74 Results for "

NPCs

" in MedChemExpress (MCE) Product Catalog:
Products (74)

74 Results for "NPCs" in MCE Product Catalog:

16
16 Publications Verification
Art. -Nr.: HY-17376
CAS. Nr.: 163222-33-1
Synonyms: SCH 58235
Target:  

Keap1-Nrf2 Autophagy

Forschungsgebiete:  

Cardiovascular Disease Cancer

Ezetimibe (SCH 58235) is a potent cholesterol absorption inhibitor. Ezetimibe is a Niemann-Pick C1-like1 (NPC1L1) inhibitor, and is a potent Nrf2 activator.
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5
5 Cited Publications
Art. -Nr.: HY-N2292
CAS. Nr.: 151870-74-5
Kinsenoside is the main active ingredient of the genus plant, and has various biological activities. Kinsenoside and Nrf2 depend on the protection of nuclear cells (NPCs), which significantly reduces their ability to survive. Kinsenoside Active NPC Medium AKT-ERK1/2-Nrf2 Signal passage, Prevent physical decline, aging, harmonious physical function impairment. Kinsenoside can improve the puncture guide model for intermediate vertebral wall discharge (IDD).
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3
3 Cited Publications
Art. -Nr.: HY-N6954
CAS. Nr.: 76996-27-5
Garcinone C, a xanthone derivative, is a natural compound extracted from Garcinia oblongifolia that is used as an anti-inflammatory, astringency and granulation-promoting medicine, and has potential cytotoxic effects on certain cancers. Garcinone C stimulates the expression levels of ATR and 4E-BP1, arrests the cell cycle, inhibits cell viability of the human Nasopharyngeal carcinoma (NPC) cell lines CNE1, CNE2, HK1 and HONE1 in a time‑ and dose‑dependent manner through inhibition of Hedgehog signaling pathway. Garcinone C is orally active .
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2
2 Cited Publications
Art. -Nr.: HY-116815
CAS. Nr.: 501104-16-1
Reinheit:  99.75%
Forschungsgebiete:  

Infection Neurological Disease

Lalistat 1 is a potent, selective, and competitive inhibitor of lysosomal acid lipase (LAL) and against purified human LAL (phLAL) with an IC50 of 68 nM. Lalistat 1 is a inhibitor of immunoglobulin A1 protease (IgA1P) proteases for H. influenzae, has less effects on other serine hydrolases (trypsin or β-lactamase, etc.). Lalistat 1 can be used for the research of niemann-pick type C (NPC) disease .
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1
1 Cited Publications
Art. -Nr.: HY-113427
CAS. Nr.: 693-72-1
Reinheit:  ≥98.0%
trans-Vaccenic acid is a naturally occurring trans fatty acid (TFA). trans-Vaccenic acid inhibits nasopharyngeal carcinoma (NPC) cell growth and induces apoptosis through the inhibition of Bad/Akt phosphorylation. trans-Vaccenic acid is a precursor for the synthesis of saturated fatty acid in the rumen and of conjugated Linoleic acid (CLA) at the tissue level. trans-Vaccenic acid exerts hypolipidemic effects in a rat model of obesity .
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1
1 Cited Publications
Art. -Nr.: HY-W395779
CAS. Nr.: 1335113-30-8
Target:  

Filovirus

Forschungsgebiete:  

Infection

EBOV-IN-1 (com 3.47) is an adamantane dipeptide piperazine and an inhibitor of Ebola virus (EBOV). EBOV-IN-1 targets Niemann-Pick C1 (NPC1) and inhibits its binding to the EBOV glycoprotein (GP) that activates and mediates viral penetration into host cells, thereby inhibiting EBOV infection. EBOV-IN-1 inhibits pseudotyped EBOV infection with an IC50 of 13 nM .
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1
1 Cited Publications
Art. -Nr.: HY-113845
CAS. Nr.: 10285-06-0
Reinheit:  ≥99.0%
(+)-Intermedine, a pyrrolizidine alkaloid (PA), exhibits significant cytotoxicity in neural progenitor cells (NPCs) .
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Art. -Nr.: HY-P99621
CAS. Nr.: 2467411-25-0
Synonyms: NPC-21; EV2038

Target:  

CMV

Forschungsgebiete:  

Infection

Fiztasovimab (NPC-21; EV2038) is a fully human IgG1λ mAb against human cytomegalovirus (hCMV). Fiztasovimab acts neutralizing activity by binding to the antigenic domain 1 of glycoprotein B on hCMV envelope. Fiztasovimab inhibits cell-to-cell transmission of hCMV .
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Art. -Nr.: HY-W010514
CAS. Nr.: 1460-57-7
trans-Cyclohexane-1,2-diol (TCHD) is a transient dilator of the nuclear pore complex (NPC). By interacting with the hydrophobic core (FG nucleoporin) of the NPC, trans-Cyclohexane-1,2-diol can disrupt the NPC structure and reversibly increase the permeability of the nuclear pore, allowing macromolecules larger than 40 kDa (such as plasmid DNA) to enter the cell nucleus by passive diffusion, thereby enhancing the nuclear import efficiency of non-viral vectors. trans-Cyclohexane-1,2-diol can improve the efficiency of in vitro electrotransfection or lipid-mediated gene transfection, especially significantly increasing gene expression in differentiated airway epithelial cells .
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Art. -Nr.: HY-136433
CAS. Nr.: 140-79-4
Reinheit:  99.94%
Synonyms: 1,4-Dinitrosopiperazine; DNP
Target:  

Others

Forschungsgebiete:  

Cancer

N,N'-Dinitrosopiperazine (1,4-Dinitrosopiperazine; DNP) is a carcinogen with specificity for nasopharyngeal epithelium and facilitates NPC metastasis. N,N'-Dinitrosopiperazine regulates multiple signaling pathways through protein phosphorylation, including LYRIC at serine 568 .
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Art. -Nr.: HY-110028
CAS. Nr.: 16496-99-4
Reinheit:  99.06%
Leelamine hydrochloride is an orally active weakly basic amine that inhibits NPC1 and the androgen receptor AR-V7, and acts as a cannabinoid receptor agonist. Leelamine hydrochloride also functions as a lysosome affinity agent that blocks endocytosis, disrupts autophagic flux and cholesterol transport, thereby altering the RTK-AKT/STAT/MAPK signaling cascade. Leelamine hydrochloride induces cancer cell death and autophagosome accumulation, and can be used in research related to melanoma, castration-resistant prostate cancer and breast cancer .
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Art. -Nr.: HY-P99544
CAS. Nr.: 2417649-97-7
Synonyms: HBM-9167; KL-A167

Target:  

PD-1/PD-L1

Forschungsgebiete:  

Cancer

Tagitanlimab (HBM-9167) is a humanized anti-PD-L1 antibody (IgG1κ type). Tagitanlimab selectively blocks the interaction of PD-L1 and PD-1. Tagitanlimab has the potential to be studied in recurrent or metastatic nasopharyngeal carcinoma (NPC) .
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Art. -Nr.: HY-W014780
CAS. Nr.: 122-40-7
Synonyms: 2-Benzylideneheptanal; α-Pentylcinnamaldehyde
Forschungsgebiete:  

Others

α-Amylcinnamaldehyde is a ligand for the Niemann-Pick type C2 (NPC2) protein of arthropod moths and may play a key role in the identification of moth volatiles. NPC2 is a key enzyme for cholesterol transport in the body .
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Art. -Nr.: HY-136059
CAS. Nr.: 302781-98-2
Target:  

Keap1-Nrf2 Autophagy

Forschungsgebiete:  

Cardiovascular Disease Cancer

Desfluoro-ezetimibe is a desfluoro impurity of Ezetimibe. Ezetimibe is a potent, metabolically stable cholesterol absorption inhibitor. Ezetimibe is a Niemann-Pick C1-like1 (NPC1L1) inhibitor, and is a potent Nrf2 activator .
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Art. -Nr.: HY-17376S1
CAS. Nr.: 1093659-89-2
Synonyms: SCH 58235-d4-1
Ezetimibe-d4-1 is deuterium labeled Ezetimibe. Ezetimibe (SCH 58235) is a potent cholesterol absorption inhibitor. Ezetimibe is a Niemann-Pick C1-like1 (NPC1L1) inhibitor, and is a potent Nrf2 activator.
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Art. -Nr.: HY-17376R
CAS. Nr.: 163222-33-1
Synonyms: SCH 58235 (Standard)
Ezetimibe (Standard) is the analytical standard of Ezetimibe. This product is intended for research and analytical applications. Ezetimibe (SCH 58235) is a potent cholesterol absorption inhibitor. Ezetimibe is a Niemann-Pick C1-like1 (NPC1L1) inhibitor, and is a potent Nrf2 activator.
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Art. -Nr.: HY-17376S
CAS. Nr.: 1093659-90-5
Synonyms: SCH 58235-d4
Ezetimibe-d4 (SCH 58235-d4) is the deuterium labeled Ezetimibe (HY-17376). Ezetimibe (SCH 58235) is a potent cholesterol absorption inhibitor. Ezetimibe is a Niemann-Pick C1-like1 (NPC1L1) inhibitor, and is a potent Nrf2 activator.
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Art. -Nr.: HY-129980
CAS. Nr.: 141774-20-1
Target:  

PKC

Forschungsgebiete:  

Neurological Disease

NPC-15437 dihydrochloride is a selective, penetrable and reversible protein kinase C (PKC) inhibitor, with an IC50 of 19 μM. NPC-15437 dihydrochloride interferes with mechanisms underlying memory consolidation .
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Art. -Nr.: HY-P99362
CAS. Nr.: 1092658-06-4
Synonyms: Anti-MUC5AC Reference Antibody (ensituximab); NEO-102

Target:  

Mucin

Forschungsgebiete:  

Cancer

Ensituximab (NEO-102; NPC-1C) is a chimeric monoclonal IgG1 antibody targeting a variant of MUC5AC. Ensituximab shows specificity to colorectal and pancreatic cancer .
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Art. -Nr.: HY-17640
CAS. Nr.: 1269181-69-2
Forschungsgebiete:  

Metabolic Disease

Nicodicosapent is a fatty acid niacin conjugate that is also an inhibitor of the sterol regulatory element binding protein (SREBP), a key regulator of cholesterol metabolism proteins such as PCSK9, HMG-CoA reductase, ATP citrate lyase, and NPC1L1.
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