16 Results for "

human chronic myelogenous leukemia

" in MedChemExpress (MCE) Product Catalog:
Products (16)

16 Results for "human chronic myelogenous leukemia" in MCE Product Catalog:

Cat. No.: HY-Y0030
CAS No.: 874-24-8
Synonyms: 3-hydroxypyridine-2-carboxylic acid
3-Hydroxypicolinic acid is a heterocyclic carboxylic acid ligand and cytotoxin, with a MIC90 of >25 μg/mL against Mycobacterium tuberculosis H37Rv. 3-Hydroxypicolinic acid inhibits the growth of cancer cells and normal fibroblasts. 3-Hydroxypicolinic acid is applicable to research related to chronic myeloid leukemia, human lung adenocarcinoma, and tuberculosis .
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Cat. No.: HY-162608
CAS No.: 3052553-20-2
Target:  

PROTACs JAK STAT

Research Areas:  

Cancer

PROTAC JAK1 degrader 1 is a JAK1 PROTAC degrader with a DC50 of 214 nM and an IC50 of 5.2 nM. PROTAC JAK1 degrader 1 inhibits the downstream JAK-STAT signaling pathway by degrading JAK1. PROTAC JAK1 degrader 1 exhibits antiproliferative activity in cells. PROTAC JAK1 degrader 1 can be used for research on leukemia .
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Cat. No.: HY-147342
CAS No.: 156724-91-3
Target:  

Drug Metabolite IMPDH

Research Areas:  

Cancer

β-Benzamide adenine dinucleotide is a biologically active metabolite of benzamide riboside. β-Benzamide adenine dinucleotide is a competitive inhibitor of human NAD kinase with a Ki value of 90 μM, and inhibits human IMPDH with IC50 values of 0.787 μM and 0.884 μM for type I and type II, respectively. β-Benzamide adenine dinucleotide exhibits inhibitory activities against lactate dehydrogenase, glutamate dehydrogenase, and malate dehydrogenase. β-Benzamide adenine dinucleotide can be used for the study of chronic myelogenous leukemia .
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Cat. No.: HY-N6736
CAS No.: 85753-43-1
K-252c, a staurosporine analog isolated from Nocardiopsis sp., is a cell-permeable PKC inhibitor, with an IC50 of 2.45 µM. K-252c induces apoptosis in human chronic myelogenous leukemia cancer cells. K-252c also inhibits β-lactamase, chymotrypsin, and malate dehydrogenase .
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Cat. No.: HY-Y0030R
CAS No.: 874-24-8
Synonyms: 3-hydroxypyridine-2-carboxylic acid (Standard)
3-Hydroxypicolinic acid (Standard) is an analytical standard for 3-Hydroxypicolinic acid. This product is for research and analytical applications. 3-Hydroxypicolinic acid is a heterocyclic carboxylic acid ligand and cytotoxin, with a MIC90 of >25 μg/mL against Mycobacterium tuberculosis H37Rv. 3-Hydroxypicolinic acid inhibits the growth of cancer cells and normal fibroblasts. 3-Hydroxypicolinic acid is applicable to research related to chronic myeloid leukemia, human lung adenocarcinoma, and tuberculosis .
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Cat. No.: HY-125322
CAS No.: 144860-69-5
Target:  

Bacterial

Research Areas:  

Infection

Reveromycin C is a polyketide originally isolated from Streptomyces that has antifungal activity against C. albicans (MICs=2.0 and >500 μg/mL at pH 3 and 7.4, respectively). Reveromycin C inhibits EGF-induced mitogenic activity in the Balb/MK mouse epidermal cell line. It also reverses the morphology of sarcoma-virus-transformed NRK rat kidney cells (EC50=1.58 μg/mL) and inhibits proliferation of KB cells and K562 human chronic myelogenous leukemia cells (IC50=2.0 μg/mL for both).
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Cat. No.: HY-N18083
CAS No.: 123914-43-2
Gweicurculactone is a sesquiterpene and cytotoxin found in the root tuber of Curcuma wenyujin Y. H. Chen et C. Ling. Gweicurculactone exerts cytotoxic effects against human promyelocytic leukemia, hepatocellular carcinoma, chronic myelogenous leukemia, epidermoid carcinoma, and breast adenocarcinoma cells. Gweicurculactone can be used for the research of leukemia, hepatocellular carcinoma, epidermoid carcinoma of the mouth, breast adenocarcinoma .
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Cat. No.: HY-181710
Target:  

mTOR PI3K

Research Areas:  

Cancer

LASSBio-2337 is a dual pan-PI3K/mTOR inhibitor with an mTOR IC50 of 5.8 μM.LASSBio-2337 functionally modulates mTOR and all PI3K isoforms.LASSBio-2337 acts as a cytotoxic agent in leukemia cells, including multidrug-resistant populations.LASSBio-2337 spares nontumor human peripheral blood mononuclear cells.LASSBio-2337 displays moderate PAMPA-GIT permeability.LASSBio-2337 shows low metabolic stability in rat liver microsomes.LASSBio-2337 is aqueous insoluble.LASSBio-2337 can be used for the research of acute lymphoblastic leukemia, chronic myelogenous leukemia, breast cancer .
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Cat. No.: HY-N19778
CAS No.: 89946-00-9
Kaempferol 3-O-α-L-arabinofuranosyl-7-O-α-L-rhamnopyranoside is a flavonoid glycoside found in the leaves of Olax mannii .
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Cat. No.: HY-P701574
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: KBTBD11; Kelch Repeat And BTB (POZ) Domain Containing 11; Kelch Repeat And BTB Domain Containing 11; chronic myelogenous leukemia-Associated Protein; KLHDC7C; Kelch Domain-Containing Protein 7B; KIAA0711; CMLAP; Kelch Repeat And BTB Domain-Containing Prot
Species:  
Human
Source:  
Sf9 insect cells
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Cat. No.: HY-P701877
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: EXOSC5; Ribosomal RNA-Processing Protein 46; Exosome Component 5; Exosome Complex Component RRP46; RRP46; Exosome Component Rrp46; P12B; MGC12901; HRrp46p; Exosome Complex Exonuclease RRP46; Rrp46p; CABAC; RRP41B; CML28; chronic myelogenous leukemia Tumor
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-D3183
CAS No.: 1623011-10-8
AldRed 659-A is a red-shifted fluorescent substrate for aldehyde dehydrogenase (ALDH). AldRed 659-A exhibits only minimal fluorescent uptake shift in comparison with DEAB (ALDH inhibitor)-treated control .
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Cat. No.: HY-P701878
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: EXOSC5; Ribosomal RNA-Processing Protein 46; Exosome Component 5; Exosome Complex Component RRP46; RRP46; Exosome Component Rrp46; P12B; MGC12901; HRrp46p; Exosome Complex Exonuclease RRP46; Rrp46p; CABAC; RRP41B; CML28; chronic myelogenous leukemia Tumor
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-119159
CAS No.: 361465-74-9
Target:  

NAMPT Caspase Apoptosis

Research Areas:  

Cancer

AS1604498 is a highly specific competitive inhibitor of human NAMPT, with an IC50 of 44.4 nM. AS1604498 functionally inhibits NAMPT enzymatic activity, reduces nicotinamide mononucleotide production, decreases intracellular NAD levels, activates caspase 3/7 and induces cancer cell apoptosis. AS1604498 is applicable to research related to chronic myeloid leukemia .
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Cat. No.: HY-123113
CAS No.: 65886-71-7
Synonyms: Kymarabine; Ara-AC; NSC 281272
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

Fazarabine (Kymarabine; Ara-AC; NSC 281272) is an orally active, blood-brain barrier permeable DNA polymerase inhibitor and antitumor agent. Fazarabine interferes with DNA synthesis via intracellular activation into a triphosphate nucleotide that directly incorporates into DNA, inducing cytotoxicity, myelosuppression, as well as moderate nausea and vomiting. Fazarabine is resistant to deamination by cytidine-deoxycytidine deaminase and undergoes spontaneous aqueous degradation. Fazarabine exerts time-dependent, broad-spectrum activity against leukemia and solid tumors. Fazarabine can be used in research related to refractory malignancies, acute leukemia, and blast-phase chronic myeloid leukemia .
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Cat. No.: HY-183242
CAS No.: 120154-96-3
Target:  

Bacterial Parasite

Research Areas:  

Infection Neurological Disease Cancer

Eilatin is a seven-ring pyridoacridine marine alkaloid with anticancer, antibacterial, and antiparasitic activities. Eilatin acts as a DNA intercalator with selectivity for electron-deficient polycyclic purines; it can chelate Ni 2+ ions and cleave DNA via hydroxyl radical generation. Eilatin induces the SOS response in bacteria, inhibits cancer cell proliferation, and induces cancer cell differentiation and reversion of transformation. The IC50 of Eilatin against Trypanosoma brucei brucei is 1.33 μM. Eilatin can be used in research related to colon tumors, neuroblastoma, chronic myeloid leukemia, acute myeloid leukemia, and trypanosome infections .
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