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1-EBIO

CAS No.
10045-45-1
Chemical Name:
1-EBIO
Synonyms
EBIO;1-EB10;1-EBIO;Einecs 233-148-1;1-EthylbenziMidazolinone;1-ETHYL-2-BENZIMIDAZOLINONE;1-ethylbenzimidazolin-2-one;1-ETHYL-2-BENZCMIDAZOLINONE;1-Ethyl-2-benzimidazolineone;3-ethyl-1H-benzimidazol-2-one
CBNumber:
CB7146587
Molecular Formula:
C9H10N2O
Molecular Weight:
162.19
MDL Number:
MFCD00005715
MOL File:
10045-45-1.mol
Last updated:2023-06-30 15:45:59

1-EBIO Properties

Melting point 118-120 °C(Solv: ethyl acetate (141-78-6))
Density 1.161±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility DMSO: ≥20mg/mL
form powder
pka 12.29±0.30(Predicted)
color Crystalline
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.
FDA UNII M82W79SS4W

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H319
Precautionary statements  P264-P270-P280-P301+P312-P305+P351+P338-P337+P313
Hazard Codes  Xn
Risk Statements  22-36
Safety Statements  26
WGK Germany  3
HazardClass  IRRITANT
HS Code  2933998090
NFPA 704
0
2 0

1-EBIO price More Price(44)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML0034 1-EBIO ≥98% (HPLC) 10045-45-1 10mg $100 2024-03-01 Buy
Sigma-Aldrich SML0034 1-EBIO ≥98% (HPLC) 10045-45-1 50mg $404 2024-03-01 Buy
Cayman Chemical 14575 1-EBIO ≥98% 10045-45-1 5mg $32 2024-03-01 Buy
Cayman Chemical 14575 1-EBIO ≥98% 10045-45-1 10mg $50 2024-03-01 Buy
Cayman Chemical 14575 1-EBIO ≥98% 10045-45-1 50mg $193 2024-03-01 Buy
Product number Packaging Price Buy
SML0034 10mg $100 Buy
SML0034 50mg $404 Buy
14575 5mg $32 Buy
14575 10mg $50 Buy
14575 50mg $193 Buy

1-EBIO Chemical Properties,Uses,Production

Description

1-EBIO is an activator of Ca2+-sensitive K+ channels (EC50 = 490 μM in T84 human carcinoma cells).This action is sensitive to the neurotoxin charybdotoxin (Ki = 3.5 nM). In mouse colonic epithelia, 1-EBIO also activates cAMP-sensitive K+ channels, a response this is inhibited by 293B.In this type of epithelium, but not mouse nasal epithelia, 1-EBIO activates both types of channels, resulting in large Cl- secretory currents.It also activates the human intermediate conductance Ca2+-activated K+ channel (EC50 = 74 μM).1-EBIO is currently used to study the role of these types of K+ channels in diverse physiological functions.

Uses

1-EBIO stimulates Cl- secretion in secretory epithelia through direct activation of clacium potassium channels.
1-EBIO was used to study the electrical activity modulated by Ca+2-activated K+ channels in rat central neurons. The effect of 1-EBIO on human intermediate conductance channels was studied.
The K+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients

Definition

ChEBI: 1-Ethyl-2-benzimidazolinone is a member of imidazoles.

Biological Activity

Activator of epithelial K Ca channels, stimulates a large and sustained trans-epithelial Cl - secretory response across T84 monolayers. Induces hyperpolarization to the same magnitude as ACh in aortic value endothelial cells.

storage

Room temperature

References

1) Adeagbo?et al.?(1999),?1-Ethyl-2-benzimidazolinone stimulates endothelial K(Ca) channels and nitric oxide formation in rat mesenteric vessels; Eur. J. Pharmacol.,?379?151 2) Orfila?et al. (2014),?Increasing small conductance Ca2+-activated potassium channel activity reverses ischemia-induced impairment of long-term potentiation; Eur. J. Neurosci.,?40?3179 3) Allen?et al.?(2011),?SK2 channels are neuroprotective for ischemia-induced neuronal cell death; J. Cereb. Blood Flow Metab.,?31?2302 4) Muller?et al. (2012),?Ca2+ activated K channels-new tools to induce cardiac commitment from pluripotent stem cells in mice and men; Stem Cell Rev.,?8?720 5) Fay?et al.?(2006),?SK channels mediate NADPH oxidase-independent reactive oxygen species production and apoptosis in granulocytes; Proc. Natl. Acad. Sci. USA,?103?17548

95-54-5
10045-45-1
Synthesis of 1-EBIO from o-Phenylenediamine

1-EBIO Suppliers

Global( 105)Suppliers
Supplier Tel Email Country ProdList Advantage
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63711 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Hangzhou MolCore BioPharmatech Co.,Ltd.
+86-057181025280; +8617767106207 sales@molcore.com China 49739 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 57511 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131981 58
J & K SCIENTIFIC LTD. 010-82848833 400-666-7788 jkinfo@jkchemical.com China 96815 76
3B Pharmachem (Wuhan) International Co.,Ltd. 821-50328103-801 18930552037 3bsc@sina.com China 15848 69
Ascent Scientific 4401179829988 customerservice@ascentscientific.co.uk United Kingdom 279 60
Artis Chemistry (Shanghai) Co. Ltd. 86-21-60936353 China 336 58
Shanghai Topbiochem Technology Co., Ltd 021-58170097 info@topbiochem.com China 9449 58

1-EBIO Spectrum

1-Ethyl-1H-benzimidazole-2(3H)-one 1-Ethyl-2,3-dihydro-1H-benzimidazole-2-one EBIO 1-Ethyl-2-benzimidazolinone,98% Einecs 233-148-1 1-EB10 1-ethyl-1,3-dihydro-2H-benzimidazol-2-one(SALTDATA: FREE) 1-EBIO, 1-Ethyl-2-benzimidazolinone 1-Ethyl-1H-benzo[d]iMidazol-2(3H)-one 1-EthylbenziMidazolinone 1-ETHYL-2-BENZIMIDAZOLINONE 1-ETHYL-1,3-DIHYDRO-2H-BENZIMIDAZOL-2-ONE 1-EBIO 1-Ethyl-2-benzimidazolineone 1-ethylbenzimidazolin-2-one 1-ETHYL-2-BENZCMIDAZOLINONE 2H-Benzimidazol-2-one,1-ethyl-1,3-dihydro-(9CI) 3-ethyl-1H-benzimidazol-2-one 2H-Benzimidazol-2-one, 1-ethyl-1,3-dihydro- 1-Ethyl-1,3-dihydro-2H-benzo[d]imidazol-2-one 10045-45-1 BENZIMIDAZOLE Potassium channel Ion Channels