L6152

D-Luciferin

synthetic, BioXtra, ≥99% (HPLC)

• Sinónimos: (S)-2-(6-Hydroxy-2-benzothiazolyl)-2-thiazoline-4-carboxylic acid, 4,5-Dihydro-2-(6-hydroxy-2-benzothiazolyl)-4-thiazolecarboxylic acid, Firefly Luciferin
• Fórmula empírica (notación de Hill): C₁₁H₈N₂O₃S₂
• Número de CAS: 2591-17-5
• Peso molecular: 280.32
• Beilstein/REAXYS Number: 30484
• EC Number: 219-981-3
• MDL number: MFCD00042929
• UNSPSC Code: 12352204
• PubChem Substance ID: 24896428
• NACRES: NA.32

Propiedades

• biological source: synthetic
• Quality Level: 200
• product line: BioXtra
• assay: ≥99% (HPLC)
• form: powder
• solubility: DMSO: 10 mg/mL, clear, colorless to faintly yellow
• storage temp.: −20°C
• SMILES string: OC(=O)[C@H]1CSC(=N1)c2nc3ccc(O)cc3s2
• InChI: 1S/C11H8N2O3S2/c14-5-1-2-6-8(3-5)18-10(12-6)9-13-7(4-17-9)11(15)16/h1-3,7,14H,4H2,(H,15,16)/t7-/m1/s1
• InChI key: BJGNCJDXODQBOB-SSDOTTSWSA-N

Descripción

General description

D-Luciferin is mainly produced in bioluminescent organisms. It has the ability to simply circulate across the blood testis barrier, blood brain barrier and the blood placenta barrier. This small molecule is sensitive to light and oxygen. It is also sensitive to moisture in its powder form.

Application

D-Luciferin has been used in the preparation of the reaction mixture for nitric oxide determination by minescence measurement. It has also been used in the preparation of D-luciferin stock solution for luciferin assays.

Substrate for firefly luciferase with a Km of approx 2 μM.

Linkage

Highly purified grade with reduced levels of inhibitor relative to L 9504

Información de seguridad

• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)