19 Results for "

immune-modulating

" in MedChemExpress (MCE) Product Catalog:
Products (19)

19 Results for "immune-modulating" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-B0300
CAS No.: 52-67-5
Synonyms: D-(-)-Penicillamine
Penicillamine (D-(-)-Penicillamine) is a penicillin metabolic degradation product, can be used as a heavy metal chelator. Penicillamine increases free copper and increases oxidative stress. Penicillamine has effect of seizures through nitric oxide/NMDA pathways. Penicillamine is a potential immune modulator. Penicillamine can be used for the research of Wilson disease, rheumatoid arthritis, and cystinuria .
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2
2 Cited Publications
Cat. No.: HY-150724
CAS No.: 937402-51-2
Synonyms: 1018 ISS
Research Areas:  

Inflammation/Immunology

ODN 1018 (1018 ISS) is a TLR9 agonist and immune modulator. ODN 1018 exhibits adjuvant activity and augments CD8+ T cell responses with LNP-encapsulated OVA peptides. ODN 1018 triggers sustained suppression of allergic airway inflammation. ODN 1018 can be used for the research of allergic asthma and systemic lupus erythematosus .
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2
2 Cited Publications
Cat. No.: HY-150724C
Purity:  97.44%
Synonyms: 1018 ISS sodium
Research Areas:  

Inflammation/Immunology

ODN 1018 (1018 ISS) sodium is a TLR9 agonist and immune modulator. ODN 1018 sodium exhibits adjuvant activity and augments CD8+ T cell responses with LNP-encapsulated OVA peptides. ODN 1018 sodium triggers sustained suppression of allergic airway inflammation. ODN 1018 sodium can be used for the research of allergic asthma and systemic lupus erythematosus .
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Cat. No.: HY-152830
CAS No.: 2394874-66-7
Purity:  99.51%
Synonyms: Q702
Target:  

c-Fms TAM Receptor MHC

Research Areas:  

Cancer

Adrixetinib (Q702) is an orally active triple inhibitor against CSF1R, Mer, and Axl, with Kd values of 8.7 nM, 0.8 nM, and 0.3 nM, respectively. Adrixetinib acts as a potent immune modulator that remodels the tumor microenvironment. Adrixetinib increases the abundance of M1 macrophages and CD8⁺ T cells, while decreasing the levels of M2 macrophages and myeloid-derived suppressor cells (MDSCs). Adrixetinib upregulates the expression of MHC class I and E-cadherin in tumor cells. Adrixetinib shows remarkable antitumor efficacy in syngeneic mouse tumor models. Adrixetinib is suitable for the research of breast cancer, renal adenocarcinoma, colon carcinoma, and melanoma .
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Cat. No.: HY-113008A
CAS No.: 7699-35-6
Purity:  99.92%
Synonyms: (Z)-Urocanic acid; cis-UCA
Target:  

5-HT Receptor

Research Areas:  

Inflammation/Immunology

cis-Urocanic acid is a 5-HT2A receptor agonist. cis-Urocanic acid binds to 5-HT receptor with relatively high affinity (Kd=4.6 nM). cis-Urocanic acid is an immune modulator that induces immunosuppression by binding to the 5-HT2A receptor .
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Cat. No.: HY-101058A
Purity:  95.11%
Target:  

PD-1/PD-L1

Research Areas:  

Inflammation/Immunology Cancer

PD1-PDL1-IN 1 TFA (compound 16) is a potent programmed cell death 1 (PD-1) inhibitor. PD1-PDL1-IN 1 TFA is useful as immune modulator .
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Cat. No.: HY-144501
CAS No.: 2230218-36-5
Purity:  98.14%
D18 is an immune modulator. D18 acts as a TLR7/8 dual agonist (EC50 = 24 nM for hTLR7 and 10 nM for hTLR8, respectively). D18 increases PD-L1 expression through epigenetic regulation, thus sensitizing tumors to PD-1/PD-L1 blockade. D18 is a ADC cytotoxin uesd for the systhesis of ADC HE-S2 (HY-144497). D18 has strong immune activation and anti-tumor activity. D18 commonly used in cancer research, such as colon cancer .
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Cat. No.: HY-N11451
CAS No.: 25541-09-7
Synonyms: LNFP-III
Lacto-N-fucopentaose III (LNFP-III) is an immune modulator. Lacto-N-fucopentaose III reduces the severity of experimental autoimmune encephalomyelitis (EAE) and CNS inflammation .
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Cat. No.: HY-106647
CAS No.: 1446418-48-9
Purity:  99.61%
Target:  

Interleukin Related

Research Areas:  

Inflammation/Immunology

Abacavir hydroxyacetate is an orally active inhibitor of IL-20 and PRINS. Abacavir hydroxyacetate reduces proliferation rate of skin in psoriasis as an immune modulator. Abacavir hydroxyacetate can be used for the research of inflammatory skin problems .
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Cat. No.: HY-101058
CAS No.: 2005454-12-4
Target:  

PD-1/PD-L1

Research Areas:  

Inflammation/Immunology

PD1-PDL1-IN 1 (compound 16) is a potent programmed cell death 1 (PD-1) inhibitor. PD1-PDL1-IN 1 is useful as immune modulator .
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Cat. No.: HY-152830A
Purity:  99.82%
Synonyms: Q702 TFA
Target:  

c-Fms TAM Receptor MHC

Research Areas:  

Cancer

Adrixetinib (Q702) TFA is an orally active triple inhibitor against CSF1R, Mer, and Axl, with Kd values of 8.7 nM, 0.8 nM, and 0.3 nM, respectively. Adrixetinib TFA acts as a potent immune modulator that remodels the tumor microenvironment. Adrixetinib TFA increases the abundance of M1 macrophages and CD8⁺ T cells, while decreasing the levels of M2 macrophages and myeloid-derived suppressor cells (MDSCs). Adrixetinib TFA upregulates the expression of MHC class I and E-cadherin in tumor cells. Adrixetinib TFA shows remarkable antitumor efficacy in syngeneic mouse tumor models. Adrixetinib TFA is suitable for the research of breast cancer, renal adenocarcinoma, colon carcinoma, and melanoma .
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Cat. No.: HY-N12737
CAS No.: 216987-13-2
15-epi-Danshenol A is a diterpenoid with an immune-modulating activity. 15-epi-Danshenol A shows inhibitory effect on B lymphoblasts cells in a concentration-dependent manner .
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Cat. No.: HY-U00088
CAS No.: 2697-85-0
Target:  

Others

Research Areas:  

Inflammation/Immunology Cancer

3b,7a,17a-Trihydroxyandrost-5-ene is a immune modulator extracted from patent US20030060425.
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Cat. No.: HY-10863S1
CAS No.: 2260669-86-9
Synonyms: AEA-d11
Anandamide-d11 is deuterium labeled Anandamide. Anandamide is an immune modulator in the central nervous system acts via not only cannabinoid receptors (CB1 and CB2) but also other targets (e.g., GPR18/GPR55) .
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Cat. No.: HY-113008AS
Purity:  99.46%
Synonyms: (Z)-Urocanic acid-13C3; cis-UCA-13C3
cis-Urocanic acid- 13C3 is the 13C-labeled cis-Urocanic acid. cis-Urocanic acid is a 5-HT2A receptor agonist. cis-Urocanic acid binds to 5-HT receptor with relatively high affinity (Kd=4.6 nM). cis-Urocanic acid is an immune modulator that induces immunosuppression by binding to the 5-HT2A receptor .
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Cat. No.: HY-B0300R
CAS No.: 52-67-5
Synonyms: D-(-)-Penicillamine (Standard)
Penicillamine (Standard) is the analytical standard of Penicillamine. This product is intended for research and analytical applications. Penicillamine (D-(-)-Penicillamine) is a penicillin metabolic degradation product, can be used as a heavy metal chelator. Penicillamine increases free copper and increases oxidative stress. Penicillamine has effect of seizures through nitric oxide/NMDA pathways. Penicillamine is a potential immune modulator. Penicillamine can be used for the research of Wilson disease, rheumatoid arthritis, and cystinuria .
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Cat. No.: HY-107138
CAS No.: 551936-17-5
Target:  

Others

Research Areas:  

Inflammation/Immunology

AIM-102 is an immune modulating anti-inflammatory agent. AIM-102 can inhibit LPS (HY-D1056)-induced neutrophilia increase. AIM-102 can be used for the researches of inflammation and immunology, such as allergic asthma .
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Cat. No.: HY-106647R
CAS No.: 1446418-48-9
Abacavir hydroxyacetate (Standard) is the analytical standard of Abacavir hydroxyacetate (HY-106647). This product is intended for research and analytical applications. Abacavir hydroxyacetate is an orally active inhibitor of IL-20 and PRINS. Abacavir hydroxyacetate reduces proliferation rate of sKin in psoriasis as an immune modulator. Abacavir hydroxyacetate can be used for the research of inflammatory sKin problems .
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Cat. No.: HY-127158
CAS No.: 140-56-7
Target:  

Bacterial

Research Areas:  

Infection

Fenaminosulf is a plant immune modulator and mutagen. Fenaminosulf impairs plant immune recognition and signal transduction by inhibiting the activities of key kinases such as Xa21 and PBL19, thereby regulating the expression of genes related to hormone metabolism, phenylpropane biosynthesis, and plant-pathogen interactions. Fenaminosulf affects the growth and gall formation of Zizania latifolia in a concentration-dependent manner. Fenaminosulf induces mutations in bacterial systems and causes plant chromosome aberrations, but shows no mutagenic activity or lethal effect in Drosophila melanogaster. Fenaminosulf exhibits inconsistent carcinogenicity in rat studies .
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