| Identification | More | [Name]
Shikonin
| [CAS]
517-89-5 | [Synonyms]
(-)-SHIKONIN
SHIKONIN
8-dihydroxy-2-(1-hydroxy-4-methyl-3-pentenyl)-4-naphthoquinon(+)-5
c.i.75535
SHIKONIN 98+%
Shikonin (C.I. 75535)
5,8-Dihydroxy-2-[(1R)-1-hydroxy-4-methyl-pent-3-enyl]naphthalene-1,4-dione
(1-hydroxy-4-methyl-3-pentenyl)-, (R)-
1,4-Naphthalenedione, 5,8-dihydroxy-2-
GromweIl pigment
(+)-5,8-Dihydroxy-2-[(R)-1-hydroxy-4-methyl-3-pentenyl]-1,4-naphthalenedione
| [Molecular Formula]
C16H16O5 | [MDL Number]
MFCD00075680 | [Molecular Weight]
288.3 | [MOL File]
517-89-5.mol |
| Chemical Properties | Back Directory | [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); | [form ]
Red crystalline solid. | [pka]
7.34±0.20(Predicted) | [color ]
Brown | [LogP]
4.350 (est) | [CAS DataBase Reference]
517-89-5(CAS DataBase Reference) |
| Safety Data | Back Directory | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [RIDADR ]
3077 | [HS Code ]
29146990 | [Hazardous Substances Data]
517-89-5(Hazardous Substances Data) |
| Hazard Information | Back Directory | [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.
| [Chemical Properties]
Purple-brown crystals with a needle-like shape, melting at 147 ° C, with a rotativity of αD20 = +135 ° (in benzene). It dissolves readily in phenethyl ether, acetone, chloroform, methanol, ethanol, glycerol, animal and vegetable oils, and alkaline aqueous solutions, but is insoluble in water. Its color changes depending on the pH value: at pH 4-6, it turns red; at pH 8, it becomes purple; and at pH 10-12, it appears blue. It exhibits excellent resistance to light, heat, and oxidation, but is reactive to reducing agents, causing the formation of dark purple when exposed to iron ions. Additionally, Shikonin has certain antibacterial effect. | [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]
Shikonin (517-89-5) 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 2-8°C, protect from light |
| Questions And Answer | Back Directory | [Plant extract]
The purple-colored roots of red gromwell (Lithos-permum erythrorhizon), also known as “zicao” in Chinese, “jichi” in Korean, and “murasaki” in Japanese, have been used as part of traditional medicines, as adyestuff, and in cosmetics across many cultures for centuries. The responsible bioactive and pigmented compounds, shikonin—or its enantiomer, alkannin—and dozens of other acylated shikonin/alkannin derivatives, are synthesized in the root periderm of L. erythrorhizon and several other Boraginaceae species.Shikonins/alkannins are deposited into the rhizosphere where they function in plant-microbe interactions and interfere with the growth of competing plants (allelopathy), roles suggested having contributed to the invasion success of species like Echium plantagineum. The presence of alkannins was also reported in Plagiobothrysarizonicus leaves, though the physiological and/or ecological significance of their presence in aerial tissues is unclear. Shikonin is produced in the roots of Lithospermum erythrorhizon. Fig. Intact roots of L. erythrorhizon producing shikonin. Fig b. Hairy root culture of L. erythrorhizon producing shikonin[1].
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