41 Results for "

N-cadherin

" in MedChemExpress (MCE) Product Catalog:
Products (41)

41 Results for "N-cadherin" in MCE Product Catalog:

43
43 Publications Verification
Cat. No.: HY-19987
CAS No.: 853220-52-7
Target:  

Wnt

Research Areas:  

Cancer

BML-284 is a potent and cell-permeable Wnt signaling activator. BML-284 induces TCF-dependent transcriptional activity with an EC50 of 700 nM .
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10
10 Cited Publications
Cat. No.: HY-13541
CAS No.: 229971-81-7
Purity:  99.93%
Target:  

Cadherin

Research Areas:  

Cancer

ADH-1, an N-cadherin antagonist, inhibits N-cadherin mediated cell adhesion.
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10
10 Cited Publications
Cat. No.: HY-13541A
CAS No.: 1135237-88-5
Purity:  99.74%
Target:  

Cadherin

Research Areas:  

Cancer

ADH-1 trifluoroacetate is an N-cadherin antagonist, which inhibits N-cadherin mediated cell adhesion.
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3
3 Cited Publications
Cat. No.: HY-115669
CAS No.: 69640-38-6
Purity:  98.88%
Synonyms: Antibiotic A 15104 Y; PClP
Target:  

Myosin TGF-β Receptor

Research Areas:  

Cancer

Pentachloropseudilin (Antibiotic A 15104 Y; PClP) is a reversible and allosteric potent inhibitor of Myo1s (class 1 myosins) with IC50s range from 1 to 5 μM for mammalian class-1 myosins and greater than 90 μM for class-2 and class-5 myosins. Pentachloropseudilin is a potent inhibitor of transforming growth factor-β (TGF-β)-stimulated signaling, with an IC50 of 0.1 to 0.2 μM for TGF-β .
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2
2 Cited Publications
Cat. No.: HY-P80761
Synonyms: CDH2; CDHN; NCAD; cadherin-2; CDw325; Neural cadherin; N-cadherin; CD antigen CD325

Host:  

Rabbit

Application:  

WB, IP

Reactivity:  

Human, Mouse, Rat

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1
1 Cited Publications
Cat. No.: HY-123931
CAS No.: 667880-38-8
Purity:  98.78%
Research Areas:  

Cancer

ZLDI-8 is a Notch activating/cleaving enzyme ADAM-17 inhibitor and inhibits the cleavage of Notch protein. ZLDI-8 decreases the expression of pro-survival/anti-apoptosis and epithelial-mesenchymal transition (EMT) related proteins. ZLDI-8 is also a competitive and irreversible tyrosine phosphatase (Lyp) inhibitor with an IC50 of 31.6 μM and a Ki of 26.22 μM. ZLDI-8 inhibits the growth of MHCC97-H cells with an IC50 of 5.32 μM .
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1
1 Cited Publications
Cat. No.: HY-P73302
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: CDH2; N-cadherin; Prev. NCAD; Calcium-Dependent Adhesion Protein, Neuronal; CDHN; CD325 Antigen; Neural cadherin; N-cadherin 1; cadherin-2; ARVD14; CD325; ADHD8; cadherin 2, Type 1, N-cadherin (Neuronal); ACOGS; cadherin 2; CDw325
Species:  
Human
Source:  
HEK293
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1
1 Cited Publications
Cat. No.: HY-P75667
Purity:  ≥ 80%, as determined by reducing SDS-PAGE.
Synonyms: CDH12; cadherin 12, Type 2 (N-cadherin 2); cadherin 12; cadherin, Neural Type, 2; Br-cadherin; Neuronal cadherin 2; CDHB; Brain-cadherin; Neural Type cadherin 2; Brain cadherin; N-cadherin 2; BR-cadherin; cadherin-12
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-P11017
CAS No.: 1152066-26-6
Target:  

p38 MAPK Cadherin

Research Areas:  

Inflammation/Immunology

LNSMGQD is a cyclic peptide fragment derived from desmoglein 1 (amino acids 81-86), which mimics trans-interactions and acts as part of the tandem peptide binding interface of desmoglein 2. LNSMGQD not only binds to desmoglein 1 and 3, but also effectively inhibits their homophilic trans-interactions, while reducing the probability of homophilic or heterophilic binding between desmoglein 2 and Dsc2, N-cadherin and E-cadherin. LNSMGQD is applicable to the research on disease mechanisms such as Crohn's disease and pemphigus vulgaris .
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Cat. No.: HY-P11288
CAS No.: 2871680-36-1
Research Areas:  

Cancer

ANT308 is a vasoactive intestinal polypeptide (VIP receptor) antagonist. ANT308 significantly enhances the activation and proliferation of T cells. ANT308 inhibits the migration and metastasis, induces apoptosis of melanoma tumor cells by inhibiting VIP-VPAC2 signaling and reducing the expression of MCAM and N-cadherin. ANT308 can be used for the studies of acute myeloid leukemia (AML) and uveal melanoma (UVM) .
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Cat. No.: HY-P11288A
Research Areas:  

Cancer

ANT308 TFA is a vasoactive intestinal polypeptide (VIP receptor) antagonist. ANT308 TFA significantly enhances the activation and proliferation of T cells. ANT308 TFA inhibits the migration and metastasis, induces apoptosis of melanoma tumor cells by inhibiting VIP-VPAC2 signaling and reducing the expression of MCAM and N-cadherin. ANT308 TFA can be used for the study of acute myeloid leukemia (AML) and uveal melanoma (UVM) .
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Cat. No.: HY-173557
CAS No.: 3058094-83-7
Research Areas:  

Cancer

PRMT7-IN-2 (A33) is a selective PRMT7 inhibitor with an IC50 of 0.50 μM. PRMT7-IN-2 arrests cell cycle at G0/G1 phase, induces cell apoptosis, and inhibits cell growth in vivo and in vitro. PRMT7-IN-2 decreases the monomethylarginine level of PRMT7, increases expression of epithelial marker (E-cadherin, and reduces expression of mesenchymal markers such as N-cadherin, Vimentin, and ZEB2 .
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Cat. No.: HY-P11346
CAS No.: 1830290-52-2
Target:  

Cadherin

Research Areas:  

Inflammation/Immunology

N-Cadherin mimic peptide is a N-cadherin agonist. N-Cadherin mimic peptide promotes N-cadherin homodimerization via enhancing β-catenin signaling, inducing early chondrogenesis and cartilage matrix production in mesenchymal stem cells (MSCs). N-Cadherin mimic peptide is promising for research of MSC-based cartilage regeneration .
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Cat. No.: HY-P5755
Target:  

Inhibitory Antibodies

Research Areas:  

Cancer

SWELYYPLRANL-NH2 is an E-cadherin and N-cadherin antagonist. SWELYYPLRANL-NH2 inhibits phage clone binding to E- or N-cad/Fc chimeric protein (IC50: 0.7 and 0.09 μM respectively). SWELYYPLRANL-NH2 inhibits cell aggregation. SWELYYPLRANL-NH2 can be used to promote drug delivery through epithelial and endothelial permeability barriers .
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Cat. No.: HY-19987A
CAS No.: 2095432-75-8
Target:  

Wnt

Research Areas:  

Cancer

BML-284 hydrochloride is a potent and cell-permeable Wnt signaling activator. BML-284 induces TCF-dependent transcriptional activity with an EC50 of 700 nM .
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Cat. No.: HY-163709
Target:  

PROTACs FAK Akt ERK

Research Areas:  

Cancer

PROTAC FAK degrader 2 is an orally active PROTAC FAK degrader with a DC50 of 60.10 nM. PROTAC FAK degrader 2 forms a ternary complex with FAK and CRBN E3 ubiquitin ligase, driving proteasome-mediated degradation of total and phosphorylated FAK. PROTAC FAK degrader 2 inhibits phosphorylation of AKT and ERK, suppressing their downstream signaling pathways. PROTAC FAK degrader 2 reduces cancer cell viability, adhesion, migration, and invasion. PROTAC FAK degrader 2 exerts anti-tumor activity in HCT8/T tumor xenografts in mice. PROTAC FAK degrader 2 can be used for the research of breast cancer, colorectal cancer, lung cancer .
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Cat. No.: HY-N15267
CAS No.: 64280-22-4
Ovalitenone is a flavonoid compound that can be isolated from the plant Millettia peguensis. It shows no cytotoxic effects on lung cancer H460 and A549 cells, but it significantly inhibits anchorage-independent growth, CSC-like phenotypes, colony formation, and the migration and invasion capabilities of cancer cells. Ovalitenone can significantly reduce the levels of N-cadherin, snail, and slug, while increasing E-cadherin, thus inhibiting the EMT pathway. Additionally, Ovalitenone suppresses the signaling pathways regulated by focal adhesion kinase (FAK), ATP-dependent tyrosine kinase (AKT), mammalian target of rapamycin (mTOR), and cell division cycle 42 (Cdc42) .
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Cat. No.: HY-173560
Target:  

ATTECs SHP2 Apoptosis

Research Areas:  

Cancer

SHP2 ATTEC degrader-1 is a SHP2 ATTEC degrader. SHP2 ATTEC degrader-1 has degradation rate of 83.31 at 1.0 μM for 24 h in the PANC-1 cell line. SHP2 ATTEC degrader-1 inhibits cell growth in vivo and in vitro. SHP2 ATTEC degrader-1 induces apoptosis and increases the expression of the epithelial marker ( E-cadherin), and reduces the expression of interstitial markers (such as N-cadherin, Vimentin) (Pink: LC3 ligand (HY-174085); Black :linker HY-140468; Blue: SHP2 ligand (HY-174084) .
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Cat. No.: HY-P73750
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: CDH2; N-cadherin; Prev. NCAD; Calcium-Dependent Adhesion Protein, Neuronal; CDHN; CD325 Antigen; Neural cadherin; N-cadherin 1; cadherin-2; ARVD14; CD325; ADHD8; cadherin 2, Type 1, N-cadherin (Neuronal); ACOGS; cadherin 2; CDw325
Species:  
Mouse
Source:  
HEK293
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Cat. No.: HY-P703737
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.;≥ 90%, as determined by HPLC.
Synonyms: CDH2; N-cadherin; Prev. NCAD; Calcium-Dependent Adhesion Protein, Neuronal; CDHN; CD325 Antigen; Neural cadherin; N-cadherin 1; cadherin-2; ARVD14; CD325; ADHD8; cadherin 2, Type 1, N-cadherin (Neuronal); ACOGS; cadherin 2; CDw325
Species:  
Human
Source:  
HEK293
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