26 Results for "

morpholine

" in MedChemExpress (MCE) Product Catalog:
Products (26)

26 Results for "morpholine" in MCE Product Catalog:

Cat. No.: HY-147090
CAS No.: 2750350-39-9
Purity:  99.06%
Tazemetostat de(methylene morpholine)-O-C3-O-C-COOH (Compound 21b) incorporates a ligand for EZH2, and a PROTAC linker, which recruit E3 ligases. Tazemetostat de(methylene morpholine)-O-C3-O-C-COOH (Compound 21b) can be used for the research of lymphoma .
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Cat. No.: HY-147091
CAS No.: 2685873-44-1
Purity:  98.15%
Research Areas:  

Cancer

Tazemetostat de(methyl morpholine)-COOH (compound 7) is a ligand for the PROTAC target protein EZH2, which can be used to synthesis of EZH2 degraders (PROTACs). EZH2 degraders have potent cell viability inhibition in diffuse large B-cell lymphoma (DLBCL) and other subtypes of lymphoma .
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Cat. No.: HY-B0846
CAS No.: 110488-70-5
Dimethomorph is a fungicide belongs to the fungicide group of sterol biosynthesis inhibitor. Dimethomorph can inhibit fungal cell wall formation. Dimethomorph also inhibits androgen receptor (AR) activity in MDA-kb2 cells with an IC20 of 0.263 µM .
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Cat. No.: HY-W007359
CAS No.: 123-90-0
Thiomorpholine is an analogue of morpholine, can be used in various applications including synthesis .
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Cat. No.: HY-76877
CAS No.: 132833-51-3
Target:  

Drug Intermediate

Research Areas:  

Others

4-(4-Bromobenzyl)morpholine is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-107840
CAS No.: 6497-78-5
Purity:  98.78%
Target:  

Drug Derivative

Research Areas:  

Others

RGW 611 is a morpholine derivative that enhances radiation-induced cell death of hypoxic V79-379A cells. RGW 611 also stimulates fatty acid synthesis .
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Cat. No.: HY-W015887R
CAS No.: 4394-85-8
Synonyms: N-Formylmorpholine (Standard)
Target:  

Reference Standards

Morpholine-4-carbaldehyde (Standard) is the analytical standard of Morpholine-4-carbaldehyde. This product is intended for research and analytical applications.
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Cat. No.: HY-154839
CAS No.: 2299227-75-9
Target:  

c-Myc

Research Areas:  

Cancer

c-Myc inhibitor 10 (compound 17), a c-Myc inhibitor, exhibits increased cellular potency, consistent with an increase in permeability with methylation of the morpholine nitrogen .
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Cat. No.: HY-17653
CAS No.: 2243974-80-1
Target:  

Drug Intermediate

Research Areas:  

Others

Morpholino A phosphoramidite is a specialized chemical building block used to synthesize Phosphorodiamidate Morpholino Oligomers (PMOs). Morpholino A phosphoramidite contains the adenine (A) nucleobase attached to a morpholine ring, fitted with a phosphoramidite group. PMOs are synthetic gene knockdown tools heavily used in developmental biology and targeted therapeutics to inhibit gene expression or alter RNA splicing .
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Cat. No.: HY-172333
Target:  

Fluorescent Dye

Research Areas:  

Others

HCy-Lyso is a lysosome-targeting turn-on fluorescent probe based on hydrocyanine. HCy-Lyso integrates a hydrocyanine moiety for selective recognition of hydroxyl radicals (•OH) and a morpholine group for lysosome targeting. Upon reacting with •OH, HCy-Lyso undergoes an extension of its π-conjugation system, producing a strong fluorescence signal at 598 nm when excited at 510 nm .
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Cat. No.: HY-176563
CAS No.: 2227349-05-3
Target:  

ADC Linkers

Research Areas:  

Cancer

Di(4-morpholine-amide)-4-DTM-phenoxy(3,5-F)-PEG4-CH2COOH (compound BL) is a cleavable PEG-based ADC linker that can be used in the synthesis of antibody-drug conjugates (ADCs) .
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Cat. No.: HY-161836
Target:  

Adrenergic Receptor

Research Areas:  

Cardiovascular Disease

α2AR agonist 1 (compound S6a), a new morpholine-containing pyrimidinone, acts as an agonist of α2-adrenoceptor. α2AR agonist 1 induces a concentration-dependent relaxation on aortic ring pre-contracted with Phenylephrine (HY-B0769; pEC50=6.81). α2AR agonist 1 increases NOx and NO levels in HUVECs .
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Cat. No.: HY-W766136
Synonyms: 2-(R)-[1-(R)-(3,5-Bis(trifluoromethyl)phenyl)ethoxy]-3-(S)-fluorophenyl-4-[(2-N-methoxycarbonyl)acetamidrazono]morpholine-13C2,d2
Aprepitant Impurity 9- 13C2,d2 (2-(R)-[1-(R)-(3,5-Bis(trifluoromethyl)phenyl)ethoxy]-3-(S)-fluorophenyl-4-[(2-N-methoxycarbonyl)acetamidrazono]morpholine- 13C2,d2) is the deuterium labeled and 13C-labeled Aprepitant Impurity 9 (HY-Z11099).
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Cat. No.: HY-B0846R
CAS No.: 110488-70-5
Dimethomorph (Standard) is the analytical standard of Dimethomorph. This product is intended for research and analytical applications. Dimethomorph is a fungicide belongs to the fungicide group of sterol biosynthesis inhibitor. Dimethomorph can inhibit fungal cell wall formation. Dimethomorph also inhibits androgen receptor (AR) activity in MDA-kb2 cells with an IC20 of 0.263 µM .
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Cat. No.: HY-W723905
CAS No.: 1219804-24-6
Morpholine-4-carbonyl-d8 chloride is the deuterium labeled Morpholine-4-carbonyl chloride.
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Cat. No.: HY-N16306
CAS No.: 3091879-73-8
Category:  

Lipids

Target:  

Fluorescent Dye

Lyso-laurdan, a derivative of Laurdan (HY-D0080), is a fluorescent probe. Lyso-Laurdan accumulates in the lysosome via a morpholine group that is entrapped in lysosome via protonation to its cationic form in the acidic compartment. Lyso-laurdan is localized to lysosomes, allowing for the study of lysosomal membranes .
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Cat. No.: HY-149018
CAS No.: 2969213-59-8
Research Areas:  

Cancer

ATX inhibitor 22 is a novel inhibitor of ATX (autotaxin) with IC50 of 218 nM but lost its inhibitory activity of LPAR1 .
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Cat. No.: HY-W175598
CAS No.: 5625-90-1
Synonyms: N,N'-Methylene-bis-morpholine
Research Areas:  

Infection

Bis(4-morpholinyl)methane (N,N'-Methylene-bis-morpholine) is a broad-spectrum, slow-release formaldehyde-based fungicide. Bis(4-morpholinyl)methane inhibits the growth and reproduction of microorganisms, and prevents spoilage and odor generation in humid environments. Bis(4-morpholinyl)methane serves as a preservative for natural rubber latex .
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Cat. No.: HY-134096
CAS No.: 78323-98-5
Synonyms: DNS-M
Target:  

Fluorescent Dye

Research Areas:  

Others

Dansyl-morpholine (DNS-M) is a Fluorescent probe for lipid droplet imaging, cancer cell discrimination, and real-time tracking of lipid droplet dynamics. As a solvatochromic probe with a donor-π-acceptor structure, it relies on hydrophobic interaction for its mechanism of action: its good lipophilicity, confirmed by an oil-water partition coefficient LogP = 2.35, allows it to rapidly penetrate cell membranes, and it specifically localizes to the hydrophobic core of lipid droplets; its fluorescence is strongly enhanced in the nonpolar environment of lipid droplets, while it emits very weak fluorescence in polar environments like PBS buffer, and it exhibits a bathochromic shift in emission wavelength with increasing solvent polarity. It has negligible cytotoxicity, with cell viability remaining over 95% after 24-hour incubation with 100 μM of the probe, and it possesses excellent photostability, retaining over 97% of initial fluorescence intensity after 60 continuous laser scans. For cell imaging applications, its excitation/emission wavelengths for lipid droplet labeling are Ex/Em = 405/480−540 nm, and in a simulative lipid environment O/W emulsion, it has an excitation wavelength of ~346 nm and emission wavelength of ~500 nm, giving a Stokes shift of 154 nm[1].
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Cat. No.: HY-D3112
Target:  

Fluorescent Dye

Research Areas:  

Neurological Disease

P2-Aggregate is a polarity-sensitive fluorescent probe for protein aggregation, which is based on the Nile Red scaffold and modified with a morpholine ring to enhance water solubility. P2-Aggregate improves anti-precipitation ability in aqueous phase via morpholine ring modification, and enables site-specific labeling of target proteins by combining with HaloTag technology. Utilizing the property that its emission wavelength blue-shifts with decreasing local polarity (excited at 543 nm), P2-Aggregate quantitatively detects changes in local polarity during protein aggregation and polarity heterogeneity inside aggregates in living cells. P2-Aggregate can be used in the research of diseases associated with the aggregation of Htt-110Q and SOD1 proteins, such as Huntington's disease and amyotrophic lateral sclerosis .
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