| Weight | 614.65 g/mol |
|---|---|
| Formula | C23H46N6O13 |
| Hydrogen Acceptors | 19 |
| Hydrogen Donors | 13 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 9 |
Neomycin C (66-86-4)
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- Phorbol ester and neomycin dissociate bradykinin receptor-mediated arachidonic acid release and polyphosphoinositide hydrolysis in Madin-Darby canine kidney cells. Evidence that bradykinin mediates noninterdependent activation of phospholipases A2 and C. (Journal of Biological Chemistry, 1988)
- Blocking c-Jun-N-terminal kinase signaling can prevent hearing loss induced by both electrode insertion trauma and neomycin ototoxicity. (Hearing Research, 2007)
- C-13 NMR Spectra of Some Aminosugars and Sugar-Antibiotics, Neomycin and Kanamycin (Chemical & Pharmaceutical Bulletin, 1974)
- Phosphoinositide hydrolysis by phospholipase C modulated by multivalent cations La3, Al3+, neomycin, polyamines, and melittin (Journal of Lipid Mediators and Cell Signalling, 1995)
- The effects of bradykinin on K+ currents in NG10815 cells treated with U73122, a phospholipase C inhibitor, or neomycin (British Journal of Pharmacology, 1997)
- Further Characterization of Neomycin B and Neomycin C (Journal of the American Chemical Society, 1955)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C(C(C(C(C1N)OC2C(C(C(C(O2)CN)O)O)N)OC3C(C(C(O3)CO)OC4C(C(C(C(O4)CN)O)O)N)O)O)N
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InChIKeyPGBHMTALBVVCIT-UHFFFAOYSA-N
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