755 Results for "

ether

" in MedChemExpress (MCE) Product Catalog:
Products (755)

755 Results for "ether" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-125861B
CAS No.: 9004-67-5
Synonyms: MC(Viscosity:400mPa.s)
Methyl cellulose (MC) (Viscosity:400mPa.s) is a non-ionic cellulose ether with surface activity and thermogelation properties. Methyl cellulose (Viscosity:400mPa.s) is widely used as drug delivery agents, thickeners, stabilizers, emulsifiers, etc., in industries such as pharmaceuticals, food, cosmetics, and construction .
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2 Cited Publications
Cat. No.: HY-125861C
CAS No.: 9004-67-5
Synonyms: MC(Viscosity:1500mPa.s)
Methyl cellulose (MC) (Viscosity:1500mPa.s) is a non-ionic cellulose ether with surface activity and thermogelation properties. Methyl cellulose (Viscosity:1500mPa.s) is widely used as drug delivery agents, thickeners, stabilizers, emulsifiers, etc., in industries such as pharmaceuticals, food, cosmetics, and construction .
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2 Cited Publications
Cat. No.: HY-125861D
CAS No.: 9004-67-5
Purity:  ≥98.0%
Synonyms: MC(Viscosity:40000mPa.s)
Methyl cellulose (MC) (Viscosity:40000mPa.s) is a non-ionic cellulose ether with surface activity and thermogelation properties. Methyl cellulose (Viscosity:40000mPa.s) is widely used as drug delivery agents, thickeners, stabilizers, emulsifiers, etc., in industries such as pharmaceuticals, food, cosmetics, and construction .
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2 Cited Publications
Cat. No.: HY-126885
CAS No.: 2144395-59-3
Purity:  95.06%
Research Areas:  

Cancer

DBCO-PEG5-NHS ester is a PEG/Alkyl/ether-based PROTAC linker can be used in the synthesis of PROTACs. DBCO-PEG5-NHS ester is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . DBCO-PEG5-NHS ester is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.
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2 Cited Publications
Cat. No.: HY-111997
CAS No.: 1799506-07-2
Purity:  96.49%
Synonyms: HaloPROTAC 3
Research Areas:  

Others

VH285-PEG4-C4-Cl (HaloPROTAC 3) is a conjugate of ligands for E3 and 16-atom-length linker. The connector of linker is Halogen group. VH285-PEG4-C4-Cl incorporates the VH285 based VHL ligand and an alkyl/ether-based linker. VH285-PEG4-C4-Cl is a highly potent and efficacious degrader of GFP-HaloTag7 with a DC50 of 19 nM. VH285-PEG4-C4-Cl is able to induce 90 % degradation of GFP-Halotag at 625 nM. VH285-PEG4-C4-Cl binds to VHL with an IC50 of 0.54 μM .
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1 Cited Publications
Cat. No.: HY-N2411
CAS No.: 60314-89-8
Geissoschizine methyl ether is an orally active, blood-brain barrier permeable alkaloid, and a partial agonist of the 5-HT1A receptor. It can be isolated from Uncaria hook. Geissoschizine methyl ether potently inhibits the binding of [ 3H]8-OH-DPAT to the 5-HT1A receptor in a concentration-dependent manner, with an IC50 of 0.904 μM. It ameliorates isolation-induced increased aggression and reduced sociability in mice. Geissoschizine methyl ether promotes oligodendrocyte differentiation and remyelination in the medial prefrontal cortex of adult mice .
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1 Cited Publications
Cat. No.: HY-N1956
CAS No.: 7460-43-7
Rubiadin-1-methyl ether is an orally potent NF-κB p65 inhibitor and autophagy inhibitor. Rubiadin-1-methyl ether inhibits RANKL-induced phosphorylation and nuclear translocation of p65, suppresses BECN1 transcription, blocks LC3 conversion and autophagosome formation, thereby reducing the levels of BECN1 mRNA and Beclin1 protein. Rubiadin-1-methyl ether inhibits osteoclastogenesis, cell proliferation, macrophage M2 polarization and the TGF-β1 signaling pathway, and effectively alleviates pulmonary inflammation. Rubiadin-1-methyl ether is widely used in research on osteoporosis, pulmonary fibrosis, idiopathic pulmonary fibrosis, acute lung injury and other related diseases .
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1 Cited Publications
Cat. No.: HY-111911
CAS No.: 4464-33-9
Purity:  98.91%
Xanthocillin X permethyl ether is a natural compound isolated from fungal extracts, with Aβ-42 lowering activity .
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1 Cited Publications
Cat. No.: HY-D0145
CAS No.: 5725-91-7
Synonyms: Resorufin ethyl ether
7-Ethoxyresorufin (Resorufin ethyl ether) is a fluorometric substrate and competitive inhibitor of cytochrome P450, especially CYP1A1. 7-Ethoxyresorufin also inhibits NO synthase .
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1 Cited Publications
Cat. No.: HY-A0272
CAS No.: 9004-82-4
Synonyms: Sodium lauryl polyoxyethylene ether sulfate
Sodium laureth sulfate (70% in water) (Sodium lauryl polyoxyethylene ether sulfate) is an anionic active agent with excellent decontamination, emulsification, dispersion, wetting, antifungal and other properties .
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1 Cited Publications
Cat. No.: HY-N7150
CAS No.: 18103-42-9
Synonyms: 5,7-Dihydroxy-3',4',5'-trimethoxyflavone
Tricetin 3',4',5'-trimethyl ether (5,7-Dihydroxy-3',4',5'-trimethoxyflavone) is a flavone glucoside, that can be isolated the flowers of Chrysanthemum sinensea. Tricetin 3',4',5'-trimethyl ether displays xanthine oxidase competitive-type inhibitory activity, with an IC50 of 0.51 μM and a Ki of 0.37 μM .
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1 Cited Publications
Cat. No.: HY-N4167
CAS No.: 6665-74-3
Synonyms: Galangin 3-methyl ether; 3-Methylgalangin
3-O-Methylgalangin (Galangin 3-methyl ether) is a natural flavonoid compound from the rhizome of Alpinia officinarum (AO) with antibacterial activities, which also inhibits pancreatic lipase .
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1 Cited Publications
Cat. No.: HY-N7641
CAS No.: 6068-80-0
Synonyms: Quercetin 3′,4′,7-trimethyl ether
3',4',7-Trimethoxyquercetin (Quercetin 3′,4′,7-trimethyl ether) is a polymethoxyflavonoid that can be isolated from Taraxacum mongolicum. 3',4',7-Trimethoxyquercetin is also a derivative of Quercetin hydrate (HY-18085A). 3',4',7-Trimethoxyquercetin has anti-tumor activity .
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1 Cited Publications
Cat. No.: HY-148100
CAS No.: 1390630-22-4
Synonyms: NOX-E36
Target:  

CCR

Research Areas:  

Inflammation/Immunology Cancer

Emapticap pegol (NOX-E36) is a inhibitor of pro-inflammatory chemokine C-C motif-ligand 2 (CCL2). Emapticap pegol is a 40-nucleotide pegylated aptamer, displays different Spiegelmers (L-RNA aptamer) isform in human (NOX-E36) and mouse (mNOX-E36). mNOX-E36 is a murine-specific analogue of NOX-E36, an anti-MCP-1 L-RNA aptamer that was previously shown to attenuate liver fibrosis in mice .
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1 Cited Publications
Cat. No.: HY-B2221B1
CAS No.: 9004-62-0
Research Areas:  

Others

Hydroxyethyl cellulose, Viscosity(2%):150mPa.s is a class of nonionic cellulose ether gel-forming polymers with pH-independent drug release properties. When used as a tablet coating, Hydroxyethyl cellulose, Viscosity(2%):150mPa.s regulates the water permeation rate, thereby altering the drug release lag time; the higher the viscosity, the longer the drug release lag time. When used as a hydrogel thickener, it increases the dynamic viscosity of the system. Hydroxyethyl cellulose, Viscosity(2%):150mPa.s can be used in organic synthesis-related research, such as pharmaceutical excipients, hydrogel thickeners, etc.
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1 Cited Publications
Cat. No.: HY-110398
CAS No.: 973-67-1
Purity:  98.02%
Synonyms: Baicalein trimethyl ether
5,6,7-Trimethoxyflavone is a flavonoid compound that can be isolated from plants Callicarpa japonica. 5,6,7-Trimethoxyflavone exhibits antiviral and anti-inflammatory activities through inhibition of NF-κB/AP-1/STAT signaling pathway .
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1 Cited Publications
Cat. No.: HY-N8259
CAS No.: 83864-78-2
Obovatol is a biphenyl ether lignan isolated from the leaves of Magnolia obovata Thunb .
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1
1 Cited Publications
Cat. No.: HY-136159
CAS No.: 117235-10-6
Purity:  ≥95.0%
Target:  

PROTAC Linkers

Research Areas:  

Cancer

3-Mercaptopropanyl-N-hydroxysuccinimide ester is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs .
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1
1 Cited Publications
Cat. No.: HY-15254
CAS No.: 163018-26-6
Purity:  98.46%
Synonyms: 25-Hydroxy Vitamin D3 3,3’-Aminopropyl ether
Target:  

VD/VDR

Research Areas:  

Metabolic Disease

3-O-(2-Aminoethyl)-25-hydroxyvitamin D3 is a Vitamin D3 derivative.
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1 Cited Publications
Cat. No.: HY-16916
CAS No.: 448895-37-2
Research Areas:  

Cancer

NS1643 is a partial agonist of human ether-a-go-go-related gene (hERG) K + channels with an EC50 of 10.5 μM. NS1643 inhibits the growth of breast cancer tumors in TNBC mouse models. NS1643 inhibits cell migration and invasion of breast cancer cells .
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