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Catalog | name | Description | price |
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R-R-4760 | ddTTP trisodium | ddTTP trisodium is one of 2,3-dideoxyribonucleoside 5-triphosphates (ddNTPs) that acts as chain-elongating inhibitor of DNA polymerase for DNA sequencing. | price> |
R-C-3091 | TAK-593 CAS:1005780-62-0 | TAK-593 is an oral formulation containing a small-molecule receptor tyrosine kinase inhibitor of both vascular endothelial growth factor receptor (VEGFR) and platelet-derived growth factor receptor (PDGFR) with potential antineoplastic activity.Only for scientific research, not for human body. | price> |
R-R-4761 | WRN inhibitor 1 CAS No.2923008-44-8 | WRN inhibitor 1 (example 7)/CAS No.2923008-44-8 is a Wemer Syndrome ATP dependent helicase enzyme (WRN) inhibitor that inhibits WRN helicase domain activity. WRN inhibitor 1 has the potential to study cancer. | price> |
R-C-3092 | SU5402 CAS:215543-92-3 | SU5402 is a potent multi-targeted receptor tyrosine kinase inhibitor with IC50 of 20 nM, 30 nM, and 510 nM for VEGFR2, FGFR1, and PDGF-Rβ, respectively.Only for scientific research, not for human body. | price> |
R-R-4762 | Remdesivir-d5 | Remdesivir-d5 is a deuterium labeled Remdesivir. Remdesivir (GS-5734) is a nucleoside analogue, with effective antiviral activity, with EC50s of 74 nM for SARS-CoV and MERS-CoV in HAE cells, and 30 nM for murine hepatitis virus in delayed brain tumor cells. Remdesivir is highly effective in the control of 2019-nCoV (COVID-19) infection in vitro. | price> |
R-C-3093 | SAR131675 CAS:1433953-83-3 | SAR131675, a potent and selective VEGFR-3-TK inhibitor with antilymphangiogenic, antitumoral, and antimetastatic activities.Only for scientific research, not for human body. | price> |
R-R-4763 | H3B-8800 CAS No.1825302-42-8 | H3B-8800/CAS No.1825302-42-8 is a potent and orally active SF3B splicing modulator. H3B-8800 direct interaction with the SF3b complex and shows anti-cancer activity. H3B-8800 has the potential for the research of acute myeloid leukemia (AML) with SF3B1 mutant. | price> |
R-C-3094 | SU 5416 (Semaxinib) CAS: 204005-46-9 | SU 5416 is an inhibitor of vascular endothelial growth factor receptor (VEGFR) that also inhibits other tyrosine kinases KIT, MET, FLT3 and RET.Only for scientific research, not for human body. | price> |
R-R-4764 | Setrobuvir CAS No.1071517-39-9 | Setrobuvir (ANA598)/CAS No.1071517-39-9 is an orally active non-nucleosidic HCV NS5B polymerase inhibitor. ANA-598 inhibits both de novo RNA synthesis and primer extension, with IC50s between 4 and 5 nM. Setrobuvir also shows excellent binding affinity to SARS-CoV-2 RdRp and induces RdRp inhibition. | price> |
R-C-3095 | CP-547632 CAS:252003-65-9 | CP-547632 is a novel, potent vascular endothelial growth factor receptor-2 tyrosine kinase inhibitor.Only for scientific research, not for human body. | price> |
R-R-4765 | Methotrexate-d3 CAS No.432545-63-6 | Methotrexate-d3 (Amethopterin-d3)/CAS No.432545-63-6 is the deuterium labeled Methotrexate. Methotrexate (Amethopterin), an antimetabolite and antifolate agent, inhibits the enzyme dihydrofolate reductase, thereby preventing the conversion of folic acid into tetrahydrofolate, and inhibiting DNA synthesis. Methotrexate, also an immunosuppressant and antineoplastic agent, is used for the research of rheumatoid arthritis and a number of different cancers (such as acute lymphoblastic leukemia). | price> |
R-C-3096 | CP-673451 CAS:343787-29-1 | CP-673451 is a selective inhibitor of PDGFRα/β with IC50 of 10 nM/1 nM in cell-free assays, exhibits >450-fold selectivity over other angiogenic receptors, has antiangiogenic and antitumor activity.Only for scientific research, not for human body. | price> |
R-R-4766 | 7-Iodo-2,3-dideoxy-7-deaza-guanosine CAS No.114748-67-3 | 7-Iodo-2,3-dideoxy-7-deaza-guanosine/CAS No.114748-67-3 is a dideoxynucleoside that can be used in DNA synthesis and sequencing reactions. | price> |
R-C-3097 | Lucitanib(E-3810) CAS:1058137-23-7 | Lucitanib , also known as E-3810 and AL3810, is a novel dual inhibitor targeting human vascular endothelial growth factor receptors (VEGFRs) and fibroblast growth factor receptors (FGFRs) with antiangiogenic activity. VEGFR/FGFR dual kinase inhibitor E-3810 inhibits VEGFR-1, -2, -3 and FGFR-1, -2 kinases in the nM range, which may result in the inhibition of tumor angiogenesis and tumor cell proliferation, and the induction of tumor cell death. | price> |
R-R-4767 | DNA31 CAS No.845626-57-5 | DNA31/CAS No.845626-57-5 is a potent RNA polymerase inhibitor. | price> |
R-C-3098 | Aftin-4 CAS# 866893-90-5 | Aftin-4 is an amyloid-β42 inducer that electively and potently increases production of extracellular Aβ42 and decreases production of extracellular Aβ38 in cultured cells. | price> |
R-R-4768 | ZIM CAS No.301298-87-3 | ZIM/CAS No.301298-87-3, a norbornene derived from 4-Aminoantipyrine, is a potent inducer of DNA damage, causing genomic and chromosomal damage as well as inducing cell death and activating phagocytosis. ZIM has chemotherapeutic potential for use in cancer research. | price> |
R-R-4769 | WRN inhibitor 3 CAS No.2923009-48-5 | WRN inhibitor 3 (example 110)/CAS No.2923009-48-5, a cyclic vinyl sulfone compound, is a Wemer Syndrome ATP dependent helicase enzyme (WRN) inhibitor. WRN inhibitor 3 can be used for the research of cancer. | price> |
R-R-4770 | 5-Methylcytosine-d4 CAS No.1219795-15-9 | 5-Methylcytosine-d4/CAS No.1219795-15-9 is the deuterium labeled 5-Methylcytosine. 5-Methylcytosine is a well-characterized DNA modification, and is also predominantly in abundant non-coding RNAs in both prokaryotes and eukaryotes. 5-Methylcytosine in mRNA is a new epitranscriptome marker inArabidopsis, and that regulation of this modification is an integral part of gene regulatory networks underlying plant development. | price> |
R-C-3101 | TAK-981 CAS:1858276-04-6 | TAK-981 is a first in class and selective inhibitor of the SUMOylation enzymatic cascade, with potential immune-activating and antineoplastic activities. | price> |