Product Name :
Urocanic acid
Description:
Urocanic acid, produced in the upper layers of mammalian skin, is a major absorber of ultraviolet radiation (UVR).
CAS:
104-98-3
Molecular Weight:
138.12
Formula:
C6H6N2O2
Chemical Name:
(2E)-3-(1H-imidazol-5-yl)prop-2-enoic acid
Smiles :
OC(=O)/C=C/C1=CN=CN1
InChiKey:
LOIYMIARKYCTBW-OWOJBTEDSA-N
InChi :
InChI=1S/C6H6N2O2/c9-6(10)2-1-5-3-7-4-8-5/h1-4H,(H,7,8)(H,9,10)/b2-1+
Purity:
≥98% (or refer to the Certificate of Analysis)
Shipping Condition:
Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis
Storage Condition :
Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.{{Omidenepag} site|{Omidenepag} GPCR/G Protein|{Omidenepag} Technical Information|{Omidenepag} Data Sheet|{Omidenepag} custom synthesis|{Omidenepag} Cancer}
Shelf Life:
≥12 months if stored properly.
Stock Solution Storage:
0 – 4 oC for 1 month or refer to the Certificate of Analysis.
Additional information:
Urocanic acid, produced in the upper layers of mammalian skin, is a major absorber of ultraviolet radiation (UVR).{{Oligomycin} web|{Oligomycin} Metabolic Enzyme/Protease|{Oligomycin} Biological Activity|{Oligomycin} Purity|{Oligomycin} manufacturer|{Oligomycin} Epigenetic Reader Domain} |Product information|CAS Number: 104-98-3|Molecular Weight: 138.PMID:24268253 12|Formula: C6H6N2O2|Chemical Name: (2E)-3-(1H-imidazol-5-yl)prop-2-enoic acid|Smiles: OC(=O)/C=C/C1=CN=CN1|InChiKey: LOIYMIARKYCTBW-OWOJBTEDSA-N|InChi: InChI=1S/C6H6N2O2/c9-6(10)2-1-5-3-7-4-8-5/h1-4H,(H,7,8)(H,9,10)/b2-1+|Technical Data|Appearance: Solid Power|Purity: ≥98% (or refer to the Certificate of Analysis)|Solubility: DMSO : 50 mg/mL (362.00 mM; Need ultrasonic). H2O : 2 mg/mL (14.48 mM; Need ultrasonic).|Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis|Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.|Shelf Life: ≥12 months if stored properly.|Stock Solution Storage: 0 – 4 oC for 1 month or refer to the Certificate of Analysis.|Drug Formulation: To be determined|HS Tariff Code: 382200|How to use|In Vitro:|Urocanic acid (UCA) is formed in the upper layers of the epidermis where filaggrin, a histidine-rich filamentous protein produced after caspase-14 cleavage of profilaggrin, is broken down by proteinases into component amino acids.|Products are for research use only. Not for human use.|