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polyamides

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Biochemical Assay Reagents (4) CXCR (2) Drug Derivative (1) Drug Intermediate (6) Drug-Linker Conjugates for ADC (1) Environmental Pollutants (1) Fluorescent Dye (1) Insulin Receptor (1) Isotope-Labeled Compounds (3) Melanocortin Receptor (1) Neuropeptide Y Receptor (2) Parasite (1) Reference Standards (1) Trk Receptor (1)
By Research Areas:	Cancer (8) Metabolic Disease (1) Neurological Disease (3)

Inhibitors & Agonists

Biochemical Assay Reagents

Peptides

Natural
Products

Isotope-Labeled Compounds

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-P4070

Insulin icodec	Insulin Receptor	Metabolic Disease
Insulin icodec is an Insulin (HY-P0035) analog that strongly but reversibly binds to albumin. Insulin icodec has long plasma half-life. Insulin icodec modulates insulin receptor activity, controls blood glucose levels, reduces HbA_1c levels, and binds reversibly to human serum albumin. Insulin icodec can be used for the research of type 2 diabetes mellitus .

HY-153263

(Aminooxy)acetamide-Val-Cit-PAB-MMAE	Drug-Linker Conjugates for ADC	Cancer
(Aminooxy)acetamide-Val-Cit-PAB-MMAE (MMAE 5) is an intermediate used in the synthetic preparation of drug-linker conjugates for ADC. (Aminooxy)acetamide-Val-Cit-PAB-MMAE is conjugated to polyamide via oxime bond formation to form MMAE polyamide conjugate. Then MMAE polyamide conjugate can be conjugated to Trastuzumab, to make ADC .

HY-W007656

Cyclen	Biochemical Assay Reagents	Others
Cyclen is a macrocyclic tetraamine chelating agent. Cyclen is the aza analogue of crown ether, used as a precursor for MRI contrast agents, and is an intermediate for the preparation of effective macrocyclic chelates. Cyclen is employed as a structural regulator through interfacial polymerization of polyethleneimine (PEI) and trimesoyl chloride (TMC) to develop polyamide NF membrane with efficient Li ⁺/Mg ²⁺ separation performance. Cyclen has specific cavity structure and exhibits selective coordination properties for Li ⁺ ions ^[1][2].

HY-59137

1-Methylimidazole	Drug Intermediate	Cancer
1-Methylimidazole acts as a membrane performance regulator that promotes the formation of reverse osmosis membranes with a dense ultra-thin polyamide layer. Such membranes exhibit higher flux and salt rejection rate, while also conferring excellent pH stability to the membrane. 1-Methylimidazole can serve as a ligand for ruthenium (II) complexes to construct metal-based anticancer agents .

HY-P1103

CTCE-9908 1 Publications Verification	CXCR	Cancer
CTCE-9908 is a potent and selective CXCR4 antagonist. CTCE-9908 induces mitotic catastrophe, cytotoxicity and inhibits migration in CXCR4-expressing ovarian cancer cells .

HY-W144037

Valeramide Pentanimidic acid	Biochemical Assay Reagents	Others
Valeramide (Pentanimidic acid) is an important raw material for organic synthesis, which is produced by ammonolysis of Caproamide. Valeramide can be used to make polyamides, amide resins, preservatives and nylon fibers .

HY-W008721

4,4'-Biphthalic anhydride	Biochemical Assay Reagents	Others
4,4'-Biphthalic anhydride (BPDA) is a rigid symmetrical polyamide used in the production of high-performance polymers, such as polyimide products and their composites .

HY-W110905

Naphthol green B	Environmental Pollutants Fluorescent Dye	Others
Naphthol green B is an iron-complex dye. Naphthol green B can be used in wool dyeing, silk dyeing and polyamide dyeing. Naphthol green B can be used to fabricate electrochemical sensor for the detection of H₂O₂ .

HY-59137S

1-Methylimidazole-d6	Isotope-Labeled Compounds Drug Intermediate	Cancer
1-Methylimidazole-d₆ is the deuterium labeled 1-Methylimidazole. 1-Methylimidazole acts as a membrane performance regulator that promotes the formation of reverse osmosis membranes with a dense ultra-thin polyamide layer. Such membranes exhibit higher flux and salt rejection rate, while also conferring excellent pH stability to the membrane. 1-Methylimidazole can serve as a ligand for ruthenium (II) complexes to construct metal-based anticancer agents.

HY-N15601

Dermocybin NSC 257450	Biochemical Assay Reagents	Others
Dermocybin (NSC 257450) is a natural anthraquinone isolated from the fungus Derniocybe sarzgiiirzea. Dermocybin can be used as a high-temperature disperse dye for polyester and polyamide fabrics .

HY-P1103A

CTCE-9908 TFA	CXCR	Cancer
CTCE-9908 TFA is a potent and selective CXCR4 antagonist. CTCE-9908 TFA induces mitotic catastrophe, cytotoxicity and inhibits migration in CXCR4-expressing ovarian cancer cells .

HY-P4757

N1-Glutathionyl-spermidine disulfide	Parasite	Others
N1-Glutathionyl-spermidine disulfide is a substrate of trypanothione reductase .

HY-P11293

DOTA-GGNle-CycMSHhex	Melanocortin Receptor	Cancer
DOTA-GGNle-CycMSHhex is a melanocortin-1 receptor (MC1R)-targeting peptide that can be radionuclide-labeled for melanoma imaging .

HY-P1321

GR231118 1229U91; GW1229	Neuropeptide Y Receptor	Neurological Disease
GR231118, an analogue of the C-terminus of neuropeptide Y, is a potent , competitive and relative seletive antagonist at human neuropeptide Y Y receptor with a pK_i of 10.4. GR231118 a potent agonist at the human neuropeptide Y Y4 receptor (pEC₅₀=8.6; pK_i=9.6) and a weak agonist at the human and rat neuropeptide YY2 and Y5 receptors. GR231118 also has high affinity for the mouse neuropeptide Y Y6 receptor (pK_i= 8.8) .

HY-59137S1

1-Methyl-imidazole-d3	Isotope-Labeled Compounds Drug Intermediate	Cancer
1-Methylimidazole-d₃ is the deuterium labeled 1-Methylimidazole. 1-Methylimidazole acts as a membrane performance regulator that promotes the formation of reverse osmosis membranes with a dense ultra-thin polyamide layer. Such membranes exhibit higher flux and salt rejection rate, while also conferring excellent pH stability to the membrane. 1-Methylimidazole can serve as a ligand for ruthenium (II) complexes to construct metal-based anticancer agents.

HY-59137S2

1-Methylimidazole-d3-1	Isotope-Labeled Compounds Drug Intermediate	Cancer
1-Methylimidazole-d₃-1 is the deuterium labeled 1-Methylimidazole. 1-Methylimidazole acts as a membrane performance regulator that promotes the formation of reverse osmosis membranes with a dense ultra-thin polyamide layer. Such membranes exhibit higher flux and salt rejection rate, while also conferring excellent pH stability to the membrane. 1-Methylimidazole can serve as a ligand for ruthenium (II) complexes to construct metal-based anticancer agents.

HY-P1321A

GR231118 TFA 1229U91 TFA; GW1229 TFA	Neuropeptide Y Receptor	Neurological Disease
GR231118 TFA, an analogue of the C-terminus of neuropeptide Y, is a potent , competitive and relative seletive antagonist at human neuropeptide YY receptor with a pK_i of 10.4. GR231118 a potent agonist at the human neuropeptide YY4 receptor (pEC₅₀=8.6; pK_i=9.6) and a weak agonist at the human and rat neuropeptide Y Y2 and Y5 receptors. GR231118 also has high affinity for the mouse neuropeptide YY6 receptor (pK_i= 8.8) .

HY-W424255

Fmoc-Aeg-OMe	Drug Intermediate	Others
Fmoc-Aeg-OMe is a methyl ester derivative of Fmoc-protected aminoethylglycine and can be used fo polyamide nucleic acid synthesis .

HY-P11693

Fmoc-Aeg-OMe hydrochloride	Drug Intermediate	Others
Fmoc-Aeg-OMe hydrochloride is a methyl ester derivative of Fmoc-protected aminoethylglycine and can be used fo polyamide nucleic acid synthesis .

HY-N17577

Salicyloylsalicin	Drug Derivative	Others
Salicyloylsalicin is a salicylic acid glycoside natural product present in the bark of Populus balsamifera .

HY-W007656R

Cyclen (Standard)	Reference Standards	Others
Cyclen (Standard) is the analytical standard substance of Cyclen. This product is used for research and analytical applications. Cyclen is a macrocyclic tetrathiolate chelating agent. Cyclen is a nitrogen-containing analogue of crown ethers and can be used as a precursor for MRI contrast agents, as well as an intermediate for preparing highly efficient macrocyclic chelates. As a structural regulator, Cyclen can be prepared into polyamide nanofiltration membranes with efficient Li ⁺/Mg ²⁺ separation performance through the interfacial polymerization of polyethyleneimine (PEI) and meta-benzotriazole chloride (TMC). Cyclen has a unique cavity structure and exhibits selective coordination properties for Li ⁺ ions .

HY-P11480

TrkA/NGF-IN-1	Trk Receptor	Neurological Disease
TrkA/NGF-IN-1 (Peptide 19) is an inhibitor of protein-protein interactions between TrkA and NGF (IC₅₀: 21 nM for human TrkA in PathHunter assay). TrkA/NGF-IN-1 shows an analgesic effect in a rat incisional pain model .

4,4'-Biphthalic anhydride	Biochemical Assay Reagents
4,4'-Biphthalic anhydride (BPDA) is a rigid symmetrical polyamide used in the production of high-performance polymers, such as polyimide products and their composites .

Cat. No.	Product Name	Target	Research Area

HY-P4070

Insulin icodec	Insulin Receptor	Metabolic Disease
Insulin icodec is an Insulin (HY-P0035) analog that strongly but reversibly binds to albumin. Insulin icodec has long plasma half-life. Insulin icodec modulates insulin receptor activity, controls blood glucose levels, reduces HbA_1c levels, and binds reversibly to human serum albumin. Insulin icodec can be used for the research of type 2 diabetes mellitus .

HY-P1103

CTCE-9908 1 Publications Verification	CXCR	Cancer
CTCE-9908 is a potent and selective CXCR4 antagonist. CTCE-9908 induces mitotic catastrophe, cytotoxicity and inhibits migration in CXCR4-expressing ovarian cancer cells .

HY-P1103A

CTCE-9908 TFA	CXCR	Cancer
CTCE-9908 TFA is a potent and selective CXCR4 antagonist. CTCE-9908 TFA induces mitotic catastrophe, cytotoxicity and inhibits migration in CXCR4-expressing ovarian cancer cells .

HY-P4757

N1-Glutathionyl-spermidine disulfide	Parasite	Others
N1-Glutathionyl-spermidine disulfide is a substrate of trypanothione reductase .

HY-P11293

DOTA-GGNle-CycMSHhex	Melanocortin Receptor	Cancer
DOTA-GGNle-CycMSHhex is a melanocortin-1 receptor (MC1R)-targeting peptide that can be radionuclide-labeled for melanoma imaging .

HY-P1321

GR231118 1229U91; GW1229	Neuropeptide Y Receptor	Neurological Disease
GR231118, an analogue of the C-terminus of neuropeptide Y, is a potent , competitive and relative seletive antagonist at human neuropeptide Y Y receptor with a pK_i of 10.4. GR231118 a potent agonist at the human neuropeptide Y Y4 receptor (pEC₅₀=8.6; pK_i=9.6) and a weak agonist at the human and rat neuropeptide YY2 and Y5 receptors. GR231118 also has high affinity for the mouse neuropeptide Y Y6 receptor (pK_i= 8.8) .

HY-P1321A

GR231118 TFA 1229U91 TFA; GW1229 TFA	Neuropeptide Y Receptor	Neurological Disease
GR231118 TFA, an analogue of the C-terminus of neuropeptide Y, is a potent , competitive and relative seletive antagonist at human neuropeptide YY receptor with a pK_i of 10.4. GR231118 a potent agonist at the human neuropeptide YY4 receptor (pEC₅₀=8.6; pK_i=9.6) and a weak agonist at the human and rat neuropeptide Y Y2 and Y5 receptors. GR231118 also has high affinity for the mouse neuropeptide YY6 receptor (pK_i= 8.8) .

HY-W424255

Fmoc-Aeg-OMe	Drug Intermediate	Others
Fmoc-Aeg-OMe is a methyl ester derivative of Fmoc-protected aminoethylglycine and can be used fo polyamide nucleic acid synthesis .

HY-P11693

Fmoc-Aeg-OMe hydrochloride	Drug Intermediate	Others
Fmoc-Aeg-OMe hydrochloride is a methyl ester derivative of Fmoc-protected aminoethylglycine and can be used fo polyamide nucleic acid synthesis .

HY-P11480

TrkA/NGF-IN-1	Trk Receptor	Neurological Disease
TrkA/NGF-IN-1 (Peptide 19) is an inhibitor of protein-protein interactions between TrkA and NGF (IC₅₀: 21 nM for human TrkA in PathHunter assay). TrkA/NGF-IN-1 shows an analgesic effect in a rat incisional pain model .

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-W007656

Cyclen	Structural Classification Natural Products Classification of Application Fields Other Diseases Plants Menispermaceae Disease Research Fields Stephania japonica (Thunb.) Miers Source Classification	Biochemical Assay Reagents
Cyclen is a macrocyclic tetraamine chelating agent. Cyclen is the aza analogue of crown ether, used as a precursor for MRI contrast agents, and is an intermediate for the preparation of effective macrocyclic chelates. Cyclen is employed as a structural regulator through interfacial polymerization of polyethleneimine (PEI) and trimesoyl chloride (TMC) to develop polyamide NF membrane with efficient Li ⁺/Mg ²⁺ separation performance. Cyclen has specific cavity structure and exhibits selective coordination properties for Li ⁺ ions ^[1][2].

HY-N15601

Dermocybin NSC 257450	Quinones Microorganisms Anthraquinones Source Classification	Biochemical Assay Reagents
Dermocybin (NSC 257450) is a natural anthraquinone isolated from the fungus Derniocybe sarzgiiirzea. Dermocybin can be used as a high-temperature disperse dye for polyester and polyamide fabrics .

HY-N17577

Salicyloylsalicin	Glycosmis parviflora Kurz. Structural Classification Monophenols Phenols Plants Salicaceae Source Classification	Drug Derivative
Salicyloylsalicin is a salicylic acid glycoside natural product present in the bark of Populus balsamifera .

HY-W007656R

Cyclen (Standard)	Structural Classification Natural Products Plants Menispermaceae Stephania japonica (Thunb.) Miers Source Classification	Reference Standards
Cyclen (Standard) is the analytical standard substance of Cyclen. This product is used for research and analytical applications. Cyclen is a macrocyclic tetrathiolate chelating agent. Cyclen is a nitrogen-containing analogue of crown ethers and can be used as a precursor for MRI contrast agents, as well as an intermediate for preparing highly efficient macrocyclic chelates. As a structural regulator, Cyclen can be prepared into polyamide nanofiltration membranes with efficient Li ⁺/Mg ²⁺ separation performance through the interfacial polymerization of polyethyleneimine (PEI) and meta-benzotriazole chloride (TMC). Cyclen has a unique cavity structure and exhibits selective coordination properties for Li ⁺ ions .

Cat. No.	Product Name	Chemical Structure

HY-59137S

1-Methylimidazole-d6
1-Methylimidazole-d₆ is the deuterium labeled 1-Methylimidazole. 1-Methylimidazole acts as a membrane performance regulator that promotes the formation of reverse osmosis membranes with a dense ultra-thin polyamide layer. Such membranes exhibit higher flux and salt rejection rate, while also conferring excellent pH stability to the membrane. 1-Methylimidazole can serve as a ligand for ruthenium (II) complexes to construct metal-based anticancer agents.

1-Methylimidazole-d6

1-Methylimidazole-d₆ is the deuterium labeled 1-Methylimidazole. 1-Methylimidazole acts as a membrane performance regulator that promotes the formation of reverse osmosis membranes with a dense ultra-thin polyamide layer. Such membranes exhibit higher flux and salt rejection rate, while also conferring excellent pH stability to the membrane. 1-Methylimidazole can serve as a ligand for ruthenium (II) complexes to construct metal-based anticancer agents.

HY-59137S1

1-Methyl-imidazole-d3
1-Methylimidazole-d₃ is the deuterium labeled 1-Methylimidazole. 1-Methylimidazole acts as a membrane performance regulator that promotes the formation of reverse osmosis membranes with a dense ultra-thin polyamide layer. Such membranes exhibit higher flux and salt rejection rate, while also conferring excellent pH stability to the membrane. 1-Methylimidazole can serve as a ligand for ruthenium (II) complexes to construct metal-based anticancer agents.

1-Methyl-imidazole-d3

1-Methylimidazole-d₃ is the deuterium labeled 1-Methylimidazole. 1-Methylimidazole acts as a membrane performance regulator that promotes the formation of reverse osmosis membranes with a dense ultra-thin polyamide layer. Such membranes exhibit higher flux and salt rejection rate, while also conferring excellent pH stability to the membrane. 1-Methylimidazole can serve as a ligand for ruthenium (II) complexes to construct metal-based anticancer agents.

HY-59137S2

1-Methylimidazole-d3-1
1-Methylimidazole-d₃-1 is the deuterium labeled 1-Methylimidazole. 1-Methylimidazole acts as a membrane performance regulator that promotes the formation of reverse osmosis membranes with a dense ultra-thin polyamide layer. Such membranes exhibit higher flux and salt rejection rate, while also conferring excellent pH stability to the membrane. 1-Methylimidazole can serve as a ligand for ruthenium (II) complexes to construct metal-based anticancer agents.

1-Methylimidazole-d3-1

1-Methylimidazole-d₃-1 is the deuterium labeled 1-Methylimidazole. 1-Methylimidazole acts as a membrane performance regulator that promotes the formation of reverse osmosis membranes with a dense ultra-thin polyamide layer. Such membranes exhibit higher flux and salt rejection rate, while also conferring excellent pH stability to the membrane. 1-Methylimidazole can serve as a ligand for ruthenium (II) complexes to construct metal-based anticancer agents.

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polyamides

Inhibitors & Agonists

Biochemical Assay Reagents

Peptides

NaturalProducts

Isotope-Labeled Compounds

Natural
Products