86 Results for "

p50

" in MedChemExpress (MCE) Product Catalog:
Products (86)

86 Results for "p50" in MCE Product Catalog:

35
35 Publications Verification
Cat. No.: HY-N0191
CAS No.: 5508-58-7
Synonyms: Andrographis
Andrographolide is a NF-κB inhibitor, which inhibits NF-κB activation through covalent modification of a cysteine residue on p50 in endothelial cells without affecting IκBα degradation or p50/p65 nuclear translocation. Andrographolide has antiviral effects.
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16
16 Cited Publications
Cat. No.: HY-N0290
CAS No.: 4773-96-0
Mangiferin is a Nrf2 activator. Mangiferin suppresses nuclear translocation of the NF-κB subunits p65 and p50. Mangiferin exhibits antioxidant, antidiabetic, antihyperuricemic, antiviral, anticancer and antiinflammatory activities .
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3
3 Cited Publications
Cat. No.: HY-P70725
Purity:  ≥ 80%, as determined by reducing SDS-PAGE.
Synonyms: THBS1; THBS; Thrombospondin 1; Thrombospondin-1p180; TSP1; Thrombospondin-1; TSP; Glycoprotein G; THBS-1; Thrombospondin-p50; TSP-1; THBS1 Protein
Species:  
Human
Source:  
HEK293
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2
2 Cited Publications
Cat. No.: HY-148013
CAS No.: 702668-62-0
Purity:  99.94%
K284-6111 is a high-affinity and orally active CHI3L1 inhibitor, and inhibits CHI3L1 expression. K284-6111 inhibits ERK and NF-κB pathway. K284-6111 suppresses nuclear translocation of p50 and p65, and phosphorylation of IκB. K284-6111 improves memory dysfunction by alleviating amyloidogenesis and neuroinflammation, with the reduction of inflammatory proteins (eg: iNOS, COX-2, GFAP, and Iba-1). K284-6111 reduces atopic-like skin inflammation and inhibits LPS (HY-D1056) -induced liver injury. K284-6111 can be used for the study of Alzheimer's diseases and sepsis like hepatic injury .
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2
2 Cited Publications
Cat. No.: HY-P701325
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: THBS1; THBS; Thrombospondin 1; Thrombospondin-1p180; TSP1; Thrombospondin-1; TSP; Glycoprotein G; THBS-1; Thrombospondin-p50; TSP-1; THBS1 Protein
Species:  
Mouse
Source:  
E. coli
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1
1 Cited Publications
Cat. No.: HY-N6046
CAS No.: 73981-34-7
Kamebakaurin is an orally active diterpenoid compound that can be isolated from Isodon excia (Maxin.). Kamebakaurin can inhibit NF-κB activation by directly targeting the DNA-binding activity of p50. Kamebakaurin can induce apoptosis and cell cycle arrest in tumor cells. Kamebakaurin has anti-inflammatory and anti-tumor activities .
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1
1 Cited Publications
Cat. No.: HY-152177
CAS No.: 950244-33-4
Purity:  99.67%
Target:  

NF-κB

Research Areas:  

Cancer

JS6 is a Bcl3 inhibitor. JS6 attenuates the binding of Bcl3 to NF-κB1 (p50), disrupts the binding of Bcl3 to NF-κB family proteins p50 and p52, and inhibits the NF-κB signaling pathway. JS6 is applicable to breast cancer-related research .
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Cat. No.: HY-N0191R
CAS No.: 5508-58-7
Synonyms: Andrographis (Standard)
Andrographolide (Standard) is the analytical standard of Andrographolide. This product is intended for research and analytical applications. Andrographolide is a NF-κB inhibitor, which inhibits NF-κB activation through covalent modification of a cysteine residue on p50 in endothelial cells without affecting IκBα degradation or p50/p65 nuclear translocation. Andrographolide has antiviral effects.
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Cat. No.: HY-108486
CAS No.: 70563-58-5
Purity:  99%
Herbimycin A is an antibiotic and protein tyrosine kinase inhibitor. Herbimycin A directly inhibits the autophosphorylation of p210 BCR-ABL with an IC50 of approximately 5 μM, and reduces Src kinase activity. Herbimycin A also induces the degradation of receptor tyrosine kinases such as insulin-like growth factor 1 receptor (IGF-1R), insulin receptor (IR) and epidermal growth factor receptor (EGFR) via the ubiquitin-20S proteasome pathway. Herbimycin A directly modifies NF-κB p50, with the main target site involving Cys62, thereby blocking the DNA binding of p50 and NF-κB-driven gene expression. Herbimycin A can be used in studies related to tyrosine kinase signaling, chronic myeloid leukemia, NF-κB signaling, osteoclast function, apoptosis and cellular stress .
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Cat. No.: HY-N0290R
CAS No.: 4773-96-0
Mangiferin (Standard) is the analytical standard of Mangiferin. This product is intended for research and analytical applications. Mangiferin is a Nrf2 activator. Mangiferin suppresses nuclear translocation of the NF-κB subunits p65 and p50. Mangiferin exhibits antioxidant, antidiabetic, antihyperuricemic, antiviral, anticancer and antiinflammatory activities .
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Cat. No.: HY-RS00964
Research Areas:  

Others

ARHGEF7 Human Pre-designed siRNA Set A contains three designed siRNAs for ARHGEF7 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P10030
CAS No.: 1801379-22-5
Target:  

Proteasome NF-κB

Research Areas:  

Inflammation/Immunology

DPLG3 is a specific chymotryptic-like β5i subunits inhibitor, with an IC50 of 4.5 nM. DPLG3 inhibits mouse i-20S with IC50 of 9.4 nM. DPLG3 downregulates the protein levels of NF-κB p50 and p65. DPLG3 can be used for immune disease research .
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Cat. No.: HY-175397
Synonyms: DFHBI-thalidomide
Research Areas:  

Cancer

Dth (DFHBI-thalidomide) is an RNA aptamer-based PROTAC degrader. Dth can degrade a variety of endogenous proteins (such as mCherry, p50, p65 and E2F1) by replacing the 3′ module on the RNA scaffold with the RNA aptamer corresponding to the target protein. Dth upregulates IκB-α and Bax, and downregulates Bcl-2 and VEGF. Dth generates green fluorescence upon binding to the Broccoli RNA aptamer, enabling the tracing of RNA scaffolds. Dth can be used in cancer-related research .
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Cat. No.: HY-RS18543
Research Areas:  

Others

Pold2 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Pold2 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-149513
CAS No.: 2882916-73-4
Target:  

c-Myc Apoptosis

Research Areas:  

Cancer

EP12 is a c-Myc inhibitor. EP12 is a c-Myc G4 stabilizer. EP12 induces apoptosis and DNA damage in multiple myeloma cells. EP12 disrupts the nuclear translocation of P65/P50 by interfering with the NF-κB signaling pathway. EP12 inhibits multiple myeloma growth .
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Cat. No.: HY-P84215
Synonyms: p50; Bp50; CDW40; TNFRSF5

Host:  

Mouse

Application:  

WB, IHC-P, FC, ELISA

Reactivity:  

Human

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Cat. No.: HY-P84215A
Synonyms: p50; Bp50; CDW40; TNFRSF5

Host:  

Mouse

Application:  

WB, IHC-P, FC, ELISA

Reactivity:  

Human

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Cat. No.: HY-N0191S
Synonyms: Andrographis-d
Andrographolide-d (Andrographis-d) is the deuterium labeled Andrographolide (HY-N0191). Andrographolide is a NF-κB inhibitor, which inhibits NF-κB activation through covalent modification of a cysteine residue on p50 in endothelial cells without affecting IκBα degradation or p50/p65 nuclear translocation. Andrographolide has antiviral effects.
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Cat. No.: HY-183786
Research Areas:  

Cancer

Anticancer agent 327, a fluorescent Andrographolide (HY-N0191) derivative, is an NF-κB p50 inhibitor. Anticancer agent 327 covalently binds to the p50 subunit of NF-κB. Anticancer agent 327 reduces levels of multiple oncogenic p53 proteins via the autophagy/lysosome pathway. Anticancer agent 327 can be used for the research of pancreatic ductal adenocarcinoma (Ex/Em = 488/515 nm)[1].
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Cat. No.: HY-P810970
Synonyms: DCTN50, DCTN2, Dynactin subunit 2, 50 kDa dynein-associated polypeptide, Dynactin complex 50 kDa subunit, p50 dynamitin, DCTN-50

Host:  

Rabbit

Application:  

WB, IHC-P

Reactivity:  

Human, Mouse, Rat

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