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| | 5,8-Dihydroxy-2-[(1R)-1-hydroxy-4-methyl-pent-3-enyl]naphthalene-1,4-dione Basic information |
| Product Name: | 5,8-Dihydroxy-2-[(1R)-1-hydroxy-4-methyl-pent-3-enyl]naphthalene-1,4-dione | | Synonyms: | 5,8-Dihydroxy-2-[(R)-1-hydroxy-4-methyl-3-pentenyl]-1,4-naphthalenedione;Tokyo Violet;(R)-5,8-Dihydroxy-2-(1-hydroxy-4-Methylpent-3-en-1-yl)naphthalene-1,4-dione;SHIKONIN(AS);Shikonin, froM Arnebia sp.;(-)-ShikoninChina;Shikonine;Shikonin
5,8-Dihydroxy-2-[(1R)-1-hydroxy-4-methyl-pent-3-enyl]naphthalene-1,4-dione | | CAS: | 517-89-5 | | MF: | C16H16O5 | | MW: | 288.3 | | EINECS: | | | Product Categories: | Inhibitors;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Anthraquinones, Hydroquinones and Quinones | | Mol File: | 517-89-5.mol | ![5,8-Dihydroxy-2-[(1R)-1-hydroxy-4-methyl-pent-3-enyl]naphthalene-1,4-dione Structure](CAS/GIF/517-89-5.gif) |
| | 5,8-Dihydroxy-2-[(1R)-1-hydroxy-4-methyl-pent-3-enyl]naphthalene-1,4-dione Chemical Properties |
| Melting point | 148℃ | | Boiling point | 567.4±50.0 °C(Predicted) | | density | 1.373±0.06 g/cm3(Predicted) | | storage temp. | -20°C | | solubility | DMSO : ≥ 31 mg/mL (107.53 mM); | | pka | 7.34±0.20(Predicted) | | form | Red crystalline solid. | | color | Brown | | LogP | 4.350 (est) | | CAS DataBase Reference | 517-89-5(CAS DataBase Reference) |
| | 5,8-Dihydroxy-2-[(1R)-1-hydroxy-4-methyl-pent-3-enyl]naphthalene-1,4-dione Usage And Synthesis |
| Description | Shikonin could be found in the plant of Lithospermum erythrorhizon Sieb. et. Zucc
and Arnebia euchroma (Royle) Johnst. It could also be produced using plant cell
culture techniques. Shikonin is recorded in British Pharmacopoeia as a reference
compound.
Zicao, a traditional Chinese medicine firstly recorded in Shen Nong’s Herbal Classic, has long been used medically in history . Chinese Pharmacopoeia
(Edition 2015) recorded the root of Arnebia euchroma (Royle) Johnst and Arnebia
guttata Bge as Zicao, which is mainly used for inflammatory diseases such as macular
eruptions, measles, sore throat, carbuncles, and burns.
| | Description | Shikonin is a naturally occurring naphthoquinine isolated from the dried root of L. erythrorhizon, an herb used in traditional Chinese medicine. It increases glucose uptake by adipocytes and myocytes and inhibits the activity of phosphatase and tensin homolog (PTEN; IC50 = 2.7 μM). It inhibits glycolysis in cancer cells by inhibiting tumor-specific pyruvate kinase M2 (IC50 = 0.3 μM). Shikonin induces cell death consistent with necroptosis in MCF-7 and HEK293 cancer cell lines. It inhibits leukocyte migration, downregulates chemokine receptor expression, and inhibits HIV-1 replication at nanomolar concentrations. Shikonin exhibits anti-inflammatory activity, reducing joint swelling and cartilage destruction in a mouse model of collagen-induced arthritis. | | Physical properties | Appearance: purple lamellae or crystalline powder. Melting point: 147 °C. Specific
optical rotation: +138°(benzene). Solubility: soluble in ethanol, vegetable oils, and
other organic solvents. | | History | Kuroda and Majima firstly identified acetyl shikonin from L. erythrorhizon in 1922
, followed by the discovery of other shikonin derivatives, including shikonin. The
chemical structure of shikonin was not precisely identified till 1936 for its high
physicochemical similarity with naphthazarin . There have been about 500 publications
on shikonin up to now. Great attention has also been paid on the biosynthesis
of shikonin and its derivatives, and an increasing number of shikonin derivatives
have been designed and synthesized for exploring their antitumor effect. There are
two types of derivatives: one is modifications of 1′-OH with parent nucleus naphthazarin
remained and the other is modifications of both
1′-OH and parent nucleus naphthazarin, as shown in Fig. 3c, d . | | Uses | A naphthoquinone derivative with angiogenesis inhibitor properties. | | Uses | Shikonin (CI 75535) occurs as an acetyl derivative in the Japanese shikone, Lithospermum erythrorhizon, another member of the Boraginaceae family. It is the (R)-optical isomer of alkannin. Tissue cultures of L. erythrorhizon are used in Japan to manufacture shikonin mainly for cosmetic use. Both alkannin and shikonin are mordant dyes producing violet to gray colors on fabrics. In Japan, shikonin was used to dye fabrics a color known as Tokyo Violet. Shikalkin the racemate, has been synthesized. | | Definition | ChEBI: Shikonin is a hydroxy-1,4-naphthoquinone. | | General Description | This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG | | Pharmacology | Shikonin possesses anti-inflammatory, antioxidant, antiviral, cardiovascular protective,and antitumor activities.
Shikonin reduces inflammation by inhibiting the biosynthesis of leukotrienes and 5-hydroxyeicosatetraenoic acid and thus reduces synthesis of inflammation-related active molecules, which selectively block chemokine binding to CC chemokine receptor 1 .
Shikonin shows free radical scavenging and antioxidant (especially toward superoxide anion and DPPH) activities. It significantly inhibits autoxidation caused by β-carotene and linoleic acid . Its anti-HCV effects have been reported recently with an EC50 at 25 ng/mL, which is lower than that of ribavirin (2.6 μg/mL) .
Recent studies also reveal shikonin possesses cardiovascular protective effects. Shikonin inhibits the activity of TNF-α promoter, revealing its transcriptional antagonism to pro-inflammatory cytokine . Shikonin also shows antitumor potentials by inducing apoptosis and/or necrosis, inhibiting DNA topoisomerase activity and angiogenesis, and regulating proliferative signaling pathways (including MAPK, VEGF, and PTKs ). In addition, shikonin circumvents cancer drug resistance by induction of necroptotic cell death . | | Clinical Use | Shikonin and its derivatives have not been approved for clinical use yet. Studies are
confined to cellular and animal experiments. Its original plant Zicao has a long history
of medical use both orally and externally in China. Various dosage forms of
Zicao, including tablets, injections, oils, creams, tinctures, plastics, and pastes, have
been developed for different clinical applications especially in dermatology, gynecology,
pediatrics, ophthalmology, and otorhinolaryngology. Among them, puccoon
oil and lithospermum cream are the most widely used forms. | | storage | Store at -20°C |
| | 5,8-Dihydroxy-2-[(1R)-1-hydroxy-4-methyl-pent-3-enyl]naphthalene-1,4-dione Preparation Products And Raw materials |
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