270 Results for "

ECL4 loop

" in MedChemExpress (MCE) Product Catalog:
Products (270)

270 Results for "ECL4 loop" in MCE Product Catalog:

Cat. No.: HY-N2587
CAS No.: 548-76-5
Irigenin is a is a lead compound, and mediates its anti-metastatic effect by specifically and selectively blocking α9β1 and α4β1 integrins binding sites on C-C loop of Extra Domain A (EDA). Irigenin shows anti-cancer properties. It sensitizes TRAIL-induced apoptosis via enhancing pro-apoptotic molecules in gastric cancer cells .
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Cat. No.: HY-174801
CAS No.: 3117797-30-2
Research Areas:  

Inflammation/Immunology

XL-3156 is a cGAS inhibitor. XL-3156 occupies both allosteric and orthosteric sites simultaneously, and inhibits the interaction and phase separation between cGAS and DNA by stabilizing the closed conformation of the activation loop. XL-3156 can be used in the research of diseases such as autoimmune diseases and inflammation .
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Cat. No.: HY-P2931
CAS No.: 9023-78-3
Synonyms: TPI
Research Areas:  

Metabolic Disease Cancer

Triosephosphate isomerase (TPI) is a biocatalyst that interconverts dihydroxyacetone phosphate and D-glyceraldehyde-3-phosphate. Triosephosphate isomerase utilises Glu167 as catalytic base, mediates proton shuttling, and stabilises a cis-enediolate intermediate via loop-6 and loop-7 closure to shield its catalytic site. Triosephosphate isomerase can be used for the research of triosephosphate isomerase deficiency .
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Cat. No.: HY-106616
CAS No.: 55294-15-0
Purity:  99.57%
Synonyms: BAY-g 2821; Edrul
Target:  

Sodium Channel

Research Areas:  

Cardiovascular Disease

Muzolimine (BAY-g 282) is a slow and long lasting diuresis agent. Muzolimine produces a diuresis in the loop of Henle and also shows anti-hypertensive and natriuresis effects. Muzolimine can be used for the research of cardiovascular disease .
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Cat. No.: HY-P99102
CAS No.: 2417213-75-1
Synonyms: 10-1074

Target:  

HIV

Research Areas:  

Infection

Zinlirvimab is a human IgG1-λ2, HIV neutralising antibody targeting to HIV-1 gp120 envelope glycoprotein (IIIB gp120 V3 loop) .
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Cat. No.: HY-130487
CAS No.: 304880-74-8
Target:  

MicroRNA

Research Areas:  

Cancer

miR-21-IN-2 is a high-affinity miR-21 inhibitor. miR-21-IN-2 binds to the apical loop region of the pre-miR-21 hairpin, inhibits Dicer-mediated processing, and thereby blocks the biosynthesis of mature miR-21. miR-21-IN-2 can be used for the research of microRNA-related diseases .
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Cat. No.: HY-P1594A
Target:  

Opioid Receptor iGluR

Research Areas:  

Neurological Disease

Dynorphin A (1-10) (TFA), an endogenous opioid neuropeptide, binds to extracellular loop 2 of the κ-opioid receptor. Dynorphin A (1-10) (TFA) also blocks NMDA-activated current with an IC50 of 42.0 μM.
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Cat. No.: HY-W317853
CAS No.: 521972-99-6
Target:  

Proton Pump

Research Areas:  

Others

Protonstatin-1 is a selective plasma membrane (PM) H +-ATPase inhibitor (IC50 of 3.9 μM) that inhibits auxin transport. Protonstatin-1 interacts with the PM H +-ATPase central loop and may thus impede the functions of the N- and/or P-domain to inhibit the pump activity .
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Cat. No.: HY-129359
CAS No.: 160580-70-1
Purity:  98.27%
Target:  

ADC Linkers

Research Areas:  

Cancer

PDP-Pfp is a reducible ADC Linker used as an active molecule targeting the extracellular loop 1 (ECL1) of TM4SF1 .
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Cat. No.: HY-B0247S
CAS No.: 1189375-06-1
Synonyms: Torasemide-d7
Torsemide-d7 is the deuterium labeled Torsemide. Torsemide (Torasemide) is an orally active loop diuretic. Torsemide has anti-aldosterone and vasodilatory effects. Torsemide also can be used for the research of heart failure, renal disease and hepatic cirrhosis .
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Cat. No.: HY-134193
CAS No.: 396721-89-4
Target:  

Cryptochrome

Research Areas:  

Metabolic Disease

KL101, a selective cryptochrome 1 (CRY1) stabilizer, is a circadian clock modulator. KL101 can stabilize the CRY1 protein and regulate its interaction with the core feedback loop of the biological clock, thereby modulating the circadian rhythm cycle of mammals .
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Cat. No.: HY-163035
CAS No.: 1206480-93-4
Target:  

TNF Receptor IFNAR

Research Areas:  

Inflammation/Immunology

EM-163 is a summative BB-Loop analog. EM-163 can alleviate inflammation and prevent death from toxic shock by targeting the TIR domain of MyD88. EM-163 can be used in the study of SEB poisoning (SEB: Staphylococcal enterotoxin B) .
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Cat. No.: HY-B0247R
CAS No.: 56211-40-6
Synonyms: Torasemide (Standard)
Torsemide (Standard) is the analytical standard of Torsemide. This product is intended for research and analytical applications. Torsemide (Torasemide) is an orally active loop diuretic. Torsemide has anti-aldosterone and vasodilatory effects. Torsemide also can be used for the research of heart failure, renal disease and hepatic cirrhosis .
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Cat. No.: HY-P1508
CAS No.: 116229-36-8
Synonyms: Bactenecin, bovine
Bactenecin (Bactenecin, bovine) is a potent 12-aa looped antimicrobial peptide isolated from bovine neutrophils. Bactenecin inhibits the growth of bacteria and yeast, and kills the fungus Trichophyton rubrum. Bactenecin increass membrane permeability, inhibits the growth and biofilm formation of B. pseudomallei .
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Cat. No.: HY-148200
CAS No.: 1016263-75-4
Target:  

ADC Payloads Telomerase

Research Areas:  

Cancer

L2H2-6OTD, containing one to four G-quadruplex binding loops, is a telomeric inhibitor analogue. l2H2-6OTD has telomerase inhibitory activity with an IC50 value of 15 nM .
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Cat. No.: HY-P1508A
Synonyms: Bactenecin, bovine TFA
Bactenecin TFA (Bactenecin, bovine TFA) is a potent 12-aa looped antimicrobial peptide isolated from bovine neutrophils. Bactenecin TFA inhibits the growth of bacteria and yeast, and kills the fungus Trichophyton rubrum. Bactenecin TFA increass membrane permeability, inhibits the growth and biofilm formation of B. pseudomallei .
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Cat. No.: HY-P2612A
Target:  

TNF Receptor

Research Areas:  

Others Cancer

WP9QY, TNF-a Antagonist, TNF-a Antagonist is a biological active peptide. (This cyclic peptide is designed to mimic the most critical tumor necrosis factor (TNF) recognition loop on TNF receptor I. It prevents interactions of TNF with its receptor. This TNF antagonist is a useful template for the development of small molecular inhibitors to prevent both inflammatory bone destruction and systemic bone loss in rheumatoid arthritis.)
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Cat. No.: HY-P5229A
Target:  

Inhibitory Antibodies

Research Areas:  

Others

IHRIC TFA is a penta-peptide, correlated positively with hairpin DNA with tetramer loops. Therefore, IHRIC TFA joins hands with hairpin DNA (hpDNA) with improved selectivity as sensing materials in the detection system, used for surface plasmon resonance imaging (SPRi) .
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Cat. No.: HY-175419
Synonyms: trans bis-Isatoic anhydride
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

TBIA (trans bis-isatoic anhydride) is a covalent RNA crosslinker. TBIA selectively induces RNA tertiary interactions (e.g., multi-helix junctions, loop-helix packing). TBIA is promising for research of RNA higher-order structure and disease-associated RNAs (e.g., KRAS-mutant RNAs) .
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Cat. No.: HY-172400
CAS No.: 3046390-69-3
Target:  

Factor Xa

Research Areas:  

Cardiovascular Disease

FXIa-IN-16 is an orally active selective FXIa inhibitor with an IC50 of 0.19 nM. FXIa-IN-16 exerts highly selective competitive inhibition on endogenous FXIa, blocks the thrombin amplification loop to inhibit thrombosis, while preserving exogenous physiological hemostatic function. FXIa-IN-16 can be used in thrombosis-related research .
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