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Home > Encyclopedia > Hypoxanthine

Hypoxanthine

pharmaceutical raw materials
Hypoxanthine structure

Hypoxanthine 

structure
  • CAS No:

    68-94-0

  • Formula:

    C5H4N4O

  • Chemical Name:

    Hypoxanthine

  • Synonyms:

    6H-Purin-6-one,1,9-dihydro-;Hypoxanthine;6H-Purin-6-one,1,7-dihydro-;1,9-Dihydro-6H-purin-6-one;Purin-6(3H)-one;9H-Purin-6(1H)-one;Sarcine;Sarkin;Sarkine;Purin-6(1H)-one;6-Hydroxypurine;6-Oxopurine;6-Hydroxy-1H-purine;9H-Purin-6-ol;Purin-6-ol;3H-Purin-6-ol;Hypoxanthine enol;1H,7H-Hypoxanthine;NSC 129419;NSC 14665;1H,9H-Hypoxanthine;1H-Purin-6(9H)-one;1,9-Dihydro-purin-6-one;480-99-9;6535-89-3;25991-09-7;25991-08-6;25991-07-5;39464-17-0;39464-15-8;184856-40-4;51953-23-2;184856-41-5

  • Categories:

    Biochemical Engineering  >  Plant Extracts

Description

Hypoxanthine, a purine derivative, is a potential free radical generator and could be used as an indicator of hypoxia.


Solid


Hypoxanthine is a purine nucleobase that consists of purine bearing an oxo substituent at position 6. It has a role as a fundamental metabolite. It is an oxopurine, a purine nucleobase and a nucleobase analogue. It derives from an adenine.|Hypoxanthine is a purine and a reaction intermediate in the metabolism of adenosine and in the formation of nucleic acids by the salvage pathway.|Hypoxanthine is a purine-based organic compound in human muscle tissues, Hypoxanthine is formed during purine catabolism as a product of xanthine oxidase action on xanthine, and occasionally is found as a constituent of nucleic acids. The potent anti-inflammatory and cytoprotective effects of purines may be mediated by cell surface adenosine receptors. Hypoxanthine protects against oxidant-induced cell injury by inhibiting activation of nuclear poly(ADP-ribose) polymerase (PARP). (NCI04)|A purine and a reaction intermediate in the metabolism of adenosine and in the formation of nucleic acids by the salvage pathway.

Hypoxanthine Basic Attributes

136.11

136.11

5811

200-697-3

2TN51YD919

14665

DTXSID8045983

C29105

2933990090

Characteristics

70.1

-1.1

Colorless to yellow to brown, darken on storage with no loss of purity powder

1.7±0.1 g/cm3

150 °C (decomp)

533.4°C at 760 mmHg

287.0±24.6 °C

1.816

Practically insoluble in water;1 M NaOH: 25 mg/mL

2-8°C

LD50 intraperitoneal in mouse: 750mg/kg

127.1 Ų [M+H]+ [CCS Type: DT, Method: single field calibrated with Agilent tune mix (Agilent)]|135.79 Ų [M+H]+ [CCS Type: DT, Method: stepped-field]|138.88 Ų [M+Na]+ [CCS Type: DT, Method: stepped-field]|126.38 Ų [M-H]- [CCS Type: DT, Method: stepped-field]|120 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine]|127.2 Ų [M+H]+ [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|134.4 Ų [M+Na]+ [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|116.9 Ų [M-H]- [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|134.4 Ų [M+Na-2H]- [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|123.1 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]|135 Ų [M-2H+Na]-

Safety Information

NONH for all modes of transport

3

36/37/38-22-40

22-24/25-37/39-26-36

UP0791000

Xn

Harmful

Stable under normal temperatures and pressures.

P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

H315

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 11 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

Hypoxanthine

Hypoxanthine Use and Manufacturing

Methods of Manufacturing

Ethyl cyanoacetate, sodium ethoxide, and thiourea are cyclized to obtain 2-mercapto-4-amino-6-hydroxypyrimidine, which is then nitrosated, reduced, eliminated, and cyclized to produce 6-hydroxypurine.

Uses

A naturally occurring purine derivative. Pharmaceuticals, Intermediates & Fine Chemicals

6H-Purin-6-one, 1,9-dihydro-: ACTIVE

Computed Properties

Molecular Weight:136.11
XLogP3:-0.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Exact Mass:136.03851076
Monoisotopic Mass:136.03851076
Topological Polar Surface Area:70.1
Heavy Atom Count:10
Complexity:190
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Drug Function and Efficacy

Hypoxanthine is an important substance involved in human life activities. It can improve the body's material metabolism and energy metabolism, accelerate the repair of damaged tissues, and promote the restoration of normal physiological functions of pathological cells and hypoxic tissues. Hypoxanthine, in combination with small molecule peptides and amino acids, can promote the body's metabolism.

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

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