116 Results for "

IMP

" in MedChemExpress (MCE) Product Catalog:
Products (116)

116 Results for "IMP" in MCE Product Catalog:

50
50 Publications Verification
Cat. No.: HY-15310
CAS No.: 70288-86-7
Purity:  98.28%
Synonyms: MK-933; CD-5024; K-237
Ivermectin (MK-933) is a broad-spectrum anti-parasite agent. Ivermectin (MK-933) is a specific inhibitor of Impα/β1-mediated nuclear import and has potent antiviral activity towards both HIV-1 and dengue virus. It is a positive allosteric effector of P2X4 and the α7 neuronal nicotinic acetylcholine receptor (nAChRs). Ivermectin also inhibits bovine herpesvirus1 (BoHV-1) replication and inhibits BoHV-1 DNA polymerase nuclear import . Ivermectin is a candidate therapeutic against SARS-CoV-2/COVID-19 .
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9
9 Cited Publications
Cat. No.: HY-112258
CAS No.: 2059148-82-0
Purity:  99.16%
Target:  

DNA/RNA Synthesis

Research Areas:  

Infection

IMP-1088 is a potent human N-myristoyltransferases NMT1 and NMT2 dual inhibitor with IC50s of <1 nM for HsNMT1 and HsNMT2. IMP-1088 has a Kd of <210 pM for HsNMT1. IMP-1088 efficiently blocks rhinovirus replication by blocking rhinovirus virus-encoded protein (VP0) N-myristoylation. IMP-1088 protects host cells from the cytotoxic effects of viral infection .
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4
4 Cited Publications
Cat. No.: HY-108213
CAS No.: 131-99-7
Purity:  99.81%
Synonyms: 5'-IMP; IMP; Inosine 5'-dihydrogen phosphate
Inosinic acid is an endogenous metabolite. Inosinic acid is used as umami tastant, or as the dietary supplement to improve the yield and meat quality of pigs .
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4
4 Cited Publications
Cat. No.: HY-108213A
CAS No.: 352195-40-5
Purity:  99.57%
Synonyms: 5'-IMP disodiumhydrate(1:2:X); IMP disodiumhydrate(1:2:X); Inosine 5'-dihydrogen phosphate disodiumhydrate(1:2:X)
Inosinic acid (disodium)(hydrate)(1:2:X) (5'-IMP (disodium)(hydrate)(1:2:X)) is an endogenous metabolite. Inosinic acid (disodium)(hydrate)(1:2:X) is used as umami tastant, or as the dietary supplement to improve the yield and meat quality of pigs .
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1
1 Cited Publications
Cat. No.: HY-103056
CAS No.: 1215010-55-1
Purity:  99.72%
Synonyms: IMP-366
Research Areas:  

Infection

DDD85646 (IMP-366) is an orally active of trypanosoma brucei N-myristoyltransferase (TbNMT IC50=2 nM; hNMT IC50=4 nM). The enzyme N-myristoyltransferase (NMT) is a potential agent target for human African trypanosomiasis .
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1
1 Cited Publications
Cat. No.: HY-16933
CAS No.: 5854-93-3
Synonyms: NSC-153353; SDX-102
Research Areas:  

Infection Cancer

L-Alanosine (NSC-153353), an antibiotic from Streptomyces alanosinicus, has antineoplastic activity. L-Alanosine (NSC-153353) inhibits adenylosuccinate synthetase, which converts inosine monophospate (IMP) into adenylosuccinate. L-Alanosine is the inhibitor for methylthioadenosine phosphorylase (MTAP) .
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1
1 Cited Publications
Cat. No.: HY-D0887
CAS No.: 4691-65-0
Synonyms: IMP disodium salt; Disodium inosinate
Disodium 5'-inosinate (IMP disodium salt) is a nucleotide-based umami agent. Disodium 5'-inosinate can bind to umami receptors and stimulate taste nerves, allowing the brain to perceive umami. In addition, Disodium 5'-inosinate produces a transient behavioral excitement in mice .
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1
1 Cited Publications
Cat. No.: HY-138995
CAS No.: 2383117-96-0
Purity:  98.01%
Target:  

Deubiquitinase

Research Areas:  

Others

IMP-1710 is a potent and selective deubiquitylating enzyme UCHL1 inhibitor with an IC50 value of 38 nM. IMP-1710 has antifibrotic activity. IMP-1710 is a UCHL1 probe to identify and quantify target proteins in intact human cells . IMP-1710 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. IMP-1710 can be used in the research of idiopathic pulmonary fibrosis .
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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-137450
CAS No.: 1401682-78-7
Purity:  99.53%
Synonyms: IMP4297; JS109
Target:  

PARP

Research Areas:  

Cancer

Senaparib (IMP4297) is a highly potent, selective and orally active PARP1/2 inhibitor. Senaparib (IMP4297) exhibits strong antitumor activity in animal models .
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Cat. No.: HY-164285
CAS No.: 2445448-66-6
Synonyms: IMP1320
Research Areas:  

Cancer

MYX1715 is an inhibitor of N-Myristoyltransferase (NMT) with a KD value of 0.09 nM. MYX1715 inhibits the proliferation of LU0884 and LU2511 with IC50 values of 44 nM and 9 nM. MYX1715 exhibits antitumor efficacy against neuroblastoma and gastric cancer in mouse models. MYX1715 can be used as ADC toxin .
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Cat. No.: HY-148493
CAS No.: 2058151-78-1
Purity:  99.96%
Target:  

Bacterial

Research Areas:  

Infection

MK-3402 (Compound303) is a metallo-beta-lactamase inhibitor, with IC50 values of 0.53, 0.25 and 0.169 nM against IMP-1, NDM-1, and VIM-1, respectively. MK-3402 can be used in bacterial research and shows a synergistic effect when used in combination with beta-lactam antibiotics .
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Cat. No.: HY-135396
CAS No.: 1132709-14-8
Purity:  ≥96.0%
Target:  

Drug Isomer

Research Areas:  

Others

(1S,2S)-Bortezomib (Compound Imp-D (1S,2S)) is a diastereomeric impurity of Bortezomib (HY-10227) .
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Cat. No.: HY-146178
CAS No.: 1480482-51-6
Purity:  99.08%
Target:  

Insulin Receptor

Research Areas:  

Cancer

IMP2-IN-1 (compound 4) is a potent IMP2 inhibitor with IC50 value of 81.3~127.5 for IMP2 RNA sequence. IMP2-IN-1 reduces IMP2 in SW480 cells. IMP2-IN-1 significantly reduces the viability of both differentiated and non-differentiated Huh7 cells .
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Cat. No.: HY-133157
CAS No.: 13018-54-7
Purity:  85.00%
Synonyms: 5-Formamidoimidazole-4-carboxamide ribotide
Category:  

Natural Products

Target:  

DNA/RNA Synthesis

FAICAR (5-Formamidoimidazole-4-carboxamide ribotide) is a purine nucleotide and the IMP cyclohydrolase substrate of Cryptococcus neoformans ATIC. It is a key intermediate in the de novo purine synthesis pathway. FAICAR can be used in studies related to Cryptococcus neoformans infection .
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Cat. No.: HY-108213R
CAS No.: 131-99-7
Synonyms: 5'-IMP (Standard); IMP (Standard); Inosine 5'-dihydrogen phosphate (Standard)
Inosinic acid (Standard) is the analytical standard of Inosinic acid. This product is intended for research and analytical applications. Inosinic acid is an endogenous metabolite. Inosinic acid is an endogenous metabolite. Inosinic acid is used as umami tastant, or as the dietary supplement to improve the yield and meat quality of pigs .
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Cat. No.: HY-D2188
IMP-2373 is a low-toxicity activity-based probe targeting covalent pan-deubiquitinase (DUB), which modulates and monitors DUB activity via covalent binding to the catalytic cysteine and active site of DUB. IMP-2373 enables real-time tracking of dynamic intracellular DUB activity in physiologically relevant living cell systems, and quantitative analysis of activity changes induced by pharmacological inhibition or MYC dysregulation. IMP-2373 can be used for research on related diseases such as B-cell lymphoma .
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Cat. No.: HY-P991301

Target:  

LAG-3

Research Areas:  

Cancer

IMP-761 is a human IgG4 monoclonal antibody (mAb) targeting CD223/LAG3. IMP-761 binds to D1 of human LAG32. Recommend Isotype Controls: Human IgG4 kappa, Isotype Control (HY-P99003) .
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Cat. No.: HY-146179
CAS No.: 1448353-39-6
Purity:  99.93%
Target:  

Insulin Receptor

Research Areas:  

Cancer

IMP2-IN-2 (compound 6) is a potent and selective IMP2 inhibitor, with IC50s of 120.9 μM and 236.7 μM for IMP2 interaction with RNA_A and RNA_B, respectively. IMP2-IN-2 can be used for the research of 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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