Weight | 167.592 g/mol |
---|---|
Formula | C5H10ClNO3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 4 |
5-Aminolevulinic acid hydrochloride (5451-09-2)
Aminolevulinic Acid · Levulan · Delta Aminolevulinic Acid
Score:
#3309 in Biology
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#4129 in Chemistry
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- Fluorescence-guided surgery with 5-aminolevulinic acid for resection of malignant glioma: a randomised controlled multicentre phase III trial (Lancet Oncology, 2006)
- THE OCCURRENCE AND DETERMINATION OF -AMINOLEVULINIC ACID AND PORPHOBILINOGEN IN URINE (Journal of Biological Chemistry, 1956)
- 5-Aminolevulinic acid-based photodynamic therapy : Clinical research and future challenges (Cancer, 1997)
- The Induction in Vitro of the Synthesis of -Aminolevulinic Acid Synthetase in Chemical Porphyria: A Response to Certain Drugs, Sex Hormones, and Foreign Chemicals (Journal of Biological Chemistry, 1966)
- Fluorescence-guided resection of glioblastoma multiforme by using 5-aminolevulinic acid-induced porphyrins: a prospective study in 52 consecutive patients. (Journal of Neurosurgery, 2000)
- 5-Aminolevulinic Acid-Based Photodynamic Therapy: Principles and Experimental Research (Photochemistry and Photobiology, 1997)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Aminolevulinic Acid
- Levulan
- Delta Aminolevulinic Acid
- Aminolevulinic Acid Hydrochloride
- 5 Aminolevulinate
- 5-Aminolaevulinate
- 5 Aminolaevulinate
- 5-Aminolevulinate
- Delta-Aminolevulinic Acid
-
SMILESC(CC(=O)O)C(=O)CN.Cl
-
InChIKeyZLHFONARZHCSET-UHFFFAOYSA-N
- Pubchem - 5-Aminolevulinic acid hydrochloride
- Wikipedia - aminolevulinic acid hydrochloride
-Aminolevulinic acid (also dALA, -ALA, 5ALA or 5-aminolevulinic acid), an endogenous non-protein amino acid, is the first compound in the porphyrin synthesis pathway, the pathway that leads to heme in mammals and chlorophyll in plants. 5ALA is used in photo dynamic detection and photo dynamic surgery of cancer.
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