| Weight | 198.178 g/mol |
|---|---|
| Formula | C8H10N2O4 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
L-mimosine (500-44-7, 2116-55-4)
Mimosine · Leucaenol · Leucenine
Score:
#1143 in Biochemistry
,
#2903 in Biology
,
#3635 in Chemistry
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- Cell cycle blockers mimosine, ciclopirox, and deferoxamine prevent the death of PC12 cells and postmitotic sympathetic neurons after removal of trophic support (The Journal of Neuroscience, 1996)
- Mimosine Arrests Proliferating Human Cells before Onset of DNA Replication in a Dose-Dependent Manner (Experimental Cell Research, 1999)
- Mimosine Arrests DNA Synthesis at Replication Forks by Inhibiting Deoxyribonucleotide Metabolism (Journal of Biological Chemistry, 1995)
- The plant amino acid mimosine may inhibit initiation at origins of replication in Chinese hamster cells. (Molecular and Cellular Biology, 1992)
- Initiation of DNA replication in the dihydrofolate reductase locus is confined to the early S period in CHO cells synchronized with the plant amino acid mimosine. (Molecular and Cellular Biology, 1992)
- Reaction of sheep to the consumption of Leucaena glauca Benth. and to its toxic principle mimosine (Crop & Pasture Science, 1964)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Mimosine
- Leucaenol
- Leucenine
- Leucenol
- Leucaenine
-
SMILESC1=CN(C=C(C1=O)O)CC(C(=O)O)N
-
InChIKeyWZNJWVWKTVETCG-UHFFFAOYSA-N
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