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| Catalog | name | Description | price |
|---|---|---|---|
| R-C-880 | DPPE-N3 | 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-azide is widely used in medical research,drug release,nanotechnology and new material research,and cell culture.In the study of ligands,peptide synthesis carrier,graft polymer compounds,new materials,polyethylene glycol modified functional coatings and other aspects of the active compounds. | price> |
| R-R-2580 | CF53 CAS No.1808160-52-2 | CF53/CAS No.1808160-52-2 is a highly potent, selective and orally active inhibitor of BET protein, with a Ki of <1 nM, Kd of 2.2 nM and an IC50 of 2 nM for BRD4 BD1. CF53 binds to both the BD1 and BD2 domains of BRD2, BRD3, BRD4, and BRDT BET proteins with high affinities, very selective over non-BET bromodomain-containing proteins. CF53 shows potent anti-tumor activity both in vitro and in vivo. | price> |
| R-C-881 | Polydopamine monodisperse mesoporous | Dopamine is the most abundant catecholamine neurotransmitter in the brain.Dopamine,as a neurotransmitter,regulates many physiological functions of the central nervous system.Dopamine can stimulate both β-andα-adrenoceptors. It can enhance myocardial contractility,increase cardiac output,accelerate heart rate and slightly constrict peripheral blood vessels.We can also make customized special products. | price> |
| R-R-2581 | Y06036 CAS No.1832671-96-1 | Y06036/CAS No.1832671-96-1 is a potent and selective BET inhibitor, which binds to the BRD4(1) bromodomain with Kd value of 82 nM. Antitumor activity. | price> |
| R-C-882 | Cy5 labeled cRGDyK modified liposomes | Objective to construct cRGDyK cyclic peptide modified liposome loaded quantum dots for accurate imaging of glioma,and to achieve accurate tumor resection guided by intraoperative fluorescence imaging.The maximum excitation wavelength of Cy5 coupling group is 650nm,and the maximum luminescence wavelength is 670nm. | price> |
| R-R-2582 | BET-IN-14 CAS No.2243669-93-2 | BET-IN-14/CAS No.2243669-93-2 is an orally active pan BET inhibitor (IC50: 5.35 nM). BET-IN-14 has anti-cancer activity. | price> |
| R-C-883 | Peptide (YGRKKRRQRRR) modified carbon quantum dots | Polypeptides are the active substances to achieve various functions in organisms.The modification of polypeptides is mainly the modification of the main chain structure and side chain groups of peptide chain.The modified peptide drugs can significantly reduce immunogenicity,reduce toxicity, increase water solubility,prolong the action time in vivo,change the distribution in vivo and so on.The main modifiers are dextran,polyethylene glycol and tetranitroethane. Peptides can modify quantum dots,other groups,etc.,and can also customize special peptide modified products. | price> |
| R-R-2583 | iBRD4-BD1 CAS No.2839318-17-9 | iBRD4-BD1/CAS No.2839318-17-9 is selective BRD4 bromodomain inhibitor. iBRD4-BD1 has inhibition activity for BRD4 bromodomain with an IC50 value of 12 nM. iBRD4-BD1 can be used for the research of inflammation and oncology. | price> |
| R-C-884 | TAT(YGRKKRRQRRR) | TAT(YGRKKRRQRRR)(Tyr Gly Arg Lys Lys Arg Arg Gln Arg Arg Arg Arg Arg ARG) is a cell penetrating peptide derived from human immunodeficiency virus (HIV-1).It has strong cell penetrating power and can directly act on the nucleus.Tat can increase the production and solubility of heterologous proteins. | price> |
| R-R-2584 | DC-BPi-03 CAS No.2758411-46-8 | DC-BPi-03/CAS No.2758411-46-8 is a potent BPTF-BRD inhibitor with an IC50 of 698.3 nM and a Kd of 2.81 μM. | price> |
| R-C-885 | 45%PC,30%PE,10%Cholesterol,10%PS,5%PI Blank liposome100NM | Ruixibio can provide synthetic phospholipids,popular cancer raw materials, macrocyclic ligands,fluorescent quantum dots,hyaluronic acid derivatives, graphene or graphene oxide,carbon nanotubes,fullerenes,silica and mesoporous silica,polymer microspheres,near-infrared fluorescent dyes,polystyrene microspheres,up conversion nanoparticles,MRI products,fluorescent proteins and other products Fluorescent probes and so on.We can also offer special customized products. | price> |
| R-R-2585 | BRD4 Inhibitor-20 CAS No.2490311-14-1 | BRD4 Inhibitor-20/CAS No.2490311-14-1 is a potent orally active bromodomain protein 4 (BRD4) inhibitor. BRD4 Inhibitor-20 has inhibitory activity for BRD4 (BD1) and BRD4 (BD2) with IC50 values of 19 nM and 28 nM, respectively. BRD4 Inhibitor-20 also has anti-proliferation activities in cancer cell lines. BRD4 Inhibitor-20 can be used for the research of kinds of cancer, such as colon cancer. | price> |
| R-C-886 | GA-PEG3400-PLA2000 | Glycyrrhetinic acid is a pentacyclic triterpenoid,which is obtained from glycyrrhizic acid hydrolysis of Glycyrrhiza glabra.Glycyrrhetinic acid can be regarded as a derivative of β-vanillin alcohol(oleanol type),which can be used as the glycoside ligand of glycyrrhetinic acid.Polyethylene glycol(PEG)is a kind of high molecular polymer,which has no irritation,slightly bitter taste,good water solubility and good compatibility with many organic components.It has excellent lubricity,moisture retention,dispersibility and adhesive.It can be used as antistatic agent and softener | price> |
| R-R-2586 | DC-BPi-11 hydrochloride | DC-BPi-11 hydrochloride is an inhibitor of bromodomain PHD finger transcription factor (BPTF), with an IC50 value of 698 nM. DC-BPi-11 hydrochloride shows remarkable inhibition against leukemia cell proliferation. | price> |
| R-C-887 | Disulfide modified paclitaxel | Disulfide bond is a chemical bond that connects the sulfhydryl groups of two different cysteine residues in different peptide chains or the same peptide chain.Disulfide bond is a relatively stable covalent bond,which plays a role in stabilizing the spatial structure of peptide chain in protein molecules. Paclitaxel can make tubulin and tubulin dimer of microtubule lose dynamic balance,induce and promote tubulin polymerization,microtubule assembly,prevent depolymerization,so as to stabilize microtubule,inhibit the mitosis of cancer cells and trigger apoptosis,and then effectively prevent the proliferation of cancer cells and play an anti-cancer role. | price> |
| R-R-2587 | BET-BAY 002 CAS No.1588521-78-1 | BET-BAY 002/CAS No.1588521-78-1 is a potent BET inhibitor; shows efficacy in a multiple myeloma model. | price> |
| R-C-888 | A549 membrane package PLGA@DOX | Doxorubicin(DOX)can maximize the efficacy and minimize dose limiting cardiotoxicity by controlled release of PEGylated nanoparticles.Using avidin biotin coupling system,the binding of PEG to PLA nanoparticles was controlled. The particle size was about 130 nm,and DOX was loaded to 5% (wt/wt).The encapsulation of nanoparticles will not affect the efficacy of DOX. | price> |
| R-R-2588 | (R)-BAY1238097 CAS No.1564269-85-7 | (R)-BAY1238097/CAS No.1564269-85-7 is the R-isomer with lower activity of BAY1238097. BAY1238097 is a potent and selective inhibitor of BET binding to histones and has strong anti-proliferative activity in different AML (acute myeloid leukemia) and MM (multiple myeloma) models through down-regulation of c-Myc levels and its downstream transcriptome. | price> |
| R-C-889 | Glycyrrhizic acid nanoparticles(100nm) | Glycyrrhizic acid is an organic compound with the molecular formula of c42h62o16. As a drug,it has anti-inflammatory and anti allergic effects. Glycyrrhizic acid is the main active ingredient in Glycyrrhiza uralensis. Glycyrrhizic acid and its series of products can inhibit the growth of sarcoma and cancer cells,and the inhibition rate of AIDS is as high as 90%.It has a strong effect on increasing human immune function,and is also a good food additive and spice base material. | price> |
| R-R-2589 | (Rac)-BAY1238097 CAS No.1564268-19-4 | (Rac)-BAY1238097/CAS No.1564268-19-4 is a BET inhibitor, with an IC50 of 1.02 μM for BRD4. Used in cancer research. | price> |

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