| Weight | 141.174 g/mol |
|---|---|
| Formula | C6H11N3O |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
L-histidinol (4836-52-6)
Score:
#1671 in Biochemistry
,
#4721 in Chemistry
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- Hydrolytic metalloenzyme models: Enantioselective hydrolysis of long chain -amino acid esters by chiral metallomicelles composed of lipophilic l-histidinol (Journal of Molecular Catalysis A-chemical, 2003)
- L-histidinol provides effective selection of retrovirus-vector-transduced keratinocytes without impairing their proliferative potential. (Human Gene Therapy, 1991)
- Structures of Escherichia coli histidinol-phosphate aminotransferase and its complexes with histidinol-phosphate and N-(5'-phosphopyridoxyl)-L-glutamate: double substrate recognition of the enzyme. (Biochemistry, 2001)
- Crystal structure of histidinol phosphate aminotransferase (HisC) from Escherichia coli, and its covalent complex with pyridoxal-5'-phosphate and l-histidinol phosphate (Journal of Molecular Biology, 2001)
- Mechanism of action and NAD+-binding mode revealed by the crystal structure of l-histidinol dehydrogenase (Proceedings of the National Academy of Sciences of the United States of America, 2002)
- The Separation and Partial Characterization of l-Histidinol Phosphatase and an Alkaline Phosphatase of Saccharomyces cerevisiae (Journal of Biological Chemistry, 1969)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(NC=N1)CC(CO)N
-
InChIKeyZQISRDCJNBUVMM-UHFFFAOYSA-N
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