104-98-3
104-98-3
Chemical Structure
Urocanic acid
- CAS No.: 104-98-3
- Formula:C6H6N2O2
- Molecular Weight:138.13
IUPAC Name: (E)-3-(1H-imidazol-5-yl)acrylic acid
InChIKey: LOIYMIARKYCTBW-OWOJBTEDSA-N
SMILES: O=C(O)/C=C/C1=CN=CN1
Biological Activity: Urocanic acid, produced in the upper layers of mammalian skin, is a major absorber of ultraviolet radiation (UVR).
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Urocanic acid | 99.96% | Urocanic acid, produced in the upper layers of mammalian skin, is a major absorber of ultraviolet radiation (UVR). | ||||||||||||||||||||
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Urocanic acid (Standard) | 99.29% | Urocanic acid (Standard) is the analytical standard of Urocanic acid. This product is intended for research and analytical applications. Urocanic acid, produced in the upper layers of mammalian skin, is a major absorber of ultraviolet radiation (UVR). | ||||||||||||||||||||
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Urocanic acid-13C3 | Urocanic acid-13C3 is the 13C labeled Urocanic acid. Urocanic acid, produced in the upper layers of mammalian skin, is a major absorber of ultraviolet radiation (UVR). | |||||||||||||||||||||
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cis-Urocanic acid | 99.81% | cis-Urocanic acid is a 5-HT2A receptor agonist. cis-Urocanic acid binds to 5-HT receptor with relatively high affinity (Kd=4.6 nM). cis-Urocanic acid is an immune modulator that induces immunosuppression by binding to the 5-HT2A receptor. | ||||||||||||||||||||
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trans-Urocanic acid (Standard) | ≥98% | trans-Urocanic acid (Standard) is the analytical standard of trans-Urocanic acid. This product is intended for research and analytical applications. 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. | ||||||||||||||||||||
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Imidazoleacetic acid (Standard) | ≥98% | Imidazoleacetic acid (Standard) is the analytical standard of Imidazoleacetic acid (HY-113413). This product is intended for research and analytical applications. Imidazoleacetic acid (Imidazolyl-4-acetic acid) is a blood-brain barrier-permeable full agonist of the GABAA receptor. Imidazoleacetic acid forms via histamine oxidation in the mouse brain. Imidazoleacetic acid exerts multiple neurochemical and behavioral effects. Imidazoleacetic acid induces a range of centrally mediated effects, including analgesia, sedation, hypnosis, as well as reductions in blood pressure, body temperature, isolation-induced aggression and motor activity. | ||||||||||||||||||||
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Thiourocanic acid | Thiourocanic acid is a product of the reaction between ergothionase and the ergothioneine substrate. | |||||||||||||||||||||
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Imidazoleacetic acid hydrochloride (Standard) | ≥98% | Imidazoleacetic acid (hydrochloride) (Standard) is the analytical standard of Imidazoleacetic acid (hydrochloride). This product is intended for research and analytical applications. Imidazoleacetic acid hydrochloride is a γ-aminobutyric acid receptor agonist. Imidazoleacetic acid hydrochloride inhibits GABA-T in a non-competitive manner, with a Ki value of 0.34 mM. Imidazoleacetic acid hydrochloride increases total free GABA in brain. | ||||||||||||||||||||
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1H-Imidazole-4-carboxylic acid | 99.95% | 1H-Imidazole-4-carboxylic acid (4-Imidazolecarboxylic acid) is an organic compound containing an imidazole ring and a carboxyl group. 1H-Imidazole-4-carboxylic acid stabilizes specific forms of metal ions through coordination, thus influencing the progress of chemical reactions. 1H-Imidazole-4-carboxylic acid plays an important role in the hydrolysis of phosphate esters catalyzed by lanthanide metals. 1H-Imidazole-4-carboxylic acid can be used to modify dendrimers, changing the surface properties and catalytic performance of materials. | ||||||||||||||||||||
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DL-Histidine-15N | DL-Histidine-15N is a 15N-labeled DL-Histidinen (HY-W010209). DL-Histidine is a histidine derivative. | |||||||||||||||||||||
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trans-3-(3-Pyridyl)acrylic acid | 99.90% | trans-3-(3-Pyridyl) acrylic acid is an unsaturated carboxylic acid and synthetic building block, which serves as a synthetic precursor of 3-(3-pyridyl) propanoic acid. trans-3-(3-Pyridyl) acrylic acid can be used to prepare dual mutant IDH1/NAMPT inhibitors and PGE2 antagonist analogs. In addition, trans-3-(3-Pyridyl) acrylic acid exhibits antiviral activity against tobacco mosaic virus (TMV). | ||||||||||||||||||||
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Imidazole-5-propionic acid | 99.99% | Imidazole-5-propionic acid (Imidazolepropionic acid) is a urinary metabolite of L-histidine (HY-N0832). Imidazole-5-propionic acid can be used in the research of intestinal diseases and cardiovascular diseases. | ||||||||||||||||||||
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