15 Results for "

ACHN

" in MedChemExpress (MCE) Product Catalog:
Products (15)

15 Results for "ACHN" in MCE Product Catalog:

9
9 Publications Verification
Art. -Nr.: HY-112055
CAS. Nr.: 151358-47-3
Reinheit:  99.05%
Forschungsgebiete:  

Cancer

DIM-C-pPhOH is a nuclear receptor 4A1 (NR4A1) antagonist. DIM-C-pPhOH inhibits cancer cell growth and mTOR signaling, induce apoptosis and cellular stress. DIM-C-pPhOH reduces cell proliferation with IC50 values of 13.6 μM and 13.0 μM for ACHN cells and 786-O cells, respectively .
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1 Cited Publications
Art. -Nr.: HY-19936A
CAS. Nr.: 1410809-37-8
Target:  

Bacterial

Forschungsgebiete:  

Infection

ACHN-975 TFA is a selective LpxC inhibitor and exhibits a subnanomolar LpxC inhibitory activity. ACHN-975 TFA is against a wide range of gram-negative bacterias with low MIC values (≤1 μg/mL) .
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1 Cited Publications
Art. -Nr.: HY-16955A
CAS. Nr.: 1380078-95-4
Synonyms: ACHN 490 sulfate
Target:  

Antibiotic Bacterial

Forschungsgebiete:  

Infection Inflammation/Immunology

Plazomicin (ACHN 490) sulfate is a semi-synthetic aminoglycoside Antibiotic. Plazomicin sulfate acts as a substrate for Aminoglycoside acetyltransferase and Aminoglycoside phosphotransferase. Plazomicin sulfaten is not modified by various common aminoglycoside-modifying enzymes. Plazomicin sulfate selectively inhibits MATE2-K. Plazomicin sulfate exhibits activity against multidrug-resistant bacteria, including carbapenem-resistant Enterobacterales .
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Art. -Nr.: HY-19936
CAS. Nr.: 1410809-36-7
Target:  

Bacterial

Forschungsgebiete:  

Infection

ACHN-975 is a selective LpxC inhibitor and exhibits a subnanomolar LpxC inhibitory activity. ACHN-975 is against a wide range of gram-negative bacterias with low MIC values (≤1 μg/mL) .
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Art. -Nr.: HY-162520
CAS. Nr.: 797780-71-3
Target:  

Wnt

Forschungsgebiete:  

Cancer

DJ-1-IN-1 (compound 797780-71-3) is a DJ-1 inhibitor. DJ-1-IN-1 exhibits antiproliferative activity in ACHN cells with an IC50 value of 12.18 μM and can inhibit the Wnt signaling pathway. DJ-1-IN-1 can be used in cancer research .
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Art. -Nr.: HY-161740
CAS. Nr.: 2410081-60-4
Forschungsgebiete:  

Cancer

PHTPP-1304 is a PHTPP-based autophagy targeting chimera (AUTOTAC). PHTPP-1304 induces the degradation of estrogen receptor ERβ through the autophagy pathway, rather than ubiquitination (DC50 ≈ 2 nM, in HEK293T cells; < 100 nM in ACHN renal carcinoma and MCF-7 breast cancer cells). PHTPP-1304 can induce the self-oligomerization of p62. PHTPP-1304 can be used to study various cancers mediated by ERβ .
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Art. -Nr.: HY-16955
CAS. Nr.: 1154757-24-0
Synonyms: ACHN 490
Target:  

Antibiotic Bacterial

Forschungsgebiete:  

Infection Inflammation/Immunology

Plazomicin (ACHN 490) is a semi-synthetic aminoglycoside Antibiotic. Plazomicin acts as a substrate for Aminoglycoside acetyltransferase and Aminoglycoside phosphotransferase. Plazomicin is not modified by various common aminoglycoside-modifying enzymes. Plazomicin selectively inhibits MATE2-K. Plazomicin exhibits activity against multidrug-resistant bacteria, including carbapenem-resistant Enterobacterales .
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Art. -Nr.: HY-N5093
CAS. Nr.: 2446-63-1
Glucodigifucoside, a cardenolide glycoside that could be isolated from the seeds of Digitalis purpurea, exhibits potent cytotoxicity against human renal adenocarcinoma cell line ACHN .
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Art. -Nr.: HY-121532
CAS. Nr.: 303156-68-5
(-)-Rasfonin is a fungal secondary metabolite and inhibits small G proteins Ras. (-)-Rasfonin induces apoptosis, necrosis and autophagy in ACHN cells (a renal carcinoma cell line) .
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Art. -Nr.: HY-N14056
CAS. Nr.: 227606-82-8
Target:  

Bacterial

Chrolactomycin is found in the strain of Streptomyces sp. 569N-3. The IC50 of Chrolactomycin for ACHN, A431, McF-7 and T24 cells are 1.2 μM, 1.6 μM, 0.69 μM and 0.45 μM, respectively. Chrolactomycin has only anti-Gram-positive bacteria activity with the MIC of 5.2-10.4 μg/mL .
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Art. -Nr.: HY-170604
Target:  

MMP

Forschungsgebiete:  

Cardiovascular Disease Cancer

MMP-2 Inhibitor-4 (Compound 5g) is an MMP-2 inhibitor with an IC50 of 152.62 nM. MMP-2 Inhibitor-4 can reduce the levels of MMP-2 in the K562 cell line through stable binding at the MMP-2 active site, and it demonstrates strong antiangiogenic effects in the ACHN cell line. MMP-2 Inhibitor-4 holds promise for research in chronic myeloid leukemia (CML) .
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Art. -Nr.: HY-149388
CAS. Nr.: 2954795-29-8
Target:  

Microtubule/Tubulin

Forschungsgebiete:  

Cancer

Anticancer agent 139 (Compound 6h) has potent anticancer activity. Anticancer agent 139 displayed a π–cationic interaction with the residue Lys352 of Tublin. Anticancer agent 139 has good anticancer activity against SNB-19, OVCAR-8, and NCI-H40 with PGIs of 86.61, 85.26, and 75.99, respectively. Anticancer agent 139 also has moderate anticancer activity against HOP-62, SNB-75, ACHN, NCI/ADR-RES, 786-O, A549/ATCC, HCT-116, and MDA-MB-231 with PGIs of 67.55, 65.46, 59.09, 59.02, 57.88, 56.88, 56.53, 56.4, and 51.88 respectively .
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Art. -Nr.: HY-RS07530
Forschungsgebiete:  

Others

LARP6 Human Pre-designed siRNA Set A contains three designed siRNAs for LARP6 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Art. -Nr.: HY-P811989
Synonyms: La-related protein 6, Acheron, La ribonucleoprotein domain family member 6, ACHN, LARP6

Host:  

Mouse

Application:  

WB

Reactivity:  

Human, Mouse, Rat

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Art. -Nr.: HY-P811989A
Synonyms: La-related protein 6, Acheron, La ribonucleoprotein domain family member 6, ACHN, LARP6

Host:  

Mouse

Application:  

WB

Reactivity:  

Human, Mouse, Rat

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