153 Results for "

lac repressor

" in MedChemExpress (MCE) Product Catalog:
Products (153)

153 Results for "lac repressor" in MCE Product Catalog:

Cat. No.: HY-P99698
CAS No.: 2475402-56-1
Synonyms: LDP

Target:  

PD-1/PD-L1

Domaines de recherche:  

Inflammation/Immunology Cancer

Lesabelimab (LDP) is an immunoglobulin G1-kappa anti-CD274 monoclonal antibody. CD274 is an immune checkpoint ligand, represses antitumour immunity through the interaction with PDCD1 receptor .
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Cat. No.: HY-139046
CAS No.: 331948-99-3
Target:  

Adrenergic Receptor

Domaines de recherche:  

Neurological Disease

MEPB is a modulator of AF-2 of the androgen receptor. MEPB increases co-repressor binding of AR. MEPB can bind to the BF3 pocket of AR specifically, thereby modulating the binding of co-regulators to the AF2 domain. MEPB alleviates degeneration in spinal bulbar muscular atrophy mouse model .
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Cat. No.: HY-101931
CAS No.: 1637443-98-1
Pureté:  99.26%
Target:  

VEGFR

Domaines de recherche:  

Cancer

hVEGF-IN-1, a quinazoline derivative, could specifically bind to the G-rich sequence in the internal ribosome entry site A (IRES-A) and destabilize the G-quadruplex structure. hVEGF-IN-1 binds to the IRES-A (WT) with a Kd of 0.928 μM in SPR experiments. hVEGF-IN-1 could hinder tumor cells migration and repress tumor growth by decreasing VEGF-A protein expression .
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Cat. No.: HY-P3906
CAS No.: 123168-46-7
Domaines de recherche:  

Infection

Melittin free acid is a basic 26-amino-acid polypeptide, the major active ingredient of honeybee venom. Melittin free acid is an activator of phospholipase A2 (PLA2). Melittin free acid has broad-spectrum antifungal activity with MIC values of 0.4-60 μM. Melittin free acid hinders fungal growth by inducing cell apoptosis, repressing (1,3)-β-D-glucan synthase and participating in other pathways .
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Cat. No.: HY-151815
CAS No.: 246855-74-3
Target:  

ADC Linkers

Domaines de recherche:  

Others

beta-Lac-TEG-N3 is a click chemistry reagent containing an azide group. beta-Lac-TEG-N3 can be used for the research of various biochemical . It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups.
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Cat. No.: HY-116055
CAS No.: 16232-91-0
Pureté:  ≥99.0%
Synonyms: 3-O-β-D-Galactopyranosyl-sn-glycerol
Domaines de recherche:  

Others

(2R)-Glycerol-O-β-D-galactopyranoside (3-O-β-D-Galactopyranosyl-sn-glycerol) is a good substrate for all three components of the lac operon, i.e. β-galactosidase, the lactose transporter and thiogalactoside transacetylase .
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Cat. No.: HY-106162A
CAS No.: 214479-33-1
Target:  

NO Synthase

ONO-1714 is an orally active nitric oxide synthase inhibitor. ONO-1714 attenuates endotoxin-induced acute lung injury, reduces intestinal ischemia–reperfusion injury, represses biliary carcinogenesis .
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Cat. No.: HY-176866
CAS No.: 2222756-46-7
Target:  

HDAC

Domaines de recherche:  

Neurological Disease

Rodin-A is an orally active, brain-penetrant and selective histone deacetylase (HDAC)-co-repressor of repressor element-1 silencing transcription factor (CoREST) complex inhibitor with an IC50 value of 1.80 μM for the CoREST complex, 0.15 μM for HDAC1, and 0.43 μM for HDAC2. Rodin-A increases the acetylation level of histone H3K9, upregulates the expression of neuron-related genes, thereby promoting the increase in dendritic spine density, the colocalization of synaptic proteins (SV2A and PSD95), and the improvement of hippocampal long-term potentiation (LTP), exerting synaptic protection and repair activity. Rodin-A is promising for research of neurodegenerative diseases related to synaptic dysfunction, especially Alzheimer’s disease .
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Cat. No.: HY-119971
CAS No.: 337506-43-1
Domaines de recherche:  

Metabolic Disease Cancer

BIM5078 is a hepatocyte nuclear factor 4α (HNF4α) antagonist that can inhibit the expression of known HNF4α target genes. BIM5078 represses insulin promoter activity through HNF4α antagonism. BIM5078 can be used for the research of cancer and diabetes .
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Cat. No.: HY-144338
CAS No.: 2758117-74-5
Domaines de recherche:  

Cancer

PARP1/BRD4-IN-1 is a potent and high selective PARP1/BRD4 inhibitor (IC50s of 49 and 202 nM in PARP1 and BRD4, respectively). PARP1/BRD4-IN-1 represses the expression and activity of PARP1 and BRD4 to synergistically inhibit the malignant growth of pancreatic cancer cells .
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Cat. No.: HY-P11138
Synonyms: lac705α
Domaines de recherche:  

Infection

Lactocin 705α (Lac705α) is a peptide component of Lactocin 705. Lactocin 705α can interact with zwitterionic DPPC bilayers. Lactocin 705α can induce the dehydration of the bilayer interfacial region. Lactocin 705α can be used in the research of bacterial infections .
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Cat. No.: HY-150012R
CAS No.: 183241-73-8
Synonyms: lac-Phe (Standard)
N-Lactoyl-phenylalanine (Standard) is the analytical standard of N-Lactoyl-phenylalanine. This product is intended for research and analytical applications. N-Lactoyl-phenylalanine, a N-lactoyl-amino acid, is a blood-derived signaling metabolite that can be induced by exercise. N-Lactoyl-phenylalanine can reduce obesity and improve glucose tolerance .
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Cat. No.: HY-P10488
CAS No.: 2116533-34-5
Domaines de recherche:  

Cancer

cycFWRPW is a peptide inhibitor of TLE1. TLE1 is an oncogenic transcriptional co‐repressor that exerts its repressive effects through binding of transcription factors, and inhibits Wnt signaling .
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Cat. No.: HY-151471
CAS No.: 2714510-72-0
Target:  

c-Myc

Domaines de recherche:  

Cancer

Anticancer agent 84 is an anticancer agent. Anticancer agent 84 represses the transcription of c-MYC by stabilizing the G-quadruplex (G4) structure. Anticancer agent 84 can be used for the research of cancer .
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Cat. No.: HY-N10106
CAS No.: 52811-28-6
Dihydromyristicin, a plant flavonoid, has potent anti-inflammatory properties. Dihydromyristicin reduces endotoxic inflammation via repressing ROS-mediated activation of PI3K/Akt/NF-κB signaling pathways .
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Cat. No.: HY-E70128
CAS No.: 9001-61-0
Target:  

Others

Domaines de recherche:  

Others

Leucyl aminopeptidase, Porcine is a metallopeptidase that cleave N-terminal residues from proteins and peptides. Leucyl aminopeptidase serves as transcriptional repressors to control pyrimidine, alginate and cholera toxin biosynthesis, as well as mediate site-specific recombination events in plasmids and phages .
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Cat. No.: HY-161114
CAS No.: 3036752-42-5
Target:  

SARS-CoV

Domaines de recherche:  

Infection

MDOLL-0229 (compound 27) is an antiviral agent that targets SARS-CoV-2 Mac1 and repress coronavirus replication. MDOLL-0229 inhibits SARS-CoV-2 Mac1 with an IC50 of 2.1 µM .
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Cat. No.: HY-P10543
CAS No.: 857026-08-5
Target:  

BCL6

Domaines de recherche:  

Cancer

SMRT peptide is one of the co-repressors of BCL6 BTB domain interaction. SMRT peptide binds to the BTB domain of BCL6 and enhances the transcriptional repression function of BCL6. SMRT peptide can be used to study protein-protein interactions .
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Cat. No.: HY-176867
Target:  

HDAC

Domaines de recherche:  

Neurological Disease

Rodin-B is a selective histone deacetylase (HDAC)-co-repressor of repressor element-1 silencing transcription factor (CoREST) complex inhibitor with an IC50 value of 0.50 μM for the CoREST complex, 0.27 μM for HDAC1, and 0.28 μM for HDAC2. Rodin-B increases the acetylation level of histone H3K9, upregulates the expression of neuron-related genes, thereby promoting the increase in dendritic spine density, the colocalization of synaptic proteins (SV2A and PSD95), and the improvement of hippocampal long-term potentiation (LTP), exerting synaptic protection and repair activity. Rodin-B is promising for research of neurodegenerative diseases related to synaptic dysfunction, especially Alzheimer’s disease .
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Cat. No.: HY-162478
Target:  

Phosphatase

Domaines de recherche:  

Cancer

GR-28 is an inhibitor for small C-terminal domain phosphatase 1 (SCP1). GR-28 inhibits the transcriptional activity of repressor element-1 silencing transcription factor (REST), inhibits the proliferation of glioblastoma cells (IC50 is 2.9 and 10.1 µM, for cells A172 and T98G) .
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