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| Product | Description | |
|---|---|---|
| Urocanic acid | Imidazoles. Alternative Names: 2-Propenoic acid, 3-(1H-imidazol-4-yl)-;3-Imidazol-4-ylacrylic acid. CAS No. 104-98-3. Molecular formula: C6H6N2O2. Mole weight: 138.12. Appearance: White to Off-White Powder. Purity: 0.99. Catalog: ACM104983. |  |
| Urocanic acid | It is produced by the strain of Bac. subtilis var. theronophilus. Urocanic acid has an inhibitory effect on Eichner's ascites pain in animals. Synonyms: 4-imidazoleacrylic acid; trans-Urocanic acid; 5-Imidazoleacrylic acid; (2E)-3-(1H-IMIDAZOL-4-YL)ACRYLIC ACID; 3-(1H-Imidazol-4-yl)-2-propenoic acid; NSC 66357. Grades: 99%. CAS No. 104-98-3. Molecular formula: C6H6N2O2. Mole weight: 138.12. |  |
| Urocanic acid | Urocanic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 104-98-3. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C6H6N2O2. US Biological Life Sciences. |  Worldwide |
| Urocanic acid | Urocanic acid, produced in the upper layers of mammalian skin, is a major absorber of ultraviolet radiation (UVR). Uses: Scientific research. Group: Natural products. CAS No. 104-98-3. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-113008. |  |
| cis-Urocanic acid | cis-Urocanic acid is a 5-HT2A receptor agonist. cis-Urocanic acid binds to 5-HT receptor with relatively high affinity ( K d =4.6 nM). cis-Urocanic acid is an immune modulator that induces immunosuppression by binding to the 5-HT2A receptor [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (Z)-Urocanic acid; cis-UCA. CAS No. 7699-35-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-113008A. | |
| cis-Urocanic Acid | cis-Urocanic acid is an agonist of the 5-HT2A receptor. Group: Biochemicals. Grades: Highly Purified. CAS No. 7699-35-6. Pack Sizes: 10mg, 50mg. Molecular Formula: C6H6N2O2, Molecular Weight: 138.12. US Biological Life Sciences. | Worldwide |
| Cis-Urocanic acid (1,2,3-13C3) | Isotope-labeled Metabolites13C Labeled Compounds. Alternative Names: cis-UCA-[13C3]; cis-3-(1H-imidazol-4-yl)-2-propenoic acid-[13C3]. CAS No. 1173097-34-1. Molecular formula: C313C3H6N2O2. Mole weight: 141.1. Appearance: White solid. Catalog: ACM1173097341. | |
| E-Urocanic acid | E-Urocanic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 3465-72-3. Pack Sizes: 2g, 5g, 10g, 25g, 50g. US Biological Life Sciences. | Worldwide |
| trans-Urocanic acid | trans-urocanic acid (trans-UCA), a natural epidermal constituent, inhibits human natural killer cell (NK) activity in vitro. trans-urocanic acid is active in regulating an immune function [1]. Uses: Scientific research. Group: Natural products. Alternative Names: (E)-Urocanic acid; trans-UCA. CAS No. 3465-72-3. Pack Sizes: 10 mM * 1 mL; 1 g. Product ID: HY-113008B. | |
| histidine ammonia-lyase | This enzyme is a member of the aromatic amino acid lyase family, other members of which are EC 4.3.1.23 (tyrosine ammonia-lyase), EC 4.3.1.24 (phenylalanine ammonia-lyase) and EC 4.3.1.25 (phenylalanine/tyrosine ammonia-lyase). The enzyme contains the cofactor 3,5-dihydro-5-methylidene-4H-imidazol-4-one (MIO), which is common to this family. This unique cofactor is formed autocatalytically by cyclization and dehydration of the three amino-acid residues alanine, serine and glycine. This enzyme catalyses the first step in the degradation of histidine and the product, urocanic acid, is further metabolized to glutamate. Group: Enzymes. Synonyms: histidase; histidinase; histidine α-deaminase; L-histidine ammonia-lyase. Enzyme Commission Number: EC 4.3.1.3. CAS No. 9013-75-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5289; histidine ammonia-lyase; EC 4.3.1.3; 9013-75-6; histidase; histidinase; histidine α-deaminase; L-histidine ammonia-lyase. Cat No: EXWM-5289. |  |
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