| Weight | 933.139 g/mol |
|---|---|
| Formula | C47H80O18 |
| Hydrogen Acceptors | 18 |
| Hydrogen Donors | 12 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 12 |
Notoginsenoside R1 (80418-24-2)
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- Protective effects of ginsenoside Rb1, ginsenoside Rg1, and notoginsenoside R1 on lipopolysaccharide-induced microcirculatory disturbance in rat mesentery (Life Sciences, 2007)
- Notoginsenoside R1 counteracts endotoxin-induced activation of endothelial cells in vitro and endotoxin-induced lethality in mice in vivo (Arteriosclerosis, Thrombosis, and Vascular Biology, 1997)
- Notoginsenoside R1 inhibits TNF--induced fibronectin production in smooth muscle cells via the ROS/ERK pathway (Free Radical Biology and Medicine, 2006)
- Simultaneous determination of panax notoginsenoside R1, ginsenoside Rg1, Rd, Re and Rb1 in rat plasma by HPLC/ESI/MS: platform for the pharmacokinetic evaluation of total panax notoginsenoside, a typical kind of multiple constituent traditional Chinese medicine. (Biomedical Chromatography, 2007)
- Effect of notoginsenoside R1 on the synthesis of tissue-type plasminogen activator and plasminogen activator inhibitor-1 in cultured human umbilical vein endothelial cells. (Arteriosclerosis, Thrombosis, and Vascular Biology, 1994)
- Characterization of metabolism and in vitro permeability study of notoginsenoside R1 from Radix notoginseng. (Journal of Agricultural and Food Chemistry, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=CCCC(C)(C1CCC2(C1C(CC3C2(CC(C4C3(CCC(C4(C)C)O)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(CO6)O)O)O)C)O)C)OC7C(C(C(C(O7)CO)O)O)O)C
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InChIKeyLLPWNQMSUYAGQI-UHFFFAOYSA-N
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Notoginsenoside R1
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