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Catalog	name	Description	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>
R-C-2960	DSPE-TK-PEOz	DSPE(1,2-distearyl-sn-glycerin-3-phosphate ethanolamine) is a saturated 18 carbon phospholipid, which is commonly used in the synthesis of liposomes. Polyethylene glycol (PEG)-coupled DSPE is hydrophilic and can be used for drug delivery,gene transfection and biomolecular modification. At present, the mainly include synthetic phospholipids, PEG derivatives, block copolymers, gold nanoparticles, magnetic nanoparticles, mesoporous silica, reactive fluorescent dyes, fluorescent quantum dots, click chemistry and macrocyclic ligands.	price>
R-R-4630	Lapachol CAS No.84-79-7	Lapachol/CAS No.84-79-7, a natural naphthoquinone, is an orally active, potent DHODH inhibitor. Lapachol has immunosuppressive activity on lymphocytes through its direct ability to block DHODH activity and inhibit pyrimidine synthesis. Lapachol is a vitamin K antagonist with antitumor activity and can inhibit DNA and RNA synthesis in neoplastic cells. Lapachol has anti-Leishmania activity.	price>
R-C-2961	5-(4-hydroxyphenyl)-10,15,20-(4-methylphenyl) porphine	Porphyrin is a complex nitrogen-containing compound based on the structure of four pyrrole nuclei closed into ten J six rings. It is changed from animal and plant pigments (chlorophyll or heme). These pigments contain pyrrole nuclei. It mainly exists in the form of metal complexes (vanadium, nickel, iron, copper, cobalt, zinc, etc.) and they are very stable	price>
R-R-4631	DHX9-IN-1 CAS No.2973747-89-4	DHX9-IN-1 (example 160)/CAS No.2973747-89-4 is an inhibitor of ATP-dependent RNA helicase A (DHX9), with the IC50 of 9.45 nM that has antitumor activity.	price>
R-C-2962	Mp-a08 CAS：219832-49-2	Porphyrin is a complex nitrogen-containing compound based on the structure of four pyrrole nuclei closed into ten J six rings.It is changed from animal and plant pigments (chlorophyll or heme).These pigments contain pyrrole nuclei.It mainly exists in the form of metal complexes (vanadium, nickel, iron, copper, cobalt, zinc, etc.) and they are very stable.	price>
R-R-4632	Dasabuvir CAS No.1132935-63-7	Dasabuvir (ABT-333)/CAS No.1132935-63-7 is a nonnucleoside hepatitis C virus (HCV) polymerase inhibitor. Dasabuvir inhibits RNA-dependent RNA polymerase encoded by the HCV NS5B gene. Dasabuvir inhibits genotype 1a (strain H77) and 1b (strain Con1) replicons, with EC50 values of 7.7 and 1.8 nM, respectively.	price>
R-C-2963	5,10,15,20-Tetrakis(3,5-dihydroxyphenyl)porphyrin cas 145764-54-1	Porphyrin is a complex nitrogen-containing compound based on the structure of four pyrrole nuclei closed into ten J six rings. It is changed from animal and plant pigments (chlorophyll or heme).These pigments contain pyrrole nuclei. It mainly exists in the form of metal complexes (vanadium, nickel, iron, copper, cobalt, zinc, etc.) and they are very stable4634.	price>
R-R-4633	Pyrazofurin CAS No.30868-30-5	Pyrazofurin/CAS No.30868-30-5, a pyrimidine nucleoside analogue with antineoplastic activity, inhibits cell proliferation and DNA synthesis in cells by inhibiting uridine 5-phosphate (UMP) synthase. Pyrazofurin is an active, sensitive orotate-phosphoribosyltransferase inhibitor with IC50s between 0.06-0.37 µM in the three squamous cell carcinoma (SCC) cell lines Hep-2, HNSCC-14B and HNSCC-14C.	price>
R-C-2964	5,10,15,20-Tetrakis(3,5-dimethoxyphenyl )-21H,23H-porphyrin Cas:74684-34-7	Porphyrin is a complex nitrogen-containing compound based on the structure of four pyrrole nuclei closed into ten J six rings. It is changed from animal and plant pigments (chlorophyll or heme). These pigments contain pyrrole nuclei. It mainly exists in the form of metal complexes (vanadium, nickel, iron, copper, cobalt, zinc, etc.) and they are very stable.	price>
R-R-4634	ccc_R08 CAS No.2919019-72-8	ccc_R08/CAS No.2919019-72-8 is a non-cytotoxic and orally active cccDNA inhibitor that reduces cccDNA levels in the liver of HBV-infected mice. ccc_R08 can be used in the study of HBV virus (hepatitis B virus) infection.	price>
R-C-2965	SB-269970	SB269970 is a potent and selective 5-HT7 receptor antagonist.	price>
R-R-4635	R-1479 CAS No.478182-28-4	R-1479/CAS No.478182-28-4, a nucleoside analogue, is a specific inhibitor of RNA-dependent RNA polymerase (RdRp) of HCV. R-1479 inhibits HCV replication in the HCV subgenomic replicon system (IC50=1.28 μM). R-1479 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.	price>
R-C-2966	Etoricoxib CAS：202409-33-4	Etoricoxib is a synthetic, nonsteroidal anti-inflammatory drug (NSAID) with antipyretic, analgesic, and potential antineoplastic properties. Etoricoxib specifically binds to and inhibits the enzyme cyclooxygenase-2 (COX-2), resulting in inhibition of the conversion of arachidonic acid into prostaglandins. Inhibition of COX-2 may induce apoptosis and inhibit tumor cell proliferation and angiogenesis.	price>
R-R-4636	Werner syndrome RecQ helicase-IN-3 CAS No.2869954-98-1	Werner syndrome RecQ helicase-IN-3/CAS No.2869954-98-1 is a potent and orally active werner syndrome recQ helicase (WRN) inhibitor with an IC50 value of 0.06 µM. Werner syndrome RecQ helicase-IN-3 shows antiproliferative activity. Werner syndrome RecQ helicase-IN-3 shows anticancer activity.	price>
R-C-2967	Olcegepant CAS：204697-65-4	Olcegepant also known as BIBN-4096 or BIBN-4096BS is is the first potent and selective non-peptide antagonist of the calcitonin gene-related peptide 1 (CGRP1)receptor.	price>

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