326 Results for "

CAP

" in MedChemExpress (MCE) Product Catalog:
Products (326)

326 Results for "CAP" in MCE Product Catalog:

50
50 Publications Verification
Cat. No.: HY-109025A
CAS No.: 1985605-59-1
Purity:  99.68%
Synonyms: Baloxavir acid; S-033447
Target:  

Influenza Virus

Research Areas:  

Infection Cancer

Baloxavir (Baloxavir acid), derived from the proagent Baloxavir marboxil, is a first-in-class, potent and selective cap-dependent endonuclease (CEN) inhibitor within the polymerase PA subunit of influenza A and B viruses. Baloxavir inhibits viral RNA transcription and replication and has potently antiviral activity .
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13
13 Cited Publications
Cat. No.: HY-109025
CAS No.: 1985606-14-1
Purity:  99.96%
Synonyms: S-033188; RG 6152
Target:  

Influenza Virus

Research Areas:  

Infection Cancer

Baloxavir marboxil (S-033188) is a selective inhibitor of influenza cap-dependent endonuclease. Baloxavir marboxil, a potent antiviral agent, shows activity against influenza A and B virus .
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8
8 Cited Publications
Cat. No.: HY-N0086
CAS No.: 1867-73-8
Synonyms: 6-Methyladenosine; N-Methyladenosine
N6-Methyladenosine is the most prevalent internal (non-cap) modification present in the messenger RNA (mRNA) of all higher eukaryotes. N6-Methyladenosine can modifies viral RNAs and has antiviral activities.
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5
5 Cited Publications
Cat. No.: HY-15523
CAS No.: 351351-75-2
Purity:  99.51%
Research Areas:  

Cancer

Braco-19 is a potent telomerase/telomere inhibitor, preventing the capping and catalytic action of telomerase. Braco-19 acts as G-quadruplex (GQ) binding ligand, stabilizing G-quadruplexes formation at the 3V telomeric DNA overhang and produce rapid senescence or selective cell death. Braco-19 is also a HAdV virus replication inhibitor .
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5
5 Cited Publications
Cat. No.: HY-15523A
CAS No.: 1177798-88-7
Purity:  99.73%
Target:  

DNA/RNA Synthesis CMV

Research Areas:  

Infection Cancer

Braco-19 trihydrochloride is a potent telomerase/telomere inhibitor, preventing the capping and catalytic action of telomerase. Braco-19 acts as G-quadruplex (GQ) binding ligand, stabilizing G-quadruplexes formation at the 3V telomeric DNA overhang and produce rapid senescence or selective cell death. Braco-19 is also a HAdV virus replication inhibitor .
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4
4 Cited Publications
Cat. No.: HY-14427
CAS No.: 328998-25-0
Purity:  98.89%
Research Areas:  

Cancer

4E1RCat is an inhibitor of cap-dependent translation, and inhibits eIF4E:eIF4GI interaction, with an IC50 an of ~4 μM.
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3
3 Cited Publications
Cat. No.: HY-153040
CAS No.: 1325721-55-8
Purity:  99.67%
Synonyms: Bach1-IN-1
Research Areas:  

Metabolic Disease

HPPE (compound 236) is an orally active, potential Bach1 inhibitor. Bach1 is a transcription factor of the cap'n'collar type alkaline region leucine zipper factor family (CNC-bZip) that regulates mitochondrial metabolism and reduces glucose utilization. HPPE can be used for research in psoriasis, multiple sclerosis, and COPD .
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3
3 Cited Publications
Cat. No.: HY-P80774A
Synonyms: CDKN1A; CAP20; CDKN1; CIP1; MDA6; PIC1; SDI1; WAF1; Cyclin-dependent kinase inhibitor 1; CDK-interacting protein 1; Melanoma differentiation-associated protein 6; MDA-6; p21

Host:  

Rabbit

Application:  

WB, ICC/IF

Reactivity:  

Human, Mouse, Rat

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2
2 Cited Publications
Cat. No.: HY-122524
CAS No.: 20244-86-4
Purity:  98.08%
7-Methylguanosine is a modified nucleoside widely present in various RNAs and a key metabolite of the 5'-cap structure of eukaryotic mRNA. 7-Methylguanosine plays important roles in stabilizing RNA structures, regulating translation, and other aspects .
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2
2 Cited Publications
Cat. No.: HY-122524A
CAS No.: 81100-62-1
7-Methylguanosine iodide is an iodide of 7-Methylguanosine (HY-122524). 7-Methylguanosine is a modified nucleoside widely present in various RNAs and a key metabolite of the 5'-cap structure of eukaryotic mRNA. 7-Methylguanosine plays important roles in stabilizing RNA structures, regulating translation, and other aspects .
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2
2 Cited Publications
Cat. No.: HY-A0148A
CAS No.: 36167-63-2
Synonyms: SKF-102886; WR-171669 hydrochloride
Halofantrine hydrochloride (SKF-102886 hydrochloride; WR-171669 hydrochloride) is a blocker that delays the delayed rectifier potassium current by inhibiting human ERG channels, and it is a potent antimalarial agent with oral activity. Halofantrine hydrochloride inhibits the Cap1-dependent oxidative stress response of Candida albicans, suppresses ROS responses, and enhances the antifungal (Fungal) activity of oxidative damage agents. Halofantrine hydrochloride exhibits antifungal activity in the Galleria mellonella model, and shows antimalarial activity against Plasmodium strains both in vitro and in animal models. Halofantrine hydrochloride can be used in studies related to invasive candidiasis, falciparum malaria, and vivax malaria .
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2
2 Cited Publications
Cat. No.: HY-156048
CAS No.: 1854086-05-7
Purity:  99.12%
Synonyms: TFMT
Target:  

Influenza Virus

Research Areas:  

Infection

Trifluoromethyl-tubercidin (TFMT) is an inhibitor of 2'-O-ribose methyltransferase 1 (MTr1). Trifluoromethyl-tubercidin can inhibit the replication of influenza A and B viruses by interfering with the cap-snatching process of the influenza virus. Trifluoromethyl-tubercidin has antiviral activity and low toxicity .
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2
2 Cited Publications
Cat. No.: HY-P80976
Synonyms: Brd4; CAP; HUNK1; MCAP; Bromodomain containing 4; chromosome associated protein

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, IP

Reactivity:  

Human, Mouse, Rat

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2
2 Cited Publications
Cat. No.: HY-P80624
Synonyms: CASP8; MCH5; Caspase-8; CASP-8; Apoptotic cysteine protease; Apoptotic protease Mch-5; CAP4; FADD-homologous ICE/ced-3-like protease; FADD-like ICE; FLICE; ICE-like apoptotic protease 5; MORT1-associated ced-3 homolog; MACH

Host:  

Mouse

Application:  

WB, IHC-F, IHC-P, ICC/IF

Reactivity:  

Human, Mouse, Rat

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2
2 Cited Publications
Cat. No.: HY-N0086R
CAS No.: 1867-73-8
Synonyms: 6-Methyladenosine (Standard); N-Methyladenosine (Standard)
N6-Methyladenosine (Standard) is the analytical standard of N6-Methyladenosine. This product is intended for research and analytical applications. N6-Methyladenosine is the most prevalent internal (non-cap) modification present in the messenger RNA (mRNA) of all higher eukaryotes. N6-Methyladenosine can modifies viral RNAs and has antiviral activities. In Vitro: N6-methyladenosine (m6A) is selectively recognized by the human YTH domain family 2 (YTHDF2) protein to regulate mRNA degradation. N6-methyladenosine (m6A), a prevalent internal modification in the messenger RNA of all eukaryotes, is post-transcriptionally installed by m6A methyltransferase (e.g., MT-A70) within the consensus sequence of G(m6A)C (70%) or A(m6A)C (30%). N6-methyladenosine (m6A)-containing RNAs are greatly enriched in the YTHDF-bound portion and diminished in the flow-through portion . N6-methyladenosine (m6A), the most abundant internal RNA modification, functions in diverse biological processes, including regulation of embryonic stem cell self-renewal and differentiation. N6-methyladenosine (m6A) is a large protein complex, consisting in part of methyltransferase-like 3 (METTL3) and methyltransferase-like 14 (METTL14) catalytic subunits .
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1
1 Cited Publications
Cat. No.: HY-148771
CAS No.: 2488296-74-6
Purity:  99.79%
Synonyms: PROTAC AR-V7 degrader-2
Research Areas:  

Cancer

MTX-23 is an AR-based PROTAC. MTX-23 inhibits CaP cellular proliferation by degrading AR-V7 and AR-FL. MTX-23 induces apoptosis .
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1
1 Cited Publications
Cat. No.: HY-14956
CAS No.: 378746-64-6
Purity:  99.80%
Synonyms: TG-873870
Target:  

Antibiotic Bacterial

Research Areas:  

Infection Inflammation/Immunology

Nemonoxacin (TG-873870) is an orally active and potent broad-spectrum antibiotic. Nemonoxacin shows good inhibitory activity against different species of staphylococci, streptococci, and enterococci, Neisseria gonorrhoeae, and Haemophilus influenza. Nemonoxacin can be used in the study of bacterial infections and community-acquired pneumonia .
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1
1 Cited Publications
Cat. No.: HY-17452
CAS No.: 104146-53-4
Synonyms: ME 1206
Research Areas:  

Infection Inflammation/Immunology

Cefditoren sodium (ME 1206) is a broad-spectrum, third-generation, oral cephalosporin antibacterial with enhanced stability against many common β lactamases. Cefditoren sodium has activity against Gram-negative organisms and Gram-positive organisms. Cefditoren sodium can be used in the research of infection diseases such as acute exacerbations of chronic bronchitis, community-acquired pneumonia (CAP), streptococcal pharyngitis/tonsillitis, or uncomplicated skin and skin structure infections .
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1
1 Cited Publications
Cat. No.: HY-P74525A
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Transforming growth factor-beta-induced protein ig-h3; Beta ig-h3; RGD-CAP; BIGH3
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-P71625
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: CAP1; DJ-1; DJ1; DJ1 protein ; Epididymis secretory sperm binding protein Li 67p; SP22
Species:  
Source:  
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