P1132

Pterin

~95%

• Synonym(e): 2-Amino-4-hydroxypteridin, 2-Amino-4-oxodihydropteridin
• Empirische Formel (Hill-System): C₆H₅N₅O
• CAS-Nummer: 2236-60-4
• Molekulargewicht: 163.14
• Beilstein: 150294
• EG-Nummer: 218-799-1
• MDL-Nummer: MFCD00010557
• UNSPSC-Code: 12352202
• PubChem Substanz-ID: 24898158
• NACRES: NA.77

Eigenschaften

• Biologische Quelle: synthetic
• Qualitätsniveau: 200
• Assay: ~95%
• Form: powder
• Lagertemp.: 2-8°C
• SMILES String: Nc1nc(O)c2nccnc2n1
• InChI: 1S/C6H5N5O/c7-6-10-4-3(5(12)11-6)8-1-2-9-4/h1-2H,(H3,7,9,10,11,12)
• InChIKey: HNXQXTQTPAJEJL-UHFFFAOYSA-N

Beschreibung

Anwendung

Pterine has been used:

• in photochemicals assay for inducing DNA damage
• as a substrate in xanthine oxidase assay
• as a standard in thin layer chromatography (TLC) for quantifying pterine from microbes

Biochem./physiol. Wirkung

Pterine consists of pyrazine and pyrimidine with substitutions in keto and amino group. Pterine is present in all organisms including cyanobacteria. It acts as a cofactor for redox enzymes and serves as a precursor for folic acid synthesis. Pterine from the butterfly wings absorb light and elicit incoherent scattering. Pterine induces alterations in DNA by hydroxylation of deoxyguanosine.

Sicherheitshinweise

• Piktogramme: GHS07
• Signalwort: Warning
• H-Sätze: H315 - H319 - H335
• P-Sätze: P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
• Gefahreneinstufungen: Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
• Zielorgane: Respiratory system
• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable
• Persönliche Schutzausrüstung: dust mask type N95 (US), Eyeshields, Gloves