19 Results for "

fatal

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

19 Results for "fatal" in MCE Product Catalog:

27
27 Cited Publications
Cat. No.: HY-15398
CAS No.: 67-97-0
Purity:  99.94%
Synonyms: Cholecalciferol; Colecalciferol
Vitamin D3 (Cholecalciferol; Colecalciferol) is a naturally occuring form of vitamin D. Vitamin D3 induces cell differentiation and prevents proliferation of cancer cells.
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1 Cited Publications
Cat. No.: HY-N2486
CAS No.: 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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Cat. No.: HY-19934
CAS No.: 1402602-94-1
Synonyms: TAS-117
Target:  

Akt Apoptosis Autophagy

Research Areas:  

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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Cat. No.: HY-19934A
CAS No.: 2930090-28-9
Synonyms: TAS-117 hydrochloride
Target:  

Akt Apoptosis Autophagy

Research Areas:  

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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Cat. No.: HY-15398R
CAS No.: 67-97-0
Synonyms: Cholecalciferol (Standard); Colecalciferol (Standard)
Vitamin D3 (Standard) is the analytical standard of Vitamin D3. This product is intended for research and analytical applications. Vitamin D3 (Cholecalciferol; Colecalciferol) is a naturally occuring form of vitamin D. Vitamin D3 induces cell differentiation and prevents proliferation of cancer cells.
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Cat. No.: HY-W001117
CAS No.: 500-99-2
Synonyms: Phloroglucinol Dimethyl Ether
3,5-Dimethoxyphenol is a toxin metabolite, found in human consuming yew leaves .
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Cat. No.: HY-N2486R
CAS No.: 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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Cat. No.: HY-174631
Target:  

mRNA

Research Areas:  

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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Cat. No.: HY-P5724
Target:  

Bacterial

Research Areas:  

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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Cat. No.: 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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Cat. No.: HY-176233
CAS No.: 2765296-93-1
Target:  

Transthyretin (TTR)

Research Areas:  

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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Cat. No.: HY-121390
CAS No.: 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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Cat. No.: HY-156121
CAS No.: 2428478-22-0
Research Areas:  

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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Cat. No.: HY-W317408
CAS No.: 5157-89-1
Research Areas:  

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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Cat. No.: HY-181434
CAS No.: 6673-97-8
Target:  

Drug Derivative

Research Areas:  

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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Cat. No.: HY-118971
CAS No.: 236102-25-3
Target:  

Bacterial

Research Areas:  

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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Cat. No.: HY-121390A
CAS No.: 1976-49-4
Target:  

Endogenous Metabolite

Research Areas:  

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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Cat. No.: HY-106458
CAS No.: 22609-73-0
Synonyms: Bay a 7168
Target:  

Calcium Channel

Research Areas:  

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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