| Weight | 286.28 g/mol |
|---|---|
| Formula | C13H18O7 |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 5 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
salicin (138-52-3)
salicyl alcohol glucoside
Score:
#1779 in Biochemistry
,
#3897 in Biology
,
#4908 in Chemistry
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- Sigma-Aldrich - salicin37.90 - 440.00 USD
- Fisher Scientific - Search for salicin
- TCI - salicin39.00 - 118.00 USD
- Salicin from host plant as precursor of salicylaldehyde in defensive secretion of chrysomeline larvae (Physiological Entomology, 1983)
- Ecological Effects of Salicin at Three Trophic Levels: New Problems from Old Adaptations (Science, 1985)
- Pharmacokinetics of salicin after oral administration of a standardised willow bark extract. (European Journal of Clinical Pharmacology, 2001)
- THE TREATMENT OF ACUTE RHEUMATISM BY SALICIN. (The Lancet, 1876)
- Probenecid inhibits the human bitter taste receptor TAS2R16 and suppresses bitter perception of salicin. (PLOS ONE, 2011)
- Pyrazinamidase, CR-MOX agar, salicin fermentation-esculin hydrolysis, and D-xylose fermentation for identifying pathogenic serotypes of Yersinia enterocolitica. (Journal of Clinical Microbiology, 1992)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - salicyl alcohol glucoside
-
SMILESC1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O
-
InChIKeyNGFMICBWJRZIBI-UHFFFAOYSA-N
- Pubchem - salicin
- Wikipedia - salicin
Salicin is an alcoholic -glucoside. Salicin is produced in (and named after) willow (Salix) bark and acts as an anti-inflammatory agent in the human body. Salicin is also commonly found in the bark of Populus species, and the leaves of willows and poplars.
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