Home Other Building Blocks 478-08-0
478-08-0,MFCD01664482
Catalog No.:AA00DA22

478-08-0 | LUCIDIN

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
98%
in stock  
$36.00   $25.00
- +
5mg
98%
in stock  
$80.00   $56.00
- +
10mg
98%
in stock  
$119.00   $83.00
- +
25mg
98%
in stock  
$201.00   $141.00
- +
50mg
98%
in stock  
$300.00   $210.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00DA22
Chemical Name:
LUCIDIN
CAS Number:
478-08-0
Molecular Formula:
C15H10O5
Molecular Weight:
270.2369
MDL Number:
MFCD01664482
SMILES:
OCc1c(O)cc2c(c1O)C(=O)c1c(C2=O)cccc1
NSC Number:
30546
Properties
Computed Properties
 
Complexity:
421  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
20  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
1  
XLogP3:
2.4  

Downstream Synthesis Route

[1]Ford,Lauren;Rayner,ChristopherM.;Blackburn,RichardS.[DyesandPigments,2018,vol.154,p.290-295]

[2]Ayyangar;Venkataraman[JournalOfScientificandIndustrialResearch,1956,vol.15B,p.359,361,362]

[3]Jegorov,Alexandr;Cvak,Ladislav;Cejka,Jan;Kratochvil,Bohumil;Sedmera,Petr;Havlicek,Vladimir[JournalofChemicalCrystallography,2005,vol.35,#8,p.621-627]

[1]Ayyangar;Venkataraman[JournalOfScientificandIndustrialResearch,1956,vol.15B,p.359,361,362]

[1]Ayyangar;Venkataraman[JournalOfScientificandIndustrialResearch,1956,vol.15B,p.359,361,362]

[1]Joshietal.[JournalOfScientificandIndustrialResearch,1955,vol.14B,p.87,92]

[1]Briggs;Nicholls[JournaloftheChemicalSociety,1949,p.1241,1244][JournaloftheChemicalSociety,1953,p.3068]Inoue,Kenichiro;Nayeshiro,Hidekazu;Inouye,Hiroyuki;Zenk,Meinhart[Phytochemistry,1981,vol.20,#7,p.1693-1700]

[2]Locationinpatent:experimentalpartIshii,Yuji;Okamura,Toshiya;Inoue,Tomoki;Fukuhara,Kiyoshi;Umemura,Takashi;Nishikawa,Akiyoshi[ChemicalResearchinToxicology,2010,vol.23,#1,p.134-141]

Literature

Title: Determination of lucidin-specific DNA adducts by liquid chromatography with tandem mass spectrometry in the livers and kidneys of rats given lucidin-3-O-primeveroside.

Journal: Chemical research in toxicology 20120521

Title: Dietary pseudopurpurin effects on bone mineral density and bone geometry architecture in rats.

Journal: International journal of molecular sciences 20120101

Title: [Anthraquinones from the roots of Knoxia valerianoides].

Journal: Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20111101

Title: Anthraquinones from the roots of Knoxia valerianoides inhibit the formation of advanced glycation end products and rat lens aldose reductase in vitro.

Journal: Archives of pharmacal research 20100201

Title: Chemical structure determination of DNA bases modified by active metabolites of lucidin-3-O-primeveroside.

Journal: Chemical research in toxicology 20100101

Title: 1,3-Dihydr-oxy-2-methoxy-methyl-9,10-anthraquinone from Rennellia elliptica Korth.

Journal: Acta crystallographica. Section E, Structure reports online 20090601

Title: Possible contribution of rubiadin, a metabolite of madder color, to renal carcinogenesis in rats.

Journal: Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 20090401

Title: Is senna laxative use associated to cathartic colon, genotoxicity, or carcinogenicity?

Journal: Journal of toxicology 20090101

Title: Antimicrobial anthraquinones from Morinda angustifolia.

Journal: Fitoterapia 20081201

Title: Chemical constituents of Morinda citrifolia roots exhibit hypoglycemic effects in streptozotocin-induced diabetic mice.

Journal: Biological & pharmaceutical bulletin 20080501

Title: Identification and quantification of the constituents of madder root by gas chromatography and high-performance liquid chromatography.

Journal: Journal of chromatography. A 20061110

Title: Characterization of lucidin formation in Rubia tinctorum L.

Journal: Plant physiology and biochemistry : PPB 20050101

Title: [Examination of the anthraquinone composition in root-stock and root samples of Rubia tinctorium L. plants of different origins].

Journal: Acta pharmaceutica Hungarica 20040101

Title: Chemical and enzymatic hydrolysis of anthraquinone glycosides from madder roots.

Journal: Phytochemical analysis : PCA 20030101

Title: Lucidin type anthraquinone glycosides from Putoria calabrica.

Journal: Chemical & pharmaceutical bulletin 20020501

Title: Mutagenicity of natural anthraquinones from Rubia tinctorum in the Drosophila wing spot test.

Journal: Planta medica 20010301

Title: Westendorf J, et al. The genotoxicity of lucidin, a natural component of Rubia tinctorum L., and lucidinethylether, a component of ethanolic Rubia extracts. Cell Biol Toxicol. 1988 Jun;4(2):225-39.

Title: Westendorf J, et al. Carcinogenicity and DNA adduct formation observed in ACI rats after long-term treatment with madder root, Rubia tinctorum L. Carcinogenesis. 1998 Dec;19(12):2163-8.

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Tags:478-08-0 Molecular Formula|478-08-0 MDL|478-08-0 SMILES|478-08-0 LUCIDIN