UCSF

ZINC00119632

Substance Information

In ZINC since Heavy atoms Benign functionality
July 23rd, 2004 24 No

Other Names:

"Ethidium bromide, 95%"

ium

1239-45-8; C11161; Ethidium bromide; Homidium bromide

2,7-Diamino-10-Ethyl-9-Phenylphenanthridinium Bromide [1239-45-8]; (Ethidium bromide)

2,7-Diamino-10-ethyl-9-phenylphenanthridinium bromide; 2,7-Diamino-9-phenyl-10-ethylphenanthridinium bromide; 2,7-Diamino-9-phenylphenanthridine ethobromide; 3,8-Diamino-1-ethyl-6-phenylphenantridinium bromide; 3,8-Diamino-5-ethyl-6-phenylphenanthridinium

2,7-diamino-10-ethyl-9-phenylphenanthridinium bromide; 2,7-diamino-9-phenyl-10-ethylphenanthridinium bromide; Dromilac; EtBr; Ethidium bromide; Homidium bromide

2,7-DIAMINO-10-ETHYL-9-PHENYLPHENANTHRIDINIUM BROMIDE; [1239-45-8]

2,7-Diamino-9-phenyl-10-ethylphenanthridinium chloride; 3,8-Diamino-5-ethyl-6-phenylphenanthridinium chloride; Babidium chloride; EINECS 210-018-2; Ethidium chloride; Homidium chloride; LS-102877; NSC 522843; NSC-84423; Novidium chloride; Phenanthridinium

237

3,8-Diamino-5-ethyl-6-phenyl-phenanthridinium bromide

3,8-Diamino-5-ethyl-6-phenylphenanthridin-5-ium bromide

3,8-Diamino-5-ethyl-6-phenylphenanthridinium bromide

3,8-diamino-5-ethyl-6-phenylphenanthridinium; ETHIDIUM; ethidium cation; homidium

3546-21-2; CPD0-1938; ethidium; ethidium cation; homidium

5-ethyl-6-phenylphenanthridin-5-ium-3,8-diamine bromide

BRN 3627183; C21H20N3; Ethidium; Ethidium Bromide; Ethidium cation; Homidium; Homidium Bromide; LS-102876; Novidium; Phenanthridinium, 3,8-diamino-5-ethyl-6-phenyl-

DNC000623

DNC000624

Ethidinium bromide, 3,8-Diamino-5-ethyl-6-phenylphenanthridinium bromide

Ethidium

Ethidium bromide

Ethidium bromide, 95%, pure

Ethidium bromide, 98% (dry wt.)

Homidium Bromide (BAN

INN

MFCD00011724

MI)

Download: MOL2 SDF SMILES Flexibase

Annotations

Vendors

Physical Representations

Type pH range xlogP Des A‑Pol Apolar desolvation (kcal/mol) Des Pol Polar desolvation (kcal/mol) H Don H-bond donors H Acc H-bond acceptors Chg Net charge tPSA (Ų) MWT Molecular weight (g/mol) RB Rotatable bonds DL
Ref Reference (pH 7) 0.30 8.49 -20.4 4 3 1 56 314.412 2

Vendor Notes

Note Type Comments Provided By
Molecular_Solubility 6.314 Bitter DB
Mp [°C] 260 - 262 Acros Organics
M.P 260-262 °C Indofine
Purity 95% Fluorochem
Therapy antiprotozoal, intercalcate with DNA SMDC MicroSource
therap antiprotozoal, intercalcates with DNA MicroSource Spectrum
Notes Assay (by dried basis) 97+% Loss on drying < 5.0%Nucleic acid intercalator; Detects as little as 10ng of DNA under short wave UV light Apollo Scientific Bioactives
Melting_Point ca 261? dec. Alfa-Aesar
Melting_Point ca 261° dec. Alfa-Aesar
UniProt Database Links DCAM_ACACA; EBRA_BACAT; EBRA_BACLD; EBRA_BACSU; EBRB_BACAT; EBRB_BACLD; EBRB_BACSU; EBR_ECOLX; EBR_PSEAI; EBR_SALTM; EMRE_ECOLI; ETBR2_BOVIN; ETBR2_HUMAN; ETBR2_MOUSE; ETBR2_RAT; FTSH_OENOE; GEP4_YEAST; GPR37_HUMAN; HMRM_HAEIN; INIA_MYCTU; MDEP_STAAU; MDF ChEBI
UniProt Database Links DCAM_ACACA; EBRA_BACAT; EBRA_BACLD; EBRA_BACSU; EBRB_BACAT; EBRB_BACLD; EBRB_BACSU; EBR_ECOLX; EBR_PSEAI; EBR_SALTM; EMRE_ECOLI; FTSH_OENOE; GEP4_YEAST; HMRM_HAEIN; INIA_MYCTU; MDEP_STAAU; MDFA_ECOLI; MDTE_ECOLI; MDTF_ECOLI; MDTK_ECOLI; MDTK_ERWAM; MDTM_E ChEBI
Patent Database Links EP1642909; EP1710256; EP1780268; EP1782838; EP1788085; EP1793001; EP1967189; US2006115848; US2007196392; US2007253900; WO2005016343; WO2007137117 ChEBI
Notes Ethidinium bromide is an intercalating dye used in the visualisation of DNA and RNA in electrophoresis gels and caesium chloride density gradients Apollo Scientific Bioactives
SOLUBILITY H2O: 10 mg/mL, opaque, strongly red Indofine
H phrase H341: Suspected of causing genetic defects Acros Organics
H phrase H341: Suspected of causing genetic defects; H330: Fatal if inhaled; H302: Harmful if swallowed Acros Organics
P phrase P310: Immediately call a POISON CENTER or doctor/physician Acros Organics
P phrase P310: Immediately call a POISON CENTER or doctor/physician; P281: Use personal protective equipment as required; P304 + P340: IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing Acros Organics
R phrase R22: Harmful if swallowed. Acros Organics
R phrase R22: Harmful if swallowed.; R26: Very toxic by inhalation.; R68: Possible risks of irreversible effects. Acros Organics
Hazard T+: Very toxic Acros Organics
Patent Database Links US2003105066; WO2007137117 ChEBI

Activity (Go SEA)

Clustered Target Annotations
Code Description Organism Class Affinity (nM) LE (kcal/mol/atom) Type
TERT-1-E Telomerase Reverse Transcriptase (cluster #1 Of 2), Eukaryotic Eukaryotes 3300 0.32 Binding ≤ 10μM
MDTK-1-B Multidrug Resistance Protein MdtK (cluster #1 Of 1), Bacterial Bacteria 9800 0.29 Binding ≤ 10μM
Z104302-7-O Glutamate NMDA Receptor (cluster #7 Of 7), Other Other 7340 0.30 Binding ≤ 10μM
Z50643-2-O Hepatitis C Virus (cluster #2 Of 2), Other Other 810 0.36 Binding ≤ 10μM
Z50643-2-O Hepatitis C Virus (cluster #2 Of 5), Other Other 600 0.36 Functional ≤ 10μM
Z80493-1-O SK-OV-3 (Ovarian Carcinoma Cells) (cluster #1 Of 6), Other Other 4500 0.31 Functional ≤ 10μM
Z80768-1-O CH1 (Ovarian Carcinoma Cells) (cluster #1 Of 1), Other Other 400 0.37 Functional ≤ 10μM
Z81034-6-O A2780 (Ovarian Carcinoma Cells) (cluster #6 Of 10), Other Other 100 0.41 Functional ≤ 10μM
ChEMBL Target Annotations
Uniprot Swissprot Description Affinity (nM) LE (kcal/mol/atom) Type
Z50643 Z50643 Hepatitis C Virus 810 0.36 Binding ≤ 1μM
Z104302 Z104302 Glutamate NMDA Receptor 3130 0.32 Binding ≤ 10μM
Z50643 Z50643 Hepatitis C Virus 3800 0.32 Binding ≤ 10μM
MDTK_ECOLI P37340 Multidrug Resistance Protein MdtK, Ecoli 9800 0.29 Binding ≤ 10μM
TERT_HUMAN O14746 Telomerase Reverse Transcriptase, Human 2500 0.33 Binding ≤ 10μM
Z81034 Z81034 A2780 (Ovarian Carcinoma Cells) 100 0.41 Functional ≤ 10μM
Z80768 Z80768 CH1 (Ovarian Carcinoma Cells) 400 0.37 Functional ≤ 10μM
Z50643 Z50643 Hepatitis C Virus 600 0.36 Functional ≤ 10μM
Z80493 Z80493 SK-OV-3 (Ovarian Carcinoma Cells) 400 0.37 Functional ≤ 10μM

Reactome Annotations from Targets (via Uniprot)

Description Species
formation of the beta-catenin:TCF transactivating complex
Telomere Extension By Telomerase

Analogs ( Draw Identity 99% 90% 80% 70% )