6 Results for "

holoenzyme

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "holoenzyme" in MCE Product Catalog:

Cat. No.: HY-E70094
Target:  

DNA/RNA Synthesis

Research Areas:  

Others

T4 UvsX Recombinase helps initiate DNA replication on a double-stranded DNA template by catalyzing synapsis between the template and a homologous DNA single strand that serves as primer. T4 UvsX Recombinase greatly amplifies the snap-back (hairpin-primed) DNA synthesis that is catalyzed by the T4 DNA polymerase holoenzyme on linear, single-stranded DNA templates .
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Cat. No.: HY-124321
CAS No.: 53734-79-5
Target:  

CDK

Research Areas:  

Cancer

Metralindole hydrochloride is an inhibitor of human cyclin-dependent kinase CDK2 and human protein kinase CK2 holoenzyme. Metralindole hydrochloride shows good potential as a non-small cell lung cancer inhibitor .
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Cat. No.: HY-103384
CAS No.: 905105-89-7
Target:  

Casein Kinase

Research Areas:  

Cancer

TMCB is a selective, ATP-competitive CK2 (casein kinase II) inhibitor with distinct Ki values of 83 nM and 21 nM for the two different catalytic CK2 subunits α and α', respectively .
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Cat. No.: HY-124321A
CAS No.: 54188-38-4
Target:  

CDK

Research Areas:  

Cancer

Metralindole is an inhibitor of human cyclin-dependent kinase CDK2 and human protein kinase CK2 holoenzyme. Metralindole shows good potential as a non-small cell lung cancer inhibitor .
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Cat. No.: HY-102072
CAS No.: 1445801-61-5
Research Areas:  

Infection

GKL003 is a bacterial transcription inhibitor that targets the RNAP-σ interaction interface, with a Ki of 5.79 nM. GKL003 specifically binds to the RNAP β' clamp helix region at the σ A factor binding site, blocks the formation of RNAP holoenzyme, and inhibits the formation of bacterial transcription initiation complexes. GKL003 inhibits the growth of both Gram-positive and Gram-negative bacterial cells, and also exhibits activity against drug-resistant strains .
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Cat. No.: HY-184823
CAS No.: 1417634-25-3
Target:  

Casein Kinase

Research Areas:  

Cancer

CK2-IN-17 is a protein kinase CK2 inhibitor with an IC50 of 9.5 μM against human targets. CK2-IN-17 regulates the activity of protein kinase CK2 by interacting with its ATP-binding site. CK2-IN-17 can be used in studies related to protein kinase CK2-mediated pathways, such as tumors .
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