CAS 52438-12-7
:Isobutyrylshikonin
Description:
Isobutyrylshikonin is a naturally occurring compound classified as a naphthoquinone derivative, primarily extracted from the roots of the plant Lithospermum erythrorhizon, commonly known as purple gromwell. This compound exhibits a range of biological activities, including antimicrobial, anti-inflammatory, and anticancer properties, making it of interest in pharmaceutical research. Isobutyrylshikonin is characterized by its distinctive naphthoquinone structure, which contributes to its reactivity and biological efficacy. It is typically found as a reddish-brown solid and is soluble in organic solvents such as ethanol and dimethyl sulfoxide (DMSO), but has limited solubility in water. The compound's mechanism of action often involves the modulation of various cellular pathways, which can lead to apoptosis in cancer cells. Additionally, its potential applications extend to traditional medicine, where it has been used for its wound-healing properties. Overall, isobutyrylshikonin represents a significant area of study in natural product chemistry and pharmacology due to its diverse therapeutic potential.
Formula:C20H22O6
InChI:InChI=1S/C20H22O6/c1-10(2)5-8-16(26-20(25)11(3)4)12-9-15(23)17-13(21)6-7-14(22)18(17)19(12)24/h5-7,9,11,16,21-22H,8H2,1-4H3/t16-/m1/s1
InChI key:InChIKey=BVRYLTBIGIAADD-MRXNPFEDSA-N
SMILES:O=C1C=2C(C(=O)C=C1[C@H](OC(C(C)C)=O)CC=C(C)C)=C(O)C=CC2O
Synonyms:- (R)-2-Methyl-propanoic acid 1-(1,4-dihydro-5,8-dihydroxy-1,4-dioxo-2-naphthalenyl)-4-methyl-3-pentenyl ester
- Isobutylshikonin
- Isobutyroylshikonin
- Propanoic acid, 2-methyl-, (1R)-1-(1,4-dihydro-5,8-dihydroxy-1,4-dioxo-2-naphthalenyl)-4-methyl-3-penten-1-yl ester
- Propanoic acid, 2-methyl-, (1R)-1-(1,4-dihydro-5,8-dihydroxy-1,4-dioxo-2-naphthalenyl)-4-methyl-3-pentenyl ester
- Propanoic acid, 2-methyl-, 1-(1,4-dihydro-5,8-dihydroxy-1,4-dioxo-2-naphthalenyl)-4-methyl-3-pentenyl ester, (R)-
- Isobutyrylshikonin
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Found 4 products.
Isobutylshikonin
CAS:<p>Isobutylshikonin exhibits obvious antioxidant activities , it exerts very good radical scavenging activities toward ABTS+ but shows moderate inhibition of DPPH</p>Formula:C20H22O6Purity:98.75% - 99.91%Color and Shape:SolidMolecular weight:358.39



