Merck
  • 565850
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565850

Sigma-Aldrich

Shikonin

A naphthoquinone found in the Chinese herb Shiunko.

Synonym(s):
Shikonin, Pyruvate Kinase Inhibitor II
Empirical Formula (Hill Notation):
C16H16O5
CAS Number:
Molecular Weight:
288.30
MDL番号:

品質水準

アッセイ

≥98% (HPLC)

形状

solid

manufacturer/tradename

Calbiochem®

保管条件

OK to freeze
protect from light

red

溶解性

DMSO: 10 mg/mL

輸送温度

ambient

保管温度

−20°C

InChI

1S/C16H16O5/c1-8(2)3-4-10(17)9-7-13(20)14-11(18)5-6-12(19)15(14)16(9)21/h3,5-7,10,17-19H,4H2,1-2H3

InChI key

NEZONWMXZKDMKF-UHFFFAOYSA-N

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Shikonin A naphthoquinone found in the Chinese herb Shiunko.

Sigma-Aldrich

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Sigma-Aldrich

573121

SMER28

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥95% (HPLC)

form

solid

form

solid

form

solid

form

solid

manufacturer/tradename

Calbiochem®

manufacturer/tradename

Calbiochem®

manufacturer/tradename

Calbiochem®

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, protect from light

storage condition

OK to freeze, protect from light

storage condition

OK to freeze, protect from light

storage condition

OK to freeze, protect from light

color

red

color

white

color

yellow

color

pale yellow

solubility

DMSO: 10 mg/mL

solubility

DMSO: 50 mg/mL

solubility

DMSO: 10 mg/mL, methanol: soluble

solubility

ethanol: 10 mg/mL, DMSO: 100 mg/mL

詳細

A naphthoquinone found in the Chinese herb Lithospermum erythrorhizon. Possesses significant antibacterial, anti-inflammatory and antitumor activities. Inhibits TNF-α and B-16 melanoma-induced angiogenesis in mice. Blocks the expression of integrin αVβ3 and inhibits endothelial cells proliferation and migration in vitro. Also induces apoptosis in HL60 human promyelocytic leukemia cell line. Selectively blocks PKM2 (IC50<1 µM) over PKM1 and PKL activities (IC50 in the range of 10-20 µM), and inhibits cancer cell glycolysis.
A naphthoquinone found in the Chinese herb Shiunko. Possesses significant antibacterial, anti-inflammatory, and antitumor activities. Inhibits TNF-α-induced and B-16 melanoma-induced angiogenesis in mice. Blocks the expression of integrin αvβ3 and inhibits endothelial cell proliferation and migration in vitro. Also induces apoptosis in HL60 human promyelocytic leukemia cell line.

生物化学的/生理学的作用

Cell permeable: no
Primary Target
TNF-α-induced and B-16 melanoma-induced angiogenesis
Product does not compete with ATP.
Reversible: no

警告

Toxicity: Standard Handling (A)

再構成

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

その他情報

Chen, J., et al. 2011. Oncogene30, 4297.
Li, H., et al. 1999. Phytother. Res.13, 236.
Yoon, Y., et al. 1999. Planta Med.65, 532.
Hisa, T., et al. 1998. Anticancer Res. 18, 783.

法的情報

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

保管分類コード

11 - Combustible Solids

WGK

WGK 3

引火点(°F)

Not applicable

引火点(℃)

Not applicable

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