3937-56-2
3937-56-2
Chemical Structure
Nonane-1,9-diol
- CAS No.: 3937-56-2
- Formula:C9H20O2
- Molecular Weight:160.25
IUPAC Name: nonane-1,9-diol
InChIKey: ALVZNPYWJMLXKV-UHFFFAOYSA-N
SMILES: OCCCCCCCCCO
Biological Activity: Nonane-1,9-diol is a pharmaceutical intermediate. Nonane-1,9-diol is also a NMDA receptor (NR1/NR2B) inhibitor that inhibits NMDA-activated currents with an IC50 of 4.96 mM[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Nonane-1,9-diol | 99.57% | Nonane-1,9-diol is a pharmaceutical intermediate. Nonane-1,9-diol is also a NMDA receptor (NR1/NR2B) inhibitor that inhibits NMDA-activated currents with an IC50 of 4.96 mM. | ||||||||||||||||||||
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References
- [1]. Peoples RW, et al. Inhibition of N-methyl-D-aspartate receptors by straight-chain diols: implications for the mechanism of the alcohol cutoff effect. Molecular pharmacology. 2002 Jan;61(1):169-76. [Content Brief]
- [2]. Kolattukudy PE, et al. Fate of naturally occurring epoxy acids: a soluble epoxide hydrase, which catalyzes cis hydration, from Fusarium solani pisi. Arch Biochem Biophys. 1975 Feb;166(2):599-607.
- [3]. Tono-oka S, et al. Terminal diols as efficient substrates for transglycosylational activity of NAD glycohydrolase. Nucleosides & nucleotides. 1999 Jan;18(1):39-49. [Content Brief]
- [4]. Croteau R, et al. Biosynthesis of pentahydroxystearic acid of cutin from linoleic acid in Rosmarinus officinalis. Arch Biochem Biophys. 1974 Jun;162(2):458-70. [Content Brief]
