44 Results for "

MGL-IN-1

" in MedChemExpress (MCE) Product Catalog:
Products (44)

44 Results for "MGL-IN-1" in MCE Product Catalog:

Cat. No.: HY-119033
CAS No.: 1881244-28-5
Purity:  98.65%
Target:  

MAGL

Research Areas:  

Inflammation/Immunology

MGL-IN-1 is a potent and selective irreversible MGL (β-lactam-based monoacylglycerol lipase) inhibitor. MGL-IN-1 alleviates symptoms in a MS model in vivo and exhibits analgesic effects in an acute inflammatory pain model in vivo. MGL-IN-1 displays high membrane permeability and brain penetrant [1].
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Cat. No.: HY-177731
Research Areas:  

Cancer

MG-Lin1 is a molecular glucose degrading agent that targets the Lin28 protein. MG-Lin1 can significantly reduce the mRNA levels of let-7 targeting oncogenes. MG-Lin1 can significantly inhibit the migration ability of cancer cells. MG-Lin1 has no obvious cytotoxicity. MG-Lin1 can be used for cancer research [1].
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1 Cited Publications
Cat. No.: HY-128780B
CAS No.: 2408422-41-1
Purity:  99.74%
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

SPR206 acetate is a polymyxin analog with antibiotic activity against Gram-negative pathogens, including multidrug-resistant (MDR) variants. SPR206 acetate has an anti-bacterial infection effect by interacting with the bacterium’s outer membrane. The MIC values of SPR206 acetate against Pseudomonas aeruginosa Pa14 and Acinetobacter baumannii NCTC13301 are both 0.125 mg/L .
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1 Cited Publications
Cat. No.: HY-139983
CAS No.: 2685795-52-0
Purity:  99.95%
Target:  

Fungal

Research Areas:  

Infection

SDH-IN-1 (compound 4i) is a succinate dehydrogenase (SDH) inhibitor with an IC50 of 4.53 μM. SDH-IN-1 has potent antifungal activities. SDH-IN-1 displays potent activity against S. sclerotiorum (EC50 of 0.14 mg/L) .
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Cat. No.: HY-19806
CAS No.: 689293-68-3
Synonyms: CXA-101 free base; FR264205 free base
Target:  

Antibiotic Bacterial

Research Areas:  

Infection

Ceftolozane (CXA-101 free base; FR264205 free base) is a cephalosporin antibiotic with potent activity againstPseudomonas aeruginosa and strains Enterobacteriaceae, with MICs of 0.5 and 0.25-0.5 mg/L .
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Cat. No.: HY-D0862
CAS No.: 145551-16-2
DIDNTB is a dye. DIDNTB exhibits chemical sensitivity and specificity toward albumin. DIDNTB is much less affected by other proteins. DIDNTB enables the detection of urinary albumin at concentrations ≥10 mg/L .\n
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Cat. No.: HY-167887
CAS No.: 2894124-00-4
Target:  

Endogenous Metabolite

Research Areas:  

Infection

7PPD-Q is a substituted p-phenylenediamine antioxidants derivatives. 7PPD-Q has toxic to the bacterium V. fischeri (EC50 = 14.9 mg/L) .
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Cat. No.: HY-N1673
CAS No.: 1194-98-5
Synonyms: Gentisaldehyde
2,5-Dihydroxybenzaldehyde (Gentisaldehyde) is a naturally occurring antimicrobial that inhibits the growth of Mycobacterium avium subsp. paratuberculosis. 2,5-Dihydroxybenzaldehyde is active against S. aureus strains with a MIC50 of 500 mg/L .
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Cat. No.: HY-N3706
CAS No.: 15297-92-4
Target:  

Fungal

Dehydro-α-lapachone can be isolated from the methanol extract of stems of Catalpa ovata G Don. Dehydro-α-lapachone inhibits mycelial growth of Botrytis cinerea with IC50 value 0.41 mg/L .
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Cat. No.: HY-128780
CAS No.: 2407717-17-1
Synonyms: SPR206
Target:  

Bacterial

Research Areas:  

Infection Cancer

Upleganan (SPR206), a polymyxin analogue, and shows antibiotic activity against multidrug resistant Gram-negative pathogen. The MIC values of Upleganan against Pseudomonas aeruginosa Pa14 and Acinetobacter baumannii NCTC13301 are both 0.125 mg/L .
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Cat. No.: HY-W272217
CAS No.: 630-02-4
Synonyms: n-Octacosane; NSC 5549
Octacosane is an endogenous metabolite with antibacterial activity. Octacosane shows high cytotoxicity against murine melanoma B16F10-Nex2 cells besides inducing protection against a grafted subcutaneous melanoma. Octacosane has the larvicidal activity against mosquito Culex quinquefasciatus with the LC50 concentration of 7.2 mg/l .
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Cat. No.: HY-122298
CAS No.: 517875-34-2
Synonyms: XDE 777
Target:  

Antibiotic Fungal

Research Areas:  

Infection

Fenpicoxamid is a new fungicide. Fenpicoxamid inhibits the growth of the fungus Z. tritici with an EC50 value of 0.051 mg/L .
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Cat. No.: HY-N10069
CAS No.: 83162-84-9
Bonducellin is a a homoisoflavonoid, which can be isolated from Caesalpinia digyna roots. Bonducellin is a potent inhibitor of efflux pump (EP), while EP induces resistance in mycobacteria and serves as a target of anti-TB (tuberculosis) agents. Bonducellin reduces MIC of EtBr by 8-fold against M. smegmatis (MIC=62.5 mg/L) .
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Cat. No.: HY-149399
Target:  

GABA Receptor

Research Areas:  

Infection

GABA-IN-1 (Compound 6) is a GABA inhibitor. GABA-IN-1 has larvicidal activity and insecticidal effect, with mortality rates of 93% at 50 mg/L .
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Cat. No.: HY-149400
CAS No.: 2363715-13-1
Target:  

GABA Receptor

Research Areas:  

Infection

GABA-IN-2 (Compound 5) is a GABA inhibitor. GABA-IN-2 has larvicidal activity and insecticidal effect, with mortality rates of 87% at 50 mg/L .
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Cat. No.: HY-169571
CAS No.: 430444-03-4
Target:  

Bacterial

Research Areas:  

Infection

Antimicrobial agent-38 (compound 10) is a potent inhibitor of methicillin-resistant S. aureus strain ATCC 700699 and nonresistant strain ATCC 29213, with MICs of 32 and 64 mg/L .
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Cat. No.: HY-155334
CAS No.: 2987900-56-9
Target:  

Parasite

Research Areas:  

Others

RyRs activator 4 (compound B18) is an insect ryanodine receptor activator. RyRs activator 4 has a larvicidal activity of Mythimna separata with an LC50 value of 1.32 mg/L .
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Cat. No.: HY-168527
Target:  

Histone Demethylase

Research Areas:  

Cancer

Acaricide agent 1 (Compound 7l) is a potent LSD1 inhibitor. LSD1 exhibits excellent acaricidal activity against egg of T. cinnabarinus with a LC50 of 0.0035 mg/L .
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Cat. No.: HY-N9075
CAS No.: 204134-70-3
9-(4′-Hydroxyphenyl)-2-methoxyphenalen-1-one is a phytoalexin and mixed competitive α-glucosidase inhibitor of Bacillus stearothermophilus (IC50: 3.86 mg/L) .
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Cat. No.: HY-155700
CAS No.: 3010257-33-4
Target:  

Fungal

Research Areas:  

Infection

SDH-IN-6 (compound 6i) is a potent succinate dehydrogenase (SDH) inhibitor. SDH-IN-6 has antifungal activity against Valsa mali with an EC50 value of 1.77 mg/L .
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