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1-EBIO

Product Name
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
Formula Weight
162.19
MOL File
10045-45-1.mol
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1-EBIO Property

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.
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Safety

Hazard Codes 
Xn
Risk Statements 
22-36
Safety Statements 
26
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933998090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P337+P313IF eye irritation persists: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SML0034
Product name
1-EBIO
Purity
≥98% (HPLC)
Packaging
10mg
Price
$100
Updated
2024/03/01
Sigma-Aldrich
Product number
SML0034
Product name
1-EBIO
Purity
≥98% (HPLC)
Packaging
50mg
Price
$404
Updated
2024/03/01
Cayman Chemical
Product number
14575
Product name
1-EBIO
Purity
≥98%
Packaging
5mg
Price
$32
Updated
2024/03/01
Cayman Chemical
Product number
14575
Product name
1-EBIO
Purity
≥98%
Packaging
10mg
Price
$50
Updated
2024/03/01
Cayman Chemical
Product number
14575
Product name
1-EBIO
Purity
≥98%
Packaging
50mg
Price
$193
Updated
2024/03/01
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1-EBIO Chemical Properties,Usage,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

1-EBIO Preparation Products And Raw materials

Raw materials

Preparation Products

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1-EBIO Suppliers

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15848
Advantage
69
Ascent Scientific
Tel
4401179829988
Fax
4402030 700 369
Email
customerservice@ascentscientific.co.uk
Country
United Kingdom
ProdList
279
Advantage
60
Artis Chemistry (Shanghai) Co. Ltd.
Tel
86-21-60936353
Fax
86-21-60936352
Country
China
ProdList
336
Advantage
58
Shanghai Topbiochem Technology Co., Ltd
Tel
021-58170097
Email
info@topbiochem.com
Country
China
ProdList
9442
Advantage
58
Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.
Tel
025-66099280 17798518460
Fax
(1)02557626880
Email
cfzhang@aikonchem.com
Country
China
ProdList
19918
Advantage
55
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
18216
Advantage
56
TargetMol Chemicals Inc.
Tel
021-33632979 15002134094
Fax
021-33632979
Email
marketing@targetmol.com
Country
China
ProdList
7934
Advantage
58
Bide Pharmatech Ltd.
Tel
400-1647117 15221909166
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
41438
Advantage
60
Shanghai Xingui Biotechnology Co., Ltd.
Tel
17501653713 17501653715
Email
xingui2022@126.com
Country
China
ProdList
9988
Advantage
58

10045-45-1, 1-EBIORelated Search:


  • 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