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CAS No:60940-34-3
MF:C13H9NOSe
Appearance:light-yellow or yellow crystalline powder
Specification:98.5%
UN number:-
Package:1/5/10/25kgs/drum
Supply Capacity:KGS
Synonyms:2-phenyl-1,2-benzisoselenazol-;2-Phenyl-1,2-benzoselenazol-3-one;Harmokisane;2-Phenyl-1-selena-2-azaindan-3-one;DR-3305;RP-60931;Ebselen,99%;Ebselen2-Phenyl-benzo[d]isoselenazol-3-one; ebselen; 60940-34-3; 2-Phenyl-1,2-benzisoselenazol-3(2H)-one; 2-phenyl-1,2-benzoselenazol-3-one; Ebselene; Ebseleno; Ebselenum; SPI-1005; PZ 51; PZ-51; DR-3305; DR3305; DTXSID7045150; 2-phenyl-1,2-benzoisoselenazol-3(2H)-one; 40X2P7DPGH; NSC-639762; NSC-757883; SPI1005; 2-phenyl-2,3-dihydro-1,2-benzoselenazol-3-one; DTXCID5025150; CHEBI:77543; SPI 1005; 2-phenylbenzoisoselenazol-3(2H)-one; RefChem:590533; 612-054-8; 2-phenylbenzo[d][1,2]selenazol-3(2H)-one; Ebselen [INN]; Ebselene [French]; Ebselenum [Latin]; Harmokisane; Ebseleno [Spanish]; C13H9NOSe; PZ51; MLS000028488; MFCD00210937; CCRIS 3714; 1,2-Benzisoselenazol-3(2H)-one, 2-phenyl-; DR 3305; 2-Phenyl-1,2-benzisoselenazolin-3-one; SMR000058445; UNII-40X2P7DPGH; CHEMBL51085; NSC 639762; Prestwick_1057; SPI-3005; Prestwick0_000740; Prestwick1_000740; Prestwick2_000740; Prestwick3_000740; Spectrum2_001441; Spectrum3_000799; Spectrum4_000445; Spectrum5_001713; Lopac-E-3520; NSC639762; Lopac0_000541; NCGC00015412-06; 2-phenyl-1,2-benzoselenazol-3(2h)-one; BSPBio_000700; BSPBio_001342; BSPBio_002538; CPD000058445; KBioGR_000062; KBioGR_000830; KBioSS_000062; DivK1c_000951; SPBio_001301; SPBio_002639; CAS-60940-34-3; MLS001148646; BPBio1_000770; BCBcMAP01_000149; HMS502P13; KBio1_000951; KBio2_000062; KBio2_002630; KBio2_005198; KBio3_000123; KBio3_000124; KBio3_001758; NINDS_000951; E 3520; Bio2_000062; Bio2_000542; HMS1361D04; HMS1570C22; HMS1791D04; HMS1989D04; HMS2052N09; s6676; AC-1124; IDI1_000951; IDI1_033812; QTL1_000035; NCGC00015412-01; NCGC00015412-02; NCGC00015412-03; NCGC00015412-13; NCGC00024072-03; NCGC00024072-04; NCGC00024072-05; NCGC00178610-01; NCGC00178610-02; NCGC00178610-03; AB00053217; EU-0100541; MLS-0003066.0001; BRD-K29359156-001-06-1; RP 60931; 2-Phenyl-1,2-benzoselenazol-3-one (Ebselen); SR-01000003081; AC1L1FDW; Ebselen?; CID3194; 2-Phenyl-1,2-benzoisoselenazol-3(2H)-one; CCG-39161; Ebselen; Lopac E 3520; NSC 639762; PZ 51; Ebselen (C5); nchembio.109-comp1; LS-33527; SAM001247071; EBESELEN [USAN]; EBSELEN [JAN]; EBSELEN [MI]; EBSELEN [MART.]; Opera_ID_1643; EBSELEN [WHO-DD]; Ebselen, cysteine modifier; cid_3194; C042986; SCHEMBL33829; MLS001424261; MLS006010108; E3520_SIGMA; I09-1611; orb1224475; orb1310258; SCHEMBL29370082; BDBM34233; GTPL10583; HMS2097C22; HMS2235A11; HMS3394N09; HMS3402D04; HMS3649O05; HMS3714C22; HMS3873N13; HMS5086A04; KUC112559N; Pharmakon1600-01501188; EX-A1447; SPI-1005;PZ-51; Tox21_110140; 2-Phenyl-benzo[d]isoselenazol-3-one; BDBM50129950; CCG-39161; DAP001372; HB0270; NSC757883; AKOS015898841; CS-5534; DB12610; EBC-412086; FE75162; LP00541; NC00431; SDCCGSBI-0050524.P004; KSC-325-014; NCGC00015412-04; NCGC00015412-05; NCGC00015412-07; NCGC00015412-08; NCGC00015412-09; NCGC00015412-10; NCGC00015412-11; NCGC00015412-12; NCGC00015412-21; phenyl-1,2-benzisoselenazol-3(2H)-one; 2-phenyl-1,2-benzisoselazol-3(2H)-one; AS-89667; HY-13750; SY052687; SBI-0050524.P003; 2-phenyl-1,2-benzisoselenazole-3(2H)-one; DB-072873; 2-phenyl-1,2-benzoisoselenazole-3(2H)-one; NS00034501; 2-phenyl-1,2-benzoisoselenazole-3-(2H)-one; 2-Phenyl-1,2-benzoselenazol-3-one(Ebselen); 2-Phenyl-benzo[d]isoselenazol-3-one(Ebselen); C05110703-B; C75847; M01704; AB00053217_25; Q5332073; SR-01000003081-2; SR-01000003081-7; SR-01000003081-8; BRD-K29359156-001-23-6; BRD-K29359156-001-30-1; SR-01000003081-10; SR-01000003081-14
Product application:Ebselen,60940-34-3,2-Phenyl-1,2-benzisoselenazol-3(2H)-one,PZ-51,Pharmaceutical grade ebselen,Glutathione peroxidase mimic,GPx mimetic,Organoselenium catalyst,Antioxidant reagent,Neuroprotective intermediate,Cerebral ischemia reperfusion agent,Peroxynitrite scavenger,Hearing loss therapeutic API,Otoprotective intermediate,Mpro protease inhibitor,Antibiotic adjuvant,Organoselenium heterocyclic building block,Biochemical research reagent,High purity Ebselen 99.5%,CAS 60940-34-3 supplier,Ebselen manufacturer China,Suzhou Health Chemicals specialty chemicals,Ebselen wholesale bulk export
Ebselen is widely utilized across neuroprotective drug discovery, acute ischemic reperfusion therapeutics, sensorineural hearing loss intervention, antiviral and antimicrobial resistance research, and cellular redox biology sectors. In cardiovascular and central nervous system pharmacology, it operates as a standard low-toxicity, lipid-soluble glutathione peroxidase mimetic, catalyzing the rapid reduction of hydrogen peroxide and lipid peroxides while scavenging cytotoxic peroxynitrite species; this catalytic activity attenuates neuronal membrane lipid peroxidation, mitigates neuroinflammatory cascades, and protects cerebral tissue against reperfusion-induced damage following acute ischemic stroke; in otological therapeutics, it shields cochlear hair cells from intense acoustic trauma and oxidative damage, providing an effective pharmaceutical agent for preventing noise-induced and aminoglycoside-induced hearing loss; in infectious disease and medicinal chemistry development, the molecule acts as a covalent modifier targeting catalytic cysteine residues in bacterial enzymes and viral main proteases, demonstrating therapeutic utility in overcoming antibiotic resistance mechanisms; furthermore, in fundamental bioscience research, Ebselen serves as an indispensable biochemical probe for elucidating ferroptosis signaling pathways, intracellular redox balance, and microvascular endothelial integrity.
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