10 Results for "

folate-peg3-azide

" in MedChemExpress (MCE) Product Catalog:
Products (10)

10 Results for "folate-peg3-azide" in MCE Product Catalog:

Cyclo[Arg-Gly-Asp-D-Phe-Lys(Azide)]
Cyclo[Arg-Gly-Asp-D-Phe-Lys(Azide)]
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製品番号: HY-P10303
CAS 番号: 2767993-86-0
別名: Cyclo[RGDfK(azide)]
Target:  

Biochemical Assay Reagents

研究分野:  

Others

Cyclo[Arg-Gly-Asp-D-Phe-Lys(Azide)] is the derivative of Cyclo(-RGDfK) (HY-P0023). Cyclo[Arg-Gly-Asp-D-Phe-Lys(Azide)] is a click chemistry reagent containing an azide group. Click chemistry has great potential for use in binding between nucleic acids, lipids, proteins, and other molecules, and has been used in many research fields because of its beneficial characteristics, including high yield, high specificity, and simplicity .
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Azido-PEG3-DYKDDDDK TFA
Azido-PEG3-DYKDDDDK TFA
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製品番号: HY-P5112A
別名: Azido-peg3-FLAG TFA
Target:  

Biochemical Assay Reagents

研究分野:  

Others

Azido-PEG3-DYKDDDDK (azide-PEG3-FLAG) TFA is a multifunctional fusion tag for the purification of recombinant proteins. Azido-PEG3-DYKDDDDK TFA 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. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups .
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Azido-PEG3-DYKDDDDK
Azido-PEG3-DYKDDDDK
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製品番号: HY-P5112
CAS 番号: 2243206-95-1
別名: Azido-peg3-FLAG
Target:  

Biochemical Assay Reagents

研究分野:  

Others

Azido-PEG3-DYKDDDDK (azide-PEG3-FLAG) is a multifunctional fusion tag for the purification of recombinant proteins. Azido-PEG3-DYKDDDDK 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. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups .
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RP-182-PEG3-K(palmitic acid)-NH2
RP-182-PEG3-K(palmitic acid)-NH2
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製品番号: HY-169089
Target:  

Drug Derivative

研究分野:  

Cancer

RP-182-PEG3-K palmitic acid-NH2 (Compound 1a) is a fatty acid derivative of the immunomodulatory peptide RP-182. RP-182-PEG3-K palmitic acid-NH2 inhibits CD206 high M2-like macrophage (IC50 of 3.2 μM) and induces phagocytosis. RP-182-PEG3-K palmitic acid-NH2 exhibits antitumor efficacy in mouse B16 melanoma allografts .
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Relsipatide
Relsipatide
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製品番号: HY-P11270
CAS 番号: 2843676-09-3
別名: BGM0504; BG128
Target:  

Insulin Receptor GLP Receptor

研究分野:  

Metabolic Disease

Relsipatide (BG128) is a dual gastric inhibitory polypeptide (GIP) and glucagon-like peptide 1 (GLP-1) receptor agonist. Enicepatide can be studied in antidiabetic research .
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RP-182-PEG3-K(palmitic acid)-NH2 TFA
RP-182-PEG3-K(palmitic acid)-NH2 TFA
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製品番号: HY-169089A
Target:  

Drug Derivative

研究分野:  

Cancer

RP-182-PEG3-K(palmitic acid)-NH2 (Compound 1a) TFA is a fatty acid derivative of the immunomodulatory peptide RP-182. RP-182-PEG3-K(palmitic acid)-NH2 TFA inhibits CD206 high M2-like macrophage (IC50 of 3.2 μM) and induces phagocytosis. RP-182-PEG3-K(palmitic acid)-NH2 TFA exhibits antitumor efficacy in mouse B16 melanoma allografts .
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RI-STAD-2
RI-STAD-2
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製品番号: HY-P10319
Target:  

PKA

研究分野:  

Cardiovascular Disease Cancer

RI-STAD-2 is a high-affinity interfering peptide that regulates the subunit RI of protein kinase A (PKA). RI-STAD-2 interferes with the binding of AKAPs and PKA-RI by simulating the interaction between AKAPs' α-helix domain and PKA-RI's dimerization/anchoration (D/D) domain, thereby affecting PKA activity and intracellular localization. RI-STAD-2 can be used to study the role of AKAPs interaction with PKA-RI in pathological processes such as cardiovascular disease and cancer .
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RI-STAD-2 acetate
RI-STAD-2 acetate
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製品番号: HY-P10319A
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JR11-PEG3-DOTA-PSMA-03
JR11-PEG3-DOTA-PSMA-03
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製品番号: HY-P11488
Target:  

Radionuclide-Drug Conjugates (RDCs) Somatostatin Receptor PSMA

研究分野:  

Cancer

JR11-PEG3-DOTA-PSMA-03 (Compound 2) is an RDC-related compound containing the chelating agent DOTA (HY-W053583), the JR11 peptide (SSTR2 antagonist), and the PSMA ligand. JR11-PEG3-DOTA-PSMA-03 shows SSTR2-binding affinities and PSMA-binding affinities, with IC50 s of 94.0 nM, 81.8 nM, respectively. JR11-PEG3-DOTA-PSMA-03 can be radiolabeled with [ 68Ga]. [ 68Ga] radiolabeled JR11-PEG3-DOTA-PSMA-03 can be used in diagnostic studies of neuroendocrine differentiated prostate cancer .
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JR11-PEG3-HBED-CC-PSMA-03
JR11-PEG3-HBED-CC-PSMA-03
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製品番号: HY-P11485
Target:  

Radionuclide-Drug Conjugates (RDCs) Somatostatin Receptor PSMA

研究分野:  

Cancer

JR11-PEG3-HBED-CC-PSMA-03 (Compound 1) is an RDC-related compound containing the chelating agent HBED-CC, the JR11 peptide (SSTR2 antagonist), and the PSMA ligand. JR11-PEG3-HBED-CC-PSMA-03 shows SSTR2-binding affinities and PSMA-binding affinities, with IC50 s of 59.2 nM, 57.0 nM, respectively. JR11-PEG3-HBED-CC-PSMA-03 can be radiolabeled with [ 68Ga]. [ 68Ga] radiolabeled JR11-PEG3-HBED-CC-PSMA-03 can be used in diagnostic studies of neuroendocrine differentiated prostate cancer .
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Assay Types