592 Results for "

DNA binding

" in MedChemExpress (MCE) Product Catalog:
Products (592)

592 Results for "DNA binding" in MCE Product Catalog:

2
2 Cited Publications
Art. -Nr.: HY-B0278
CAS. Nr.: 1405-89-6
Synonyms: Zinc bacitracin
Forschungsgebiete:  

Infection

Bacitracin Zinc is a complex formed by the binding of Bacitracin (HY-107193) with zinc ions. Bacitracin Zinc is an orally active polypeptide antibiotic with bactericidal properties. Bacitracin Zinc can cause DNA and deoxyribose damage, as well as improve the gut microbiota of broiler and beef cattle .
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2
2 Cited Publications
Art. -Nr.: HY-B0268
CAS. Nr.: 74011-58-8
Synonyms: AT 2266; CI 919
Forschungsgebiete:  

Infection Cancer

Enoxacin (AT 2266), a fluoroquinolone, interferes with DNA replication and inhibits bacterial DNA gyrase (IC50=126 µg/ml) and topoisomerase IV (IC50=26.5 µg/ml). Enoxacin is a miRNA processing activator and enhances siRNA-mediated mRNA degradation and promotes the biogenesis of endogenous miRNAs. Enoxacin has potent activities against gram-positive and -negative bacteria. Enoxacin is a cancer-specific growth inhibitor that acts by enhancing TAR RNA-binding protein 2 (TRBP)-mediated microRNA processing .
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2
2 Cited Publications
Art. -Nr.: HY-B0268A
CAS. Nr.: 84294-96-2
Synonyms: Enoxacin sesquihydrate; AT-2266 hydrate; CI-919 hydrate
Forschungsgebiete:  

Infection Cancer

Enoxacin hydrate (Enoxacin sesquihydrate), a fluoroquinolone, interferes with DNA replication and inhibits bacterial DNA gyrase (IC50=126 µg/ml) and topoisomerase IV (IC50=26.5 µg/ml). Enoxacin hydrate is a miRNA processing activator and enhances siRNA-mediated mRNA degradation and promotes the biogenesis of endogenous miRNAs. Enoxacin hydrate has potent activities against gram-positive and -negative bacteria. Enoxacin hydrate is a cancer-specific growth inhibitor that acts by enhancing TAR RNA-binding protein 2 (TRBP)-mediated microRNA processing .
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2
2 Cited Publications
Art. -Nr.: HY-131031
CAS. Nr.: 315702-75-1
Reinheit:  99.95%
Forschungsgebiete:  

Neurological Disease Cancer

KCC-07 is a potent and brain-penetrant MBD2 (methyl-CpG-binding domain protein 2) inhibitor. KCC-07 prevents binding of MBD2 to methylated DNA and activates brain specific angiogenesis inhibitor 1 (BAI1) inducing anti-proliferative BAI1/p53/p21 signaling . KCC-07 is a TRACER (transcriptional regulation via active control of epigenetic reprogramming) that can stimulate ER transcriptional activity . KCC-07 can be used for the stduy of breast cancer .
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2
2 Cited Publications
Art. -Nr.: HY-138113
CAS. Nr.: 477888-48-5
Reinheit:  98.61%
Pyrrothiogatain is a transcription factor GATA3 inhibitor with an IC50 of 54.7 μM. Pyrrothiogatain inhibits the DNA-binding activity of GATA3 and inhibits the T helper 2 (Th2) cell differentiation and expression of Th2 cytokines. Pyrrothiogatain shows anti-infection effect by inhibiting ACE2 expression. Pyrrothiogatain can be used for the researches of inflammation, immunology, infection and cancer, such as colon cancer and SARS-CoV-2 infection .
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2
2 Cited Publications
Art. -Nr.: HY-144878
CAS. Nr.: 2361742-30-3
Reinheit:  99.93%
Target:  

c-Myc

Forschungsgebiete:  

Cancer

VPC-70619 is a potent N-Myc inhibitor. VPC-70619 blocks the binding of the N-Myc-Max heterocomplex to the DNA E-box and exhibits potent inhibitory activity against N-Myc-dependent cell lines. VPC-70619 can partially reverse paclitaxel (HY-B0015) resistance in cells by reducing MYCN expression. VPC-70619 can be used for cancer research (e.g., neuroblastoma and thyroid cancer) .
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2
2 Cited Publications
Art. -Nr.: HY-B0837
CAS. Nr.: 155569-91-8
Synonyms: MK-244
Emamectin Benzoate (MK-244) is an orally active nervoussystem toxicant by binding g-aminobutyric (GABA) receptor in insects. Emamectin Benzoate is one of semi-synthetic derivative of Avermectin (HY-15311) with a broadspectrum of insecticidal and acaricidal activity. Emamectin Benzoate induces ROS-mediated DNA damage and cell apoptosis. Emamectin Benzoate, a mixture of the natural Emamectin B1a benzoate and Emamectin B1b benzoate, has the main component of Emamectin B1a benzoate .
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2
2 Cited Publications
Art. -Nr.: HY-111832
CAS. Nr.: 79886-50-3
Reinheit:  99.08%
Synonyms: TeGG
1,2,3,6-Tetragalloylglucose (TEgG) is a competitive inhibitor of UDP-glucuronyltransferase UGT1A1, targeting the competitive substrate binding site of UGT1A1. 1,2,3,6-Tetragalloylglucose inhibits UGT1A1-mediated β-estradiol 3-glucuronidation and SN-38 glucuronidation with IC50 of 6.01 μM and 4.31 μM, respectively, and binds to UGT1A1 with Ki of 3.55 μM. 1,2,3,6-Tetragalloylglucose also induces tumor cell apoptosis, inhibit cell proliferation, activates caspase-3 and induces DNA fragmentation in HL-60 cells. 1,2,3,6-Tetragalloylglucose also inhibits HIV integrase and reverse transcriptase, and inhibits HCV protease .
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1
1 Cited Publications
Art. -Nr.: HY-15620
CAS. Nr.: 188247-01-0
Reinheit:  98.90%
Methylproamine is a DNA-binding radioprotector, acts by repair of transient radiation-induced oxidative species on DNA. Methylproamine also protects against ionizing radiation by preventing DNA double-strand breaks .
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1
1 Cited Publications
Art. -Nr.: HY-P71788
Reinheit:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: TARDBP; TDP43; TAR DNA binding Protein; TAR DNA binding Protein, Isoform CRA_c; TDP-43; TAR DNA-binding Protein-43; TAR DNA-binding Protein 43; TDP43 Isoform F; ALS10
Species:  
Human
Source:  
E. coli
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1
1 Cited Publications
Art. -Nr.: HY-P71497
Reinheit:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: DNA-binding protein HU-alpha; HU-2; NS2; hupA; Z5576; ECs4923
Species:  
E.coli
Source:  
E. coli
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1
1 Cited Publications
Art. -Nr.: HY-118581
CAS. Nr.: 38989-38-7
Reinheit:  98.30%
Target:  

Topoisomerase

Forschungsgebiete:  

Cancer

Coralyne chloride is a protoberberine alkaloid with potent anti-cancer activities. Coralyne chloride acts as a potent topoisomerase I poison and induces Top I mediated DNA cleavage . Coralyne chloride can be used for preparing coralyne derivatives as DNA binding fluorescent probes .
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1
1 Cited Publications
Art. -Nr.: HY-19639
CAS. Nr.: 858102-78-0
Target:  

DNA/RNA Synthesis

Forschungsgebiete:  

Others

E-982 is a steroid used for the on-line screening of the DNA unwinding element binding protein (DUE-B) immobilized protein column .
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1
1 Cited Publications
Art. -Nr.: HY-116940
CAS. Nr.: 365542-77-4
Reinheit:  99.37%
Target:  

Oct3/4 Notch STAT

Forschungsgebiete:  

Cancer

Sm4 is a selective and orally active SOX18 inhibitor. Sm4 inhibits SOX18-DNA binding (IC50 = 97.5 μM); Sm4 disrupts the SOX18-RBPJ protein-protein interaction (IC50 = 42.3 μM). Sm4 blocks SOX18 DNA binding, disrupts multiple SOX18 protein-protein interactions with RBPJ, DDX1, DDX17, ILF3, SOX7 and STAT1, modulates SOX18 chromatin binding dynamics. Sm4 exerts anti‑angiogenic and anti‑lymphangiogenic effects, reduces tumor vascular density, triggers vascular defects in zebrafish, prolongs survival in mouse metastatic cancer models. Sm4 can be used for the research of breast cancer .
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1
1 Cited Publications
Art. -Nr.: HY-P80936
Synonyms: YBX1; NSEP1; YB1; Nuclease-sensitive element-binding protein 1; CCAAT-binding transcription factor I subunit A; CBF-A; DNA-binding protein B; DBPB; Enhancer factor I subunit A; EFI-A; Y-box transcription factor; Y-box-binding protein 1; YB-

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, IP

Reactivity:  

Human, Mouse, Rat

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1
1 Cited Publications
Art. -Nr.: HY-128904
CAS. Nr.: 2055896-98-3
Reinheit:  98.77%
Forschungsgebiete:  

Cancer

MC-Val-Cit-PAB-duocarmycin chloride is a agent-linker conjugate for ADC with potent antitumor activity by using Duocarmycin (a DNA minor groove binding alkylating agent), linked via the ADC linker MC-Val-Cit-PAB.
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1
1 Cited Publications
Art. -Nr.: HY-124676A
CAS. Nr.: 1366126-19-3
Reinheit:  99.13%
Target:  

Apoptosis

Forschungsgebiete:  

Cancer

DB2115 tetrahydrochloride is a highly selective PU.1 inhibitor that suppresses the binding of PU.1 to DNA (IC50: 2.3 nM). DB2115 tetrahydrochloride can inhibit tumor cell proliferation and induce apoptosis. DB2115 tetrahydrochloride can be used in the research of tumors such as leukemia .
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1
1 Cited Publications
Art. -Nr.: HY-125471
Reinheit:  99.88%
Target:  

EBV

Forschungsgebiete:  

Infection Inflammation/Immunology Cancer

VK-1727 is a selective small molecule inhibitor of EBNA1. VK-1727 can reduce EBNA1 DNA binding activity. VK-1727 selectively blocks the proliferation and metabolic activity of EBV+ cells, instead of EBV- cells. VK-1727 is used in multiple sclerosis research .
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1
1 Cited Publications
Art. -Nr.: HY-N6046
CAS. Nr.: 73981-34-7
Kamebakaurin is an orally active diterpenoid compound that can be isolated from Isodon excia (Maxin.). Kamebakaurin can inhibit NF-κB activation by directly targeting the DNA-binding activity of p50. Kamebakaurin can induce apoptosis and cell cycle arrest in tumor cells. Kamebakaurin has anti-inflammatory and anti-tumor activities .
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1
1 Cited Publications
Art. -Nr.: HY-P72229
Reinheit:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: HNRNPA1; Heterogeneous Nuclear Ribonucleoprotein A1B Protein; Prev. HNRPA1; Nuclear Ribonucleoprotein Particle A1 Protein; HnRNP-A1; Single-Strand DNA-binding Protein UP1; ALS20; HnRNP Core Protein A1-Like 3; Epididymis Secretory Sperm binding Protein; Hn
Species:  
Human
Source:  
E. coli
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