aromatic prenyltransferases in fungi and can be catalyzed to undergo a regiospecific prenylation reaction. 2,7-Dihydroxynaphthalene can undergo reactions such as oxidation and substitution[1][2].
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2,7-Dihydroxynaphthalene | 99.27% | 2,7-Dihydroxynaphthalene (2,7-DHN) is a substrate of a new group of aromatic prenyltransferases in fungi and can be catalyzed to undergo a regiospecific prenylation reaction. 2,7-Dihydroxynaphthalene can undergo reactions such as oxidation and substitution. | ||||||||||||||||||||
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2,7-Dihydroxynaphthalene (Standard) | ≥98% | 2,7-Dihydroxynaphthalene (Standard) (2,7-DHN (Standard)) is the analytical standard of 2,7-Dihydroxynaphthalene (HY-W015451). This product is intended for research and analytical applications. 2,7-Dihydroxynaphthalene (2,7-DHN) is a substrate of a new group of aromatic prenyltransferases in fungi and can be catalyzed to undergo a regiospecific prenylation reaction. 2,7-Dihydroxynaphthalene can undergo reactions such as oxidation and substitution. | ||||||||||||||||||||
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References
- [1]. Haug-Schifferdecker E, et al. A new group of aromatic prenyltransferases in fungi, catalyzing a 2,7-dihydroxynaphthalene 3-dimethylallyl-transferase reaction. J Biol Chem. 2010 May 28;285(22):16487-94. [Content Brief]
- [2]. Bloom CR, et al. Binding of 2,6- and 2,7-dihydroxynaphthalene to wild-type and E-B13Q insulins: dynamic, equilibrium, and molecular modeling investigations. Biochemistry. 1997 Oct 21;36(42):12746-58. [Content Brief]
