Catalog |
name |
Description |
price |
R-R-0025 |
Nitidine chloride Cas: 13063-04-2 |
Nitidine chloride, a potential anti-malarial lead compound derived from Zanthoxylum nitidum (Roxb) DC, exerts potent anticancer activity through diverse pathways, including inducing apoptosis, inhibiting STAT3 signaling cascade, DNA topoisomerase 1 and 2A, ERK and c-Src/FAK associated signaling pathway. Nitidine chloride inhibits LPS-induced inflammatory cytokines production via MAPK and NF-kB pathway. |
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R-R-0032 |
N-(3-Aminopropyl)methacrylamide hydrochloride |
N-(3-Aminopropyl)methacrylamide hydrochloride (NAPM-HCl) is used in many scientific and industrial applications. It is an important component of many synthetic polymers, and is also used as a surfactant, a lubricant, and a catalyst. NAPM-HCl has been used in a variety of biomedical, pharmacological, and biotechnological research applications, as well as in laboratory experiments. |
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R-R-0036 |
VH032-NH-CO-CH2-Br CAS: 2379404-33-6 |
(S,R,S)-AHPC-CO-CI-Br/VH032-NH-CO-CH2-Br/CAS:2379404-33-6.Proteolysis targeting chimera (PROTAC) building block. Contains (S,R,S)-AHPC as von Hippel-Lindau (VHL) ligand with alkyl linker and a halide group. Ready for conjugation to a target protein ligand to form PROTACs containing (S,R,S)-AHPC as E3 ligase ligand. |
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R-R-0037 |
FMOC-RGD |
FMOC-RGD/Fmoc-Arg-Gly-Asp is a peptide sequence that combines the FMOC protecting group with the RGD motif. It is commonly used for studying cell adhesion and as a component in the design of biomaterials and peptides for tissue engineering and drug delivery applications. |
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R-R-0039 |
Tetrazine-Amine |
Tetrazine-Amine/(4-(1,2,4,5-Tetrazin-3-yl)phenyl)methanamine/Tetrazine-NH2.Tetrazine-Amine is a tetrazine linker that can be used to covalently label live cells through a cycloaddition.At equivalent molar concentrations, both the salt and free forms of a compound exhibit comparable biological activity. Nevertheless, the salt form (Tetrazine-Amine monohydrochloride) usually boasts enhanced water solubility and stability. |
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R-R-0044 |
Maltose cholesterol |
Maltose-Cholesterol, also known as cholesterol-maltoside, refers to a compound that consists of a cholesterol molecule conjugated with a maltose sugar unit. Cholesterol is a sterol molecule that is an essential component of cell membranes and plays a crucial role in various biological processes. |
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R-L-051 |
Flupirtine,cas56995-20-1 |
Flupidine is an analgesic drug that acts on the center and has no opioid effect such as respiratory inhibition or antitussive effect. It acts on the center, but has no opioid characteristics such as respiratory inhibition or antitussive. It is used for short-term treatment of pain caused by surgery, trauma, burns and toothache. |
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R-R-0052 |
Mitoxantrone Hydrochloride |
1,4-dihydroxy-5,8-bis[[2-[(2-hydroxyethyl)amino]ethyl]amino]-9,10-anthracenedione, dihydrochloride/ Mitozantrone (dihydrochloride).Mitoxantrone dihydrochloride is an antiviral, antibacterial, antiprotozoal, immunomodulating, and antineoplastic cytostatic anthraquinone derivative. Induces DNA damage by intercalating into DNA and inhibiting Topo II (topoisomerase II). Mitoxantrone dihydrochloride induces interstrand DNA cross-links and DNA-protein cross-links in cellular systems. Mitoxantrone dihydrochloride has recently been shown to be an inhibitor of DNA methylation. |
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R-R-0053 |
Doxorubicin-SPDP |
Doxorubicin-SPDP refers to the conjugation of the chemotherapy drug doxorubicin and the bifunctional cross-linker N-succinimidyl 3-(2-pyridyldithio)propionate (SPDP). When doxorubicin is conjugated to SPDP, other molecules, such as targeting ligands or polymers, can be attached to doxorubicin. This combination can enhance drug stability, solubility, and target specificity. |
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R-R-0054 |
DSPE acyl hydrazone bond PEG5000-MAL |
DSPE acyl hydrazone bond PEG5000-MAL refers to the conjugation of distearyl phosphatidylethanolamine (DSPE) with a polyethylene glycol (PEG) polymer containing a maleimide (MAL) group through an acyl hydrazone bond. DSPE acyl hydrazone bond PEG5000-MAL conjugation offers a versatile approach for the modification of lipid-based drug delivery systems, providing improved stability, enhanced pharmacokinetics, and the opportunity for further functionalization. |
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