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Urocanic acid
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Urocanic acid

CAS: 104-98-3

Ref. 3D-FU29984

5g
172.00 €
10g
248.00 €
25g
363.00 €
50g
518.00 €
100g
739.00 €
Estimated delivery in United States, on Monday 3 Feb 2025

Product Information

Name:
Urocanic acid
Synonyms:
  • (2E)-3-(1H-imidazol-5-yl)prop-2-enoate
  • (2E)-3-(1H-imidazol-5-yl)prop-2-enoic acid
  • (2Z)-3-(1H-imidazol-5-yl)prop-2-enoic acid
  • 2-Propenoic acid, 3-(1H-imidazol-4-yl)-
  • 2-Propenoic acid, 3-(1H-imidazol-5-yl)-
  • 3-(1H-Imidazol-4-yl)-2-propenoic acid
  • 3-(1H-Imidazol-4-yl)acrylic acid
  • 3-(1H-Imidazol-5-yl)-2-propenoic acid
  • 3-(1H-imidazol-5-yl)prop-2-enoic acid
  • 3-(4-Imidazolyl)acrylic acid
  • See more synonyms
  • 4-Imidazoleacrylic acid
  • 4-Imidazolylacrylic acid
  • 5-Imidazoleacrylic acid
  • Imidazole-4-acrylic acid
  • NSC 66357
  • Urocaninic acid
Description:

Urocanic acid is a metabolite of the amino acid tryptophan. It is found in human urine and has been shown to have high affinity for proteins and nucleic acids, which may be due to its basic structure. Urocanic acid has been shown to have an antiviral effect against picolinic acid-induced herpes simplex virus type 1 (HSV-1) infection in mice. The antiviral effect of urocanic acid is thought to be due to its ability to inhibit HSV-1 DNA polymerase activity and deplete cellular thiocyanate levels. Urocanic acid can also inhibit the growth of cells infected with wild-type strains of human papillomavirus (HPV).

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
138.12 g/mol
Formula:
C6H6N2O2
Purity:
Min. 95%
Color/Form:
Beige Powder
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+
InChI key:
InChIKey=LOIYMIARKYCTBW-OWOJBTEDSA-N
SMILES:
O=C(O)/C=C/c1cnc[nH]1
MDL:
Melting point:
Boiling point:
Flash point:
Density:
Concentration:
EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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