CAS 182004-65-5
:2-[4-[(4-Nitrophenyl)methoxy]phenyl]ethyl carbamimidothioate methanesulfonate (1:1)
Description:
2-[4-[(4-Nitrophenyl)methoxy]phenyl]ethyl carbamimidothioate methanesulfonate (1:1), with CAS number 182004-65-5, is a chemical compound characterized by its complex structure, which includes a carbamimidothioate functional group and a methanesulfonate salt. This compound features a nitrophenyl moiety, which is known for its electron-withdrawing properties, potentially influencing the compound's reactivity and solubility. The presence of the methoxy group enhances its lipophilicity, which may affect its biological activity and interaction with various biological targets. The methanesulfonate component contributes to the overall solubility in polar solvents, making it suitable for various applications in medicinal chemistry and research. Additionally, the compound may exhibit specific pharmacological properties due to its unique structural features, which could be explored in drug development or as a biochemical probe. As with many chemical substances, safety and handling precautions should be observed, given the potential toxicity associated with nitro groups and other reactive functionalities.
Formula:C16H17N3O3S·CH4O3S
InChI:InChI=1S/C16H17N3O3S.CH4O3S/c17-16(18)23-10-9-12-3-7-15(8-4-12)22-11-13-1-5-14(6-2-13)19(20)21;1-5(2,3)4/h1-8H,9-11H2,(H3,17,18);1H3,(H,2,3,4)
InChI key:InChIKey=WGIKEBHIKKWJLG-UHFFFAOYSA-N
SMILES:C(OC1=CC=C(CCSC(=N)N)C=C1)C2=CC=C(N(=O)=O)C=C2.S(C)(=O)(=O)O
Synonyms:- 2-(2-(4-(4-Nitrobenzyloxy)Phenyl)Ethyl)Isothiourea, Methane Sulfonate
- 2-[4-[(4-Nitrophenyl)methoxy]phenyl]ethyl carbamimidothioate methanesulfonate (1:1)
- 2-{4-[(4-Nitrobenzyl)Oxy]Phenyl}Ethyl Carbamimidothioate Methanesulfonate (1:1)
- Carbamimidothioic acid, 2-[4-[(4-nitrophenyl)methoxy]phenyl]ethyl ester, methanesulfonate (1:1)
- Carbamimidothioic acid, 2-[4-[(4-nitrophenyl)methoxy]phenyl]ethyl ester, monomethanesulfonate
- Kb-R 7943
- Kb-R7943
- Kb-R7943 Mesylate
- KB-R 7943 mesylate
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Found 8 products.
CARBAMIMIDOTHIOIC ACID, 2-[4-[(4-NITROPHENYL)METHOXY]PHENYL]ETHYL ESTER, METHANESULFONATE (1:1)
CAS:Formula:C17H21N3O6S2Purity:98%Color and Shape:SolidMolecular weight:427.4951S-[4-[(4-Nitrobenzyl)Oxy]Phenethyl]Isothiourea Methanesulfonate
CAS:S-[4-[(4-Nitrobenzyl)Oxy]Phenethyl]Isothiourea MethanesulfonatePurity:99%Molecular weight:427.49g/molKB-R7943 mesylate
CAS:<p>KB-R7943 mesylate is a widely used inhibitor of the reverse Na+/Ca2+ exchanger (NCXrev) with IC50 of 5.7±2.1 μM.</p>Formula:C17H21N3O6S2Purity:99.88% - ≥95%Color and Shape:SolidMolecular weight:427.5KB-R 7943
CAS:Formula:C16H17N3O3S·CH4O3SPurity:>98.0%(HPLC)Color and Shape:White to Yellow to Green powder to crystalMolecular weight:427.49KB-R7943 Mesylate
CAS:Controlled Product<p>Applications KB-R7943 Mesylate is a selective inhibitor of the reverse mode of Na+/Ca2+ exchange in cells expressing NCX1.<br>References Iwamoto, T. et al.: J. Biol. Chem., 271, 22391 (1996)<br></p>Formula:C16H17N3O3S·(CH4O3S)Color and Shape:NeatMolecular weight:331.39 + (96.11)KB-R7943
CAS:<p>KB-R7943 is a polymerase chain inhibitor that has been shown to be effective in the treatment of atrial fibrillation. It inhibits the activity of DNA polymerase, which is required for replication and transcription of DNA. KB-R7943 also has been shown to increase intracellular calcium levels and inhibit mitochondrial membrane potential, leading to cardioprotective effects. KB-R7943 has inhibitory properties on the ryanodine receptor and exchangers, which are involved in cardiac excitation–contraction coupling. KB-R7943 also has been shown to reduce myocardial infarction size and improve heart function following an injury.</p>Formula:C17H21N3O6S2Purity:Min. 95%Molecular weight:427.49 g/mol






