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Psoralen

Catalog No. T2942   CAS 66-97-7
Synonyms: Ficusin, Furocoumarin, psoralene

Psoralen (Ficusin) is a furocoumarin that intercalates with DNA, inhibiting DNA synthesis and cell division.

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Psoralen Chemical Structure
Psoralen, CAS 66-97-7
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20 mg In stock $ 50.00
1 mL * 10 mM (in DMSO) In stock $ 50.00
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Purity: 100%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Psoralen (Ficusin) is a furocoumarin that intercalates with DNA, inhibiting DNA synthesis and cell division.
In vitro Psoralen inhibits the proliferation of MCF-7/ADR cells as shown by G0/G1 phase arrest rather than encouraging apoptosis. Psoralen reverses MDR(multidrug resistance) through inhibiting ATPase activity rather than reducing P-gp expression. Psoralen inhibits the migration abilities of MCF-7/ADR cells by repressing EMT possibly through inhibiting the activation of NF-κB. Psoralens are photoactive compounds that readily alkylate DNA when activated by longwave ultraviolet light. Proliferation has been significantly promoted in MCF-7/ADR cells treated with low concentration of psoralen (<10.75 μM) and inhibited with high concentration(>21.5 μM). Psoralen can inhibit metastasis of breast cancer. Psoralen mediates a variety of cell processes including cell death, proliferation, inflammation and migration[1].
In vivo Psoralen has been characterized as a tumor suppressor in various tumors[1]. Psoralen ameliorates sex hormone deficiency-induced osteoporosis in female and male mice. It has antiosteoporosis effect in ovariectomy-induced osteoporotic rats via stimulating osteoblastic differentiation from bone mesenchymal stem cells[2].
Cell Research The effects of psoralen on cell proliferation are measured by MTT assay. MCF-10A and MCF-7/ADR cells are cultured in 96-well plates at a cell density of 2&times;104 cells per well for 48 h. The medium is then removed and replaced by fresh medium containing different concentrations of psoralen (0, 21.5, 43.0, 64.5, 86.0, 107.5 &mu;M) for 48 h. Cells in the negative control group are incubated with RPMI-1640 culture medium supplemented with 0.1% dimethyl sulfoxide (DMSO). Cells are incubated with 10 &micro;L MTT (5 mg/mL) for 4 h, and then discarded the medium and added 200 &micro;L DMSO. The spectrophotometric absorbance is measured at 490 nm with enzyme-labeling instrument after the crystals were fully dissolved. (Only for Reference)
Source
Synonyms Ficusin, Furocoumarin, psoralene
Molecular Weight 186.16
Formula C11H6O3
CAS No. 66-97-7

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

H2O: < 1 mg/mL (insoluble or slightly soluble)

Ethanol: < 1 mg/mL (insoluble or slightly soluble)

DMSO: 35 mg/mL (188 mM)

TargetMolReferences and Literature

1. Wang X, et al. Biol Pharm Bull. 2016, 39(5):815-22. 2. Xiaomei Yuan, et al. BioMed Research International. 2016, 2016:6869452.

TargetMolCitations

1. Ma X, Li H, Gong Y, et al. Psoralen inhibits hepatitis B viral replication by down-regulating the host transcriptional machinery of viral promoters. Virologica Sinica. 2022

Related compound libraries

This product is contained In the following compound libraries:
Anti-Cancer Active Compound Library EMA Approved Drug Library Anti-Cancer Clinical Compound Library Anti-Cancer Drug Library Anti-Cancer Approved Drug Library Drug Repurposing Compound Library Traditional Chinese Medicine Monomer Library Natural Product Library for HTS Food as Medicine Compound Library Bioactive Compound Library

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Keywords

Psoralen 66-97-7 Apoptosis Cell Cycle/Checkpoint DNA Damage/DNA Repair Microbiology/Virology Proteases/Proteasome Influenza Virus DNA/RNA Synthesis HIV Protease Ficusin inhibit Furocoumarin Inhibitor Human immunodeficiency virus HIV psoralene inhibitor

 

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