59 Results for "

Rin

" in MedChemExpress (MCE) Product Catalog:
Products (59)

59 Results for "Rin" in MCE Product Catalog:

10
10 Publications Verification
Cat. No.: HY-137471
CAS No.: 2682114-39-0
Purity:  99.80%
Synonyms: Rin1
Target:  

Notch

Research Areas:  

Cancer

RBPJ Inhibitor-1 (RIN1), the first RBPJ inhibitor, blocks the functional interaction of RBPJ with SHARP. RBPJ Inhibitor-1 (RIN1) inhibits NOTCH-dependent tumor cell proliferation .
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1 Cited Publications
Cat. No.: HY-101774
CAS No.: 2095849-04-8
Purity:  98.11%
Target:  

c-Fms

Research Areas:  

Cancer

CSF1R-IN-1 is a CSF1R inhibitor with an with an IC50 of 0.5 nM.
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1 Cited Publications
Cat. No.: HY-139990
CAS No.: 2760584-90-3
Purity:  98.26%
Target:  

c-Fms

Research Areas:  

Cancer

CSF1R-IN-3 (compound 21) is a potent and orally active CSF-1R inhibitor (IC50=2.1 nM). CSF1R-IN-3 is a potent antiproliferative activity against colorectal cancer cells. CSF1R-IN-3 inhibits the progression of colorectal cancer by suppressing the migration of macrophages, reprograming M2-like macrophages to the M1 phenotype, and enhancing the antitumor immunity .
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Cat. No.: HY-P1840
CAS No.: 142846-71-7
Galanin Receptor Ligand M35 is a high-affinity ligand and antagonist of galanin receptor (Kd=0.1 nM). Galanin Receptor Ligand M35 exerts a Ki values of 0.11 and 2.0 nM for human galanin receptor type 1 and 2, respectively .
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Cat. No.: HY-160842
CAS No.: 3024322-57-1
Target:  

c-Fms

Research Areas:  

Neurological Disease

CSF1R-IN-24 (Example 134) is an orally active CSF1R inhibitor. CSF1R-IN-24 significantly inhibits the survival of human ipSC-derived microglia (hiPSC-MG) .
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Cat. No.: HY-147615
CAS No.: 2361556-35-4
Purity:  98.75%
Target:  

c-Fms

Research Areas:  

Cancer

CSF1R-IN-12 (compound 1) is a potent inhibitor of CSF1R. Colony stimulating factor 1 (CSF-1, also known as macrophage colony stimulating factor, M-CSF) is an important growth factor that controls bone marrow progenitor cells, monocytes, macrophages, and giants. CSF1R-IN-12 has the potential for the research of cancer diseases .
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Cat. No.: HY-168954
Target:  

c-Fms Apoptosis Akt ERK STAT

Research Areas:  

Inflammation/Immunology Cancer

CSF1R-IN-26 (Compound III-1) is the inhibitor for CSF-1R with an IC50 of 20.07 nM. CSF1R-IN-26 promotes the polarization of M2 macrophages to M1 macrophages, thereby inducing apoptosis in MC-38 cancer cell. CSF1R-IN-26 inhibits the activation of AKT/ERK/STAT3 signaling pathway. CSF1R-IN-26 reconstructs the tumor immune microenvironment and exhibits antitumor activity in mouse models. CSF1R-IN-26 exhibits pharmacokinetics characteristics in SD rats with a half-life 1.86 hours, and an oral bioavailability of 79.22% .
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Cat. No.: HY-144041
CAS No.: 2716184-93-7
Target:  

c-Fms

Research Areas:  

Cancer

CSF1R-IN-5 is a potent inhibitor of CSF1R. CSF-1R is expressed in macrophages, and the survival and differentiation of macrophages depends on the CSF-1/CSF-1R signaling pathway. CSF1R-IN-5 affects the exchange of inflammatory factors between TAMs and glioma cells. CSF1R-IN-5 has the potential for the research of cancer disease (extracted from patent WO2021197276A1, compound 11) .
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Cat. No.: HY-147609
CAS No.: 2765301-60-6
Target:  

c-Fms

Research Areas:  

Cancer

CSF1R-IN-8 (Compound 22) is a CSF-1R inhibitor with an IC50 of 0.012 μM .
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Cat. No.: HY-147611
CAS No.: 2765301-88-8
Target:  

c-Fms

Research Areas:  

Cancer

CSF1R-IN-10 (Compound 48) is a CSF-1R inhibitor with an IC50 of 0.005 μM .
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Cat. No.: HY-155001
CAS No.: 2925744-43-8
Target:  

c-Fms

Research Areas:  

Others

CSF1R-IN-15 (compound 23) is an inhibitor targeting CSF1R. The colony-stimulating factor-1 receptor (CSF1R) is a tyrosine kinase embedded in the cell membrane of macrophages. The receptor is activated by colony-stimulating factor-1 (CSF-1) and interleukin-34, and signaling via CSF1R is crucial for the differentiation, proliferation, and survival of macrophages .
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Cat. No.: HY-RS11982
Research Areas:  

Others

RIN1 Human Pre-designed siRNA Set A contains three designed siRNAs for RIN1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS11983
Research Areas:  

Others

RIN2 Human Pre-designed siRNA Set A contains three designed siRNAs for RIN2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS11984
Research Areas:  

Others

RIN3 Human Pre-designed siRNA Set A contains three designed siRNAs for RIN3 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS17055
Research Areas:  

Others

Rin1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Rin1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P5796
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

FS-2 is a potent and specific L-type CaV channel inhibitor. FS-2 inhibits high K + or glucose induced L-type Ca 2+ influx in RIN beta cells .
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Cat. No.: HY-RS12004
Research Areas:  

Others

RIT2 Human Pre-designed siRNA Set A contains three designed siRNAs for RIT2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-157422
CAS No.: 1819989-27-9
Target:  

c-Fms

Research Areas:  

Cancer

CSF1R-IN-19 is a potent inhibitor of CSF1R. CSF1R-IN-19 affects the exchange of inflammatory factors between TAMs and glioma cells. CSF1R-IN-19 has the potential for the research of cancer .
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Cat. No.: HY-176546
Target:  

Neurokinin Receptor

Research Areas:  

Endocrinology

NK3R-IN-2 is an orally active NK3R inhibitor with an IC50 of 330.50 nM for human NK3R. NK3R-IN-2 can pass through the blood-brain barrier. NK3R-IN-2 has excellent NK3R binding affinity (IC50 = 87.31 nM) in CHO-K1 cells. NK3R-IN-2 effectively inhibits the level of luteinizing hormone (LH). NK3R-IN-2 can be used for research on hormone related conditions .
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Cat. No.: HY-149014
CAS No.: 2639148-08-4
Research Areas:  

Neurological Disease

OX2R-IN-1 (compound 15) is a low cytotoxicity profile OX2R-IN-1 antagonist (a potential OX2R binder) with an IC50 value of 484 μM. OX2R-IN-1 (compound 15) can cross the BBB into the brain with a short half-life .
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