| Weight | 194.139 g/mol |
|---|---|
| Formula | C6H10O7 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 5 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 5 |
d-iduronic acid (3402-98-0)
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- Biosynthesis of L-iduronic acid in heparin: Epimerization of D-glucuronic acid on the polymer level (Biochemical and Biophysical Research Communications, 1972)
- Application of a radical reaction to the synthesis of L-iduronic acid derivatives from D-glucuronic acid analogues (Carbohydrate Research, 1986)
- Structure of a highly acidic O-specific polysaccharide of lipopolysaccharide of Pseudoalteromonas haloplanktis KMM 223 (44-1) containing l-iduronic acid and d-QuiNHb4NHb (Carbohydrate Research, 1998)
- A synthetic heparan sulfate pentasaccharide, exclusively containing l-iduronic acid, displays higher affinity for FGF-2 than its d-glucuronic acid-containing isomers (Bioorganic & Medicinal Chemistry, 1999)
- Biosynthesis of heparin. Loss of C-5 hydrogen during conversion of d-glucuronic to l-iduronic acid residues (Biochemical and Biophysical Research Communications, 1976)
- Synthesis and transformations of d-glucuronic and l-iduronic acid glycals (Tetrahedron Letters, 2001)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(=O)C(C(C(C(C(=O)O)O)O)O)O
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InChIKeyIAJILQKETJEXLJ-UHFFFAOYSA-N
- Pubchem - d-iduronic acid
- Wikipedia - Iduronic acid
L-Iduronic acid (IdoA) is the major uronic acid component of the glycosaminoglycans (GAGs) dermatan sulfate, and heparin. It is also present in heparan sulfate although here in a minor amount relative to its carbon-5 epimer glucuronic acid. IdoA is a hexapyranose sugar.
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