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Catalog | name | Description | price |
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R-C-3075 | KU-0060648 CAS:881375-00-4 | KU-0060648 is a dual inhibitor of DNA-PK and PI3Kα, PI3Kβ, PI3Kδ with IC50 of 8.6 nM and 4 nM, 0.5 nM, 0.1 nM respectively, less inhibition of PI3Kγ with IC50 of 0.59 μM. Only for scientific research, not for human body. | price> |
R-R-4745 | Laflunimus CAS No.147076-36-6 | Laflunimus (HR325)/CAS No.147076-36-6 is an immunosuppressive agent and an analogue of the Leflunomide-active metabolite A77 1726. Laflunimus is an orally active inhibitor of dihydroorotate dehydrogenase (DHODH). Laflunimus suppresses immunoglobulin (Ig) secretion, with IC50 values of 2.5 and 2 µM for IgM and IgG, respectively. Laflunimus also is a prostaglandin endoperoxide H synthase (PGHS) -1 and -2 inhibitor. | price> |
R-C-3076 | SU 5205 CAS:3476-86-6 | SU5205 is an inhibitor of VEGF receptor 2 (VEGFR2/FLK-1) with IC50 of 9.6 µM.Only for scientific research, not for human body. | price> |
R-R-4746 | Adenine-d CAS No.109923-52-6 | Adenine-d/CAS No.109923-52-6 is the deuterium labeled Adenine. Adenine (6-Aminopurine), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine acts as a chemical component of DNA and RNA. Adenine also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis. | price> |
R-C-3077 | SU-5408 CAS:15966-93-5 | SU5408 (VEGFR2 Kinase Inhibitor I) is a potent and selective inhibitor of VEGFR2 Kinase with IC50 of 70 nM.Only for scientific research, not for human body. | price> |
R-R-4747 | MMV688845 CAS No.2208962-35-8 | MMV688845/CAS No.2208962-35-8 is a nontuberculous mycobacteria (NTM) RNA polymerase inhibitor with bactericidal activity against Mycobacterium abscessus and anti-tuberculosis efficacy. | price> |
R-C-3078 | SU 5214 CAS:186611-04-1 | SU5214 is a inhibitor of VEGF receptor 2 (VEGFR2/FLK-1) with IC50 of 14.8 µM and EGFR with IC50 of 36.7 µm, respectively.Only for scientific research, not for human body. | price> |
R-R-4748 | 7-TFA-ap-7-Deaza-dA CAS No.178420-75-2 | 7-TFA-ap-7-Deaza-dA/CAS No.178420-75-2 is a modified nucleoside. 7-TFA-ap-7-Deaza-dA can be used in the synthesis of deoxyribonucleic acid or nucleic acid. 7-TFA-ap-7-Deaza-dA is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. | price> |
R-C-3079 | Ranibizumab cas:347396-82-1 | Ranibizumab is a monoclonal antibody that inhibits angiogenesis by inhibiting Vascular endothelial growth factor A.Only for scientific research, not for human body. | price> |
R-R-4749 | Methylproamine CAS No.188247-01-0 | Methylproamine/CAS No.188247-01-0 is a DNA-binding radioprotector, acts by repair of transient radiation-induced oxidative species on DNA. Methylproamine also protects against ionizing radiation by preventing DNA double-strand breaks. | price> |
R-C-3080 | ACC-789(NVP-ACC789) | ACC-789, also known as NVP-ACC789 and ZK-202650, is a potent, selective and orally active inhibitor of the VEGF receptor tyrosine kinases with potential anticancer activity.Only for scientific research, not for human body. | price> |
R-R-4750 | SCR7 CAS No.1533426-72-0 | SCR7/CAS No.1533426-72-0 is an unstable form that can be autocyclized into a stable form SCR7 pyrazine. SCR7 pyrazine is a DNA ligase IV inhibitor that blocks nonhomologous end-joining (NHEJ) in a ligase IV-dependent manner. SCR7 pyrazine is also a CRISPR/Cas9 enhancer which increases the efficiency of Cas9-mediated homology-directed repair (HDR). SCR7 pyrazine induces cell apoptosis and has anticancer activity. | price> |
R-C-3081 | JI-101 CAS NO. 900573-88-8 | JI-101 is an orally active inhibitor of vascular endothelial growth factor receptor 2 (VEGFR2), platelet-derived growth factor receptor beta (PDGFRβ), and the ephrin B4 receptor B4 (EphB4) with potential antiangiogenic and antineoplastic activities.Only for scientific research, not for human body. | price> |
R-R-4751 | Deoxycytidine triphosphate CAS No.2056-98-6 | Deoxycytidine triphosphate (dCTP)/CAS No.2056-98-6 is a nucleoside triphosphate that can be used for DNA synthesis. Deoxycytidine triphosphate has many applications, such as real-time PCR, cDNA synthesis, and DNA sequencing. | price> |
R-C-3082 | SU1498 CAS:168835-82-3 | SU1498, a powerful inhibitor of KDR (IC50=0.7μM), stimulates accumulation of phosphorylated ERK1/2 in endothelial cells.Only for scientific research, not for human body. | price> |
R-R-4752 | Novobiocin CAS No.303-81-1 | Novobiocin (Albamycin)/CAS No.303-81-1 is a potent and orally active antibiotic. Novobiocin also is a DNA gyrase inhibitor and a heat shock protein 90 (Hsp90) antagonist. Novobiocin has the potential for the research of highly beta-lactam-resistant pneumococcal infections. Novobiocin shows anti-orthopoxvirus activity.The free form of the compound is prone to instability, it is advisable to consider the stable salt form (Novobiocin sodium) that retains the same biological activity. | price> |
R-C-3083 | GW806742X CAS:579515-63-2 | GW806742X is a Mixed Lineage Kinase Domain-Like protein (MLKL)inhibitor which binds the MLKL pseudokinase domain with a Kd value of 9.3μM and has anti-necroptosis activity.GW806742X has activity against VEGFR2. Only for scientific research, not for human body. | price> |
R-R-4753 | Crisnatol CAS No.96389-68-3 | Crisnatol (BWA770U)/CAS No.96389-68-3 is an orally active and anticancer agent, and a member of the arylmethylaminopropanediol class of DNA intercalators. Crisnatol shows in vitro cytotoxicity against human breast cancer cells, but not normal human skin fibroblasts. | price> |
R-C-3084 | GW842166X CAS:666260-75-9 | GW842166X is a potent and highly selective agonist of cannabinoid receptor CB2 receptor with EC50 of 63 nM,shows no significant activity at CB1 receptor.Only for scientific research, not for human body. | price> |
R-R-4754 | Herboxidiene CAS No.142861-00-5 | Herboxidiene (GEX1A)/CAS No.142861-00-5 is a potent phytotoxic polyketide from Streptomyces sp. A7847 with a diverse range of activities, including herbicidal, anti-cholesterol, anti-tumor effects. Herboxidiene inhibits the pre-mRNA splicing process by binding to spliceosome-associated protein (SAP) 155, a subunit of SF3b, in the splicesome. | price> |