2-Isopropyl-6-methyl-4-pyrimidinol

CAS: 2814-20-2

Ref. 3D-FI37652

Product Information

• Name: 2-Isopropyl-6-methyl-4-pyrimidinol
• Synonyms: 2-Isopropyl-4-Methyl-6-Hydroxypyrimidine, 2-Isopropyl-4-hydroxy-6-methylpyrimidine, 2-Isopropyl-4-methyl-6-oxypyrimidine, 2-Isopropyl-4-methyl-6-pyrimidinone, 2-Isopropyl-4-methylpyrimidin-6-ol, 2-Isopropyl-6-methyl-3H-pyrimidin-4-one, 2-Isopropyl-6-methyl-4(3H)-pyrimidone, 2-Isopropyl-6-methyl-4-hydroxypyrimidine, 2-Isopropyl-6-methyl-4-pyrimidone, 2-Isopropyl-6-methylpyrimidin-4-ol, 4(1H)-Pyrimidinone, 2-isopropyl-6-methyl-, 4(1H)-Pyrimidinone, 6-methyl-2-(1-methylethyl)-, 4(3H)-Pyrimidinone, 6-methyl-2-(1-methylethyl)-, 4-Hydroxy-2-Iso-Propyl-6-Methyl Pyrimidine, 4-Hydroxy-2-isopropyl-6-methylpyrimidine, 4-Pyrimidinol, 2-isopropyl-6-methyl-, 6-Methyl-2-(1-methylethyl)-4(1H)-pyrimidinone, 6-Methyl-2-(1-methylethyl)-4(3H)-pyrimidinone, 6-methyl-2-(propan-2-yl)pyrimidin-4(1H)-one, G 27550, Pyrimidinol

Description

2-Isopropyl-6-methyl-4-pyrimidinol is a potential drug that is a metal chelate. It has been shown to inhibit HIV replication in tissue culture and has anti-inflammatory effects. 2-Isopropyl-6-methyl-4-pyrimidinol reduces the acetylcholinesterase activity in the body, which may be due to its ability to inhibit phosphodiesterase enzymes on the surface of cells. The chemical structure of this compound can be synthesized from chiral building blocks and it can be used as an analytical method for measuring the content of various target enzymes.
2I6MP4P binds tightly to phosphate groups, rendering them unavailable for enzymatic reactions. This inhibition is reversible and concentration dependent with a redox potential near zero volts.

• Brand: Biosynth

Chemical properties

• Purity: Min. 95%