| Weight | 212.252 g/mol |
|---|---|
| Formula | C13H12N2O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
1,3-Diphenylurea (102-07-8)
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- Activation of Human ether-a-go-go-Related Gene Potassium Channels by the Diphenylurea 1,3-Bis-(2-hydroxy-5- trifluoromethyl-phenyl)-urea (NS1643) (Molecular Pharmacology, 2005)
- Dual-target-directed 1,3-diphenylurea derivatives: BACE 1 inhibitor and metal chelator against Alzheimer's disease. (Bioorganic & Medicinal Chemistry, 2010)
- N6-1,3-diphenylurea derivatives of 2-phenyl-9-benzyladenines and 8-azaadenines: synthesis and biological evaluation as allosteric modulators of A2A adenosine receptors. (European Journal of Medicinal Chemistry, 2008)
- Conformational preferences in model antiviral compounds: A spectroscopic and computational study of phenylurea and 1,3-diphenylurea (Physical Chemistry Chemical Physics, 2004)
- Potent Activation of Large-Conductance Ca2+-Activated K+ Channels by the Diphenylurea 1,3-Bis-[2-hydroxy-5-(trifluoromethyl)phenyl]urea (NS1643) in Pituitary Tumor (GH3) Cells (Molecular Pharmacology, 2008)
- Antiprotozoal activity and DNA binding of N- Substituted N-phenylbenzamide and 1,3- Diphenylurea Bisguanidines (European Journal of Medicinal Chemistry, 2014)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)NC(=O)NC2=CC=CC=C2
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InChIKeyGWEHVDNNLFDJLR-UHFFFAOYSA-N
- Pubchem - 1,3-Diphenylurea
- Wikipedia - 1,3-diphenylurea
1,3-Diphenylurea is a phenylurea-type cytokinin, a type of plant hormone that induces flower development. Folke Skoog discovered the effects of cytokinins using coconut milk in the 1940s at the University of WisconsinMadison. 1,3-Diphenylurea is a compound that has been thereafter identified in coconut milk.
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1,3-Diphenylurea
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