489 Results for "

H. influenza

" in MedChemExpress (MCE) Product Catalog:
Products (489)

489 Results for "H. influenza" in MCE Product Catalog:

80
80 Publications Verification
Cat. No.: HY-10964
CAS No.: 117570-53-3
Purity:  99.93%
Synonyms: DMXAA; ASA-404
Research Areas:  

Infection Cancer

Vadimezan (DMXAA), the tumor vascular disrupting agent (tumor-VDA), is a murine agonist of the stimulator of interferon genes (STING) and also a potent inducer of type I IFNs and other cytokines. Vadimezan is unable to activate human STING. Vadimezan has anti-influenza virus H1N1-PR8 activities.
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50
50 Cited Publications
Cat. No.: HY-13317
CAS No.: 196618-13-0
Purity:  99.94%
Synonyms: GS 4104
Target:  

Influenza Virus

Research Areas:  

Infection Cancer

Oseltamivir (GS 4104) is an orally active influenza virus neuraminidase inhibitor (NAI). Oseltamivir inhibits influenza A/H3N2, A/H1N2, A/H1N1, and B viruses with mean IC50s of 0.67, 0.9, 1.34 and 13 nM, respectively .
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44
44 Cited Publications
Cat. No.: HY-15230
CAS No.: 30562-34-6
Purity:  99.78%
Geldanamycin is a Hsp90 inhibitor with antimicrobial activity against many Gram-positive and some Gram-negative bacteria. Geldanamycin has anti-influenza virus H5N1 activities.
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15
15 Cited Publications
Cat. No.: HY-N0540
CAS No.: 5373-11-5
Synonyms: Luteolin 7-glucoside; Luteolin 7-O-β-D-glucoside
Cynaroside (Luteolin 7-glucoside) is a flavonoid compound that exhibits anti-oxidative capabilities. Cynaroside is also a potent influenza RNA-dependent RNA polymerase inhibitor with an IC50 of 32 nM. Cynaroside also is a promising inhibitor for H2O2-induced apoptosis, has cytoprotection against oxidative stress-induced cardiovascular diseases. Cynaroside also has antibacterial, antifungal and anticancer activities, antioxidant and anti-inflammatory activities .
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12
12 Cited Publications
Cat. No.: HY-N0736
CAS No.: 6020-18-4
Coptisine chloride is an alkaloid from Chinese goldthread, and acts as an efficient uncompetitive IDO inhibitor with a Ki value of 5.8 μM and an IC50 value of 6.3 μM. Coptisine chloride is a potent H1N1 neuraminidase (NA-1) inhibitor with an IC50 of 104.6?μg/mL and can be used for influenza A (H1N1) infection.
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11
11 Cited Publications
Cat. No.: HY-107201
CAS No.: 7585-39-9
Purity:  99.95%
Synonyms: Betadex
Target:  

Influenza Virus

Research Areas:  

Infection

β-Cyclodextrin is a cyclic polysaccharide composed of seven units of glucose (α-D-glucopyranose) linked by α-(1,4) type bonds. β-Cyclodextrin has often been used to enhance the solubility of agents. β-Cyclodextrin has anti-influenza virus H1N1 activities.
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9
9 Cited Publications
Cat. No.: HY-14818
CAS No.: 203120-17-6
Purity:  99.27%
Synonyms: R 125489
Target:  

Influenza Virus

Research Areas:  

Infection

Laninamivir (R 125489) is a potent influenza neuraminidase (NA) inhibitor with IC50s of 0.90 nM, 1.83 nM and 3.12 nM for avian H12N5 NA (N5), pH1N1 N1 NA (p09N1) and A/RI/5+/1957 H2N2 N2 (p57N2), respectively .
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7
7 Cited Publications
Cat. No.: HY-N0243
CAS No.: 4670-05-7
Theaflavin is a suitable natural inhibitor against influenza A (H1N1) neuraminidase.
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7
7 Cited Publications
Cat. No.: HY-N0638
CAS No.: 2115-91-5
Dendrobine is an alkaloid isolated from Dendrobium nobile. Dendrobine possesses antiviral activity against influenza A viruses, with IC50s of 3.39 μM, 2.16 μM and 5.32 μM for A/FM-1/1/47 (H1N1), A/Puerto Rico/8/34 H274Y (H1N1) and A/Aichi/2/68 (H3N2), respectively. Dendrobine activates the JNK/p38/Nrf2 signaling pathway. Dendrobine exhibits antiviral, antitumor, anti-inflammatory, and neuroprotective properties .
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4
4 Cited Publications
Cat. No.: HY-B0157
CAS No.: 34580-13-7
Synonyms: HC 20-511
Ketotifen (HC 20-511) is an orally active second-generation noncompetitive histamine 1 (H1) receptor blocker and mast cell stabilizer. Ketotifen can block 6-phosphogluconate dehydrogenase (PGD) in vitro. Ketotifen also has antiviral activity against SARS-CoV-2 and Influenza virus. Ketotifen can be used to the research of autoimmune encephalomyelitis (EAE) and asthma attack prevention .
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4
4 Cited Publications
Cat. No.: HY-B0157A
CAS No.: 34580-14-8
Synonyms: HC 20511 fumarate
Ketotifen (HC 20-511) fumarate is an orally active second-generation noncompetitive histamine 1 (H1) receptor blocker and mast cell stabilizer. Ketotifen fumarate can block 6-phosphogluconate dehydrogenase (PGD) in vitro. Ketotifen fumarate also has antiviral activity against SARS-CoV-2 and Influenza virus. Ketotifen fumarate can be used to the research of autoimmune encephalomyelitis (EAE) and asthma attack prevention .
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2
2 Cited Publications
Cat. No.: HY-116815
CAS No.: 501104-16-1
Purity:  99.75%
Research Areas:  

Infection Neurological Disease

Lalistat 1 is a potent, selective, and competitive inhibitor of lysosomal acid lipase (LAL) and against purified human LAL (phLAL) with an IC50 of 68 nM. Lalistat 1 is a inhibitor of immunoglobulin A1 protease (IgA1P) proteases for H. influenzae, has less effects on other serine hydrolases (trypsin or β-lactamase, etc.). Lalistat 1 can be used for the research of niemann-pick type C (NPC) disease .
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2
2 Cited Publications
Cat. No.: HY-N0540R
CAS No.: 5373-11-5
Synonyms: Luteolin 7-glucoside (Standard); Luteolin 7-O-β-D-glucoside (Standard)
Cynaroside (Standard) is the analytical standard of Cynaroside. This product is intended for research and analytical applications. Cynaroside (Luteolin 7-glucoside) is a flavonoid compound that exhibits anti-oxidative capabilities. Cynaroside is also a potent influenza RNA-dependent RNA polymerase inhibitor with an IC50 of 32 nM. Cynaroside also is a promising inhibitor for H2O2-induced apoptosis, has cytoprotection against oxidative stress-induced cardiovascular diseases. Cynaroside also has antibacterial, antifungal and anticancer activities, antioxidant and anti-inflammatory activities .
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1
1 Cited Publications
Cat. No.: HY-B1589A
CAS No.: 3505-38-2
Carbinoxamine maleate salt is a blood-brain barrier-permeable histamine H1 receptor antagonist. Carbinoxamine maleate salt blocks the action of histamine on H1 receptors, reducing symptoms such as sneezing, rhinitis, rhinorrhea, erythema, pruritus and urticaria. Carbinoxamine maleate salt inhibits influenza virus entry into cells via endocytosis, targets the early stage of the viral life cycle, and simultaneously reduces viral replication levels in the lungs, alleviating pathological damage and inflammatory responses in lung tissues. Carbinoxamine maleate salt can be used in research on allergic rhinitis, influenza, etc.
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1
1 Cited Publications
Cat. No.: HY-P76447
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: influenza A H1N1 (A/California/04/2009) Hemagglutinin / HA0 Protein
Species:  
Virus
Source:  
Sf9 insect cells
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1
1 Cited Publications
Cat. No.: HY-P77026
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: influenza A H3N2 (A/Babol/36/2005) Hemagglutinin / HA0 Protein
Species:  
Virus
Source:  
Sf9 insect cells
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1
1 Cited Publications
Cat. No.: HY-P77034
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: influenza A H8N4 (A/pintail duck/Alberta/114/1979) Hemagglutinin / HA Protein (His)
Species:  
Virus
Source:  
HEK293
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Cat. No.: HY-P99853
CAS No.: 1393659-46-5
Synonyms: CR6261

Target:  

Influenza Virus

Research Areas:  

Infection

Diridavumab is a monoclonal anti-HA stalk antibody. Diridavumab stabilizes the prefusion HA structure and prevents pH-dependent fusion of cellular and viral membranes in endosomes. Diridavumab can be used in research of H2 influenza virus .
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Cat. No.: HY-P99750
CAS No.: 1443004-16-7
Synonyms: CT-P23

Target:  

Influenza Virus

Research Areas:  

Infection

Navivumab (CT-P23) is a monoclonal antibody targeting the hemagglutinin (HA) of influenza A virus. Navivumab binds to the HA2 stem fusion domain and the low-variability HA2 region of influenza viruses. Navivumab neutralizes influenza A viruses of subtypes H1, H2, H5, and H9. Navivumab is applicable to research related to influenza and influenza A .
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Cat. No.: HY-132894
CAS No.: 2365473-17-0
Purity:  99.53%
Synonyms: TG-1000
Research Areas:  

Infection

Pixavir marboxilo (TG-1000) is an orally active prodrug of TG-0527 and an analog of Baloxavir marboxil (HY-109025). Pixavir marboxilo undergoes conversion to its active metabolite and inhibits the cap‑dependent endonuclease of Influenza Virus, reduces pulmonary viral titers, and suppresses the proliferation of influenza A, influenza B, H7N9 avian influenza, and neuraminidase‑resistant strains. Pixavir marboxilo can be used in influenza-related research .
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