| Weight | 822.942 g/mol |
|---|---|
| Formula | C42H62O16 |
| Hydrogen Acceptors | 13 |
| Hydrogen Donors | 8 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 7 |
Glycyrrhizic acid (1405-86-3)
Glycyrrhizin · Glycyrrhizinic Acid · Diammonium Glycyrrhizinate
Score:
#833 in Biochemistry
,
#2238 in Biology
,
#2754 in Chemistry
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- Glycyrrhizin, an active component of liquorice roots, and replication of SARS-associated coronavirus (The Lancet, 2003)
- The long term efficacy of glycyrrhizin in chronic hepatitis C patients (Cancer, 1997)
- GLYCYRRHIZIC ACID INHIBITS VIRUS GROWTH AND INACTIVATES VIRUS PARTICLES (Nature, 1979)
- Glycyrrhizin Binds to High-Mobility Group Box 1 Protein and Inhibits Its Cytokine Activities (Chemistry & Biology, 2007)
- Risk and safety assessment on the consumption of Licorice root (Glycyrrhiza sp.), its extract and powder as a food ingredient, with emphasis on the pharmacology and toxicology of glycyrrhizin (Regulatory Toxicology and Pharmacology, 2006)
- GLYCYRRHIZIN AS A POTENTIAL TREATMENT FOR CHRONIC HEPATITIS C. (Alimentary Pharmacology & Therapeutics, 1998)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Glycyrrhizin
- Glycyrrhizinic Acid
- Diammonium Glycyrrhizinate
- Dipotassium Glycyrrhizinate
- Zinc Glycyrrhizate
-
SMILESCC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)C)C(=O)C=C6C3(CCC7(C6CC(CC7)(C)C(=O)O)C)C)C)C
-
InChIKeyLPLVUJXQOOQHMX-UHFFFAOYSA-N
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