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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T37591 | IMP-1710 | DUB | |
IMP-1710 is a selective UCH-L1 inhibitor with an IC50 value of 38 nM in a fluorescence polarization assay. | |||
T9350 | IMP-1088 | Others , DNA/RNA Synthesis | |
IMP-1088 is a potent inhibitor of human N-myristoyltransferases NMT1 and NMT2 dual. | |||
T73362 | C-di-IMP | Cyclic-di-IMP | |
Cyclic-di-IMP (C-di-IMP), a STING agonist, serves as a research tool in tumor studies. | |||
T37729 | IMP-1700 | ||
IMP-1700 is an inhibitor of bacterial DNA repair.1It potentiates the activity of the quinolone antibiotic ciprofloxacin against methicillin-resistantS. aureus(MRSA) with a combination index value of 0.7. IMP-1700 inhibit... | |||
T82760 | C-di-IMP disodium | Cyclic-di-IMP disodium | STING |
C-di-IMP disodium, a STING agonist, is utilized in tumor research [1]. | |||
T68322 | IMP-321 | ||
IMP-321 is a soluble dimeric recombinant form of LAG-3 and first-in-class antigen presenting cell activator. | |||
T4685 | INOSINIC ACID | Inosine 5′-monophosphate,IMP,I-5'-P | Endogenous Metabolite |
Inosinic acid (IMP) is a purine nucleotide which has hypoxanthine as the base and one phosphate group esterified to the sugar moiety. Inosinic acid is a nucleotide present in muscle and other tissues. It is formed by the... | |||
TMS1830 | Disodium 5'-inosinate | Disodium Inosinate,Sodium Inosinate,5'-IMP disodium salt | Others |
Disodium 5'-inosinate (5'-IMP disodium salt) is a flavor agent. | |||
T36984 | Cyclic di-IMP (sodium salt) | ||
Cyclic di-IMP (sodium salt) (c-di-IMP) is a synthetic second messenger structurally related to the bacterial second messengers cyclic di-GMP and cyclic di-AMP . C-di-IMP has adjuvant properties when co-administered with ... | |||
T5073 | Inosine 5'-monophosphate disodium salt hydrate | Inosine 5'-monophosphate disodium salt,5'-IMP-Na2,Disodium 5'-inosinate monohydrate | Others , Endogenous Metabolite |
Inosine 5'-monophosphate disodium salt hydrate (Inosine 5'-monophosphate disodium salt), or inosinic acid, is the ribonucleotide of hypoxanthine and the first nucleotide formed during purine synthesis. | |||
T9593 | Senaparib | IMP4297 | PARP |
Senaparib (IMP4297) is a novel highly potent and selective oral PARP1/2 inhibitor with strong antitumor activity. | |||
T78247 | Ieramilimab | IMP701,LAG525 | |
Ieramilimab (LAG525; IMP701) is a humanized IgG4 monoclonal antibody that targets LAG-3, disrupting its interaction with MHC-II molecules [1]. | |||
T78332 | Eftilagimod alfa | IMP321,LAG-3Ig | |
Eftilagimod alfa (IMP321), a recombinant LAG-3Ig fusion protein, binds to MHC class II and mediates the activation of antigen-presenting cells (APCs), which in turn activates CD8 T-cells. It is utilized in the research o... | |||
T70760 | NVP018 | ||
NVP018, also known as BC 556, is a potent inhibitor of hepatitis B virus, hepatitis C virus (HCV), and HIV-1 replication, shows minimal inhibition of major drug transporters, and has a high barrier to generation of both... | |||
T16028 | IMB-XH1 | Mcl1-IN-2 | BCL , Antibacterial |
IMB-XH1 (Mcl1-IN-2) is a myeloid cell factor 1 (Mcl-1) inhibitor. | |||
T9042 | Teriflunomide impurity 3 | 4-Amino-N-(4-trifluoromethylphenyl)benzamide | COX |
Teriflunomide impurity 3 (4-Amino-N-(4-trifluoromethylphenyl)benzamide) is a selective COX-1 inhibitor(IC50 of 30 μM). It is less active against COX-2 (IC50>100 μM). | |||
T1689 | Enalapril IMpurity B | (+)-N-[1-(S)-Ethoxycarbonxyl-3-phenylpropyl]-L-alanine | Others |
Enalapril IMpurity B ((+)-N-[1-(S)-Ethoxycarbonxyl-3-phenylpropyl]-L-alanine) is Moexipril intermediate and is the main metabolite of Imidapril. | |||
T61326 | AIMP2-DX2-IN-1 | Others | |
AIMP2-DX2-IN-1 is a potent AIMP2-DX2 inhibitor with potential antitumor activity for the study of lymphoma. | |||
T1698 | Carvedilol EP IMpurity E | Carvedilol USP E,Carvedilol Impurity E | Others |
Carvedilol EP IMpurity E (Carvedilol USP E) is used as a pharmaceutical intermediate. | |||
T12962 | Sofosbuvir impurity G | HCV Protease | |
Sofosbuvir impurity G is a diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity. |