1-Ethylbenzimidazolinone - Moligand™, ≥98% , Activator of K Ca2.1;Activator of K Ca2.2;Activator of K Ca2.3;Activator of K Ca3.1, CAS No.10045-45-1, Activator of K Ca2.1;Activator of K Ca2.2;Activator of K Ca2.3;Activator of K Ca3.1

CAS: 10045-45-1 Cat. No.: E178702 Formula: C9H10N2O Peso molecolare: 162.2 Numero EC: 233-148-1
Disponibile su ordine
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
2(1H)-Quinolinone, 6-hydroxy- | 2-chloro-1-(2,3-dihydro-1H-indol-1-yl)ethan-1-one | SCHEMBL12397237 | HMS1779F03 | HMS3267A18 | MFCD00005715 | Z57114989 | 1-EBIO, >=98% (HPLC) | 1-ethyl-1,3-dihydro-benzimidazol-2-one | 3-ethyl-1H-benzimidazol-2-one. | A89
Storage
Conservare a 2-8°C
Shipped In
Ghiaccio umido
★
Size
Germania (EU)
USA*
Price
Qty
1g
E178702-1g
—
3 Disponibile

32,02€

48,51€
Salva 16,49 € (33.99%)
5g
E178702-5g
—
1 Disponibile

102,31€

153,50€
Salva 51,20 € (33.35%)
10g
E178702-10g
—
2 Disponibile

183,01€

274,99€
Salva 91,98 € (33.45%)
25g
E178702-25g
—
1 Disponibile

347,01€

520,56€
Salva 173,55 € (33.34%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Conservare a 2-8°C Ships Ghiaccio umido Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 11 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinonimi
2(1H)-Quinolinone, 6-hydroxy- | 2-chloro-1-(2,3-dihydro-1H-indol-1-yl)ethan-1-one | SCHEMBL12397237 | HMS1779F03 | HMS3267A18 | MFCD00005715 | Z57114989 | 1-EBIO, >=98% (HPLC) | 1-ethyl-1,3-dihydro-benzimidazol-2-one | 3-ethyl-1H-benzimidazol-2-one. | A89
Specifiche e purezza
Moligand™, ≥98%
Meccanismi biochimici e fisiologici
Attivatore dei canali K + attivati dal Ca 2+ a conduttanza piccola e intermedia (SK). Attiva anche il canale CFTR a conduttanza Cl- della membrana apicale.
Condizioni di conservazione di stoccaggio
Conservare a 2-8°C
Spedito in
Ghiaccio umido
Grado
Moligand™
Tipo di azione
ACTIVATOR
Meccanismo d'azione
Activator of K Ca2.1;Activator of K Ca2.2;Activator of K Ca2.3;Activator of K Ca3.1
Nota
Per quanto possibile, si consiglia di preparare e utilizzare le soluzioni lo stesso giorno. Tuttavia, se è necessario preparare in anticipo le soluzioni di riserva, si consiglia di conservarle in aliquote in fiale ben chiuse a -20°C. In genere, queste possono essere utilizzate per un mese. In genere, queste soluzioni sono utilizzabili fino a un mese. Prima dell'uso e dell'apertura della fiala, si consiglia di lasciare che il prodotto si equilibri a temperatura ambiente per almeno 1 ora. Avete bisogno di ulteriori consigli su solubilità, uso e manipolazione? Per ulteriori informazioni, visitare la pagina delle domande frequenti (FAQ).
Purezza
≥98%
Nomi e identificatori
Pubchem Sid508807269
Sorrisi canoniciCCN1C2=CC=CC=C2NC1=O
IUPAC Name3-ethyl-1H-benzimidazol-2-one
InChIKeyCXUCKELNYMZTRT-UHFFFAOYSA-N
INCHI1S/C9H10N2O/c1-2-11-8-6-4-3-5-7(8)10-9(11)12/h3-6H,2H2,1H3,(H,10,12)
Isomeri SMILES CCN1C2=CC=CC=C2NC1=O
WGK Germania 3
Peso molecolare 162.2
Reaxy-Rn 137120
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=137120&ln=

Documentazione

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClasseBenzimidazoles
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzimidazoles
Alternative Parents N-substituted imidazoles  Benzenoids  Heteroaromatic compounds  Ureas  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Benzimidazole - N-substituted imidazole - Benzenoid - Heteroaromatic compound - Azole - Imidazole - Urea - Azacycle - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as benzimidazoles. These are organic compounds containing a benzene ring fused to an imidazole ring (five member ring containing a nitrogen atom, 4 carbon atoms, and two double bonds).
External Descriptors imidazoles
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
KCNN4 Tchem Intermediate conductance calcium-activated potassium channel protein 4 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNN1 Tchem Small conductance calcium-activated potassium channel protein 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNN3 Tchem Small conductance calcium-activated potassium channel protein 3 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNN2 Tchem Small conductance calcium-activated potassium channel protein 2 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Obiettivi associati (non umani)
Kcnn3 Small conductance calcium-activated potassium channel protein 3 (210 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot NumberCertificate TypeDataOggetto
I2617011Certificate of AnalysisSep 28, 2026 E178702
H2330401Certificate of AnalysisSep 07, 2023 E178702
H2330402Certificate of AnalysisSep 07, 2023 E178702
H2330448Certificate of AnalysisSep 07, 2023 E178702
H2330476Certificate of AnalysisSep 07, 2023 E178702
Proprietà chimiche e fisiche
Peso molecolare162.190 g/mol
XLogP31.100
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count1
Exact Mass162.079 Da
Monoisotopic Mass162.079 Da
Topological Polar Surface Area32.299 Ų
Heavy Atom Count12
Formal Charge0
Complexity193.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Riferimenti
1. Guiyuan Liu, Yinliang Bai, Guangxian Leng, Hanwei Ma, Yin Kong, Liuqing Guo, Fahong Wu, Fengxian Wei, Yi Pang, Youcheng Zhang.  (2023)  Rhubarb Anthraquinones Ameliorates Inflammatory Lung Injury by Enhancing Alveolar Epithelium Tight Junction Proteins through RhoA/ROCK1 Signalling.  Pharmacognosy Magazine,      [PMID:] [10.1177/09731296231158697]
2. Dongya Wang, Qianqian Zhao, Jingcan Qin, Yuanyuan Guo, Chuan Zhang, Yuehua Li.  (2022)  Urokinase loaded black phosphorus nanosheets for sequential thrombolysis and reactive oxygen species scavenging in ischemic stroke treatment.  Biomaterials Science,  10  (16): (4656-4666).  [PMID:35801526] [10.1039/D2BM00746K]
3. Pan Cheng, Cancan Ji, Wei Hu, Peng Huang, Qihao Guo, Ming Xia, Qin Cheng, Jia Xu, Ke Liu, Dong Wang.  (2022)  Facile fabrication of nanofibrous ion-exchange chromatography membrane with aminated surface for highly efficient RNA separation and purification.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2022.129160]
4. Yuemiao Lai, Zhengtian Pu, Peng Liu, Fangliang Li, Jie Zeng, Xueming Yang, Qing Guo.  (2022)  Low-Temperature C–H Bond Activation: Ethylbenzene-to-Styrene Conversion on Rutile TiO2(110).  Journal of Physical Chemistry C,      [PMID:] [10.1021/acs.jpcc.2c00244]
5. Zhenxing Cai, Hui Zhao, Xin Zhou, Xiaobo Chen, Chaohe Yang.  (2021)  Determination and modeling of binary solid-liquid equilibria of para-xylene/meta-xylene, para-xylene/ortho-xylene by DSC method.  FLUID PHASE EQUILIBRIA,      [PMID:] [10.1016/j.fluid.2021.113325]
6. Shenling Wang, Yanling Geng, Xiaowei Sun, Rongyu Wang, Zhenjia Zheng, Shenghuai Hou, Xiao Wang, Wenhua Ji.  (2020)  Molecularly imprinted polymers prepared from a single cross-linking functional monomer for solid-phase microextraction of estrogens from milk.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:32823105] [10.1016/j.chroma.2020.461400]
7. Sun Qian, Song Xueying, Gao Li, Chen Wei, Li Yamin, Mao Liqun, Yang Jing-He.  (2018)  Heterogeneous liquid phase oxidation of ethylbenzene to acetophenone with graphene carbon-based catalyst.  CHEMICAL PAPERS,  72  (9): (2203-2214).  [PMID:] [10.1007/s11696-018-0432-8]
8. Xuying Nan, Yi Huang, Jianzhong Shao, Huiqiong Yan, Mingshu Wu, Yuhua Yao.  (2018)  Co-initiating function of silk peptide in free radical photopolymerization.  POLYMER ENGINEERING AND SCIENCE,  58  (12): (2185-2191).  [PMID:] [10.1002/pen.24833]
9. Yan Li, Cheng Chen, Jinlong Wu, Xiangxiang Jia, Yufan Lu, Fangjuan Chen, Lijian Liu.  (2016)  Copolymerization of alkyl diazoacetates with α,β-unsaturated aldehydes: synthesis and application.  Polymer Chemistry,  7  (47): (7216-7222).  [PMID:] [10.1039/C6PY01666A]
10. Xuying Nan, Yi Huang, Qinguo Fan, Jianzhong Shao, Yuhua Yao.  (2015)  Efficient visible photoinitiator with high-spectrum stability in an acid medium for free-radical and free-radical-promoted cationic photopolymerization based on erythrosine B derivatives.  JOURNAL OF APPLIED POLYMER SCIENCE,  133  (10):   [PMID:] [10.1002/app.43035]
11. Xuying Nan, Yi Huang, Qinguo Fan, Jianzhong Shao.  (2015)  Efficient visible photoinitiator containing linked dye-coinitiator and iodonium salt for free radical polymerization.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2014.12.013]
Calcolatori di soluzioni
Recensioni

Recensioni dei clienti

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.