66 Results for "

caged

" in MedChemExpress (MCE) Product Catalog:
Products (66)

66 Results for "caged" in MCE Product Catalog:

Cat. No.: HY-103526
CAS No.: 927866-58-8
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

DPNI-GABA is a nitroindoline cage compound that inhibits GABA(A) receptors and reduces GABA-evoked peak responses with an IC50 value of 0.5 mM .
loading...
    loading...
Cat. No.: HY-N10256
CAS No.: 1623451-72-8
Varioxepine A is a 3H-oxepine-containing alkaloid with a new oxa-cage found in the marine algal-derived endophytic fungus Paecilomyces variotii. Varioxepine A inhibits plant pathogenic fungus Fusarium graminearum .
loading...
    loading...
Cat. No.: HY-161005
CAS No.: 2107375-54-0
Target:  

Hapten

Research Areas:  

Metabolic Disease

TETS-Methyl benzoate(compound 2j) is a haptendirectly conjugated to the carrier protein via carboxylic acid function using the standard activated ester method .
loading...
    loading...
Cat. No.: HY-N7502R
CAS No.: 17241-59-7
2-(Hydroxymethyl)anthraquinone is used as a photoremovable protecting group (PRPG) to chemically cage sex pheromone (e.g. (Z)-11-hexadecen-1-ol (sex pheromone of Chilo infuscatellussnellen)) .
loading...
    loading...
Cat. No.: HY-131019
CAS No.: 2341841-03-8
Target:  

mGluR

Research Areas:  

Neurological Disease

JF-NP-26, an inactive photocaged derivative of raseglurant, is the first caged mGlu5 receptor negative allosteric modulator. Uncaging of JF-NP-26 is elicited with light pulses in the visible spectrum (405 nm). JF-NP-26 induces light-dependent analgesia in models of inflammatory and neuropathic pain in freely behaving animals .
loading...
    loading...
Cat. No.: HY-131885
CAS No.: 2417096-44-5
Purity:  82.94%
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

RuBi-Glutamate hexafluorophosphate sodium is a neuronal activator. RuBi-Glutamate hexafluorophosphate sodium photocleaves to release glutamate upon one- or two-photon excitation, activating glutamate receptors in cortical pyramidal neurons. RuBi-Glutamate hexafluorophosphate sodium reduces peak amplitude of evoked GABAergic inhibitory postsynaptic currents in its caged form. RuBi-Glutamate hexafluorophosphate sodium can be used for the research of Huntington's disease .
loading...
    loading...
Cat. No.: HY-131001
Target:  

nAChR

Research Areas:  

Neurological Disease

DPNB-ABT594 is a nitrobenzyl-caged ABT594 (HY-14316A) and activates nAChRs containing the α4β2 subunits with good selectivity than the α7 subunit. DPNB-ABT594 can be used to map the distribution of nAChRs on neurons of the medial habenula (MHb) and helps to gain a deeper understanding of the nAChR-mediated Ca 2+ signalling in the MHb .
loading...
    loading...
Cat. No.: HY-108578
CAS No.: 851956-02-0
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

RuBi-4AP, a derivative of 4-aminopyridine (4AP; HY-B0604), is a caged Kv channel blocker. RuBi-4AP contains a photolabile protecting group, allowing its effect to be controlled precisely in both space and time with light. RuBi-4AP can be used for the research of neuronal excitability, synaptic transmission, and signal propagation .
loading...
    loading...
Cat. No.: HY-149328
CAS No.: 3033545-34-2
phoBET1 is a photolabile PROTAC molecule that, upon photoactivation, functions as a BRD4 PROTAC degrader to trigger BRD4 degradation via the ubiquitin-proteasome system. Activated phoBET1 induces cancer cell apoptosis and inhibits tumor growth in xenograft mouse models. In its inactive caged state, phoBET1 exhibits only extremely low antiproliferative activity against cancer cells. phoBET1 can be applied in studies related to acute myeloid leukemia .
loading...
    loading...
Cat. No.: HY-D2984
CAS No.: 1308789-62-9
Synonyms: SNAP-PEG-NH2
Target:  

Fluorescent Dye

Research Areas:  

Others

BG-PEG-NH2 (SNAP-PEG-NH2) is an amino-terminal fluorescent probe building block and a precursor for site-specific labeling of SNAP-tag fusion proteins. BG-PEG-NH2 undergoes one-step coupling with activated carboxyl esters to form customized SNAP-tag substrates, which covalently bind to SNAP tags via a thioether bond formed at the Cys145 site. After coupling with a caged carboxyfluorescein, BG-PEG-NH2 forms a probe with Ex/Em = 500/524 nm following ultraviolet uncaging. Coupling of BG-PEG-NH2 with SeTau-647-NHS enables visualization of GPCR signal transduction. BG-PEG-NH2 is suitable for coupling reactions in aqueous phases or buffers, conjugation of labels, and labeling of intracellular or cell-surface proteins .
loading...
    loading...
Cat. No.: HY-155817
Research Areas:  

Others

UNC7096 (compound 53) is a biotinylated affinity reagent. The phenyl ring of UNC7096 replaces the pyrimidine ring in UNC6934 (HY-145103) and introduces biotin at the para position of the phenyl ring, which has a high binding affinity to the NSD2-PWWP1 domain (Kd=46 nM). UNC7096 blocks the interaction between NSD2-PWWP1 and nucleosomal H3K36me2 by occupying the methyl-lysine binding pocket of NSD2-PWWP1. This binding is achieved by covalent binding through the formation of hydrogen bonds and a specific aromatic cage structure. UNC7096 can be used to capture proteins that interact with the NSD2-PWWP1 domain to further analyze the biological significance of these interactions .
loading...
    loading...
Cat. No.: HY-182128
CAS No.: 1325717-65-4
Research Areas:  

Others

DEACM caged-dG-CE phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
loading...
    loading...
Cat. No.: HY-182134
CAS No.: 942218-71-5
Research Areas:  

Others

NPOM caged-dT-CE phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
loading...
    loading...
Cat. No.: HY-P11782
CAS No.: 254732-11-1
Target:  

GSK-3 CDK Apoptosis

Research Areas:  

Cancer

GTGKT is a CAGE inhibitor. GTGKT binds to CAGE and blocks the binding of CAGE to GSK3β. GTGKT alters the localization of CAGE and inhibits the binding of CAGE to the promoter sequence of Cyclin D1. GTGKT enhances the Apoptotic effect of anticancer agents. GTGKT reduces the expression of Cyclin D1. GTGKT decreases the tumorigenic potential of melanoma and hepatocellular carcinoma cells .
loading...
    loading...
Cat. No.: HY-122783A
CAS No.: 942623-57-6
Target:  

Others

Research Areas:  

Others

(S)-Isogambogic acid is a caged xanthone isolated from the resin of Garcinia hanburyi that exhibits cytotoxic activity. (S)-Isogambogic acid serves as a detection marker for the quality control of Garcinia hanburyi .
loading...
    loading...
Cat. No.: HY-182461
CAS No.: 1064-34-2
Deoxymorellin is a caged xanthone found in resins and fruits of Garcinia hanburyi hook. f.. Deoxymorellin exhibits cytotoxicity. Deoxymorellin can be used for research of Methicillin (HY-121544)-resistant or Methicillin-susceptible Staphylococcus aureus .
loading...
    loading...
Cat. No.: HY-N7890
CAS No.: 1240792-57-7
Isomoreollic acid is a cage xanthonoid. Isomoreollic acid exhibits cytotoxicity against colon cancer cells, with an IC50 > 10 μM for proteasome inhibition. Isomoreollic acid is present in the stem bark of Garcinia lateriflora. Isomoreollic acid can be used in colon cancer research .
loading...
    loading...
Cat. No.: HY-P10761A
NOTA-DPI-4452 TFA is a trifluoroacetate derivative with DPI-4452 (HY-P10761) as the parent peptide. DPI-4452 is a CAIX-targeting cyclic peptide with a DOTA cage that can chelate with radionuclides and is used to express CAIX tumors for PET-CT imaging and research .
loading...
    loading...
Cat. No.: HY-183603
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

FRC-222 is a CHD1 tandem chromodomain inhibitor with a Kd of 0.15 μM and an IC50 of 0.18 μM. FRC-222 binds to the H3K4me3 binding site of CHD1 tandem chromodomain via aromatic cage interactions and extended ligand contacts. FRC-222 can be used for the research of prostate cancer[1].
loading...
    loading...
Cat. No.: HY-168992A
Research Areas:  

Others

UNC6535 TFA is a covalent ligand targeting the triple Tudor domain (3TD) of SETDB1. UNC6535 TFA reversibly binds to the aromatic cages of both TD2 and TD3 within SETDB1 3TD simultaneously, weakly inhibits the methyltransferase activity of SETDB1, and displaces the H3K9Me2K14Ac peptide from SETDB1 3TD .
loading...
    loading...