Carteolol
Based on 2 publication(s) in Google Scholar
Carteolol is a non-selective β-adrenoceptor antagonist. Carteolol induces apoptosis via a caspase activated and mitochondrial-dependent pathway. Carteolol can be used for glaucoma research.
연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.
- CAS No.: 51781-06-7
- 화학식: C16H24N2O3
- 분자량:292.37
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications Citing Use of MedChemExpress (MCE) Carteolol
MoreAll Adrenergic Receptor Isoforms
MoreAll Caspase Isoforms
More
Biological Activity
Carteolol (0-2%; 0-28 hours; HCECs) has cytotoxicity and decreases cell viability in a dose- and time-dependent manner[1].
Carteolol (0.25%; 4-12 hours; HCECs) induces apoptosis and necroptotic protein expression in HCECs[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:HCECs
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Concentration:0.00390625-2%
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Incubation Time:0, 2, 4, 8, 16, 20,24 and 28 hours
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Result:Decreased cell viability with the concentrations above 0.0015625% in a dose- and time-dependent manner.
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Cell Line:HCECs
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Concentration:0.25%
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Incubation Time:4, 8 and 12 hours
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Result:Dampened expression of the anti-apoptotic protein Bcl-2 and Bcl-xL, enhanced expression of the pro-apoptotic proteins Bax and Bad, and mitochondrial-released pro-apoptotic proteins Cyt.c and AIF.
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Cell Line:HCECs
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Concentration:0.25%
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Incubation Time:4, 8 and 12 hours
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Result:Increased the number of G1 phase of the cell cycle, whereas decreased S phase.
| NCT Number | Sponsor | Condition | Start Date |
Phase
|
|---|---|---|---|---|
| NCT01329991 | Plexxikon| | 2011-05 | PHASE1 |
Chemical Information
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CAS No. 51781-06-7
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분자량 292.37
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화학식 C16H24N2O3
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SMILES
O=C1NC2=C(C(OCC(O)CNC(C)(C)C)=CC=C2)CC1
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Synonyms
OPC-1085
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications (2)
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Journal Impact Factor
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Most Recent
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ACS Omega
Computational and Experimental Approaches Identify Beta-Blockers as Potential SARS-CoV-2 Spike Inhibitors. [Abstract]2022 Aug 8;7(32):27950-27958. PMID: 35983371 -
J Pharm Biomed Anal
Screening method of mildronate and over 300 doping agents by reversed-phase liquid chromatography-high resolution mass spectrometry. [Abstract]2021 Feb 20:195:113870. PMID: 33453569
순도&문서
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)