Structure of Bezafibrate
CAS No.: 41859-67-0
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Bezafibrate is the agonist of PPAR and the EC50 for PPAR⍺, PPARβ, PPARẟ is 50 , 20, and 60 nM respectively. It has hypolipidemic effect.
Synonyms: BM15075; Benzofibrate; Bezafibratum
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| CAS No. : | 41859-67-0 |
| Formula : | C19H20ClNO4 |
| M.W : | 361.82 |
| SMILES Code : | CC(C)(OC1=CC=C(CCNC(C2=CC=C(Cl)C=C2)=O)C=C1)C(O)=O |
| Synonyms : |
BM15075; Benzofibrate; Bezafibratum
|
| MDL No. : | MFCD00078970 |
| InChI Key : | IIBYAHWJQTYFKB-UHFFFAOYSA-N |
| Pubchem ID : | 39042 |
| GHS Pictogram: |
|
| Signal Word: | Warning |
| Hazard Statements: | H302 |
| Precautionary Statements: | P264-P270-P301+P312+P330-P501 |
In Vitro:
|
Cell Line
|
Concentration | Treated Time | Description | References |
| INS-1 832/13 β-cells | 1–100 nM | 5 minutes | To evaluate the effect of compounds on insulin secretion. Results showed that tazarotenic acid, efaproxiral, and bezafibrate significantly increased insulin secretion at nanomolar concentrations, with EC50 values of 5.73 nM, 14.2 nM, and 13.5 nM, respectively. | J Enzyme Inhib Med Chem. 2021 Dec;36(1):377-383. |
| MDA-MB-231 | 10 μM | 48 h | Bezafibrate inhibits PKCβII expression and reduces NMHC-IIA phosphorylation | Acta Pharm Sin B. 2023 Mar;13(3):1053-1070. |
| LM-MCF-7 | 10 μM | 48 h | Bezafibrate inhibits PKCβII expression and reduces NMHC-IIA phosphorylation | Acta Pharm Sin B. 2023 Mar;13(3):1053-1070. |
| MC3T3-E1 cells | 100 μM | 7-28 days | Bezafibrate enhanced differentiation and mineralization of MC3T3-E1 cells, increasing mRNA expression of ALP, collagen I and osteocalcin | Acta Pharmacol Sin. 2011 May;32(5):591-600. |
| MC3T3-E1 cells | 1-1000 μM | 24-72 h | Bezafibrate increased the viability and proliferation of MC3T3-E1 cells in a dose- and time-dependent manner | Acta Pharmacol Sin. 2011 May;32(5):591-600. |
| MO3.13 cells | 500 µM and 1000 µM | 24 or 48 h | To evaluate the effect of sulfite on the viability of MO3.13 cells. Results showed that sulfite significantly decreased cell viability, and Bezafibrate (1 µM) prevented this effect after 24 h incubation. | Cells. 2023 Jun 6;12(12):1557. |
In Vivo:
|
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
| BALB/c nude mice | Breast cancer metastasis model | Oral gavage | 25 mg/kg | Once daily for 55 days | Bezafibrate inhibits breast cancer metastasis by suppressing PKCβII-mediated NMHC-IIA phosphorylation | Acta Pharm Sin B. 2023 Mar;13(3):1053-1070. |
| TallyHo mice | Early diabetes (ED) and late diabetes (LD) models | Dietary supplementation | 0.5% (w/w) | 8 weeks | Bezafibrate markedly reduced plasma lipid and glucose levels, accompanied by elevated insulin sensitivity index and glucose tolerance. Additionally, Bezafibrate increased islet area in the pancreas, improved energy expenditure and metabolic flexibility. In the liver, Bezafibrate ameliorated steatosis, modified lipid composition, increased mitochondrial mass, and reduced hepatic gluconeogenesis. | Mol Metab. 2017 Jan 6;6(3):256-266 |
| Wistar rats | Sulfite-induced neuroinflammation and oxidative stress model | Oral | 30 or 100 mg/kg | Once daily for 7 days | To evaluate the protective effects of Bezafibrate against sulfite-induced neuroinflammation and oxidative stress. Results showed that Bezafibrate mitigated sulfite-induced myelin disruption, neuroinflammation, and oxidative stress. | Cells. 2023 Jun 6;12(12):1557. |
| Mice | Ndufs4 KO mouse model | Dietary administration | 0.5% BEZ | Continuous administration from p25 | BEZ significantly extended the survival of Ndufs4 KO mice and attenuated disease progression. Decreased oxidative stress and stunted growth were also observed. | Neurotherapeutics. 2022 Apr;19(3):994-1006 |
Clinical Trial:
| NCT Number | Conditions | Phases | Recruitment | Completion Date | Locations |
| NCT02584504 | Hypercholesterolemia | Phase 3 | Completed | - | Japan ... More >> Investigational Site Number 392028 Ageo-Shi, Japan Investigational Site Number 392007 Chuo-Ku, Japan Investigational Site Number 392029 Chuo-Ku, Japan Investigational Site Number 392014 Fukui-Shi, Japan Investigational Site Number 392023 Hachioji-Shi, Japan Investigational Site Number 392013 Itoshima-Shi, Japan Investigational Site Number 392010 Kanazawa-Shi, Japan Investigational Site Number 392024 Kasuga-Shi, Japan Investigational Site Number 392004 Kawanishi-Shi, Japan Investigational Site Number 392015 Kitakyushu-Shi, Japan Investigational Site Number 392005 Komatsu-Shi, Japan Investigational Site Number 392032 Matsudo-Shi, Japan Investigational Site Number 392017 Matsumoto-Shi, Japan Investigational Site Number 392003 Mito-Shi, Japan Investigational Site Number 392018 Morioka-Shi, Japan Investigational Site Number 392009 Moriya-Shi, Japan Investigational Site Number 392006 Nagoya-Shi, Japan Investigational Site Number 392011 Nagoya-Shi, Japan Investigational Site Number 392019 Nagoya-Shi, Japan Investigational Site Number 392025 Nagoya-Shi, Japan Investigational Site Number 392027 Osaka-Shi, Japan Investigational Site Number 392030 Sakura-Shi, Japan Investigational Site Number 392016 Shinagawa-Ku, Japan Investigational Site Number 392001 Shinjuku-Ku, Japan Investigational Site Number 392008 Shinjuku-Ku, Japan Investigational Site Number 392012 Shizuoka-Shi, Japan Investigational Site Number 392002 Suita-Shi, Japan Investigational Site Number 392031 Suita-Shi, Japan Investigational Site Number 392020 Toyonaka-Shi, Japan Investigational Site Number 392022 Yao-Shi, Japan Less << |
| NCT02584504 | - | Completed | - | - | |
| NCT03031821 | Prostate Cancer ... More >> Metabolic Syndrome Less << | Phase 3 | Not yet recruiting | June 1, 2023 | Canada, British Columbia ... More >> BC Cancer Agency - Vancouver Cancer Centre Not yet recruiting Vancouver, British Columbia, Canada, V5Z 4E6 Contact: Bernie Eigl, MD 604-877-6000 bernie.eigl@bccancer.bc.ca Principal Investigator: Bernie Eigl, MD Less << |
| NCT02984982 | Hypercholesterolemia ... More >> Acute Coronary Syndrome Less << | Phase 4 | Completed | - | Japan ... More >> Investigational Site Number 392026 Bunkyoku-ku, Japan Investigational Site Number 392022 Chiyoda-ku, Japan Investigational Site Number 392032 Fujisawa-shi, Japan Investigational Site Number 392004 Fukui-shi, Japan Investigational Site Number 392007 Fukuoka-shi, Japan Investigational Site Number 392048 Fukuoka-shi, Japan Investigational Site Number 392008 Gifu-shi, Japan Investigational Site Number 392039 Hiroshima-shi, Japan Investigational Site Number 392028 Isehara-shi, Japan Investigational Site Number 392036 Itabashi-ku, Japan Investigational Site Number 392037 Itabashi-ku, Japan Investigational Site Number 392024 Izumisano-shi, Japan Investigational Site Number 392013 Izunokuni-shi, Japan Investigational Site Number 392020 Kawaguchi-shi, Japan Investigational Site Number 392041 Kisarazu-shi, Japan Investigational Site Number 392009 Kitakyushu-shi, Japan Investigational Site Number 392034 Kitakyushu-shi, Japan Investigational Site Number 392044 Kochi-shi, Japan Investigational Site Number 392002 Kumamoto-shi, Japan Investigational Site Number 392011 Kumamoto-shi, Japan Investigational Site Number 392003 Kurashiki-shi, Japan Investigational Site Number 392018 Matsuyama-shi, Japan Investigational Site Number 392021 Morioka-shi, Japan Investigational Site Number 392017 Nagakute-shi, Aichi, Japan Investigational Site Number 392047 Nagaoka-shi, Japan Investigational Site Number 392038 Nagoya-shi, Japan Investigational Site Number 392042 Nagoya-shi, Japan Investigational Site Number 392033 Okayama-shi, Japan Investigational Site Number 392006 Osaka-shi, Japan Investigational Site Number 392010 Osaka-shi, Japan Investigational Site Number 392045 Osaka-shi, Japan Investigational Site Number 392046 Osaka-shi, Japan Investigational Site Number 392015 Sagamihara-shi, Japan Investigational Site Number 392019 Sakai-shi, Japan Investigational Site Number 392035 Sapporo-shi, Japan Investigational Site Number 392001 Tenri-shi, Japan Investigational Site Number 392016 Toyoake-shi, Japan Investigational Site Number 392025 Tsukuba-shi, Japan Investigational Site Number 392040 Tsukuba-shi, Japan Investigational Site Number 392005 Wakayama-shi, Japan Investigational Site Number 392027 Yokohama-shi, Japan Investigational Site Number 392043 Yokohama-shi, Japan Less << |
| NCT00506298 | Type 2 Diabetes | Phase 2 | Completed | - | Canada, British Columbia ... More >> Chilliwack, British Columbia, Canada Vancouver, British Columbia, Canada Canada, Manitoba Winnipeg, Manitoba, Canada Canada, Newfoundland and Labrador Bay Roberts, Newfoundland and Labrador, Canada Holyroad, Newfoundland and Labrador, Canada St. Johns, Newfoundland and Labrador, Canada Canada, Ontario Aylmer, Ontario, Canada Burlington, Ontario, Canada Collingwood, Ontario, Canada Corunna, Ontario, Canada Robarts Research Institute London, Ontario, Canada London, Ontario, Canada Newmarket, Ontario, Canada Sarnia, Ontario, Canada Sudbury, Ontario, Canada Toronto, Ontario, Canada Canada, Quebec Montreal, Quebec, Canada Canada, Saskatchewan Saskatoon, Saskatchewan, Canada Less << |
| NCT01527318 | Neutral Lipid Storage Disease | Phase 4 | Completed | - | Netherlands ... More >> Maastricht University Medical Center Maastricht, Limburg, Netherlands, 6200MD Less << |
| NCT02548832 | Mixed Dyslipidemia | Phase 2 | Unknown | July 2016 | Mexico ... More >> Institute of Experimental and Clinical Therapeutics (INTEC), CUCS, University of Guadalajara Recruiting Guadalajara, Jalisco, Mexico, 44340 Contact: Esperanza Martínez Abundis, PhD Science (33) 1058-5200 ext 34211 esperanzamartnezabundi@yahoo.com Less << |
| NCT02481245 | Bipolar Disorder|Depressive Ep... More >>isode Less << | PHASE2 | UNKNOWN | 2025-06-23 | The Dauten Family Center for B... More >>ipolar Treatment Innovation at Massachusetts General Hospital, Boston, Massachusetts, 02114, United States Less << |
| NCT00336167 | Carnitine Palmitoyl Transferas... More >>e 2 Deficiency Less << | Phase 3 | Unknown | July 2007 | France ... More >> Jean Paul Bonnefont Recruiting Paris, France, 75015 Contact: Jean-Paul Bonnefont, MD; PhD bonnefont@necker.fr Less << |
| NCT03649269 | Hypertriglyceridemia | Not Applicable | Completed | - | - |
| NCT01165060 | X-linked Adrenoleukodystrophy|... More >>Adrenomyeloneuropathy Less << | COMPLETED | 2025-08-11 | Academisch Medisch Centrum, Am... More >>sterdam, NH, 1100 DD, Netherlands Less << | |
| NCT02701166 | Primary Biliary Cholangitis ... More >> Primary Sclerosing Cholangitis Secondary Sclerosing Cholangitis Less << | Phase 3 | Unknown | April 2018 | Netherlands ... More >> Academic Medical Center Recruiting Amsterdam, Netherlands Contact: Ulrich Beuers, prof. dr. +31205662422 u.h.beuers@amc.uva.nl Contact: Ruth Bolier +31205668701 a.r.bolier@amc.uva.nl Principal Investigator: Ulrich Beuers, prof. dr. Sub-Investigator: Elsemieke de Vries Vrije Universiteit Medisch Centrum Recruiting Amsterdam, Netherlands Contact: Karin van Nieuwkerk, dr. +31-20-4440613 cmj.vannieuwkerk@vumc.nl Contact: Ineke Jansen +31-20-4449455 a.jansen1@vumc.nl Universitair Medisch Centrum Groningen Recruiting Groningen, Netherlands Contact: Marleen de Vree, dr. +31-6-55256255 j.m.l.de.vree@umcg.nl Contact: Lyda Engelsman +31-50-3614996 a.f.engelsman@umcg.nl Leids Universitair Medisch Centrum Recruiting Leiden, Netherlands Contact: Bart van Hoek, prof. dr. +31-71-5263507 b.van_hoek@lumc.nl Contact: Lida Beneken Kolmer +31-71-5261188 a.beneken_kolmer@lumc.nl Maastricht Universitair Medisch Centrum Recruiting Maastricht, Netherlands Contact: Peter Jansen, prof. dr. +31-43-3876543 plm.jansen@maastrichtuniversity.nl Contact: Tine Horsten +31-43-3874436 t.horsten@mumc.nl Radboud Universitair Medisch Centrum Recruiting Nijmegen, Netherlands Contact: Joost Drenth, prof. dr. +31-24-3613999 joostphdrenth@cs.com Contact: Sonja Cuppen +31-24-3619190 researchunit.mdl@radboudumc.nl Erasmus Medisch Centrum Recruiting Rotterdam, Netherlands Contact: Henk van Buuren, dr. +31-10-7035942 h.vanbuuren@erasmusmc.nl Contact: Maren Harms +31-10-7038922 m.h.harms@erasmusmc.nl Universitair Medisch Centrum Utrecht Recruiting Utrecht, Netherlands Contact: Karel van Erpecum, dr. +31-88-7555555 k.j.vanerpecum@umcutrecht.nl Contact: Janneke van den Brink +31-88-7557973 j.vandenbrink@umcutrecht.nl Spain University of Barcelona Not yet recruiting Barcelona, Spain Contact: Albert Parés, dr. +34-93-2275753 pares@ub.edu Less << |
| NCT00983788 | Carnitine Palmitoyltransferase... More >> II Deficiency Very Long Chain Acyl Coa Dehydrogenase Deficiency Less << | Phase 2 | Completed | - | Denmark ... More >> Neuromusculare Research Unit, Rigshospitalet Copenhagen, Denmark, 2100 Less << |
| NCT02398201 | Mitochondrial Diseases | PHASE2 | COMPLETED | 2017-03-23 | Clinical Research Facility, Ro... More >>yal Victoria Infirmary, Newcastle upon Tyne, Tyne and Wear, NE1 4LP, United Kingdom Less << |
| NCT02937012 | Primary Biliary Cirrhosis | Phase 3 | Recruiting | December 2019 | Mexico ... More >> Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran Recruiting Mexico City, Mexico, 14000 Contact: Edgardo Eric Lopez Mendez, MD (01)(55) 54870900 ext 2710 ericlopezmendez@yahoo.com.mx Contact: Sergio Gabriel Munoz Martinez, MD (01)(55) 54870900 ext 2710 sergio_sg@hotmail.com Principal Investigator: Edgardo Eric Lopez Martinez, MD Sub-Investigator: Sergio Gabriel Munoz Martinez, MD Sub-Investigator: Ignacio Garcia Juarez, MD Sub-Investigator: Ernesto Marquez Guillen, MD Sub-Investigator: Carlos Moctezuma Velazquez, MD Sub-Investigator: Alejandra Tepox Padron, MD Less << |
| NCT02291796 | Acute Myocardial Infarction | PHASE4 | COMPLETED | 2025-12-13 | - |
| NCT01654731 | PBC | Phase 3 | Completed | - | France ... More >> Hepatology department - Hopital Saint Antoine Paris, France, 75012 Less << |
| Bio Calculators | ||||
| Preparing Stock Solutions | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.76mL 0.55mL 0.28mL |
13.82mL 2.76mL 1.38mL |
27.64mL 5.53mL 2.76mL |
|
Tags: Bezafibrate | BM15075 | BM 15075 | BM-15075 | PPARα Agonist | PPARγ Agonist | PPARδ Agonist | Peroxisome Proliferator-Activated Receptor | PPARs | nuclear receptor | lipid metabolism | glucose homeostasis | adipogenesis | inflammation | peroxisome proliferator response element | PPREs | 41859-67-0
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| H231 | May react explosively even in the absence of air at elevated pressure and/or temperature |
| H240 | Heating may cause an explosion |
| H241 | Heating may cause a fire or explosion |
| H242 | Heating may cause a fire |
| H250 | Catches fire spontaneously if exposed to air |
| H251 | Self-heating; may catch fire |
| H252 | Self-heating in large quantities; may catch fire |
| H260 | In contact with water releases flammable gases which may ignite spontaneously |
| H261 | In contact with water releases flammable gas |
| H270 | May cause or intensify fire; oxidizer |
| H271 | May cause fire or explosion; strong oxidizer |
| H272 | May intensify fire; oxidizer |
| H280 | Contains gas under pressure; may explode if heated |
| H281 | Contains refrigerated gas; may cause cryogenic burns or injury |
| H290 | May be corrosive to metals |
Health hazards | |
| Code | Phrase |
| H300 | Fatal if swallowed |
| H301 | Toxic if swallowed |
| H302 | Harmful if swallowed |
| H303 | May be harmful if swallowed |
| H304 | May be fatal if swallowed and enters airways |
| H305 | May be harmful if swallowed and enters airways |
| H310 | Fatal in contact with skin |
| H311 | Toxic in contact with skin |
| H312 | Harmful in contact with skin |
| H313 | May be harmful in contact with skin |
| H314 | Causes severe skin burns and eye damage |
| H315 | Causes skin irritation |
| H316 | Causes mild skin irritation |
| H317 | May cause an allergic skin reaction |
| H318 | Causes serious eye damage |
| H319 | Causes serious eye irritation |
| H320 | Causes eye irritation |
| H330 | Fatal if inhaled |
| H331 | Toxic if inhaled |
| H332 | Harmful if inhaled |
| H333 | May be harmful if inhaled |
| H334 | May cause allergy or asthma symptoms or breathing difficulties if inhaled |
| H335 | May cause respiratory irritation |
| H336 | May cause drowsiness or dizziness |
| H340 | May cause genetic defects |
| H341 | Suspected of causing genetic defects |
| H350 | May cause cancer |
| H351 | Suspected of causing cancer |
| H360 | May damage fertility or the unborn child |
| H361 | Suspected of damaging fertility or the unborn child |
| H361d | Suspected of damaging the unborn child |
| H362 | May cause harm to breast-fed children |
| H370 | Causes damage to organs |
| H371 | May cause damage to organs |
| H372 | Causes damage to organs through prolonged or repeated exposure |
| H373 | May cause damage to organs through prolonged or repeated exposure |
Environmental hazards | |
| Code | Phrase |
| H400 | Very toxic to aquatic life |
| H401 | Toxic to aquatic life |
| H402 | Harmful to aquatic life |
| H410 | Very toxic to aquatic life with long-lasting effects |
| H411 | Toxic to aquatic life with long-lasting effects |
| H412 | Harmful to aquatic life with long-lasting effects |
| H413 | May cause long-lasting harmful effects to aquatic life |
| H420 | Harms public health and the environment by destroying ozone in the upper atmosphere |
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