36 Results for "

inosine monophosphate

" in MedChemExpress (MCE) Product Catalog:
Products (36)

36 Results for "inosine monophosphate" in MCE Product Catalog:

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17
17 Publications Verification
Cat. No.: HY-B0421
CAS No.: 24280-93-1
Synonyms: Mycophenolate
Mycophenolic acid is a potent uncompetitive inosine monophosphate dehydrogenase (IMPDH) inhibitor with an EC50 of 0.24 µM. Mycophenolic acid demonstrates antiviral effects against a wide range of RNA viruses including influenza. Mycophenolic acid is an immunosuppressive agent. Antiangiogenic and antitumor effects .
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17
17 Publications Verification
Cat. No.: HY-B0421A
CAS No.: 37415-62-6
Synonyms: Mycophenolate sodium
Mycophenolic acid sodium is a potent uncompetitive inosine monophosphate dehydrogenase (IMPDH) inhibitor with an EC50 of 0.24 µM. Mycophenolic acid sodium demonstrates antiviral effects against a wide range of RNA viruses including influenza. Mycophenolic acid sodium is an immunosuppressive agent. Antiangiogenic and antitumor effects .
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14
14 Cited Publications
Cat. No.: HY-B0199
CAS No.: 128794-94-5
Synonyms: RS 61443; TM-MMF
Mycophenolate mofetil (RS 61443) is the morpholinoethylester proagent of Mycophenolic acid. Mycophenolate mofetil inhibits de novo purine synthesis via the inhibition of inosine monophosphate dehydrogenase (IMPDH). Mycophenolate mofetil shows selective lymphocyte antiproliferative effects involve both T and B cells, preventing antibody formation .
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6
6 Cited Publications
Cat. No.: HY-13560
CAS No.: 297730-17-7
Purity:  99.89%
Synonyms: VX-944
AVN-944 (VX-944) is an orally active, potent, selective, noncompetitive and specific inhibitor of IMPDH (inosine monophosphate dehydrogenase). AVN-944 is an essential rate-limiting enzyme in de novo guanine nucleotide synthesis. AVN-944 is also an inhibitor of arenavirus RNA synthesis, and blocks arenavirus infection. AVN-944 has broad anti-cancer activities, and can be used for multiple myeloma (MM) and acute myeloid leukemia (AML) research .
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2
2 Cited Publications
Cat. No.: HY-13986
CAS No.: 198821-22-6
Purity:  99.27%
Synonyms: VX-497; MMPD
Research Areas:  

Infection Cancer

Merimepodib (VX-497) is a noncompetitive and oral inhibitor of inosine monophosphate dehydrogenase (IMPDH) with broad spectrum antiviral activities.
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2
2 Cited Publications
Cat. No.: HY-B0421S
CAS No.: 1185242-90-3
Synonyms: Mycophenolate-d3
Mycophenolic acid-d3 (Mycophenolate-d3) is deuterium labeled Mycophenolic acid (HY-B0421). Mycophenolic acid is a potent uncompetitive inosine monophosphate dehydrogenase (IMPDH) inhibitor with an EC50 of 0.24 μM. Mycophenolic acid demonstrates antiviral effects against a wide range of RNA viruses including influenza. Mycophenolic acid is an immunosuppressive agent. Antiangiogenic and antitumor effects.
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2
2 Cited Publications
Cat. No.: HY-W010759
CAS No.: 20813-76-7
Inosine-5'-monophosphate disodium salt octahydrate is a purine nucleotide that can be used as an umami tastant as well as a precursor of GMP and AMP .
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1
1 Cited Publications
Cat. No.: HY-150252A
CAS No.: 3067165-96-9
Purity:  99.96%
Research Areas:  

Cancer

ATIC-IN-1 (compound 14) acetate is an inhibitor targeting to Aminoimidazole carboxamide ribonucleotide transformylase/inosine monophosphate cyclohydrolase (ATIC) dimerization with a Ki value of 685 nM, whcich catalyzes de novo purine biosynthesis. ATIC dimerization is crucial for its aminoimidazole carboxamide ribonucleotide (AICAR) transformylase activity. ATIC-IN-1 acetate exhibits anti-tumor activity via reduction in cell numbers and cell division rates .
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Cat. No.: HY-13986A
CAS No.: 2748420-50-8
Purity:  96.93%
Synonyms: (R)-VX-497; (R)-MMPD
Target:  

IMPDH

Research Areas:  

Infection

(R)-Merimepodib is the isomer of Merimepodib (HY-13986), and can be used as an experimental control. Merimepodib (VX-497) is a noncompetitive and oral inhibitor of inosine monophosphate dehydrogenase (IMPDH) with broad spectrum antiviral activities.
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Cat. No.: HY-145286
CAS No.: 1434517-02-8
Purity:  99.73%
Target:  

Bacterial IMPDH

Research Areas:  

Infection

IMPDH2-IN-2 is an inhibitor of Mycobacterium tuberculosis inosine 5′-monophosphate dehydrogenase 2 (MtbIMPDH2) with a Ki,app value of 14 nM. IMPDH2-IN-2 blocks guanine nucleotide biosynthesis and exhibits antibacterial activity against Mycobacterium tuberculosis. IMPDH2-IN-2 can be used for research on tuberculosis .
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Cat. No.: HY-W700392
CAS No.: 31858-65-8
Target:  

IMPDH

Research Areas:  

Cancer

IMPDH-IN-2 (compound 2) is an inhibitor of inosine monophosphate dehydrogenase (IMPDH) with IC50Values are 0.15 and 0.17 μM, respectively. IMPDH-IN-2 has antitumor activity .
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Cat. No.: HY-10545A
CAS No.: 40372-00-7
Purity:  99.89%
Target:  

HBV HCV

Research Areas:  

Infection

Taribavirin hydrochloride is an orally active inosine monophosphate dehydrogenase inhibitor, has activity against a wide range of viruses, especially the hepatitis C virus and influenza virus. Taribavirin hydrochloride is a Ribavirin proagent, is designed to concentrate within the liver to target HCV-infected hepatocytes while minimizing distribution within red blood cells (RBCs) and the development of hemolytic anemia .
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Cat. No.: HY-117124
CAS No.: 267645-83-0
Target:  

IMPDH

Research Areas:  

Others

BMS-337197 is an inosine monophosphate dehydrogenase (IMPDH) inhibitor .
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Cat. No.: HY-B0421R
CAS No.: 24280-93-1
Synonyms: Mycophenolate (Standard)
Mycophenolic acid (Standard) is the analytical standard of Mycophenolic acid. This product is intended for research and analytical applications. Mycophenolic acid is a potent uncompetitive inosine monophosphate dehydrogenase (IMPDH) inhibitor with an EC50 of 0.24 μM.?Mycophenolic acid demonstrates antiviral effects against a wide range of RNA viruses including influenza. Mycophenolic acid is an immunosuppressive agent. Antiangiogenic and antitumor effects .
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Cat. No.: HY-161712
CAS No.: 2427862-70-0
Target:  

IMPDH

Research Areas:  

Cancer

IMPDH-IN-4 is a derivative of N-pyridinylthiophene carboxamid that exhibits activity against peripheral nerve sheath carcinoma cells. IMPDH-IN-4 is metabolized by NAMPT and NMNAT1 to an adenine dinucleotide (AD) derivative, which is an NAD analog and can inhibit inosine monophosphate dehydrogenase (IMPDH), leading to the accumulation of inosine monophosphate (IMP) in cells. IMPDH-IN-4 has good blood-brain barrier permeability and can be used in the study of central and peripheral nervous system cancers .
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Cat. No.: HY-168509
CAS No.: 3094970-14-3
Target:  

Bacterial

Research Areas:  

Infection

IMPDH-IN-1 (compound 44) is a bacterial inosine 5'-monophosphate dehydrogenase (IMPDH) inhibitor. IMPDH-IN-1 specifically binds to the catalytic domain of IMPDH. IMPDH-IN-1 potently inhibits the IMPDH of Pseudomonas aeruginosa, Staphylococcus aureus and Escherichia coli .
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Cat. No.: HY-29244
CAS No.: 67095-44-7
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

ATIC-IN-2 (Compound 1) is a competitive inhibitor for the bifunctional enzyme AICAR Tfase/IMPCH (ATIC), that binds to inosine monophosphate cyclohydrolase (IMPCH) with a Ki of 0.13 μM .
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Cat. No.: HY-134375
CAS No.: 1507367-51-2
Synonyms: Cyclic Adenosine-inosine monophosphate
Target:  

NF-κB IFNAR

Research Areas:  

Inflammation/Immunology

cAIMP (Cyclic Adenosine-Inosine Monophosphate) is an effective synthetic cyclic dinucleotide. cAIMP activates IRF and NF-κB in the THP1 human monocyte reporter cell line (THP1-Dual). cAIMP induces the secretion of IFNs and pro-inflammatory cytokines in vitro in human blood, with an EC50 of 6.4 μmol/L .
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Cat. No.: HY-10545
CAS No.: 119567-79-2
Target:  

HBV HCV

Research Areas:  

Infection

Taribavirin is an orally active inosine monophosphate dehydrogenase inhibitor, has activity against a wide range of viruses, especially the hepatitis C virus and influenza virus. Taribavirin, is a ribavirin proagent, is designed to concentrate within the liver to target HCV-infected hepatocytes while minimizing distribution within red blood cells (RBCs) and the development of hemolytic anemia .
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Cat. No.: HY-150252
CAS No.: 1402453-15-9
Target:  

Others

Research Areas:  

Cancer

ATIC-IN-1(compound 14) is an inhibitor targeting to Aminoimidazole carboxamide ribonucleotide transformylase/inosine monophosphate cyclohydrolase (ATIC) dimerization with a Ki value of 685 nM. ATIC dimerization is crucial for its aminoimidazole carboxamide ribonucleotide (AICAR) transformylase activity. ATIC-IN-1 exhibits anti-tumor activity via reduction in cell numbers and cell division rates .
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