| Weight | 388.207 g/mol |
|---|---|
| Formula | C15H15Cl2N3O5 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
Clonitralid (1420-04-8)
Niclosamide · Bayluscide · Yomesan
Score:
#812 in Biochemistry
,
#2193 in Biology
,
#2696 in Chemistry
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- Antineoplastic Mechanisms of Niclosamide in Acute Myelogenous Leukemia Stem Cells: Inactivation of the NF-B Pathway and Generation of Reactive Oxygen Species (Cancer Research, 2010)
- The biology and toxicology of molluscicides, bayluscide (Pharmacology & Therapeutics, 1982)
- Antihelminth Compound Niclosamide Downregulates Wnt Signaling and Elicits Antitumor Responses in Tumors with Activating APC Mutations (Cancer Research, 2011)
- The Anti-Helminthic Niclosamide Inhibits Wnt/Frizzled1 Signaling (Biochemistry, 2009)
- Comparison of the aqueous solubilization of practically insoluble niclosamide by polyamidoamine (PAMAM) dendrimers and cyclodextrins (International Journal of Pharmaceutics, 2005)
- Niclosamide Inhibits Androgen Receptor Variants Expression and Overcomes Enzalutamide Resistance in Castration-Resistant Prostate Cancer (Clinical Cancer Research, 2014)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Niclosamide
- Bayluscide
- Yomesan
- Niclocide
- Bayer 73
- Trdmine
- Fenasal
- Phenasal
- Radewerm
- Bayer 2353
- Clonitralide
- Niclosamide, 2-Aminoethanol (1:1)
-
SMILESC1=CC(=C(C=C1[N+](=O)[O-])Cl)NC(=O)C2=C(C=CC(=C2)Cl)O.C(CO)N
-
InChIKeyXYCDHXSQODHSLG-UHFFFAOYSA-N
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