11 Results for "

mPEG3400-SH

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "mPEG3400-SH" in MCE Product Catalog:

Azido-PEG3-DYKDDDDK TFA
Azido-PEG3-DYKDDDDK TFA
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Referencia número: HY-P5112A
Synonyms: Azido-PEG3-FLAG TFA
Target:  

Biochemical Assay Reagents

Áreas de investigación:  

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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Palopegteriparatide
Palopegteriparatide
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Referencia número: HY-P10277
No. CAS: 2222514-07-8
Synonyms: Transcon PTH; ACP-014
Target:  

Peptides

Áreas de investigación:  

Endocrinology

Palopegteriparatide (Transcon PTH) is a prodrug of parathyroid hormone PTH 1-34, which can maintain normal and stable calcium concentrations without the need for calcium and active vitamin D replacement. Palopegteriparatide can be used in research on hypoparathyroidism .
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m-PEG3400-thiol
m-PEG3400-thiol
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Referencia número: HY-W591476A
No. CAS: 134874-49-0
Synonyms: mPEG3400-SH
m-PEG3400-thiol modifies DNA thiolation for the synthesis of gold nanorods (AuNRs). Thiolated DNA can be loaded onto AuNR by the mPEG-SH/Tween 20 assisted method (Tween 20 and mPEG-SH repeatedly displace CTAB on the AuNR surface). DNA AuNRs have been widely used in nanostructure assembly, gene therapy, biosensing, and drug delivery.
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Azido-PEG3-DYKDDDDK
Azido-PEG3-DYKDDDDK
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Referencia número: HY-P5112
No. CAS: 2243206-95-1
Synonyms: Azido-PEG3-FLAG
Target:  

Biochemical Assay Reagents

Áreas de investigación:  

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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Referencia número: HY-169089
Target:  

Drug Derivative

Áreas de investigación:  

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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Referencia número: HY-P11270
No. CAS: 2843676-09-3
Synonyms: BGM0504; BG128
Target:  

Insulin Receptor GLP Receptor

Áreas de investigación:  

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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Referencia número: HY-169089A
Target:  

Drug Derivative

Áreas de investigación:  

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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Referencia número: HY-P10319
Target:  

PKA

Áreas de investigación:  

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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Referencia número: HY-P10319A
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JR11-PEG3-DOTA-PSMA-03
JR11-PEG3-DOTA-PSMA-03
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Referencia número: HY-P11488
Target:  

Radionuclide-Drug Conjugates (RDCs) Somatostatin Receptor PSMA

Áreas de investigación:  

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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Referencia número: HY-P11485
Target:  

Radionuclide-Drug Conjugates (RDCs) Somatostatin Receptor PSMA

Áreas de investigación:  

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