37 Results for "

macrophage migration inhibitory factor

" in MedChemExpress (MCE) Product Catalog:
Products (37)

37 Results for "macrophage migration inhibitory factor" in MCE Product Catalog:

25
25 Publications Verification
Cat. No.: HY-16692
CAS No.: 478336-92-4
Synonyms: MIF Antagonist
ISO-1 is a macrophage migration inhibitory factor (MIF) antagonist with an IC50 of 7 μM.
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11
11 Cited Publications
Cat. No.: HY-110063
CAS No.: 41270-96-6
Purity:  99.46%
Synonyms: 4-Iodo-6-phenylpyrimidine
4-IPP (4-Iodo-6-phenylpyrimidine) is a specific suicide substrate and irreversible inhibitor of macrophage migration inhibitory factor (MIF) .
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10
10 Cited Publications
Cat. No.: HY-P7387
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: MIF; L-Dopachrome Isomerase; Prev. GLIF; Glycosylation-Inhibiting factor; Phenylpyruvate Tautomerase; MMIF; GIF; Epididymis Secretory Sperm Binding Protein; L-Dopachrome Tautomerase; macrophage migration inhibitory factor; macrophage migration inhibitory
Species:  
Human
Source:  
E. coli
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5
5 Cited Publications
Cat. No.: HY-17009
CAS No.: 123663-49-0
Synonyms: T614
Iguratimod is an antirheumatic agent, acts as an inhibitor of COX-2, with an IC50 of 20 μM (7.7 μg/mL), but shows no effect on COX-1. Iguratimod also inhibits macrophage migration inhibitory factor (MIF) with an IC50 of 6.81 μM.
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3
3 Cited Publications
Cat. No.: HY-110095
CAS No.: 1309793-47-2
Purity:  99.64%
(±)-CPSI-1306 is an orally available antagonist of macrophage migration inhibitory factor (MIF).
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3
3 Cited Publications
Cat. No.: HY-P7388
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: MIF; L-Dopachrome Isomerase; Prev. GLIF; Glycosylation-Inhibiting factor; Phenylpyruvate Tautomerase; MMIF; GIF; Epididymis Secretory Sperm Binding Protein; L-Dopachrome Tautomerase; macrophage migration inhibitory factor; macrophage migration inhibitory
Species:  
Mouse
Source:  
E. coli
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2
2 Cited Publications
Cat. No.: HY-110084
CAS No.: 99420-15-2
Purity:  99.69%
BTZO-1, a chemical probe, binds to Macrophage migration inhibitory factor (MIF) with a Kd value of 68.6 nM, and its binding requires the N-terminal Pro1. BTZO-1 can activate antioxidant response element (ARE)-mediated gene expression and suppress oxidative stress-induced cardiomyocyte apoptosis in vitro .
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1
1 Cited Publications
Cat. No.: HY-147390
CAS No.: 1208448-95-6
Purity:  99.88%
MIF098 is a macrophage migration inhibitory factor (MIF) antagonist. MIF098 inhibits proliferation, migration and fibrosis of pulmonary smooth muscle cells. MIF098 can be used for immunoinflammation-related disease research .
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1
1 Cited Publications
Cat. No.: HY-P82167
Synonyms: MIF; GLIF; MMIF; macrophage migration inhibitory factor; MIF; Glycosylation-inhibiting factor; GIF; L-dopachrome isomerase; L-dopachrome tautomerase; Phenylpyruvate tautomerase

Host:  

Rabbit

Application:  

WB, IP, FC

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-W019710
CAS No.: 1396841-57-8
Target:  

HDAC

Research Areas:  

Neurological Disease

(E,E)-RGFP966 is a selective and CNS permeable HDAC3 inhibitor that can be used for the research of Huntington’s disease .
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Cat. No.: HY-148117
CAS No.: 2758431-97-7
Purity:  99.96%
MD13 is a MIF PROTAC degrader with a DC50 of approximately 100 nM. MD13 induces ubiquitination and degradation of MIF by recruiting the Cereblon Cullin RING E3 ubiquitin ligase complex. MD13 inactivates the MAPK pathway and induces G2/M phase cell cycle arrest. MD13 exhibits antiproliferative effects in 3D tumor spheroid models. MD13 can be used in lung cancer-related research .
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Cat. No.: HY-D0039
CAS No.: 19088-73-4
Target:  

Fluorescent Dye

Research Areas:  

Others

3-Cyanoumbelliferone is a coumarin derivative, acting as molecular probe and fluorescent dye. 3-Cyanoumbelliferone is also a macrophage migration inhibitory factor (MIF) tautomerase inhibitor with a Ki of 2.9 μM .
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Cat. No.: HY-144190
CAS No.: 851095-20-0
MIF-IN-1 (compound 14) is a potent macrophage migration inhibitory factor (MIF) inhibitor (pIC50=6.87) .
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Cat. No.: HY-144196
CAS No.: 2489514-05-6
Research Areas:  

Cancer

MIF-IN-4 hydrochloride is potent macrophage migration inhibitory factor (MIF) inhibitor (pIC50=5.01-6). MIF is a cytokine originally found to play a role in inhibiting macrophage migration .
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Cat. No.: HY-16692R
CAS No.: 478336-92-4
Synonyms: MIF Antagonist (Standard)
ISO-1 (Standard) is the analytical standard of ISO-1. This product is intended for research and analytical applications. ISO-1 is a macrophage migration inhibitory factor (MIF) antagonist with an IC50 of 7 μM.
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Cat. No.: HY-115887
CAS No.: 1985622-33-0
Purity:  99.90%
Research Areas:  

Cancer

R110 is a potent, competitive inhibitor of macrophage migration inhibitory factor 2 (MIF2) tautomerase with an IC50 of 15 μM. R110 has the potential for the research of cancer diseases .
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Cat. No.: HY-146318
CAS No.: 2582755-31-3
MIF-IN-5 (compound 1d) is a potent and reversible macrophage migration inhibitory factor (MIF) competitive inhibitor with an IC50 of 4.8 μM and a Ki value of 3.3 μM, respectively .
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Cat. No.: HY-121356S
CAS No.: 1189661-02-6
Carebastine-d5 is the deuterium labeled Carebastine. Carebastine is the active metabolite of Ebastine. Carebastine is a histamine H1 receptor antagonist. Carebastine inhibits VEGF-induced HUVEC and HPAEC proliferation, migration and angiogenesis in a dose-dependent manner . Carebastine suppresses the expression of macrophage migration inhibitory factor .
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Cat. No.: HY-121356S1
CAS No.: 1190019-51-2
Carebastine-d5 Methyl Ester is the deuterium labeled Carebastine. Carebastine is the active metabolite of Ebastine. Carebastine is a histamine H1 receptor antagonist. Carebastine inhibits VEGF-induced HUVEC and HPAEC proliferation, migration and angiogenesis in a dose-dependent manner . Carebastine suppresses the expression of macrophage migration inhibitory factor .
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Cat. No.: HY-146319
CAS No.: 2582758-61-8
MIF-IN-6 (compound 2d) is a potent macrophage migration inhibitory factor (MIF) inhibitor with an IC50 of 1.4 μM and a Ki value of 0.96 μM, respectively. MIF-IN-6 attenuates MIF-induced ERK phosphorylation and inhibits proliferation of A549 cells .
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