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Lucidin

Cat. No. M15000

All AbMole products are for research use only, cannot be used for human consumption.

Lucidin Structure
Synonym:

NSC 30546

Size Price Availability Quantity
5mg USD 200  USD200 In stock
10mg USD 330  USD330 In stock
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Quality Control & Documentation
Biological Activity

Lucidin (NSC 30546) is a natural component of Rubia tinctorum L. lucidin is mutagenic in bacteria and mammalian cells. IC50 Value: Target: in vitro: Lucidin was mutagenic in five Salmonella typhimurium strains without metabolic activation, but the mutagenicity was increased after addition of rat liver S9 mix. In V79 cells, lucidin was mutagenic at the hypoxanthine-guanine phosphoribosyl transferase gene locus and active at inducing DNA single-strand breaks and DNA-protein cross-links as assayed by the alkaline elution method. Lucidin also induced DNA repair synthesis in primary rat hepatocytes and transformed C3H/M2-mouse fibroblasts in culture. HPLC analysis of 32P-labelled DNA adducts revealed a peak co-migrating with an adduct obtained after in vitro treatment of deoxyguanosine-3'-phosphate with lucidin. in vivo: Dose-dependent increases in benign and malignant tumour formation were observed in the liver and kidneys of treated animals. 32P-post-labelling analysis showed an increase in the overall level of DNA adducts observed in the liver, kidney and colon of rats treated with 10% madder root in the diet for 2 weeks. Toxicity: lucidin is mutagenic in bacteria and mammalian cells. Clinical trial:

Chemical Information
Molecular Weight 270.24
CAS Number 478-08-0
Solubility (25°C) DMSO 6.67 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Younglim Son, et al. Phytomedicine. Lucidin 3-methyl ether from Rubia philippinensis suppresses the proliferation of multiple myeloma cells through the promotion of β-catenin degradation

[2] Yuji Ishii, et al. J Appl Toxicol. Effects of inhibition of hepatic sulfotransferase activity on renal genotoxicity induced by lucidin-3-O-primeveroside

[3] Jian-Hua Zhang, et al. J Ethnopharmacol. Morinda officinalis How. - A comprehensive review of traditional uses, phytochemistry and pharmacology

[4] Oliver P Yockey, et al. Chem Res Toxicol. Mechanism of Error-Free DNA Replication Past Lucidin-Derived DNA Damage by Human DNA Polymerase κ

[5] Ihsan Caliş, et al. Chem Pharm Bull (Tokyo). Lucidin type anthraquinone glycosides from Putoria calabrica

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Keywords: Lucidin, NSC 30546 supplier, Others, inhibitors, activators

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