113639-01-3

5-Aminolevulinic acid-<sup>13</sup>C<sub>2</sub>,<sup>15</sup>N hydrochloride Chemical Structure
113639-01-3

Chemical Structure

5-Aminolevulinic acid-13C2,15N hydrochloride

Synonym(s): 5-ALA-13C2,15N hydrochloride; δ-Aminolevulinic acid-13C2,15N hydrochloride; 5-Amino-4-oxopentanoic acid-13C2,15N hydrochloride

  • CAS No.: 113639-01-3
  • Formula:C313C2H10Cl15NO3
  • Molecular Weight:170.57

IUPAC Name: 5-(amino-15N)-4-oxopentanoic-4,5-13C2 acid hydrochloride

InChIKey: ZLHFONARZHCSET-MBIZCHBVSA-N

SMILES: O=C(O)CC[13C]([13CH2][15NH2])=O.Cl

Biological Activity: 5-Aminolevulinic acid-13C2,15N (5-ALA-13C2,15N; δ-Aminolevulinic acid-13C2,15N) is 13C- and 15N-labeled 5-Aminolevulinic acid (HY-W000450)[1].

Cat. No. Product Name Purity Description Pricing
HY-W749251
5-Aminolevulinic acid-13C2,15N hydrochloride 99.94% 5-Aminolevulinic acid-13C2,15N (5-ALA-13C2,15N; δ-Aminolevulinic acid-13C2,15N) is 13C- and 15N-labeled 5-Aminolevulinic acid (HY-W000450).
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HY-W000450S
5-Aminolevulinic acid-13C 5-Aminolevulinic acid-13C is the 13C-labeled 5-Aminolevulinic acid. 5-Aminolevulinic acid (5-ALA) is a non-protein amino acid that plays a rate-limiting role in heme biosynthesis.
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HY-W000450
5-Aminolevulinic acid 99.92% 5-Aminolevulinic acid (5-ALA; δ-Aminolevulinic acid; 5-Amino-4-oxopentanoic acid) is an orally active heme precursor. 5-Aminolevulinic acid promotes aerobic energy metabolism and increases ATP levels by enhancing the activity of cytochrome c oxidase. 5-Aminolevulinic acid enhances LPS-induced proinflammatory cytokine production and gene activation, and restores the phagocytic activity and ROS generation capacity of neutrophils. 5-Aminolevulinic acid selectively accumulates protoporphyrin IX in tumor cells; as a photosensitizer and radiosensitizer, it induces ROS burst upon light or X-ray irradiation to inhibit tumor growth. 5-Aminolevulinic acid can be applied to the research of septic shock, melanoma, and cancer radiotherapy.
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