Scientific Reviews
Product Guides
Blogs
Topics
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
318 Results for "
CE
" in MedChemExpress (MCE) Product Catalog:
Products (318)
318 Results for "CE" in MCE Product Catalog:
Cat. No.: HY-169434
Synonyms: Lon-TK-BMS-1
Target:
Research Areas:
LTB is a prodrug formed by coupling glycolysis inhibitor (Lonidamine (HY-B0486)) with PD1/PDL1 blocker (BMS-1 (HY-19991)) by thioketal linkage. LTB can further encapsulate photosensitizer chlorine e6 (Ce6) (HY-13594) to construct a co-delivery photodynamic nanoplatform (LTB-6 NPs) by self-assembly .
Cat. No.: HY-140735
Purity: ≥95.0%
DSPE-PEG5000-Amine (DSPE-PEG5000-ammonium) is an amino-functionalized PEGylated lipid. DSPE-PEG5000-Amine can be conjugated with chlorin e6 (Ce6) via EDC/NHS coupling. It can also be conjugated with FITC to prepare DSPE-PEG-FITC. DSPE-PEG5000-Amine is applicable to research related to PEGylated lipid functionalization and bioconjugation .
Cat. No.: HY-P702224
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: RHD; Rhesus Blood Group Antigen CE; Prev. RH; Rhesus Blood Group D Antigen; SLC42A5; Rhesus System D Polypeptide; CD240D; Rh Blood Group, D Anitgen; DIIIc; RhD Blood Group D Antigen; RhPI; Rh Blood Group, D Antigen; RhII; Rh Blood Group CE Antigen; Rh4; R
Species:
Human
Source:
E. coli Cell-free
Cat. No.: HY-120042
CAS No.: 23560-59-0
Research Areas:
Heptenophos is an inhibitor of AChE and plasma carboxylesterase (CES). By inhibiting AChE activity, Heptenophos causes the accumulation of acetylcholine at cholinergic synapses, thereby triggering typical symptoms of organophosphate poisoning. Heptenophos exhibits rapid lethal toxicity in male albino mice, but its toxic effects are effectively antagonized by obidoxime, and Memantine (HY-B0591) further enhances the detoxification efficacy of obidoxime. Therefore, Heptenophos is commonly used in studies related to the mechanism of organophosphate poisoning and detoxification strategies .
Research Areas:
WWL229 is a selective inhibitor of carboxylesterase 3 (CES3) with an IC50 1.94 μM. WWL229 attenuates LPS (HY-D1056)-induced pro-inflammatory cytokine mRNA levels, inhibits lipolysis and adipose thermogenesis, impairs mitochondrial function, and promotes lipid storage. WWL229 can be used for the research of obesity, insulin resistance, type 2 diabetes, and lung inflammation .
Cat. No.: HY-W013059S
CAS No.: 2483830-15-3
Synonyms: DA-CE phosphoramidite-13C10,15N5
Cat. No.: HY-155907
CAS No.: 474922-26-4
Synonyms: DSPE-PEG5000-NH2 ammonium
DSPE-PEG5000-Amine ammonium (DSPE-PEG5000-NH2 ammonium) is an amino-functionalized PEGylated lipid. DSPE-PEG5000-Amine ammonium can be conjugated with chlorin e6 (Ce6) via EDC/NHS coupling. It can also be conjugated with FITC to prepare DSPE-PEG-FITC. DSPE-PEG5000-Amine ammonium is applicable to research related to PEGylated lipid functionalization and bioconjugation .
Cat. No.: HY-D1603
CAS No.: 209541-26-4
Cat. No.: HY-N10686
CAS No.: 61077-78-9
Target:
Cat. No.: HY-N8353
CAS No.: 149598-71-0
Category:
Target:
Target:
Research Areas:
Hemicellulase is a hemicellulose-targeting hydrolase that breaks down the binding of glucose and polymers to water molecules present in plant fibers. Hemicellulase specifically degrades hemicellulose (such as xylan and mannan) in plant cell walls by hydrolyzing β-1,4-xylosidic bonds and ester bonds (such as acetyl and ferulic acid ester bonds). Hemicellulase relies on the synergistic action of the glycoside hydrolase (GH) and carbohydrate esterase (CE) families to achieve efficient hydrolysis through acid-base catalysis (such as Glu/Asp residues) and substrate binding pockets. Hemicellulase can be used in the food industry (such as improving bread texture)， biofuel production (lignocellulose pretreatment) and paper industry (biobleaching) .
Cat. No.: HY-121032
CAS No.: 1848233-59-9
Research Areas:
DO53 is a serine hydrolase inhibitor that targets ABHD6, PAFAH2, PLA2G7, ABHD2 and CES1C. DO53 reduces LPS (HY-D1056A1)-induced cytokine production in the mouse brain, decreases fasting-induced refeeding behavior, and induces hypoactivity in mice. As a DAGL negative control, DO53 shows no activity against DAGLα/β in vivo, and does not affect brain lipid levels, DSE/DSI synaptic plasticity or LPS-induced anhidrosis in mice . DO53 can be used in studies related to LPS-induced neuroinflammation and fasting-induced refeeding .
Cat. No.: HY-P76528
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: OPCML; CDNA, FLJ79172, Highly Similar To Opioid-Binding Protein/CEll Adhesion Moleculeprecursor; Opioid Binding Protein/CEll Adhesion Molecule Like; Opioid Binding Protein/CEll Adhesion Molecule-Like Preprotein Isoform A; IGLON1; Opioid Binding Protein/CE
Species:
Human
Source:
HEK293
Cat. No.: HY-P77114
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: OPCML; CDNA, FLJ79172, Highly Similar To Opioid-Binding Protein/CEll Adhesion Moleculeprecursor; Opioid Binding Protein/CEll Adhesion Molecule Like; Opioid Binding Protein/CEll Adhesion Molecule-Like Preprotein Isoform A; IGLON1; Opioid Binding Protein/CE
Species:
Mouse
Source:
HEK293
Cat. No.: HY-P77115
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: OPCML; CDNA, FLJ79172, Highly Similar To Opioid-Binding Protein/CEll Adhesion Moleculeprecursor; Opioid Binding Protein/CEll Adhesion Molecule Like; Opioid Binding Protein/CEll Adhesion Molecule-Like Preprotein Isoform A; IGLON1; Opioid Binding Protein/CE
Species:
Rat
Source:
HEK293
Cat. No.: HY-P73884
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: IL32; Interleukin-32; Interleukin 32; Interleukin-32 Small; TAIF; Interleukin-32 Eta; NK4; IL-32alpha; TAIFb; IL-32delta; TAIFd; IL-32gamma; Tumor Necrosis Factor Alpha-Inducing Factor; IL-32beta; Natural Killer CEll Transcript 4; TAIFa; Natural Killer CE
Species:
Human
Source:
HEK293
Cat. No.: HY-P700124AF
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: IL32; Interleukin-32; Interleukin 32; Interleukin-32 Small; TAIF; Interleukin-32 Eta; NK4; IL-32alpha; TAIFb; IL-32delta; TAIFd; IL-32gamma; Tumor Necrosis Factor Alpha-Inducing Factor; IL-32beta; Natural Killer CEll Transcript 4; TAIFa; Natural Killer CE
Species:
Human
Source:
E. coli
Cat. No.: HY-P701780
Purity: ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: SCYL3; PACE-1; SCY1 Like Pseudokinase 3; SCY1-Like, Kinase-Like 3; PACE1; Ezrin-Binding Partner PACE-1 (PACE-1); Protein-Associating With The Carboxyl-Terminal Domain Of Ezrin; Ezrin-Binding Partner PACE-1; Ezrin-Binding Protein PACE-1; SCY1-Like 3 (S. CE
Species:
Human
Source:
Sf9 insect cells
-
-
Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
