10217 Results for "

dauer-inducing activity

" in MedChemExpress (MCE) Product Catalog:
Products (10217)

10217 Results for "dauer-inducing activity" in MCE Product Catalog:

67
67 Cited Publications
Cat. No.: HY-N0184
CAS No.: 1405-86-3
Synonyms: Glycyrrhizin
Glycyrrhizic acid is a triterpenoid saponinl, acting as a direct HMGB1 antagonist, with anti-tumor, anti-diabetic activities.
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67
67 Cited Publications
Cat. No.: HY-76225
CAS No.: 53956-04-0
Synonyms: Monoammonium glycyrrhizinate; Glycyrrhizic acid ammonium salt; Ammonium glycyrrhizate
Ammonium glycyrrhizinate (Monoammonium glycyrrhizinate) has various pharmacological actions such as anti-inflammatory, antiallergic, antigastriculcer, and antihepatitis activities.
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67
67 Cited Publications
Cat. No.: HY-N0184A
CAS No.: 68797-35-3
Synonyms: Glycyrrhizic acid dipotassium; Dipotassium glycyrrhizate
Dipotassium glycyrrhizinate is a HMGB1 inhibitor, inhibits atopic dermatitis-related gene expression with anti-anti-inflammatory activity .
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67
67 Cited Publications
Cat. No.: HY-101085
CAS No.: 909089-13-0
Purity:  99.68%
Target:  

Wnt β-catenin

Research Areas:  

Cancer

SKL2001 is an agonist of the Wnt/β-catenin pathway, with anti-cancer activity. SKL2001 stabilizes intracellular β-catenin via disruption of the Axin/β-catenin interaction .
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66
66 Cited Publications
Cat. No.: HY-12289
CAS No.: 1073154-85-4
Purity:  99.87%
Synonyms: VS-6063; PF-04554878
Target:  

FAK

Research Areas:  

Cancer

Defactinib (VS-6063; PF-04554878) is a novel FAK inhibitor with potential antiangiogenic and antineoplastic activities.
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65
65 Cited Publications
Cat. No.: HY-15145A
CAS No.: 2468639-77-0
Purity:  99.19%
Target:  

Sirtuin Autophagy

Research Areas:  

Metabolic Disease

SRT 1720 dihydrochloride is a selective and orally active activator of SIRT1 with an EC50 of 0.10 μM, and shows less potent activities on SIRT2 and SIRT3 .
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65
65 Cited Publications
Cat. No.: HY-15145
CAS No.: 2060259-60-9
Purity:  99.37%
Target:  

Sirtuin Autophagy

Research Areas:  

Metabolic Disease

SRT 1720 monohydrochloride is a selective and orally active activator of SIRT1 with an EC50 of 0.10 μM, and shows less potent activities on SIRT2 and SIRT3 .
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63
63 Cited Publications
Cat. No.: HY-B0434
CAS No.: 36791-04-5
Synonyms: Ribasphere
Research Areas:  

Infection Cancer

Ribavirin (ICN-1229) is an antiviral agent against a broad spectrum of viruses including HCV, HIVl, and RSV. Ribavirin also has anti-orthopoxvirus and anti-variola activities.
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61
61 Cited Publications
Cat. No.: HY-13004
CAS No.: 376348-65-1
Purity:  99.88%
Synonyms: UK-427857
Target:  

CCR HIV

Maraviroc (UK-427857) is a selective CCR5 antagonist with activity against human HIV.
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61
61 Cited Publications
Cat. No.: HY-B0356
CAS No.: 85721-33-1
Synonyms: Bay-09867
Ciprofloxacin (Bay-09867) is a potent, orally active topoisomerase IV inhibitor. Ciprofloxacin induces mitochondrial DNA and nuclear DNA damage and lead to mitochondrial dysfunction, ROS production. Ciprofloxacin has anti-proliferative activity and induces apoptosis. Ciprofloxacin is a fluoroquinolone antibiotic, exhibiting potent antibacterial activity .
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58
58 Cited Publications
Cat. No.: HY-111783
CAS No.: 2230820-11-6
Purity:  99.86%
Research Areas:  

Cancer

AZD-7648 is a potent, orally active, selective DNA-PK inhibitor with an IC50 of 0.6 nM. AZD-7648 induces apoptosis and shows antitumor activity .
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58
58 Cited Publications
Cat. No.: HY-P9905
CAS No.: 205923-56-4
Synonyms: C225; IMC-C225
Research Areas:  

Cancer

Cetuximab (C225) is a human IgG1 monoclonal antibody that inhibits epidermal growth factor receptor (EGFR), with a Kd of 0.201 nM for EGFR by SPR. Cetuximab has potent antitumor activity .
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56
56 Cited Publications
Cat. No.: HY-A0107
CAS No.: 60-54-8
Tetracycline is a broad-spectrum antibiotic with oral activity. Tetracycline exhibits activity against a wide range of bacteria including gram-positive, gram-negative bacteria, chlamydiae, mycoplasmas and rickettsiae. Tetracycline can be used for the research of infections .
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56
56 Cited Publications
Cat. No.: HY-B0474
CAS No.: 64-75-5
Tetracycline hydrochloride is a broad-spectrum antibiotic with oral activity. Tetracycline hydrochloride exhibits activity against a wide range of bacteria including gram-positive, gram-negative bacteria, chlamydiae, mycoplasmas and rickettsiae. Tetracycline hydrochloride can be used for the research of infections .
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56
56 Cited Publications
Cat. No.: HY-16589
CAS No.: 579-13-5
Synonyms: MCH 32
Oligomycin A (MCH 32), created by Streptomyces, acts as a mitochondrial F0F1-ATP synthase inhibitor, with a Ki of 1 μM; Oligomycin A shows anti-fungal activity.
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55
55 Cited Publications
Cat. No.: HY-114481
CAS No.: 1801530-11-9
Purity:  99.77%
Synonyms: IKE
Target:  

Ferroptosis

Research Areas:  

Cancer

Imidazole ketone erastin is a potent, selective, and metabolically stable inhibitor of the cystine-glutamate antiporter, system xc - and an activator of ferroptosis. Imidazole ketone erastin has anti-tumor activity .
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53
53 Cited Publications
Cat. No.: HY-15845
CAS No.: 307543-71-1
Purity:  ≥98.0%
Target:  

IRE1

Research Areas:  

Cancer

STF-083010 is a specific IRE1α inhibitor. STF-083010 inhibits Ire1 endonuclease activity, without affecting its kinase activity, after endoplasmic reticulum stress.
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53
53 Cited Publications
Cat. No.: HY-10159
CAS No.: 641571-10-0
Purity:  99.94%
Synonyms: AMN107
Target:  

Bcr-Abl Autophagy

Research Areas:  

Cancer

Nilotinib is an orally available Bcr-Abl tyrosine kinase inhibitor with antineoplastic activity.
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53
53 Cited Publications
Cat. No.: HY-K1090

MCE Cytotoxicity LDH Assay Kit can detect LDH activity in the culture supernatant, which is indicative of cytotoxicity.

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53
53 Cited Publications
Cat. No.: HY-10320A
CAS No.: 1283526-53-3
Synonyms: BIRB 796 hydrochloride
Target:  

Autophagy Raf p38 MAPK

Research Areas:  

Inflammation/Immunology

Doramapimod hydrochloride (BIRB 796 hydrochloride) is an anti-inflammatory compound with biological activity through inhibition of p38 MAPK. Doramapimod hydrochloride can significantly inhibit the activities of TNF-α and IL-1β induced by LPS, LTA and PGN. Doramapimod hydrochloride showed a stronger inhibitory effect on inflammation induced by all three bacterial toxins, which was more significant compared with the effects of other compounds. Doramapimod hydrochloride can be used in the research of autoimmune diseases .
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