![4,5-DIHYDRO-2[6-AMINO-2-BENZTHIAZOLYL]-4-THIAZOLE CARBOXYLIC ACID](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F281117-45-dihydro-2-6-amino-2-benzthiazolyl-4-thiazole-carboxylic-acid.webp&w=3840&q=75)
CAS 118969-27-0: 4,5-DIHYDRO-2[6-AMINO-2-BENZTHIAZOLYL]-4-THIAZOLE CARBOXYLIC ACID
Formula:C11H9N3O2S2
InChI:InChI=1/C11H9N3O2S2/c12-5-1-2-6-8(3-5)18-10(13-6)9-14-7(4-17-9)11(15)16/h1-3,7H,4,12H2,(H,15,16)
SMILES:c1cc2c(cc1N)sc(C1=NC(CS1)C(=O)O)n2
Synonyms:- ADL
- 6-Amino-6-Deoxyluciferin
- 6-Amino-D-Luciferin
- 6-Amino Luciferin
- 6-Amino-6-Deoxyluciferin (Adl)
- 2-(6-Amino-1,3-Benzothiazol-2-Yl)-4,5-Dihydro-1,3-Thiazole-4-Carboxylic Acid
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6-Amino-6-deoxyluciferin
CAS:6-Amino-6-deoxyluciferin is a synthetic analog of luciferin. It is used as a substrate for bacterial luciferase and in immunoassays to detect neutrophils, infectious diseases, and various protease activities. 6-Amino-6-deoxyluciferin is synthesized by the condensation of an amide with a hydroxyl group from acetaldehyde. This reaction requires the use of a coupling agent such as dicyclohexylcarbodiimide or 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC), which are often used to form amides from carboxylic acids and amines. The conjugation of 6-amino-6-deoxyluciferin with antibodies can be accomplished by chemical crosslinking methods, such as glutaraldehyde, which react thiol groups on the antibodyFormula:C11H9N3O2S2Purity:Min. 95%Color and Shape:Yellow SolidMolecular weight:279.34 g/mol