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24502-79-2,MFCD00143687
Catalog No.:AA002OA0

24502-79-2 | 2-Butenoic acid, 3-methyl-, (1R)-1-(1,4-dihydro-5,8-dihydroxy-1,4-dioxo-2-naphthalenyl)-4-methyl-3-penten-1-yl ester

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5mg
>90%(HPLC)
in stock  
$150.00   $105.00
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25mg
>90%(HPLC)
in stock  
$299.00   $209.00
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100mg
>90%(HPLC)
in stock  
$597.00   $418.00
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  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA002OA0
Chemical Name:
2-Butenoic acid, 3-methyl-, (1R)-1-(1,4-dihydro-5,8-dihydroxy-1,4-dioxo-2-naphthalenyl)-4-methyl-3-penten-1-yl ester
CAS Number:
24502-79-2
Molecular Formula:
C21H22O6
Molecular Weight:
370.3958
MDL Number:
MFCD00143687
SMILES:
CC(=CC[C@H](C1=CC(=O)c2c(C1=O)c(O)ccc2O)OC(=O)C=C(C)C)C
Properties
Properties
 
BP:
587.3°C at 760 mmHg  
Form:
Solid  
MP:
103°C  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
706  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
27  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
6  
XLogP3:
5  

Literature

Title: Exploration of natural compounds as sources of new bifunctional scaffolds targeting cholinesterases and beta amyloid aggregation: the case of chelerythrine.

Journal: Bioorganic & medicinal chemistry 20121115

Title: Naphthoquinones from Onosma paniculata induce cell-cycle arrest and apoptosis in melanoma Cells.

Journal: Journal of natural products 20120525

Title: Ionization of shikonin derivatives using negative-ion electrospray mass spectrometry: [M-H]- versus [M + e]•-.

Journal: Journal of mass spectrometry : JMS 20120501

Title: Selective and slow-binding inhibition of shikonin derivatives isolated from Lithospermum erythrorhizon on glycosyl hydrolase 33 and 34 sialidases.

Journal: Bioorganic & medicinal chemistry 20120301

Title: Effect of β,β-dimethylacrylshikonin on inhibition of human colorectal cancer cell growth in vitro and in vivo.

Journal: International journal of molecular sciences 20120101

Title: Determination of the active constituents in Arnebia euchroma (Royle) Johnst. by ionic liquid-based ultrasonic-assisted extraction high-performance liquid chromatography.

Journal: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20110615

Title: The anti-proliferation effect of Aikete injection on hepatocellular carcinoma in vitro and in vivo.

Journal: Pharmaceutical biology 20110501

Title: Quantitative determination of beta,beta-dimethylacrylshikonin (DASK) in rat whole blood by liquid chromatography-tandem mass spectrometry with pre-column derivation and its pharmacokinetic application.

Journal: Biomedical chromatography : BMC 20090401

Title: Evaluation of the anti-inflammatory and cytotoxic activities of naphthazarine derivatives from Onosma leptantha.

Journal: Phytomedicine : international journal of phytotherapy and phytopharmacology 20060301

Title: Zeng Z, et al. Arnebin-1 promotes angiogenesis by inducing eNOS, VEGF and HIF-1α expression through the PI3K-dependent pathway. Int J Mol Med. 2015 Sep;36(3):685-97.

Title: Sidhu GS, et al. Arnebin-1 accelerates normal and hydrocortisone-induced impaired wound healing. J Invest Dermatol. 1999 Nov;113(5):773-81.

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Tags:24502-79-2 Molecular Formula|24502-79-2 MDL|24502-79-2 SMILES|24502-79-2 2-Butenoic acid, 3-methyl-, (1R)-1-(1,4-dihydro-5,8-dihydroxy-1,4-dioxo-2-naphthalenyl)-4-methyl-3-penten-1-yl ester