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Catalog	name	Description	price
R-C-3981	DOX-HYD-PEG750-DSPE	1,2-distearoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol is a PEG-modified lipids.so the drug stability is better,even by hemodilution,can maintain the integrity of the micelle particle,has certain targeting,easy accumulation in solid tumors.Suitable for the development of long circulating liposomes.It can connect peptides and other groups.Doxorubicin is an anti-tumor antibiotic,which can inhibit the synthesis of RNA and DNA.It has the strongest inhibitory effect on RNA and has a wide anti-tumor spectrum.It has an effect on a variety of tumors.It is a cycle nonspecific drug and can kill tumor cells in various growth cycles.	price>
R-R-5660	4-(2-Pyridin-4-ylethynyl)benzoic acid CAS No.:212138-35-7	4-(2-Pyridin-4-ylethynyl)benzoic acid/CAS No.:212138-35-7 is a versatile chemical compound used in scientific research. It exhibits intriguing properties and finds applications in various fields like materials science, pharmaceuticals, and catalysis. Its unique structure makes it an exciting compound for investigating new possibilities in scientific exploration.	price>
R-M-1535	PMAP36	PMAP36 exerts antimicrobial activity against both Gram-positive and negative bacteria. Its activity appears to be mediated by its ability to damage bacterial membranes.	price>
R-R-5661	[3,3-Bipyridine]-2,2-dicarboxylic acid CAS No.:3723-32-8	[3,3-Bipyridine]-2,2-dicarboxylic acid/CAS No.:3723-32-8, also known as bipyridine dicarboxylic acid (BPDA), is a versatile compound widely used in various scientific fields. BPDA is a chelating agent that can form coordination complexes with metal ions, making it useful in a range of applications.	price>
R-M-1536	Rat Renin FRET Substrate (5-FAM/CPQ2 520)	Over the past decade, a number of structurally different synthetic renin inhibitors of excellent potency have been described. To facilitate high throughput screening of renin inhibitors, we have developed the FRET pair, 5-FAM/CPQ2, that quenches at 520 nm and shows superior sensitivity compared to that of FRET pairs Dnp/Amp and EDANS/Dabcyl.	price>
R-C-3982	DSPE-PEG350-Desthiobiotin	Desthiobiotin is a single ring,sulfur-free biotin.It binds to streptomycin and has almost the same specificity,but its affinity is smaller than biotin(Kd=1011 and 1015m).DSPE-PEG is a PEG-modified lipids.Suitable for the development of long circulating liposomes.It can connect peptides and other groups.	price>
R-R-5662	5-(Pyridin-4-ylmethoxy)isophthalic acid CAS No.:1240327-15-4	5-(Pyridin-4-ylmethoxy)isophthalic acid/CAS No.:1240327-15-4 is a versatile chemical compound used in scientific research. Its unique structure allows for diverse applications in fields like materials science and pharmaceuticals, making it a valuable tool for advancing innovation.	price>
R-M-1537	UCI-1	UCI-1 (University of California, Irvine Coronavirus Inhibitor-1) is a first-in-class cyclic peptide that inhibits SARS-CoV main protease (Mpro, also known as 3CLpro). UCI-1 was developed by Professor James S. Nowick and designed to mimic the autolytic cleavage site of SARS-CoV Mpro.	price>
R-C-3983	DSPE-polyethylene glycol550-Desthiobiotin	Desthiobiotin is a single ring,sulfur-free biotin.It binds to streptomycin and has almost the same specificity,but its affinity is smaller than biotin(Kd=1011 and 1015m).DSPE-PEG is a PEG-modified lipids.Suitable for the development of long circulating liposomes.It can connect peptides and other groups.	price>
R-R-5663	3-(1H-pyrazol-4-yl)benzoic Acid CAS No.:1002535-21-8	3-(1H-pyrazol-4-yl)benzoic Acid/CAS No.:1002535-21-8 is a chemical compound commonly used in scientific research. This versatile material finds applications in various fields such as pharmaceuticals, organic synthesis, and material science. Its unique structure and properties make it an essential component in many studies aiming to develop new drugs or explore novel materials.	price>
R-M-1538	(Cys39)-Tissue Factor (33-53),CAS :313642-01-2	Tissue factor (TF) is a transmembrane protein, enables cells to initiate the blood coagulation cascades in vivo, functions as the high-affinity receptor for the coagulation factor VII. This peptide specially inhibit theTF dependent clotting cascade.	price>
R-C-3984	Desthiobiotin-PEG750-DSPE	Desthiobiotin is a single ring,sulfur-free biotin.It binds to streptomycin and has almost the same specificity,but its affinity is smaller than biotin(Kd=1011 and 1015m).DSPE-PEG is a PEG-modified lipids.Suitable for the development of long circulating liposomes.It can connect peptides and other groups.	price>
R-R-5664	Gilteritinib (ASP2215) Liposomes CAS No.1254053-43-4	Gilteritinib (ASP2215)/CAS No.1254053-43-4 is a small-molecule inhibitor of FLT3/AXL with IC50 values of 0.29 nM and 0.73 nM for FLT3 and AXL, respectively. Gilteritinib (ASP2215) is a highly selective FLT3 inhibitor that demonstrates activity against both FLT3-ITD and FLT3-TKD mutation subtypes and selectively inhibits FLT3 at concentrations roughly 800-fold lower than those required to inhibit c-Kit (230 nM). This product is a pre-formulated liposomal version of Gilteritinib (ASP2215) which is supplied ready to use in vitro or in vivo. The liposomes are PEGylated for optimal in vivo performance; the lipid composition of the liposomes is the same as Doxil. For preclinical research use only.	price>
R-M-1539	(Gly106)-Cytochrome C (92-107) (Manduca sexta),CAS :213260-63-0	This peptide is an antigenic peptide that prevents the development of mature 2B4 TCRhi CD4+8+ thymocytes, competitively blocks antigen induced IL-2 production plays major role in T-cell selection.	price>
R-C-3985	DSPE-PEG350-sucrose	DSPE-PEG is a PEG-modified lipids.so the drug stability is better,even by hemodilution,can maintain the integrity of the micelle particle,has certain targeting,easy accumulation in solid tumors.Suitable for the development of long circulating liposomes.It can connect peptides and other groups.Sucrose,organic compound,molecular weight 342.3.Colorless crystal,with optical rotation,but no variable rotation.	price>
R-R-5665	HSPC/Chol/DSPE-mPEG2000/DSPE-mPEG2000-maleimide (50/45/4/1, mol/mol) Liposomes	HSPC/Chol/DSPE-mPEG2000/DSPE-mPEG2000-maleimide (50/45/4/1, mol/mol) Liposomes. PEGylated liposomes containing free maleimide functional group for maleimide-thiol conjugation. The liposomes are co-formulated with 1 mol% DSPE-mPEG2000-maleimide, and supplied in a pH-optimized buffer for direct conjugation of the thiol-containing molecule of choice. Conjugation can be achieved by incubating the liposomes with the activated thiol-containing compound which has been reduced by a disulfide bond reducing agent such as (tris(2-carboxyethyl)phosphine) (TCEP), which can be purchased as an add-on.	price>
R-M-1540	(Trp63,Trp64)-C3a (63-77),CAS:130154-64-2	(Trp63,Trp64)-C3a (63-77), synthetic superagonist analog of complement 3a, was 12-15 times more active than natural C3a.	price>
R-C-3986	DSPE-polyethylene glycol550-sucrose	DSPE-PEG is a PEG-modified lipids.so the drug stability is better,even by hemodilution,can maintain the integrity of the micelle particle,has certain targeting,easy accumulation in solid tumors.Suitable for the development of long circulating liposomes.It can connect peptides and other groups.Sucrose,organic compound,molecular weight 342.3.Colorless crystal,with optical rotation,but no variable rotation.	price>
R-R-5666	Tanespimycin (17-AAG) Liposomes, Formulation XT28.1	Tanespimycin (17-AAG) Liposomes, Formulation XT28.1. PEGylated liposomes containing Hsp90 inhibitor Tanespimycin (17-AAG). Tanespimycin exhibits 100-fold higher binding affinity to HSP90 derived from tumor cells vs normal cells, and induces apoptosis, necrosis, autophagy, and mitophagy. Tanespimycin is insoluble in aqueous media. This product is a pre-formulated liposomal version of Tanespimycin which is supplied ready to use in vitro or in vivo. The liposomes are PEGylated for optimal in vivo performance. For preclinical research use only.	price>
R-M-1541	[Ala9] Autocamtide 2,CAS:167114-91-2	Highly specific and potent inhibitor of calmodulin-dependent protein Kinase II (IC50= 40 nM) that does not affect cycle AMP-dependent protein kinase, protein kinase C and calmodulin-dependent protein kinase IV.	price>

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