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Chemical Structure| 484-20-8 Chemical Structure| 484-20-8

Structure of Bergapten
CAS No.: 484-20-8

Chemical Structure| 484-20-8

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5-Methoxypsoralen, a naturally occurring linear furocoumarin, has been successfully used in combination with ultraviolet (UV) A irradiation [psoralen plus UV (PUVA)] to manage psoriasis and vitiligo and inhibits proliferation in the human hepatocellular carcinoma cell line.

Synonyms: 5-Methoxypsoralen; 5-MOP; NSC 95437

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Product Details of Bergapten

CAS No. :484-20-8
Formula : C12H8O4
M.W : 216.19
SMILES Code : O=C1C=CC2=C(O1)C=C(OC=C3)C3=C2OC
Synonyms :
5-Methoxypsoralen; 5-MOP; NSC 95437
MDL No. :MFCD00010272
InChI Key :BGEBZHIAGXMEMV-UHFFFAOYSA-N
Pubchem ID :2355

Safety of Bergapten

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335-H351-H361
Precautionary Statements:P261-P305+P351+P338

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
SW620 354.5 µM (IC50) 96 hours Inhibited cell proliferation Int J Mol Sci. 2023 Oct 25;24(21):15555.
HT-29 332.4 µM (IC50) 96 hours Inhibited cell proliferation Int J Mol Sci. 2023 Oct 25;24(21):15555.
HOS 257.5 µM (IC50) 96 hours Inhibited cell proliferation Int J Mol Sci. 2023 Oct 25;24(21):15555.
Saos-2 40.05 µM (IC50) 96 hours Inhibited cell proliferation, induced apoptosis Int J Mol Sci. 2023 Oct 25;24(21):15555.
RPMI8226 1272 µM (IC50) 96 hours Inhibited cell proliferation Int J Mol Sci. 2023 Oct 25;24(21):15555.
HFOB 200-400 µM 48 hours To evaluate cytotoxicity Int J Mol Sci. 2023 Oct 25;24(21):15555.
HSF 200-400 µM 48 hours To evaluate cytotoxicity Int J Mol Sci. 2023 Oct 25;24(21):15555.
U266 1190 µM (IC50) 96 hours Inhibited cell proliferation Int J Mol Sci. 2023 Oct 25;24(21):15555.
HUVEC cells 2.5-40 µM 12 or 24 hours To evaluate the biocompatibility of Ber-lipo, results showed that Ber-lipo had good biocompatibility and Lipo significantly reduced the cytotoxicity of bergapten. Bioact Mater. 2024 Oct 1;43:406-422.
RAW264.7 cells 2.5-40 µM 12 or 24 hours To evaluate the biocompatibility of Ber-lipo, results showed that Ber-lipo had good biocompatibility and Lipo significantly reduced the cytotoxicity of bergapten. Bioact Mater. 2024 Oct 1;43:406-422.
Bone marrow-derived macrophages (BMDMs) 20 µM 2 hours Inhibited NLRP3 inflammasome activation, evidenced by attenuated cleaved caspase-1 and mature IL-1β release, as well as reduced ASC speck formation and subsequent gasdermin D (GSDMD)-mediated pyroptosis. Acta Pharmacol Sin. 2023 Sep;44(9):1867-1878.
J774A.1 cells 20 µM 2 hours Inhibited NLRP3 inflammasome activation, evidenced by attenuated cleaved caspase-1 and mature IL-1β release, as well as reduced ASC speck formation and subsequent gasdermin D (GSDMD)-mediated pyroptosis. Acta Pharmacol Sin. 2023 Sep;44(9):1867-1878.
RAW264.7 macrophages 62.5, 125, 250 µM 24 hours To evaluate the effect of Bergapten on NO and PGE2 production in RAW264.7 cells. Results showed that Bergapten significantly inhibited LPS-induced NO and PGE2 production. Int J Mol Sci. 2022 May 22;23(10):5813.
Recombinant human CYP3A4 (rCYP3A4) 1.424 µM (IC50) 30 minutes Bergapten significantly inhibited the metabolism of tofacitinib in recombinant human CYP3A4, showing competitive inhibition corylifolia on the pharmacokinetic profile of tofacitinib and the underlying mechanism. Front Pharmacol.
Human liver microsomes (HLMs) 2.647 µM (IC50) 30 minutes Bergapten significantly inhibited the metabolism of tofacitinib in human liver microsomes, showing competitive inhibition corylifolia on the pharmacokinetic profile of tofacitinib and the underlying mechanism. Front Pharmacol.
Rat liver microsomes (RLMs) 2.619 µM (IC50) 30 minutes Bergapten significantly inhibited the metabolism of tofacitinib in rat liver microsomes, showing competitive inhibition corylifolia on the pharmacokinetic profile of tofacitinib and the underlying mechanism. Front Pharmacol.
B16F10 melanoma cells 6.25, 12.5, 25 µM 48 hours To evaluate the effect of Bergapten on the expression of melanogenesis-related proteins, results showed that Bergapten significantly increased the protein expression levels of MITF, tyrosinase, TRP-1, and TRP-2. Molecules. 2022 Apr 19;27(9):2613.
B16F10 melanoma cells 6.25, 12.5, 25 µM 48 hours To evaluate the effect of Bergapten on the expression of melanogenesis-related proteins, results showed that Bergapten increased the expression of MITF, tyrosinase, TRP-1, and TRP-2. Molecules. 2022 Apr 19;27(9):2613.
ZR-75 20 µM and 50 µM 6 to 16 hours Bergapten induces autophagy by up-regulating PTEN expression, increasing Beclin1, PI3KIII, UVRAG, AMBRA expression and conversion of LC3-I to LC3-II Mol Cancer. 2015 Jul 7;14:130.
MCF-7 20 µM and 50 µM 6 to 16 hours Bergapten induces autophagy by up-regulating PTEN expression, increasing Beclin1, PI3KIII, UVRAG, AMBRA expression and conversion of LC3-I to LC3-II Mol Cancer. 2015 Jul 7;14:130.
B16F10 melanoma cells 6.25, 12.5, 25 µM 72 hours To evaluate the effect of Bergapten on melanogenesis, results showed that Bergapten significantly increased melanin content and tyrosinase activity. Molecules. 2022 Apr 19;27(9):2613.
B16F10 melanoma cells 1, 10, or 100 µM To evaluate the effect of Bergapten on melanin content and tyrosinase activity, results showed that Bergapten dose-dependently increased melanin content and tyrosinase activity in B16F10 cells J Adv Res. 2019 Oct 10;21:57-64.
Rabbit jejunum 0.0026 mg/ml Bergapten exhibited concentration-dependent relaxation of both spontaneous and K+-induced contractions, similar to the effect of papaverine Front Pharmacol. 2022 Nov 16;13:1005154.

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Mice High-fat diet and streptozotocin-induced diabetic mice Dietary supplementation 0.02% (w/w) For 10 weeks To evaluate whether bergapten and methoxsalen could prevent diabetes-induced osteoporosis and its underlying mechanism. Results showed that both bergapten and methoxsalen significantly reversed the decrease in serum osteocalcin, bone-alkaline phosphatase, and femur BMD, increased bone volume density and trabecular number, while decreasing the structure model index of femur tissue in diabetic mice. Additionally, these derivatives significantly reduced the number and formation of osteoclasts in diabetic bone tissue and downregulated the expression of osteoclast-related genes. Int J Mol Sci. 2019 Mar 14;20(6):1298
C57BL/6 mice Vitiligo model Transdermal administration 1% (w/w) Once daily for 12 days To evaluate the effect of Bergapten on hair pigmentation in vitiligo model mice, results showed that Bergapten significantly improved hair pigmentation J Adv Res. 2019 Oct 10;21:57-64.
C57/B6 mice High-fat diet-induced diabetes-related osteoporosis model Oral 10 mg/kg/day and 20 mg/kg/day Once daily for 20 weeks Bergapten significantly inhibited RANKL-RANK signaling transduction, and suppressed the activation of the PI3K/AKT, JNK/MAPK and NF-κB signaling pathways, thus protecting trabecular structure and decreasing osteoclastogenic differentiation Int J Mol Med. 2016 Dec;38(6):1661-1672
Sprague Dawley rats Drug interaction model Oral 20 mg/kg and 50 mg/kg Single dose Bergapten significantly increased the plasma exposure (AUC) and maximum concentration (Cmax) of tofacitinib and decreased clearance (CLz/F), indicating inhibition of tofacitinib metabolism in vivo corylifolia on the pharmacokinetic profile of tofacitinib and the underlying mechanism. Front Pharmacol.
C57BL/6J mice Escherichia coli-induced sepsis model Intraperitoneal injection 50 mg/kg 24 hours and 1 hour before injection Significantly ameliorated tissue inflammation and injury. Acta Pharmacol Sin. 2023 Sep;44(9):1867-1878.
Mice Castor oil-induced diarrhea model Oral 50, 100, 200 mg/kg Single dose, observed for 4 hours Bergapten at doses of 50-200 mg/kg effectively reduced diarrheal secretions and intestinal secretions, showing antidiarrheal and antisecretory effects Front Pharmacol. 2022 Nov 16;13:1005154.

Clinical Trial:

NCT Number Conditions Phases Recruitment Completion Date Locations
NCT00533195 Atopic Dermatitis Phase 3 Completed - Austria ... More >> Medical University of Vienna; University Clinic of Dermatology; Division of Special and Environmental Dermatology Vienna, Austria, 1090 Less <<
NCT00811005 Pustular Palmoplantar Psoriasi... More >>s Less << Phase 3 Unknown October 2010 Austria ... More >> Medical University of Vienna; University Clinic of Dermatology; Division of Special and Environmental Dermatology Vienna, Austria, 1180 Less <<

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

4.63mL

0.93mL

0.46mL

23.13mL

4.63mL

2.31mL

46.26mL

9.25mL

4.63mL

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