kojic acid

Synonyms: "5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one", "5-hydroxy-2-(hydroxymethyl)-4-pyrone", "5-hydroxy-2-hydroxymethyl-4-pyrone", "5-hydroxy-2-(hydroxymethyl)pyran-4-one", "2-(Hydroxymethyl)-5-hydroxy-4H-pyran-4-one", "5-hydroxy-2-hydroxymethyl-4H-4-pyranone", "pyran-4-one, 5-hydroxy-2-(hydroxymethyl)", "5-Hydroxy-2-hydroxymethyl-4H-pyran-4-on"

Source: Kojic acid is used as a key ingredient in the preparation of skin care products because it acts as a skin lightening and depigmenting agent

Identifiers:

IUPAC Name: 5-hydroxy-2-(hydroxymethyl)pyran-4-one
CAS Number: 501-30-4
PubChem ID: 3840
InChiKey: BEJNERDRQOWKJM-UHFFFAOYSA-N
Canonical SMILES: C1=C(OC=C(C1=O)O)CO

Structural Properties:

Molecular Formula: C6H6O4
Molecular Weight: 142.110

Pharmacophore Features:

Number of bond donors: 2
Number of bond acceptors: 4
Number of atoms different from hydrogen: 10

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Evidence Supporting This Chemical as an Endocrine Disruptor
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Fujimoto, N., Watanabe, H., Nakatani, T., Roy, G. and Ito, A., 1998. Induction of thyroid tumours in (C57BL/6NA? C3H/N) F1 mice by oral administration of kojic acid. Food and chemical toxicology, 36(8), pp.697-703. DOI: https://doi.org/10.1016/S0278-6915(98)00030-1. URL: https://www.sciencedirect.com/science/article/pii/S0278691598000301.
Higa, Y., Ohkubo, A., Kitajima, S., Moriyasu, M. and Kariya, K., 2002. Effects of kojic acid on thyroidal functions in rats by single-dose administration and in cultured rat thyroid cells (FRTL-5 cells). The Journal of toxicological sciences, 27(5), pp.423-431. DOI: https://doi.org/10.2131/jts.27.423. URL: https://www.jstage.jst.go.jp/article/jts/27/5/27_5_423/_article/-char/ja/.
Ota, Y., Imai, T., Onose, J.I., Takami, S., Cho, Y.M., Hirose, M. and Nishikawa, A., 2009. A 55-week chronic toxicity study of dietary administered kojic acid (KA) in male F344 rats. The Journal of toxicological sciences, 34(3), pp.305-313. DOI: https://doi.org/10.2131/jts.34.305. URL: https://www.jstage.jst.go.jp/article/jts/34/3/34_3_305/_article/-char/ja/.

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