![]() Clamikalant sodium structure
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Common Name | Clamikalant sodium | ||
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CAS Number | 261717-22-0 | Molecular Weight | 493.96000 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C19H21ClN3NaO5S2 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of Clamikalant sodiumClamikalant sodium (HMR 1098) is an ATP-sensitive potassium (KATP) channel blocker. Clamikalant sodium can be used for the research of arrhythmia[1]. |
Name | Sodium (5-chloro-2-methoxybenzoyl)(2-{4-methoxy-3-[(methylcarbamo thioyl)sulfamoyl]phenyl}ethyl)azanide |
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Description | Clamikalant sodium (HMR 1098) is an ATP-sensitive potassium (KATP) channel blocker. Clamikalant sodium can be used for the research of arrhythmia[1]. |
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Related Catalog | |
In Vitro | Clamikalant sodium (HMR 1098; 40 μM) prevents improvement effect of Levosimendam on left ventricular developed pressure (LVDP) recovery rate, abolishes the inhibitory effect of Levosimendan on hypothermic preservation-induced activation of calpain, cleavage of Bid, and apoptosis[2]. Clamikalant sodium (HMR 1098; 30 µM, 24 hours) reduces cellular viability, increases the apoptosis of Neonatal rat cardiomyocytes (NRCs) [3]. Clamikalant sodium (30 µM) decreases the Bcl-2 protein level and increases the Bax protein level in the LPS-exposed NRCs[3]. Cell Viability Assay[3] Cell Line: Neonatal rat cardiomyocytes (NRCs) Concentration: 30 µM Incubation Time: 24 hours Result: Reduced cellular viability to 42.8±6.3% compared with the LPS group. Western Blot Analysis[3] Cell Line: Neonatal rat cardiomyocytes (NRCs) Concentration: 30 µM Incubation Time: 24 hours Result: Decreased the Bcl-2 protein level and increased the Bax protein level. |
In Vivo | Clamikalant sodium (HMR 1098; 6.0 mg/kg; 5 min prior to EET administration) completely abolishes the cardioprotection produced by epoxyeicosatrienoic acid (EET)[1]. |
References |
Molecular Formula | C19H21ClN3NaO5S2 |
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Molecular Weight | 493.96000 |
Exact Mass | 493.05100 |
PSA | 141.24000 |
LogP | 4.77940 |