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Filtered Search Results
eMolecules 58-27-5 | Ambeed | 2-Methylnaphthalene-14-dione | 1g | 592282229 | A129193 | MFCD00001681 | 172.183 | C11H8O2
Ambeed | 2-Methylnaphthalene-14-dione | 1g | 592282229 | A129193 | 58-27-5 | MFCD00001681 | 172.183 | C11H8O2
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![eMolecules 518990-00-6 | 3-Cyano-4-fluorophenylzinc bromide, 0.50 M in THF | Synthonix | MFCD02260165 | 265.390 | C7H3BrFNZn | 0.000 | [Br-].Fc1ccc([Zn+])cc1C#N | 100ml | 532652691](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502696292.jpg-250.jpg)
eMolecules 518990-00-6 | 3-Cyano-4-fluorophenylzinc bromide, 0.50 M in THF | Synthonix | MFCD02260165 | 265.390 | C7H3BrFNZn | 0.000 | [Br-].Fc1ccc([Zn+])cc1C#N | 100ml | 532652691
3-Cyano-4-fluorophenylzinc bromide, 0.50 M in THF | Synthonix | 518990-00-6 | MFCD02260165 | 265.390 | C7H3BrFNZn | 0.000 | [Br-].Fc1ccc([Zn+])cc1C#N | 100ml | 532652691
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(CCCC)c1nccs1 | 1g | 525923779](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502696594.jpg-250.jpg)
eMolecules 121359-48-6 | 2-(Tributylstannyl)thiazole | Synthonix - Stock | MFCD01319057 | 374.170 | C15H29NSSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1nccs1 | 1g | 525923779
2-(Tributylstannyl)thiazole | Synthonix - Stock | 121359-48-6 | MFCD01319057 | 374.170 | C15H29NSSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1nccs1 | 1g | 525923779
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AdipoGen Loxistatin acid
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Chemical. CAS 76684-89-4. Formula C15H26N2O5. Molecular Weight 314.4. E-64c is a potent cell-impermeable epoxysuccinyl peptide inhibitor of calpain and other cysteine proteases, such as papain, cathepsin B, H and L. Does not inhibit the serine proteases trypsin, chymotrypsin or elastase. E-64c is an active metabolite of the protease inhibitor E-64d Prod. No. AG-CR1-3737, and a synthetic analog of E-64 Prod. No. AG-CP3-7006. Studies indicate that E-64c is a more potent inhibitor of cathepsins B and L compared to E-64. E-64c has in vitro antiviral, antiparasitic and immunomodulatory properties. It reduces the autocatalytic activity of the foot-and-mouth-disease virus FMDV leader protease, reduces infection of HEK293T cells by an HIV-based virus system pseudotyped with SARS-CoV spike glycoprotein in a concentration-dependent manner, inhibits human rotavirus replication, and exhibits entry-blocking effects against MERS-CoV.
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(CCCC)c1ccnc2ccccc12 | 5g | 525924408](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502696490.JPG-250.jpg)
eMolecules 1272412-64-2 | 4-(Tributylstannyl)quinoline | Synthonix - Stock | MFCD18325178 | 418.212 | C21H33NSn | 90.000 | CCCC[Sn](CCCC)(CCCC)c1ccnc2ccccc12 | 5g | 525924408
4-(Tributylstannyl)quinoline | Synthonix - Stock | 1272412-64-2 | MFCD18325178 | 418.212 | C21H33NSn | 90.000 | CCCC[Sn](CCCC)(CCCC)c1ccnc2ccccc12 | 5g | 525924408
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Medchemexpress LLC Benzocaine hydrochloride | 23239-88-5 | MFCD00012999 | 201.65 | C9H12ClNO2 | 500mg
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Benzocaine (hydrochloride) is an orally active local agent that can suppress or relieve pain that acts on voltage-gated Na channels at a common receptor with an IC50 value of 0 8 mM at 30 mV Additionally Benzocaine (hydrochloride) non-competitively inhibits Ca-ATPase binding with Ca2 with an IC50 of 47 1 mM Benzocaine (hydrochloride) can be used in research within the field of neuromuscular regulation[1][2][3]
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5000428526 BI-27 SUPPLEMENT 50 10ML
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Medchemexpress LLC Flecainide hydrochloride | 57415-44-8 | 99.93% | 450.80 | 1 ML
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Flecainide hydrochloride is an orally active antiarrhythmic agent that blocks sodium channels and inhibits calcium ion release mediated by the cardiac ryanodine receptor (RyR2). It can be used in the research of diseases such as catecholaminergic polymorphic ventricular tachycardia (CPVT).
- Significantly reduces irregular Ca2+ release in single cardiomyocytes derived from ATS-iPSCs.
- Completely inhibits catecholamine-induced ventricular arrhythmias in Casq2 knockout mice.
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5000379148 NEPICASTAT HYDROCHL 10MM 1ML
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5000586623 VONOPRAZAN HYDROCHL 100MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000586630 VONOPRAZAN HYDROCHL 10MM/1ML
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![eMolecules 352530-43-9 | 2,5-Dichlorophenylzinc iodide, 0.50 M in THF | Synthonix | MFCD02260175 | 338.270 | C6H3Cl2IZn | 0.000 | [I-].Clc1ccc(Cl)c([Zn+])c1 | 50ml | 532652756](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502696232.jpg-250.jpg)
eMolecules 352530-43-9 | 2,5-Dichlorophenylzinc iodide, 0.50 M in THF | Synthonix | MFCD02260175 | 338.270 | C6H3Cl2IZn | 0.000 | [I-].Clc1ccc(Cl)c([Zn+])c1 | 50ml | 532652756
2,5-Dichlorophenylzinc iodide, 0.50 M in THF | Synthonix | 352530-43-9 | MFCD02260175 | 338.270 | C6H3Cl2IZn | 0.000 | [I-].Clc1ccc(Cl)c([Zn+])c1 | 50ml | 532652756
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5000383504 ETHACIZINE HYDROCHL 25MG
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![eMolecules 1029128-52-6 | 4-Fluorophenethylzinc bromide, 0.50 M in THF | Synthonix268.430 | C8H8BrFZn | 0.000 | [Br-].Fc1ccc(CC[Zn+])cc1 | 50ml | 532652845](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502696146.jpg-250.jpg)
eMolecules 1029128-52-6 | 4-Fluorophenethylzinc bromide, 0.50 M in THF | Synthonix268.430 | C8H8BrFZn | 0.000 | [Br-].Fc1ccc(CC[Zn+])cc1 | 50ml | 532652845
4-Fluorophenethylzinc bromide, 0.50 M in THF | Synthonix | 1029128-52-6268.430 | C8H8BrFZn | 0.000 | [Br-].Fc1ccc(CC[Zn+])cc1 | 50ml | 532652845
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Medchemexpress LLC Fomepizole (hydrochloride) | 56010-88-9 | 99.9% | 25 MG
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Fomepizole hydrochloride (4-Methylpyrazole hydrochloride) is a potent and orally active cytochrome P450 (CYP2E1) inhibitor. It acts as a competitive inhibitor of the enzyme alcohol dehydrogenase, preventing the conversion of methanol and ethylene glycol into toxic metabolites. It is considered a potential antidote for ethylene glycol or methanol poisoning.
- Potent and orally active cytochrome P450 (CYP2E1) inhibitor.
- Competitive inhibitor of alcohol dehydrogenase.
- Blocks conversion of methanol and ethylene glycol to toxic metabolites.
- Potential antidote for ethylene glycol or methanol poisoning.
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