14 Results for "

IMP dehydrogenase

" in MedChemExpress (MCE) Product Catalog:
Products (14)

14 Results for "IMP dehydrogenase" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-114570
CAS No.: 60084-10-8
Purity:  99.84%
Synonyms: NSC 286193; Riboxamide
Tiazofurin (NSC 286193) is a synthetic nucleoside analogue with antineoplastic activity. Tiazofurin is anabolized intracellularly to tiazole-4-carboxamide adenine dinucleotide (TAD), a potent inhibitor of IMP dehydrogenase (IMPDH). Tiazofurin enhances the autosecretion of IL-6 in K562 cells. Tiazofurin also has anti-orthopoxvirus and anti-variola activities. Tiazofurin can be used for the study of leukemia and lung cancer .
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Cat. No.: HY-129972
CAS No.: 66983-94-6
Synonyms: RMP dilithium
Ribavirin 5'-monophosphate dilithium is an active form of ribavirin that inhibits IMP dehydrogenase, and ribavirin itself is a broad-spectrum antiviral agent .
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Cat. No.: HY-136498A
CAS No.: 2096342-42-4
Purity:  95.34%
Target:  

Drug Metabolite

Research Areas:  

Infection

T-705RMP (ammonium) is the ammonium form of T-705RMP. T-705RMP (ammonium)’s the inhibition of IMP dehydrogenase (IMPDH) activity is weak .
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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-P10563
CAS No.: 2580150-96-3
Synonyms: BHV-1100
Target:  

CD38 IFNAR

Research Areas:  

Cancer

Noraramtide (BHV-1100) is an antibody-recruiting molecule. Noraramtide binds to CD38 and recruits natural killer (NK) cells to mediate antibody-dependent cellular cytotoxicity. Noraramtide enhances the capacity of autologous cytokine-induced memory-like (CIML) NK cells to produce IFNγ and CD107a, thereby improving their cytotoxicity against multiple myeloma cells. Noraramtide can be used in the research of multiple myeloma .
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Cat. No.: HY-164434
CAS No.: 523-98-8
Synonyms: 5'-Xanthylic acid
Target:  

Endogenous Metabolite

Research Areas:  

Others

Xanthosine-5'-monophosphate can be obtained by catalyzing inosine 5'-monophosphate (IMP) with inosine 5'-monophosphate dehydrogenase (IMPDH) .
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Cat. No.: HY-10250
CAS No.: 61966-08-3
Synonyms: TCN-P
Target:  

ATP Synthase

Research Areas:  

Metabolic Disease Cancer

Triciribine phosphate (TCN-P) inhibits amidophosphoribosyltransferase by an allosteric mechanism which affects the first committed step of de novo purine biosynthesis. Triciribine phosphate also inhibits  IMP dehydrogenase which is the first committed step of guanosine nucleotide synthesis. Tricilibine phosphate does not affect ligase activity .
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Cat. No.: HY-136498
CAS No.: 356783-08-9
Target:  

Drug Metabolite

Research Areas:  

Infection

T-705RMP, a phosphorylated metabolite of T-705, exhibits a very weak inhibitory effect on the IMP dehydrogenase (IMPDH) activities of the host cells, with an IC50 of 601 μM .
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Cat. No.: HY-P3820
[Dehydro-Pro4] Substance P (4-11) is a peptide fragment of Substance P. Substance P is a peptide mainly secreted by neurons. Substance P takes part in many biological processes, including nociception, inflammation and immunity .
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Cat. No.: HY-10250A
Purity:  99.82%
Synonyms: TCN-P sodium
Target:  

ATP Synthase

Research Areas:  

Metabolic Disease Cancer

Triciribine phosphate sodium inhibits amidophosphoribosyltransferase by an allosteric mechanism which affects the first committed step of de novo purine biosynthesis. Triciribine phosphate sodium also inhibits IMP dehydrogenase which is the first committed step of guanosine nucleotide synthesis. Tricilibine phosphate does not affect ligase activity .
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Cat. No.: HY-118061
CAS No.: 1278553-16-4
Target:  

Bacterial

Research Areas:  

Infection

VCC234718 is a molecule with mycobacterial growth inhibitory activity, specifically targeting Mycobacterium tuberculosis (Mtb). The primary molecular target of VCC234718 is inosine monophosphate dehydrogenase (GuaB2), and it inhibits the growth of Mtb by affecting the function of this enzyme. VCC234718 inhibits GuaB2 with a K value of 100 nM and exhibits non-competitive inhibition with IMP and NAD+. VCC234718 exerts its inhibitory effect by directly interacting with IMP and binding at the NAD+ site .
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Cat. No.: HY-P702799
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: IMPDH2; IMPD2; Inosine Monophosphate dehydrogenase 2; IMP (Inosine Monophosphate) dehydrogenase 2; IMP (Inosine 5'-Monophosphate) dehydrogenase 2; Epididymis Secretory Sperm Binding Protein; Inosine-5'-Monophosphate dehydrogenase Type II; Inosine-5'-Monop
Species:  
Source:  
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Cat. No.: HY-P703151
Purity:  ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: IMPDH1; IMPD 1; Prev. RP10; IMPD; SWSS2608; Retinitis Pigmentosa 10 (Autosomal Dominant); LCA11; IMP (Inosine Monophosphate) dehydrogenase 1; IMP (Inosine 5'-Monophosphate) dehydrogenase 1; Inosine-5'-Monophosphate dehydrogenase; Inosine-5'-Monophosphate
Species:  
Source:  
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Cat. No.: HY-E70516
CAS No.: 9028-93-7
Target:  

Others

Research Areas:  

Others

Inosine-5'-monophosphate dehydrogenase, Microorganism (EC 1.1.1.205) catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate-limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth .
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