18 Results for "

fatal

" in MedChemExpress (MCE) Product Catalog:
Products (18)

18 Results for "fatal" in MCE Product Catalog:

1
1 Cited Publications
Referencia número: HY-N2486
No. CAS: 30197-14-9
Desoxyrhaponticin is a kind of oral drug that inhibits effective fatty acid synthesis (FASN), and has a fatal effect on cancer cells. Desoxyrhaponticin has the ability to inhibit glucose uptake, improve oral glucose tolerance as a diabetic agent, and possess anti-diabetic effects.
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Referencia número: HY-19934
No. CAS: 1402602-94-1
Synonyms: TAS-117
Target:  

Akt Apoptosis Autophagy

Áreas de investigación:  

Cancer

Pifusertib (TAS-117) is a potent, selective, orally active allosteric Akt inhibitor (with IC50s of 4.8, 1.6, and 44 nM for Akt1, 2, and 3, respectively). Pifusertib triggers anti-myeloma activities and enhances fatal endoplasmic reticulum (ER) stress induced by proteasome inhibition. Pifusertib induces apoptosis and autophagy .
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Referencia número: HY-19934A
No. CAS: 2930090-28-9
Synonyms: TAS-117 hydrochloride
Target:  

Akt Apoptosis Autophagy

Áreas de investigación:  

Cancer

Pifusertib (TAS-117) hydrochloride is a potent, selective, orally active allosteric Akt inhibitor (with IC50s of 4.8, 1.6, and 44 nM for Akt1, 2, and 3, respectively). Pifusertib hydrochloride triggers anti-myeloma activities and enhances fatal endoplasmic reticulum (ER) stress induced by proteasome inhibition. Pifusertib hydrochloride induces apoptosis and autophagy .
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Referencia número: HY-N2486R
No. CAS: 30197-14-9
Desoxyrhaponticin (Standard) is the analytical standard of Desoxyrhaponticin. This product is intended for research and analytical applications. Desoxyrhaponticin is a kind of oral drug that inhibits effective fatty acid synthesis (FASN), and has a fatal effect on cancer cells. Desoxyrhaponticin has the ability to inhibit glucose uptake, improve oral glucose tolerance as a diabetic agent, and possess anti-diabetic effects .
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Referencia número: HY-174631
Target:  

mRNA

Áreas de investigación:  

Inflammation/Immunology

Human IL18 mRNA encodes the human interleukin 18 (IL18) protein, a proinflammatory cytokine of the IL-1 family. IL18 is constitutively found as a precursor within the cytoplasm of a variety of cells including macrophages and keratinocytes. This cytokine has been implicated in the injury of different organs, and in potentially fatal conditions characterized by a cytokine storm.
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Referencia número: HY-P5724
Target:  

Bacterial

Áreas de investigación:  

Infection

Nv-CATH is an antibacterial peptide of frog origin. Nv-CATH has broad-spectrum antibacterial activity against gram-positive and gram-negative bacteria. Nv-CATH significantly protects mice from fatal infections caused by Staphylococcus aureus. Nv-CATH protects mice from bacterial infection through antimicrobial immunoregulatory duality .
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Referencia número: HY-P11250
HVF18-a3-d is an antimicrobial peptide. HVF18-a3-d reduces NO production. HVF18-a3-d inhibits the production of TNF-α and IL-6, reduces ROS production, and suppresses the TLR4 signaling pathway, as well as LPS-induced phosphorylation of ERK, JNK, and p38 MAPK. HVF18-a3-d exhibits antimicrobial activity against a variety of bacteria by disrupting their outer and inner membranes. HVF18-a3-d protects mice from fatal septic shock induced by Acinetobacter baumannii resistant to Carbapenem. HVF18-a3-d shows anti-inflammatory and antioxidant effects .
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Referencia número: HY-176233
No. CAS: 2765296-93-1
Target:  

Transthyretin (TTR)

Áreas de investigación:  

Cardiovascular Disease

Transthyretin-IN-4 (Compound B26) is a bivalent inhibitor of transthyretin (TTR) amyloidosis (bIC50: 0.09 µM, pIC50: 1.4 µM). Transthyretin-IN-4 is used in the study of fatal heart failure with preserved ejection fraction (HFpEF) and fatal arrhythmias .
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Referencia número: HY-121390
No. CAS: 303-34-4
Lasiocarpine, a hepatotoxic pyrrolizidine alkaloid (PA), causes fatal liver veno-occlusive disease in vivo. Lasiocarpine is toxic only after its metabolic conversion to the toxic intermediate, including dehydrolasiocarpine and N-oxide .
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Referencia número: HY-156121
No. CAS: 2428478-22-0
Áreas de investigación:  

Inflammation/Immunology Cancer

NLRP3-IN-20 (compound 11) is an orally available inhibitor of the NLRP3 inflammasome with an IC50 of 25 nM for IL-1β secretion. NLRP3-IN-20 has excellent pharmacokinetic properties and demonstrated significant efficacy in models of non-alcoholic steatohepatitis, fatal septic shock, and colitis .
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Referencia número: HY-W317408
No. CAS: 5157-89-1
Áreas de investigación:  

Others

(+)-Menthyl acetate is a compound isolated from natural Cunila angustifolia Benth essential oil. The selectivity of (+)-Menthyl acetate is higher than that of MCF-7 cell line, IC50=34.0 μg?mL -1, and lower than that of SK-Mel-28 cell line, IC50=279.9 μg?mL -1, on A549 cell without fatal .
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Referencia número: HY-181434
No. CAS: 6673-97-8
Target:  

Drug Derivative

Áreas de investigación:  

Endocrinology

Spiroxasone is an orallyactive thioacetyl-containing steroid. Spiroxasone can prevent fatal renal damage and nephrocalcinosis associated with acute mercuric chloride intoxication. Spiroxasone can be used for the research of acute HgCl2 poisoning .
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Referencia número: HY-118971
No. CAS: 236102-25-3
Target:  

Bacterial

Áreas de investigación:  

Infection

CHIR-29498 is an antibacterial peptoid. CHIR-29498 is active against both Gram-positive and Gram-negative bacteria. CHIR-29498 can be used for the study of fatal Staphylococcus aureus .
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Referencia número: HY-121390A
No. CAS: 1976-49-4
Target:  

Endogenous Metabolite

Áreas de investigación:  

Cancer

Lasiocarpine hydrochloride, a hepatotoxic pyrrolizidine alkaloid (PA), causes fatal liver veno-occlusive disease in vivo. Lasiocarpine hydrochloride is toxic only after its metabolic conversion to the toxic intermediate, including dehydrolasiocarpine and N-oxide .
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Referencia número: HY-106458
No. CAS: 22609-73-0
Synonyms: Bay a 7168
Target:  

Calcium Channel

Áreas de investigación:  

Cardiovascular Disease

Niludipine (Bay a 7168) is an orally active calcium channel blocker and vasodilator with antihypertensive effects. Niludipine can improve early fatal ventricular arrhythmias induced by acute myocardial ischemia in rats. Niludipine can reduce left ventricular systolic and diastolic loads during pacing-induced angina pectoris. Niludipine can be used in the research of cardiovascular diseases such as coronary heart disease and myocardial ischemia .
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Referencia número: HY-P78023
Pureza:  ≥ 95%, as determined by Bis-Tris PAGE.
Synonyms: PRNP; PrP27-30; Prev. PRIP; ASCR; Prev. CJD; Gerstmann-Strausler-Scheinker Syndrome; Prev. GSS; Creutzfeldt-Jakob Disease; AltPrP; fatal Familial Insomnia; PRP; Prion Protein (P27-30); Alternative Prion Protein; Prion-Related Protein; Major Prion Protein
Species:  
Mouse
Source:  
HEK293
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Referencia número: HY-P74619A
Pureza:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: PRNP; PrP27-30; Prev. PRIP; ASCR; Prev. CJD; Gerstmann-Strausler-Scheinker Syndrome; Prev. GSS; Creutzfeldt-Jakob Disease; AltPrP; fatal Familial Insomnia; PRP; Prion Protein (P27-30); Alternative Prion Protein; Prion-Related Protein; Major Prion Protein
Species:  
Human
Source:  
HEK293
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Referencia número: HY-P74619
Pureza:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: PRNP; PrP27-30; Prev. PRIP; ASCR; Prev. CJD; Gerstmann-Strausler-Scheinker Syndrome; Prev. GSS; Creutzfeldt-Jakob Disease; AltPrP; fatal Familial Insomnia; PRP; Prion Protein (P27-30); Alternative Prion Protein; Prion-Related Protein; Major Prion Protein
Species:  
Human
Source:  
HEK293
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