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6-Pteridinemethanol, 2-amino-7,8-dihydro-4-hydroxy-, also known as 2-amino-4-hydroxy-7,8-dihydropteridine-6-methanol, is a heterocyclic organic compound belonging to the pteridine family. It features a pteridine core structure with a hydroxyl group at the 4-position, an amino group at the 2-position, and a hydroxyl group at the 6-position. 6-Pteridinemethanol, 2-amino-7,8-dihydro-4-hydroxy- is significant in the field of biochemistry and medicinal chemistry due to its potential role as an intermediate in the synthesis of various biologically active compounds, such as folic acid and its derivatives, which are essential for various metabolic processes in the human body. The compound's structure and properties make it a subject of interest for researchers studying the synthesis and applications of pteridine-based compounds in pharmaceuticals and other related fields.

3672-03-5

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3672-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3672-03-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,7 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3672-03:
(6*3)+(5*6)+(4*7)+(3*2)+(2*0)+(1*3)=85
85 % 10 = 5
So 3672-03-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H9N5O2/c8-7-11-5-4(6(14)12-7)10-3(2-13)1-9-5/h13H,1-2H2,(H4,8,9,11,12,14)

3672-03-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-6-(hydroxymethyl)-7,8-dihydro-1H-pteridin-4-one

1.2 Other means of identification

Product number -
Other names dihydropterin-CH2OH

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3672-03-5 SDS

3672-03-5Relevant articles and documents

A point mutation converts dihydroneopterin aldolase to a cofactor-independent oxygenase

Wang, Yi,Scherperel, Gwynyth,Roberts, Kade D.,Jones, A. Daniel,Reid, Gavin E.,Yan, Honggao

, p. 13216 - 13223 (2008/03/11)

Dihydroneopterin aldolase (DHNA) catalyzes the conversion of 7,8-dihydroneopterin (1) to 6-hydroxymethyl-7,8-dihydropterin (4) in the folate biosynthetic pathway. Substitution of a conserved tyrosine residue at the active site of DHNA by phenylalanine converts the enzyme to a cofactor-independent oxygenase, which generates mainly 7,8-dihydroxanthopterin (6) rather than 4. 6 is generated via the same enol intermediate as in the wild-type enzyme-catalyzed reaction, but this species undergoes an oxygenation reaction to form 6. The conserved tyrosine residue plays only a minor role in the formation of the enol reaction intermediate but a critical role in the protonation of the enol intermediate to form 4.

Determination of Pterins in Biological Samples by Liquid Chromatography/Electrochemistry with a Dual-Electrode Detector

Lunte, Craig E.,Kissinger, Peter T.

, p. 1458 - 1462 (2007/10/02)

The pterins are a family of compounds that are currently of great interest in medicine and biology.Biopterin, in its reduced form, serves as the cofactor to the enzyme which catalyze the rate-limiting reactions in the biosynthesis of the catecholamines and serotonin.As such, it may serve a role in the regulation of the neurotransmitters.Abnormal pterin concentrations have been observed in the urine and serum of patiens with several diseases.No currently available analytical method is totally satisfactory for the determination of pterins in biological samples.They lack either specificity or the ability to detect both the oxidzed and reduced forms of the pterins.Liquid chromatography/electrochemistry (LCEC) using a dual-electrode detector can overcome both of these problems.A method has been developed that is capable of determining several pterin species and their various oxidation states in biological samples.The dual-electrode detector used in a parallel-adjacent configuration is also capable of enhancing peak identity assignments and selectively determining easily oxidized compounds in the presence of harder to oxidize compounds.

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