Recettore di Ephrin
Gli inibitori del recettore Ephrin sono diretti ai recettori Eph, una famiglia di tirosina chinasi recettoriali che interagiscono con ligandi ephrin legati alla membrana. La segnalazione ephrin è cruciale per il posizionamento cellulare, la modellazione dei tessuti e l'angiogenesi. La disregolazione di questa via è implicata nel cancro, nelle malattie neurodegenerative e nei disturbi dello sviluppo. Presso CymitQuimica, offriamo inibitori dei recettori Ephrin per supportare la tua ricerca in biologia dello sviluppo, oncologia e neurobiologia.
Trovati 37 prodotti per "Recettore di Ephrin".
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ALW-II-49-7
CAS:ALW-II-49-7 is a selective and potent inhibitor of EphB2 kinase with an EC50 value of 40 nM in cell.Formula:C21H17F3N4O2Purezza:99.72%Colore e forma:SolidPeso molecolare:414.3805SA-PA
SA-PA, a self-assembled intracellular PROTAC leveraging azide-alkyne click chemistry, selectively degrades VEGFR-2, PDGFR-β, and EphB4 proteins within U87 cellsFormula:C40H32ClF3N10O8Purezza:98%Colore e forma:SolidPeso molecolare:873.19AZ12672857
CAS:AZ12672857 is an inhibitor of EphB4 with IC50 of 1.3 nM.Formula:C26H30N8O2Purezza:98.99%Colore e forma:Red SolidPeso molecolare:486.5688(123B9)2-Motif
(123B9)2-Motif is a selective agonist of the EphA2 receptor with a dissociation constant (Kd) of 4.9 μM and does not bind to EphA4. It functions by inducing phosphorylation and oligomerization of the EphA2 receptor, promoting receptor activation and internalization. (123B9)2-Motif is primarily used in research on targeted drug delivery for cancers overexpressing EphA2, such as breast cancer, to reduce circulating tumor cells and inhibit metastasis.AWL-II-38.3
CAS:AWL-II-38.3 is a highly potent EphA3 inhibitor with potent kinase inhibitory activity against EphA3.Cost-effective and quality-assured.Formula:C23H18F3N5O3Purezza:99.03% - 99.57%Colore e forma:SolidPeso molecolare:469.4159KYL peptide
CAS:EphA4 inhibitor, Kd 0.8 μM, blocks EphA4-EphrinA5; avoids AβO damage, preserves spines & LTP; long half-life (8-12h), neuroprotective.Formula:C74H108N14O17Purezza:98%Colore e forma:SolidPeso molecolare:1465.75(123B9)2-L2-PTX
(123B9)2-L2-PTX is an EphA2 agonist peptide-drug conjugate (PDC). It consists of dimer 123B9 and Paclitaxel. This compound significantly reduces circulating tumor cells and inhibits lung metastasis in a breast cancer metastasis mouse model. (123B9)2-L2-PTX is applicable in cancer research, including studies on melanoma, ovarian cancer, and breast cancer.Colore e forma:Odour SolidAPY-d3
APY-d3 is an EphA4-LBD antagonist peptide with a Kd value of 138 nM. It is constrained in a biologically active β-hairpin conformation through a disulfide bond linking its ends. APY-d3 is applicable for research in cancers such as gastric and pancreatic cancer, as well as in neurodegenerative diseases like amyotrophic lateral sclerosis and Alzheimer's disease.UniPR1449
UniPR1449 is an EphA2 receptor antagonist with a KD of 3.8±2.4 μM, which is significant in cancer pathophysiology [1].Purezza:98%Colore e forma:Odour SolidTargefrin
Targefrin: potent EphA2 antagonist, binds with 21nM Kd, IC50 of 10.8nM, induces receptor degradation in pancreatic cancer cells.Formula:C85H116F3N19O15Peso molecolare:1700.94UniPR1454
UniPR1454 targets the EphA2 receptor and inhibits the interaction between EphA2 and ephrin A1, with an IC50 of 2.6 μM. Furthermore, UniPR1454 suppresses the proliferation of glioblastoma U251 cells.Colore e forma:Odour SolidEphA2 agonist 1
CAS:Compound 7bg is a potent, selective EphA2 agonist targeting overexpressed glioblastoma cells.Formula:C50H58N12O12Colore e forma:SolidPeso molecolare:1019.07A11 acetate
A11 (ANXA1-derived 11 amino acid-long peptide) acetate is an ANXA1-EphA2 interaction inhibitor peptide. It reduces the binding of ANXA1 to EphA2 and enhances the binding of Cbl (E3 ubiquitin ligase of EphA2) to EphA2. A11 acetate effectively lowers EphA2 levels, significantly increases its ubiquitination, facilitates EphA2 internalization, and promotes colocalization of EphA2 and Cbl in nasopharyngeal carcinoma (NPC) cells. Additionally, A11 acetate inhibits NPC cell proliferation, migration, invasion, and angiogenesis.123B9
CAS:123B9 is a tumor-homing agent characterized as a potent and selective agonist for EphA2 with a dissociation constant (Kd) of 4.0 μM. It specifically targets the ligand-binding domain of the EphA2 tyrosine kinase receptor. Notably, 123B9 does not significantly inhibit the ligand-binding domains of closely related receptors EphA3 and EphA4.Formula:C58H82ClFN12O20Peso molecolare:1321.79Anti-Human EphB2 Antibody
Anti-EphB2 Antibody serves as a functional therapeutic tool specifically designed to enable the precise detection and neutralization of the EphB2 protein which plays a pivotal role in the orchestration of cell positioning and cancer progression during strictly monitored laboratory observation periods and molecular investigations to evaluate the pharmacological potential of targeted RTK inhibition.Peso molecolare:146.99 kDa (Predicted)Eph inhibitor 2
CAS:Eph inhibitor 2 is an Eph family tyrosine kinase inhibitor targeting Eph receptors.Formula:C18H15N5OPurezza:99.01%Colore e forma:White SolidPeso molecolare:317.3446NVP-BHG712 isomer
CAS:NVP-BHG712 isomer shows conserved non-bonded binding to EPHA2 and EPHB4.Formula:C26H20F3N7OPurezza:99.14%Colore e forma:White SolidPeso molecolare:503.4785JI-101
CAS:JI-101 (CGI-1842) is an oral multi-kinase inhibitor that targets VEGFR-2, PDGFR-β, and EphB4.Formula:C22H20BrN5O2Purezza:99.41% - 99.97%Colore e forma:SolidPeso molecolare:466.331NVP-BHG712
CAS:NVP-BHG712 is a specific EphB4 inhibitor with ED50 of 25 nM that discriminates between VEGFR and EphB4 inhibition; also shows activity against c-Raf, c-Src andFormula:C26H20F3N7OPurezza:97.32% - 98.63%Colore e forma:SolidPeso molecolare:503.48KYL acetate
EphA4 inhibitor, Kd: 0.8 μM, IC50: 6.34 μM. Protects synapses and spines, maintains LTP. Long half-life: 8-12h. Neuroprotective.Formula:C76H112N14O19Purezza:99.75%Colore e forma:SolidPeso molecolare:1525.78
