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Imidazoles

Aromatic organic heterocyclic compounds that consist of a diazole with non-adjacent nitrogen atoms with the formula: C3N2H4.
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1-Methyl-3-propylimidazolium Bis(trifluoromethanesulfonyl)imide 98.0+%, TCI America™

CAS: 216299-72-8 Molecular Formula: C9H13F6N3O4S2 Molecular Weight (g/mol): 405.33 MDL Number: MFCD15071469 InChI Key: CDWUIWLQQDTHRA-UHFFFAOYSA-N PubChem CID: 12040508 IUPAC Name: bis(trifluoromethylsulfonyl)azanide;1-methyl-3-propylimidazol-1-ium SMILES: CCCN1C=C[N+](=C1)C.C(F)(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F

PubChem CID 12040508
CAS 216299-72-8
Molecular Weight (g/mol) 405.33
MDL Number MFCD15071469
SMILES CCCN1C=C[N+](=C1)C.C(F)(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F
IUPAC Name bis(trifluoromethylsulfonyl)azanide;1-methyl-3-propylimidazol-1-ium
InChI Key CDWUIWLQQDTHRA-UHFFFAOYSA-N
Molecular Formula C9H13F6N3O4S2
2

Medchemexpress LLC (Z)-Urocanic acid; cis-UCA | 7699-35-6 | 99.9% | 138.12 | 1 ML
SDP

cis-Urocanic acid is a 5-HT2A receptor agonist. It binds to the 5-HT receptor with relatively high affinity (Kd=4.6 nM) and acts as an immune modulator, inducing immunosuppression by binding to the 5-HT2A receptor.

  • Target: 5-HT Receptor
  • Pathway: GPCR/G Protein; Neuronal Signaling
  • In vitro activity: Treatment with 100 μg/mL cis-Urocanic acid completely suppresses IL-6 and IL-8 secretion, decreases caspase-3 activity, and improves cell viability against UV-B irradiation.
  • Cell lines for assays: Human corneal epithelial cells (HCE-2) and human conjunctival epithelial cells (HCECs)
  • Concentrations for assays: 10, 100, 1,000, and 5,000 μg/mL
  • Incubation time for assays: 24, 48, or 72 hours

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