ROMK-IN-1
ROMK-IN-1 is an orally active inhibitor of ROMK (Kir1.1) with an IC50 of 0.073 μM. ROMK-IN-1 exhibits no activity against Kir2.1, Kir4.1, Kir7.1, Nav1.5, Cav1.2, as well as the enzymes CYP3A4, CYP2D6, and CYP2C9. ROMK-IN-1 can be used in research related to hypertension.
For research use only. We do not sell to patients.
- CAS No.: 1443735-02-1
- Formula: C23H23FN8O2
- Molecular Weight:462.49
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
IC50 & Target
[1]|
Kir1.1 0.073 μM (IC50) |
Cellular Effect
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| CHO | IC50 |
0.073 μM
Compound: 25
|
Inhibition of human ROMK expressed in CHO cells after 6 mins at -70 mV holding potential by electrophysiology method
Inhibition of human ROMK expressed in CHO cells after 6 mins at -70 mV holding potential by electrophysiology method
|
[PMID: 27839686] |
| HEK293 | IC50 |
0.073 μM
Compound: 16
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Inhibition of human ROMK1 expressed in HEK293 cells by Tl+ flux assay
Inhibition of human ROMK1 expressed in HEK293 cells by Tl+ flux assay
|
[PMID: 31034224] |
In Vitro
ROMK-IN-1 (10 μM) exhibits high selectivity for ROMK in a screening panel comprising 115 off-target enzyme and binding assays, with only the somatostatin receptor subtype 2 being inhibited, showing an IC50 of 4.1 μM[1].
ROMK-IN-1 (up to 50 μM) exhibits no significant inhibitory effect on CYP3A4, CYP2D6 or CYP2C9 enzymes, with an IC50 value greater than 50 μM[1].
ROMK-IN-1 (incubated for 45 min) exhibits high microsomal stability in both preclinical species and humans, with 72-89% of the parent drug remaining after 45 min of incubation[1].
ROMK-IN-1 (incubated for 90 min) exhibits extremely low in vitro metabolic levels in rhesus monkey and human hepatocytes, with 92-99% of the parent drug remaining after 90 min of incubation[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Parmacokinetics
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Spontaneously Hypertensive Rats[1]
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Dosage:3 mg/kg; 10 mg/kg; 30 mg/kg
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Administration:p.o.; once daily for 3 days
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Result:Produced 24-hour diuresis fold-increases of 1.4, 1.6, and 1.8 at 3, 10, and 30 mg/kg, respectively.
Reduced systolic blood pressure by 9 mmHg at 3 mg/kg, 16 mmHg at 10 mg/kg, and 16 mmHg at 30 mg/kg on day 3.
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Animal Model:Guinea Pigs (anesthetized)[1]
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Dosage:Maximal average peak unbound plasma concentration of 83 μM
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Administration:i.v. infusion
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Result:Showed no significant change in QTc interval.
Chemical Information
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CAS No. 1443735-02-1
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Molecular Weight 462.49
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Formula C23H23FN8O2
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SMILES
CC1=C([C@@H]2CN3[C@](CO2)(CN(C(CC4=CC=C(C=N4)N5C=NN=N5)=O)CC3)[H])C=CC(F)=C1C#N
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)