204 Results for "

cluster

" in MedChemExpress (MCE) Product Catalog:
Products (204)

204 Results for "cluster" in MCE Product Catalog:

Cat. No.: HY-117123
CAS No.: 37206-04-5
Convulxin is a toxin found in a tropical rattlesnake. Convulxin stimulates platelet aggregation, and clusters GPVI to trigger Src family kinase activation, Fc receptor γ chain phosphorylation, and p72SYK signaling. Convulxin interacts with Dectin-2 to induce IL-10 production, activates monocytes to generate ROS and NLRP3 inflammasome-mediated IL-1β secretion, and induces mitochondrial ROS. Convulxin causes transient arterial blood pressure changes in dogs. Convulxin can be used for research related to coagulation .
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Cat. No.: HY-149035
PAA4 is a hypercoordinate carbon-centered tetranuclear gold (I) cluster prodrug . PAA4 releases active Au (I) ions upon triggering by GSH (HY-D0187), and this process is accelerated in the acidic microenvironment of bladder cancer cells with high GSH expression. PAA4 inhibits the activities of cytosolic TrxR1 and mitochondrial TrxR2, inducing ROS accumulation, lipid peroxidation, ferroptosis, loss of mitochondrial membrane potential and DNA damage. PAA4 can be used in bladder cancer-related research .
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Cat. No.: HY-P0131A
CAS No.: 2828432-44-4
Synonyms: Laminin (925-933) TFA
Target:  

Drug Intermediate

Research Areas:  

Neurological Disease Cancer

Laminin peptide CDPGYIGSR TFA (Laminin (925-933) TFA) is a peptide fragment derived from the laminin B1 chain that binds to laminin receptors, and acts as a ligand for the laminin receptor. Laminin peptide CDPGYIGSR TFA mediates cell spreading, induces the clustering of receptors with vinculin and α-actinin, regulates the actin cytoskeleton, promotes the formation of stress fibers, and enhances epithelial cell adhesion. Laminin peptide CDPGYIGSR TFA can be used in studies related to tumor metastasis and nerve injury .
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Cat. No.: HY-P991529

Target:  

TNF Receptor

Research Areas:  

Inflammation/Immunology Cancer

AGEN-2373 is a conditionally active agonist antibody targeting the co-stimulatory receptor CD137. GEN-2373 binds to CD137 without disruption of ligand binding. AGEN-2373 stimulates CD137 under receptor clustering conditions. AGEN-2373 can enhance T cell activity when combined with other checkpoint modulators (e.g. PD-1 antagonist and OX40 agonist). AGEN-2373 can be studied in research for human malignancies .
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Cat. No.: HY-P72328
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: H2AC4; Histone H2A Type 1-B/E; Prev. HIST1H2AB; Histone H2A/M; Prev. H2AFM; HIST1H2AE; H2A/M; Histone H2A/A; Histone cluster 1 H2A Family Member B; Histone H2A.2; H2A Histone Family, Member M; Histone H2A; Histone cluster 1, H2ab; H2AFA; H2A clustered His
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P703142
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: H2BC5; Histone H2B.K; Prev. HIST1H2BD; DJ221C16.6; Prev. H2BFB; HIST1H2BI; H2B/B; HIST1H2BG; Histone cluster 1 H2B Family Member D; HIST1H2BF; H2B Histone Family, Member B; HIST1H2BC; HIRA-Interacting Protein 2; HIST1H2BE; Histone cluster 1, H2bd; H2B.1B
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-100847
CAS No.: 1825345-52-5
Target:  

PARP

Research Areas:  

Cancer

AZ0108 is an inhibitor for poly ADP-ribose polymerase (PARP), which inhibits PARP1, PARP2, PARP3, PARP6, TNKS1, TNKS2, with IC50s of <0.03, <0.03, 2.8, 0.083, 3.2, >3 μM, respectively. AZ0108 prevents centrosome clustering with an EC50 of 0.053 μM, and exhibits cytotoxicity in cell OCI-LY-19 with GI50 of 0.017 μM. AZ0108 exhibits good in vivo pharmacokinetic characters in rat/mouse models .
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Cat. No.: HY-156533
CAS No.: 2708279-78-9
Target:  

5-HT Receptor

Research Areas:  

Cancer

5-HT2 agonist-1 (Compound 24) is a 5-HT2A & 5-HT2B & 5-HT2C agonist, with IC50s of 10 nM, 8.3, and 1.6 nM respectively. 5-HT2 agonist-1 free base can be used for research of depression, alcoholism, tobacco and cocaine addiction, inflammation, cluster headache, PTSD, seizure disorders and other CNS disorders .
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Cat. No.: HY-156533A
CAS No.: 2708279-77-8
5-HT2 agonist-1 (Compound 24) free base is a 5-HT2A & 5-HT2B & 5-HT2C agonist, with IC50s of 10 nM, 8.3, and 1.6 nM respectively. 5-HT2 agonist-1 free base can be used for research of depression, alcoholism, tobacco and cocaine addiction, inflammation, cluster headache, PTSD, seizure disorders and other CNS disorders .
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Cat. No.: HY-P99431
CAS No.: 2489390-15-8
Synonyms: Alomfilimab; SAR 445256

Target:  

CD28

Research Areas:  

Inflammation/Immunology Cancer

KY-1044 (Alomfilimab; SAR 445256) is a fully human IgG1 antibody targeting inducible costimulatory receptor (ICOS). KY-1044 depletes ICOS high cells via antibody-dependent cellular cytotoxicity (ADCC) through the engagement of FcgRIIIa. KY-1044 act as a costimulatory molecule on cells expressing lower ICOS levels, such as CD8 + TEff cells (through FcgR-dependent clustering). KY-1044 exploit the differential expression of ICOS on T-cell subtypes to improve the intratumoral immune contexture and restore an antitumor immune response .
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Cat. No.: HY-P86668
Synonyms: CD34 antigen; CD34 molecule; cluster designation 34; Hematopoietic progenitor cell antigen CD34; HPCA1; CD34_HUMAN.

Host:  

Rabbit

Application:  

WB, IHC-P, IHC-F, IF-Tissue, IP

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-156534
CAS No.: 1640-02-4
5-HT2A&5-HT2C agonist-1 (Example 2) is a 5-HT2A & 5-HT2C agonist, with IC50s of 196 nM and 0.9 nM respectively. 5-HT2A&5-HT2C agonist-1 can be used for research of depression, alcoholism, tobacco and cocaine addiction, inflammation, cluster headache, PTSD, seizure disorders and other CNS disorders .
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Cat. No.: HY-16031A
CAS No.: 468719-53-1
Synonyms: NSC710464
AFP464 (NSC710464) is a prodrug of Aminoflavone (HY-132974) and an agonist of the aryl hydrocarbon receptor (AhR). AFP464 downregulates the expression of α6-integrin (α6-integrin), inhibits breast tumor growth, reduces the population of tumor-initiating cells, disrupts mammosphere structure, induces the formation of mucin lake clusters, triggers DNA damage, and exerts antiproliferative activity. AFP464 is rapidly converted to Aminoflavone by nonspecific esterases in plasma and cell culture media. AFP464 is applicable to research related to breast cancer .
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Cat. No.: HY-16031B
Synonyms: NSC710464 dihydrochloride
AFP464 (NSC710464) dihydrochloride is a prodrug of Aminoflavone (HY-132974) and an agonist of the aryl hydrocarbon receptor (AhR). AFP464 dihydrochloride downregulates the expression of α6-integrin (α6-integrin), inhibits breast tumor growth, reduces the population of tumor-initiating cells, disrupts mammosphere structure, induces the formation of mucin lake clusters, triggers DNA damage, and exerts antiproliferative activity. AFP464 dihydrochloride is rapidly converted to Aminoflavone by nonspecific esterases in plasma and cell culture media. AFP464 dihydrochloride is applicable to research related to breast cancer .
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Cat. No.: HY-P5912
Target:  

iGluR Calcium Channel

Research Areas:  

Neurological Disease

GluN1 (356-385) is a polypeptide targeting NMDAR GluN1. GluN1 (356-385) induces the production of autoantibodies, which reduce the density of cell surface NMDAR clusters, impair long-term potentiation, and decrease NMDAR-mediated Ca 2+ influx. As an immunogen, GluN1 (356-385) induces symptoms similar to anti-NMDAR encephalitis, including memory loss, in mice. GluN1 (356-385) can be used to establish a mouse model that mimics the pathogenesis of anti-NMDAR encephalitis. GluN1 (356-385) is applicable to research related to anti-NMDAR encephalitis .
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Cat. No.: HY-P72335
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: H3C1; Histone H3/C; Prev. HIST1H3A; HIST1H3J; Prev. H3FA; HIST1H3I; H3/A; HIST1H3H; Histone cluster 1 H3 Family Member A; HIST1H3G; H3 Histone Family, Member A; HIST1H3F; Histone cluster 1, H3a; HIST1H3E; Histone 1, H3a; HIST1H3D; Histone H3.1; HIST1H3B;
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P72336
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: H4C1; H4/B; Prev. HIST1H4A; H4/G; Prev. H4FA; H4FI; Histone H4; H4/I; Histone cluster 1 H4 Family Member A; H4/A; H4 Histone Family, Member A; H4/J; Histone cluster 1, H4a; H4FJ; Histone 1, H4a; H4/C; HIST1H4J; H4FC; HIST1H4D; H4/H; HIST1H4C; H4FH; HIST1H
Species:  
Xenopus laevis Human
Source:  
E. coli
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Cat. No.: HY-P72798
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: H3C1; Histone H3/C; Prev. HIST1H3A; HIST1H3J; Prev. H3FA; HIST1H3I; H3/A; HIST1H3H; Histone cluster 1 H3 Family Member A; HIST1H3G; H3 Histone Family, Member A; HIST1H3F; Histone cluster 1, H3a; HIST1H3E; Histone 1, H3a; HIST1H3D; Histone H3.1; HIST1H3B;
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P71005
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: SLAMF9; CD2F10; SLAM Family Member 9; Signaling Lymphocytic Activation Molecule Family Member 2001; CD2F-10; Signaling Lymphocytic Activation Molecule Family Member 9; CD84-H1; cluster Of Differentiation 2 Antigen Family Member 10; SF2001; cluster Of Diff
Species:  
Mouse
Source:  
HEK293
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Cat. No.: HY-P99605
CAS No.: 2218515-90-1
Synonyms: PRS 343

Target:  

EGFR TNF Receptor

Research Areas:  

Cancer

Cinrebafusp alfa (PRS 343) is a high affinity CD137/HER2 bispecfic anticalin-based drug. Cinrebafusp alfa binds to recombinant human HER2 (Kd=0.3 nM) and human monomeric CD137 (4-1BB; Kd=5 nM). Cinrebafusp alfa facilitates T-cell costimulation by tumor-localized, HER2-dependent 4-1BB clustering and activation, further enhancing T-cell receptor-mediated activity and leading to tumor destruction. Cinrebafusp alfa has the potential for HER2+ solid tumors research .
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