16 Results for "

Tetrazole

" in MedChemExpress (MCE) Product Catalog:
Products (16)

16 Results for "Tetrazole" in MCE Product Catalog:

Cat. No.: HY-W054424
CAS No.: 1638767-25-5
Target:  

Drug Intermediate

Research Areas:  

Others

tert-Butyl (3-aminobicyclo[1.1.1]pentan-1-yl) carbamate is a pharmaceutical intermediate used in the synthesis of various active compounds, such as for the preparation of tetrazole-based eIF2B activators .
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Cat. No.: HY-W004131
CAS No.: 4916-55-6
Target:  

Drug Intermediate

Research Areas:  

Others

3-Bromomethylpyridine hydrobromide is an intermediate that can be used for the preparation of 1,5-disubstituted tetrazole-based P2X7 antagonists .
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Cat. No.: HY-23269
CAS No.: 3441-00-7
Target:  

Drug Intermediate

Research Areas:  

Others

5-(M-Tolyl)tetrazole is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-W010517S
CAS No.: 345909-96-8
1-Methyl-5-mercapto-1,2,3,4-tetrazole-d3 is the deuterium labeled 1-Methyl-1H-tetrazole-5-thiol .
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Cat. No.: HY-143335
CAS No.: 2901064-06-8
Target:  

Fungal

Research Areas:  

Infection

Antifungal agent 52 (compound 6c) is a tetrazole derivative. Antifungal agent 52 inhibits the synthesis of Ergosterol (HY-N0181). Antifungal agent 52 exhibit a significant antifungal activity against Candida albicans. Antifungal agent 52 affects C. albicans sessile cell membrane permeabilization .
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Cat. No.: HY-153934
CAS No.: 873874-16-9
Target:  

GHR

Research Areas:  

Endocrinology

Tetrazole-C15-(N-acetylsulfamoyl)butanoic acid (Ligand 1) improves the pharmacokinetic properties of therapeutic peptides and proteins through non-covalent binding with human serum albumin (HSA). Tetrazole-C15-(N-acetylsulfamoyl)butanoic acid can be used for synthesis of long-acting human growth hormone (HGH) analog somapacitan .
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Cat. No.: HY-134953
CAS No.: 916923-10-9
Target:  

Potassium Channel

Research Areas:  

Cancer

Mephetyl tetrazole is a potassium channel Kv1.5 blocker, with an IC50 of 330 nM. Mephetyl tetrazole can be used for the research of cancer .
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Cat. No.: HY-174353
Target:  

Cytochrome P450 Fungal

Research Areas:  

Infection

CYP51-IN-22, the non-deuterated analog of CYP51-IN-23-d3 (HY-174353S), is a potent and broad-spectrum CYP51 inhibitor.CYP51-IN-22 inhibits Aspergillus fumigatum with a MIC80 of 1 μg/mL. CYP51-IN-22 can prevent fungal phase transformation and biofilm formation. CYP51-IN-22 exhibits anti-drug resistance activity and fungal activity, and shows excellent safety for cells and significant pharmacological activity in mice. CYP51-IN-22 can be used for the study of invasive fungal infections (IFIs) .
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Cat. No.: HY-174353S
CYP51-IN-23-d3 is a potent and broad-spectrum CYP51 inhibitor with a MIC80 of 1 μg/mL against Aspergillus fumigatum. CYP51-IN-23-d3 can prevent fungal phase transformation and biofilm formation. CYP51-IN-23-d3 exhibits anti-drug resistance activity and fungal activity, and shows excellent safety for cells and significant pharmacological activity in mice. CYP51-IN-23-d3 can be used for the study of invasive fungal infections (IFIs) .
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Cat. No.: HY-117742
CAS No.: 380382-38-7
Target:  

Bacterial

Research Areas:  

Infection

DA-7867 is an antibacterial compound with activity against a wide range of bacteria, including drug-resistant bacteria. DA-7867 shows promising antibacterial activity against some clinically important pathogens, including drug-resistant bacteria. It is an amide analog of Tedizolid (HY-14855), reflecting the potential use of tetrazoles in the development of new antibacterial agents .
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Cat. No.: HY-155152
CAS No.: 3052839-42-3
Target:  

P-glycoprotein BCRP

Research Areas:  

Cancer

P-gp/BCRP-IN-2 (compound 15) is an oxadiazole derivative and a dual inhibitor of the ABC transporter P-glycoprotein (IC50: 1.6 nM) and BCRP (IC50: 600 nM). P-gp/BCRP-IN-2 also enhances the anti-proliferative effects of Doxorubicin (HY-15142A) in drug-resistant human adenocarcinoma colon cancer cell lines HT29/DX and MDCK-MDR1 cells .
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Cat. No.: HY-149376
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

Tubulin inhibitor 38 (compound 14) is a tetrazole-based Tubulin inhibitor with antiproliferative potencies. Tubulin inhibitor 38 (100 nM,24 h) mediates mitotic arrest,blocks cell cycle at G2/M phase and induces apoptosis. Tubulin inhibitor 38 exhibits high cytotoxicity with high selectivity index among HeLa,MCF7,and U87 MG cells .
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Cat. No.: HY-W010517R
CAS No.: 13183-79-4
Target:  

Reference Standards

1-Methyl-1H-tetrazole-5-thiol (Standard) is the analytical standard of 1-Methyl-1H-tetrazole-5-thiol. This product is intended for research and analytical applications.
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Cat. No.: HY-W743814
2-(5-Mercaptotetrazole-1-yl)ethanol-d4 is the deuterium labeled 1-(2-Hydroxyethyl)-1H-tetrazole-5(2H)-thione (HY-W105679).
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Cat. No.: HY-124255R
CAS No.: 120568-11-8
Synonyms: Losartan impurity 4 (Standard)
Target:  

Reference Standards

Losartan impurity E (Standard) is the analytical standard of Losartan impurity E. This product is intended for research and analytical applications.
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Cat. No.: HY-182024
Target:  

SARS-CoV Virus Protease

Research Areas:  

Infection

SARS-CoV-2 3CLpro-IN-36 is a SARS-CoV-2 3CLpro inhibitor and antiviral agent with a human sub-micromolar IC50 against SARS-CoV-2 3CLpro.SARS-CoV-2 3CLpro-IN-36 forms a covalent bond with catalytic Cys145 of SARS-CoV-2 3CLpro; its tetrazole core occupies the S1 pocket and interacts with His163, while its chloroacetamide carbonyl forms hydrogen bonds with the backbone amides of Gly143 and Ser144 in the oxyanion hole.SARS-CoV-2 3CLpro-IN-36 reduces SARS-CoV-2 replication in infected cells.SARS-CoV-2 3CLpro-IN-36 can be used for the research of SARS-CoV-2 infection .
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