38 Results for "

hPD-1

" in MedChemExpress (MCE) Product Catalog:
Products (38)

38 Results for "hPD-1" in MCE Product Catalog:

4
4 Cited Publications
Cat. No.: HY-P81169A
Synonyms: Programmed cell death protein 1; CD279; CD279 antigen; hPD 1; hPD-1; hSLE1; PD 1; PD1; PDCD 1; PDCD1; PDCD1_HUMAN; Programmed cell death 1; Protein PD 1; Protein PD-1; SLEB2; Systemic lupus erythematosus susceptibility 2.

Host:  

Mouse

Application:  

WB, IHC-P, ICC/IF, FC

Reactivity:  

Human

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1
1 Cited Publications
Cat. No.: HY-P73344A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.;≥ 90%, as determined by HPLC.
Synonyms: CD279; hPD-1; PDCD1; Programmed cell death 1; SLEB2
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-P73724
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Programmed cell death protein 1; PD1; CD279; PDCD1
Species:  
Source:  
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Cat. No.: HY-176763
CAS No.: 2376747-46-3
Target:  

Sec61

Research Areas:  

Cancer

KZR-261 is a Sec61 translocase inhibitor. KZR-261 binds directly to the Sec61 channel, thereby inhibiting the biosynthesis of certain Sec61 substrate proteins, including oncogenic factors. KZR-261 activates the endoplasmic reticulum stress response. KZR-261 exhibits broad in vitro anticancer activity. KZR-261 shows antitumor efficacy in mouse models of cancer. KZR-261 can be used for the research of multiple myeloma, colorectal cancer, small cell lung cancer, pancreatic cancer, prostate cancer, non-Hodgkin's lymphoma, and mantle cell lymphoma [1].
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Cat. No.: HY-135767
CAS No.: 352010-68-5
Purity:  99.95%
Research Areas:  

Metabolic Disease

Bicyclopyrone is an inhibitor of 4-hydroxyphenylpyruvate dioxygenase (Hpd) .
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Cat. No.: HY-174830
CAS No.: 3099808-68-8
Target:  

PD-1/PD-L1

Research Areas:  

Cancer

GJ19 is a PD-L1 inhibitor with an IC50 of 32.06 nM. GJ19 can effectively bind to human/murine PD-L1 protein with Kd values of 171 and 290 nM, respectively. GJ19 concentration-dependently promotes HepG2 cell mortality in a co-culture model of HepG2/hPD-L1 and Jurkat T/hPD-1 cells. GJ19 effectively suppresses tumor growth in a B16-F10 melanoma mouse model. GJ19 can be used for the study of tumor immunotherapy [1].
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Cat. No.: HY-P2478
CAS No.: 2815311-61-4
Target:  

PD-1/PD-L1

Research Areas:  

Inflammation/Immunology

Human PD-L1 inhibitor V, a human PD-1 protein binding peptide with a Kd value of 3.32 μM. Human PD-L1 inhibitor V inhibit the interaction of hPD-1/hPD-L1 [1].
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Cat. No.: HY-P2474
CAS No.: 2135542-86-6
Target:  

PD-1/PD-L1

Research Areas:  

Cancer

Human PD-L1 inhibitor I is a hPD-1 peptide ligand, with a KD of 3.39 μM. Human PD-L1 inhibitor I may disturb the binding of hPD-L1 to hPD-1 [1].
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Cat. No.: HY-P2477
CAS No.: 2135542-83-3
Target:  

PD-1/PD-L1

Research Areas:  

Inflammation/Immunology

Human PD-L1 inhibitor IV, a polypeptide, is a competitive human PD-1 protein inhibitor with a Kd value of 1.38 μM. Human PD-L1 inhibitor IV inhibits the interaction of hPD-1/hPD-L1 [1].
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Cat. No.: HY-P2478A
Target:  

PD-1/PD-L1

Research Areas:  

Inflammation/Immunology

Human PD-L1 inhibitor V TFA, a human PD-1 protein binding peptide with a Kd value of 3.32 μM. Human PD-L1 inhibitor V TFA inhibit the interaction of hPD-1/hPD-L1 [1].
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Cat. No.: HY-135767R
CAS No.: 352010-68-5
Research Areas:  

Metabolic Disease

Bicyclopyrone (Standard) is the analytical standard of Bicyclopyrone. This product is intended for research and analytical applications. Bicyclopyrone is an inhibitor of 4-hydroxyphenylpyruvate dioxygenase (Hpd) .
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Cat. No.: HY-184989
PD-L1-IN-12 is an orally active and potent selenium-containing small-molecule PD-L1 inhibitor (KD = 9.06 nM). PD-L1-IN-12 can mediate the internalization of PD-L1 and strongly block hPD-1 and hPD-L1 interaction (IC50 = 5.2 nM). PD-L1-IN-12 can be used in colorectal cancer immunology research [1].
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Cat. No.: HY-P84582
Synonyms: PDCD1; PD-1; CD279; SLEB2; hPD-1; hPD-l; hSLE1

Host:  

Mouse

Application:  

WB, FC, ELISA

Reactivity:  

Human

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Cat. No.: HY-P70525
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Programmed cell death protein 1; hPD-1; PDCD1; CD279
Species:  
Source:  
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Cat. No.: HY-163837
Target:  

PD-1/PD-L1

Research Areas:  

Cancer

PD-1/PD-L1-IN-48 (compound HD10) is a potent inhibitor of PD-1/PD-L1 interaction, with an IC50 of 3.1 nM. PD-1/PD-L1-IN-48 plays an important role in cancer research [1].
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Cat. No.: HY-P72406
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Programmed cell death protein 1; hPD-1; PDCD1; CD279
Species:  
Source:  
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Cat. No.: HY-P705070
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Programmed cell death protein 1; hPD-1; PDCD1; CD279
Species:  
Source:  
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Cat. No.: HY-P73342A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: CD279; hPD-1; PDCD1; Programmed cell death 1; SLEB2
Species:  
Source:  
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Cat. No.: HY-P70766
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Programmed cell death protein 1; hPD-1; PDCD1; CD279
Species:  
Source:  
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Cat. No.: HY-P704840
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Programmed cell death protein 1; PDCD1; PD-1; hPD-1; CD279
Species:  
Source:  
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