18 Results for "

NODAL

" in MedChemExpress (MCE) Product Catalog:
Products (18)

18 Results for "NODAL" in MCE Product Catalog:

141
141 Publications Verification
Cat. No.: HY-10432
CAS No.: 909910-43-6
Purity:  99.33%
Research Areas:  

Cancer

A 83-01 is a potent inhibitor of TGF-β type I receptor ALK5 kinase, type I nodal receptor ALK4 and type I nodal receptor ALK7, with IC50s of 12 nM, 45 nM and 7.5 nM against the transcription induced by ALK5, ALK4 and ALK7, respectively .
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4
4 Cited Publications
Cat. No.: HY-A0016
CAS No.: 141626-36-0
Synonyms: SR 33589
Dronedarone (SR 33589), a derivative of amiodarone (HY-14187), is a class III antiarrhythmic agent for the study of atrial fibrillation (AF) and atrial flutter. Dronedarone is a potent blocker of multiple ion currents, including potassium current, sodium current, and L-type calcium current, and exhibits antiadrenergic effects by noncompetitive binding to β-adrenergic receptors. Dronedarone is a substrate for and a moderate inhibitor of CYP3A4 .
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2
2 Cited Publications
Cat. No.: HY-P700025AF
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: NODAL
Species:  
Source:  
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Cat. No.: HY-106577
CAS No.: 53267-01-9
Purity:  95.08%
Synonyms: Cifenline; Ro 22-7796
Cibenzoline is a class Ia antiarrhythmic active molecule with low anticholinergic activity. Cibenzoline is a KATP channel inhibitor, acting through the pore forming subunit Kir6.2, with an IC50 of 22.2 μM. Cibenzoline inhibits IKr and IKs currents with IC50 values of 8.8 μM and 12.3 μM, respectively. Cibenzoline is used in the study of cardiac diseases. In addition, Cibenzoline can induce hypoglycemia .
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Cat. No.: HY-10432R
CAS No.: 909910-43-6
Research Areas:  

Cancer

A 83-01 (Standard) is the analytical standard of A 83-01 (HY-10432). This product is intended for research and analytical applications. A 83-01 is a potent inhibitor of TGF-β type I receptor ALK5 kinase, type I nodal receptor ALK4 and type I nodal receptor ALK7, with IC50s of 12 nM, 45 nM and 7.5 nM against the transcription induced by ALK5, ALK4 and ALK7, respectively .
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Cat. No.: HY-RS09409
Research Areas:  

Others

NODAL Human Pre-designed siRNA Set A contains three designed siRNAs for NODAL gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS19222
Research Areas:  

Others

Nodal Mouse Pre-designed siRNA Set A contains three designed siRNAs for Nodal gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-106577R
CAS No.: 53267-01-9
Synonyms: Cifenline (Standard); Ro 22-7796 (Standard)
Cibenzoline (Standard) is the analytical standard of Cibenzoline. This product is intended for research and analytical applications. Cibenzoline is a class Ia antiarrhythmic active molecule with low anticholinergic activity. Cibenzoline is a KATP channel inhibitor, acting through the pore forming subunit Kir6.2, with an IC50 of 22.2 μM. Cibenzoline inhibits IKr and IKs currents with IC50 values of 8.8 μM and 12.3 μM, respectively. Cibenzoline is used in the study of cardiac diseases. In addition, Cibenzoline can induce hypoglycemia .
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Cat. No.: HY-123196
CAS No.: 342419-09-4
Target:  

Adenosine Receptor

Research Areas:  

Cardiovascular Disease

CVT-2759 is a potent inhibitor of A1-ADOR, with the IC50 values of 0.18 μM and 9.5 μM to reduce the binding of [3H]CPX in the absence and presence of 1 mM GTP. CVT-2759 plays an important role in slowing AV nodal conduction and thereby ventricular rate without causing AV block, bradycardia, atrial arrhythmias, or vasodilation .
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Cat. No.: HY-P704126
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: HTX5; NODAL; NODAL homolog
Species:  
Source:  
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Cat. No.: HY-A0016R
CAS No.: 141626-36-0
Synonyms: SR 33589 (Standard)
Dronedarone (Standard) is the analytical standard of Dronedarone. This product is intended for research and analytical applications. Dronedarone (SR 33589), a derivative of amiodarone (HY-14187), is a class III antiarrhythmic agent for the study of atrial fibrillation (AF) and atrial flutter. Dronedarone is a potent blocker of multiple ion currents, including potassium current, sodium current, and L-type calcium current, and exhibits antiadrenergic effects by noncompetitive binding to β-adrenergic receptors. Dronedarone is a substrate for and a moderate inhibitor of CYP3A4 .
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Cat. No.: HY-RS25711
Research Areas:  

Others

Nodal Rat Pre-designed siRNA Set A contains three designed siRNAs for Nodal gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P79080
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: NODAL; Tg.413d
Species:  
Source:  
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Cat. No.: HY-P810344
Synonyms: NODAL homolog, NODAL

Host:  

Mouse

Application:  

WB, ICC/IF, IF-Tissue, IHC-P, IP, ELISA

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-10321G
CAS No.: 219580-11-7
PD173074 GMP is PD173074 (HY-10321) produced by using GMP guidelines. GMP small molecules works appropriately as an auxiliary reagent for cell therapy manufacture. PD173074 is an orally active FGFR inhibitor that targets the transphosphorylation of FGFR1 and FGFR2 and blocks the FGF signaling pathway. By reducing the phosphorylation level of SMAD2 and altering the expression of Nodal/Activin target genes, PD173074 eliminates endothelial differentiation potential, thereby inhibiting the formation of capillary-like structures. PD173074 blocks the proliferation and colony formation of tumor cells and increases intratumoral cell apoptosis. PD173074 successfully reverses FGF-2-induced chemoresistance to enhance the effect of cisplatin (HY-17394) in small cell lung cancer models. PD173074 can be applied to research related to critical limb ischemia and small cell lung cancer .
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Cat. No.: HY-P81665
Synonyms: HTX5

Host:  

Rabbit

Application:  

WB, FC

Reactivity:  

Human, Rat

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Cat. No.: HY-P81665A
Synonyms: HTX5

Host:  

Rabbit

Application:  

WB, FC

Reactivity:  

Human, Rat

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Cat. No.: HY-180334
CAS No.: 120004-07-1
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease

S-312 is a calcium antagonist with a bicyclic dihydrothienopyridine structure. S-312 can relax the helical strips of various isolated rabbit arteries procontracted with high potassium depolarizaiton. S-312 competitively imhibits calcium-induced contractions in depolarized basilar and femoral arteries. S-312 increases AV nodal conduction time in Langenedorff-perfused isolated rabbit hearts. S-312 exhibits vasculoselectivity, particularly for cerebral vessel .
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