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Catalog | name | Description | price |
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R-C-2949 | PAMAM G1-NH2 | PAMAM is a polyamide amine dendrimer with colorless to yellowish transparent liquid.As a carrier of drugs,genes and vaccines in the field of biomedicine,it is used for drug sustained-release and targeted release;it is used for in-vitro diagnosis,in vitro gene transfer,gene therapy,nuclear magnetic resonance imaging and other applications. | price> |
R-R-4619 | JH-RE-06 CAS No.1361227-90-8 | JH-RE-06/CAS No.1361227-90-8, a potent REV1-REV7 interface inhibitor (IC50=0.78 μM; Kd=0.42 μM), targets REV1 that interacts with the REV7 subunit of POLζ. JH-RE-06 disrupts mutagenic translesion synthesis (TLS) by preventing recruitment of mutagenic POLζ. JH-RE-06 improves chemotherapy. | price> |
R-C-2950 | PAMAM G2-NH2 | PAMAM is a polyamide amine dendrimer with colorless to yellowish transparent liquid.As a carrier of drugs,genes and vaccines in the field of biomedicine,it is used for drug sustained-release and targeted release;it is used for in-vitro diagnosis,in vitro gene transfer,gene therapy,nuclear magnetic resonance imaging and other applications. | price> |
R-R-4620 | Zoliflodacin CAS No.1620458-09-4 | Zoliflodacin (ETX0914;AZD0914)/CAS No.1620458-09-4 is a novel spiropyrimidinetrione bacterial DNA gyrase/topoisomerase inhibitor. Zoliflodacin has potent in vitro antibacterial activity against Gram-positive and Gram-negative organisms, including S. aureus with the MIC90 of 0.25 μg/mL. | price> |
R-C-2951 | PAMAM G3-NH2 | PAMAM is a polyamide amine dendrimer with colorless to yellowish transparent liquid.As a carrier of drugs,genes and vaccines in the field of biomedicine,it is used for drug sustained-release and targeted release;it is used for in-vitro diagnosis,in vitro gene transfer,gene therapy,nuclear magnetic resonance imaging and other applications. | price> |
R-R-4621 | 116-9e CAS No.831217-43-7 | 116-9e (MAL2-11B)/CAS No.831217-43-7 is a Hsp70 co-chaperone DNAJA1 inhibitor. 116-9e inhibits Simian Virus 40 (SV40) replication and DNA synthesis. | price> |
R-C-2952 | Poly-L-lysine (MW:20-40k) | ε- Polylysine is polymerized from 25 ~ 30 lysine residues. It has strong antibacterial ability and can be used as a preservative for food preservation. ε- Polylysine has a wide antibacterial spectrum and has a certain antibacterial effect on Gram-positive bacteria, Gram-negative bacteria, yeasts and molds in acidic and slightly acidic environment. | price> |
R-R-4622 | DDD85646 CAS No.1215010-55-1 | DDD85646 (IMP-366)/CAS No.1215010-55-1 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. | price> |
R-C-2953 | Gamma-PGA MW:20-40k | Gamma PGA is a natural occurring, multi-functional, and biodegradable biopolymer. It is produced through fermentation by Bacillus subtilis using glutamic acid. PGA is consists of glutamic acid monomers crosslinked between α-amino and γ-carboxyl groups, and the molecular weight of PGA is usually between 100~1000 kDa. | price> |
R-R-4623 | Fialuridine CAS No.69123-98-4 | Fialuridine/CAS No.69123-98-4 is a nucleoside analog with antiviral activity. Fialuridine shows anti-orthopoxvirus activity. | price> |
R-C-2954 | Oligoarginine-FITC Labeled | Isothiocyanate fluorescent orange red,isothiocyanate fluorescent yellow,isothiocyanate fluorescent red, isothiocyanate fluorescein isomer I, 5-isothiocyanate fluorescein. Its form is yellow powder with hygroscopicity. It is a biochemical reagent. | price> |
R-R-4624 | L82 CAS No.329227-30-7 | L82/CAS No.329227-30-7 is a selective and uncompetitive DNA ligase 1 (DNA Lig1) inhibitor (hLig1 IC50=12 μM). L82 shows anti-proliferative activity to breast cancer cells | price> |
R-C-2955 | Oligoarginine-TAMRA Labeled | RuixiBiotechCo.Ltd sells research regeats related to nano targeted drug delivery system, including synthetic phospholipid, polyethylene glycol derivatives, block copolymers, gold nanoparticles, magnetic nanoparticles and fluorescent dyes. | price> |
R-R-4625 | COH29 CAS No.1190932-38-7 | COH29 (RNR Inhibitor COH29)/CAS No.1190932-38-7 is a potent ribonucleotide reductase (RNR) inhibitor with anticancer activity. COH29 inhibits α and β subunit of RNR with IC50s of 16 μM. | price> |
R-R-4626 | L189 CAS No.64232-83-3 | L189/CAS No.64232-83-3 is a DNA ligase inhibitor. L189 has inhibition effect for DNA Ligase I, III and IV with IC50 values of 5 μM, 9 μM and 5 μM, respectively. L189 has no cytotoxicity and individually increase cell death. L189 can be used for the research of cancer. | price> |
R-C-2958 | PLA-PEOz-SH | Poly(D,L-lactide)-Poly(2-ethyl-2-oxazoline)is an amphiphilic AB block copolymer,it can be used to prepare PH responsivemicelle for drug delivery,PLA can choose DLLA or LLA.It is a pH responsive amphiphilic copolymer product | price> |
R-R-4627 | APE1-IN-1 CAS No.524708-03-0 | APE1-IN-1/CAS No.524708-03-0 is a potent and blood-brain barrier (BBB) penetrant apurinic/apyrimidinic (AP) endonuclease 1 (APE1) inhibitor with an IC50 value of 2 μM. APE1-IN-1 can potentiate the cytotoxicity of the alkylating agents Methylmethane sulfonate and Temozolomide (HY-17364) to cancer cells. | price> |
R-R-4628 | Galidesivir hydrochloride CAS No.222631-44-9 | Galidesivir (BCX4430) hydrochloride/CAS No.222631-44-9, an adenosine analog and a direct-acting antiviral agent, disrupts viral RNA-dependent RNA polymerase (RdRp) activity. Galidesivir hydrochloride is active in vitro against many RNA viral pathogens, including the filoviruses and emerging infectious agents such as MERS-CoV, SARS-CoV, and SARS-CoV-2. Galidesivir hydrochloride inhibits some negative-sense RNA viruses with EC50s ranging from ~3 to ~68 μM. | price> |
R-C-2959 | PLGA-PEOz-MAL | Poly(L-lactide-co-glycolide)-Poly(2-ethyl-2-oxazoline)is an amphiphilic AB block copolymer,it can be used to prepare PH responsivemicelle for drug delivery, LA:GA:75:25/50:50. | price> |
R-R-4629 | Bractoppin CAS No.2290527-07-8 | Bractoppin/CAS No.2290527-07-8 is a potent and selective agent-like inhibitor of phosphopeptide recognition by the human BRCA1 tandem(t) BRCT domain (binding IC50: 74 nM). Bractoppin diminishes BRCA1 recruitment to DNA breaks, in turn suppressing damage-induced G2 arrest and assembly of the recombinase, RAD51. Bractoppin preferentially inhibits BRCA1 tBRCT-dependent steps in the DNA damage response. | price> |