229 Results for "

Anemone flaccida Fr. Schmidt

" in MedChemExpress (MCE) Product Catalog:
Products (229)

229 Results for "Anemone flaccida Fr. Schmidt" in MCE Product Catalog:

106
106 Publications Verification
Art. -Nr.: HY-13756
CAS. Nr.: 104987-11-3
Reinheit:  99.93%
Synonyms: FK506; Fujimycin; FR900506
Tacrolimus (FK506), a molecular glue, a macrocyclic lactone, binds to FK506 binding protein (FKBP) to form a complex. Tacrolimus inhibits calcineurin phosphatase, which inhibits T-lymphocyte signal transduction and IL-2 transcription. Immunosuppressive properties .
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106
106 Publications Verification
Art. -Nr.: HY-13756A
CAS. Nr.: 109581-93-3
Reinheit:  99.67%
Synonyms: FK506 monohydrate; Fujimycin monohydrate; FR900506 monohydrate
Tacrolimus (FK506) monohydrate, a molecular glue, a macrocyclic lactone, binds to FK506 binding protein (FKBP) to form a complex. Tacrolimus monohydrate inhibits calcineurin phosphatase, which inhibits T-lymphocyte signal transduction and IL-2 transcription. Immunosuppressive properties .
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75
75 Cited Publications
Art. -Nr.: HY-15149
CAS. Nr.: 128517-07-7
Reinheit:  99.87%
Synonyms: FK 228; FR 901228; NSC 630176
Target:  

HDAC Apoptosis

Forschungsgebiete:  

Cancer

Romidepsin (FK 228) is a Histone deacetylase (HDAC) inhibitor with anti-tumor activities. Romidepsin (FK 228) inhibits HDAC1, HDAC2, HDAC4, and HDAC6 with IC50s of 36 nM, 47 nM, 510 nM and 1.4 μM, respectively . Romidepsin (FK 228) is produced by Chromobacterium violaceum, induces cell G2/M phase arrest and apoptosis .
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32
32 Cited Publications
Art. -Nr.: HY-12686
CAS. Nr.: 253863-19-3
Reinheit:  99.30%
Synonyms: FR148083; L783279; LL-Z 1640-2
5Z-7-Oxozeaenol is a natural anti-protozoan compound from fungal origin, acting as a potent irreversible and selective inhibitor of TAK1 and VEGF-R2, with IC50s of 8 nM and 52 nM, respectively.
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26
26 Cited Publications
Art. -Nr.: HY-12275
CAS. Nr.: 865362-74-9
Reinheit:  99.91%
Forschungsgebiete:  

Cancer

FR 180204 is an ATP-competitive and selective ERK inhibitor. FR 180204 inhibits ERK1 and ERK2 with IC50s of 0.51 μM (Ki=0.31 μM) and 0.33 μM (Ki=0.14 μM), respectively .
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16
16 Cited Publications
Art. -Nr.: HY-19332
CAS. Nr.: 109944-15-2
Synonyms: FR-900494
Kifunensine, a potent and selective inhibitor of class I α-mannosidases isolated from Actinomycete, prevents α-mannosidases I from trimming mannose residues on glycoproteins. Kifunensine inhibits ERAD .
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12
12 Cited Publications
Art. -Nr.: HY-N6707
CAS. Nr.: 76896-80-5
Synonyms: WS 1228A; FR 900190
Triacsin C (WS 1228A), is an orally active and intracellular long-chain acyl-CoA synthetases (ACSL) inhibitor, which can be isolated from Streptomyces aureofaciens. Triacsin C inhibits TAG accumulation into lipid droplets (LD) by suppressing ACSL activity . Triacsin C exhibits highly inhibitory effect against rotavirus replication .
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9
9 Cited Publications
Art. -Nr.: HY-B1381
CAS. Nr.: 79350-37-1
Synonyms: FR-17027; FK-027; CL-284635
Target:  

Antibiotic Bacterial

Forschungsgebiete:  

Infection Cancer

Cefixime (FR-17027) is an orally active antibiotic and a third generation cephalosporin antibiotic, useful for the treatment of a number of bacterial infections .
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9
9 Cited Publications
Art. -Nr.: HY-B1381A
CAS. Nr.: 125110-14-7
Synonyms: FR-17027 trihydrate; FK-027 trihydrate; CL-284635 trihydrate
Target:  

Antibiotic Bacterial

Forschungsgebiete:  

Infection Inflammation/Immunology Cancer

Cefixime trihydrate (FR-17027 trihydrate) is an antibiotic and a third generation cephalosporin antibiotic, useful for the treatment of a number of bacterial infections .
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9
9 Cited Publications
Art. -Nr.: HY-108599
CAS. Nr.: 28399-31-7
Reinheit:  ≥98.0%
Synonyms: FR236924
Forschungsgebiete:  

Neurological Disease

DCP-LA (FR236924), a linoleic acid derivative, selectively and directly activates PKCε. DCP-LA activates Ca( 2+)/calmodulin-dependent protein kinase II (CaMKII) and inhibits protein phosphatase-1 (PP-1) to stimulate AMPA receptor exocytosis. DCP-LA inhibits activation of caspase-3/-9 and protects neurons at least in part from oxidative stress-induced apoptosis .
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6
6 Cited Publications
Art. -Nr.: HY-13557
CAS. Nr.: 104987-12-4
Reinheit:  ≥98.0%
Synonyms: Immunomycin; FR-900520; FK520
Ascomycin (Immunomycin; FR-900520; FK520) is an ethyl analog of Tacrolimus (FK506) with strong immunosuppressant properties. Ascomycin is also a macrocyclic polyketide antibiotic with multiple biological activities such as anti-malarial, anti-fungal and anti-spasmodic. Ascomycin prevents graft rejection and has potential for varying skin ailments research .
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4
4 Cited Publications
Art. -Nr.: HY-117037
CAS. Nr.: 107530-18-7
Reinheit:  99.90%
FR900359 is a depsipeptide selective inhibitor of q/11/14 in mammalia, can inhibits ERK pathway. FR900359 suppresses the proliferation of melanoma cells and decreases of blood pressure. FR900359 also protected against airway hyperreactivity in murine models of allergen sensitization in Ovalbumin, low endotoxin (HY-W250978A)-induced sensitization model of asthma. FR900359 can be used for cancer and cardiovascular disease research .
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3
3 Cited Publications
Art. -Nr.: HY-132258A
CAS. Nr.: 1453084-37-1
Reinheit:  99.71%
Synonyms: IMGN853 (solution)
Forschungsgebiete:  

Cancer

Mirvetuximab soravtansine (IMGN853) solution is an anti-folate receptor α (FRα) antibody drug-conjugate (ADC) consisting of the cytotoxic maytansinoid, DM4, covalently linked to the humanized monoclonal antibody M9346A, and the drug-linker conjugate for ADC is sulfo-SPDB-DM4 (HY-101141). Mirvetuximab soravtansine selectively binds to folate receptor 1 (FOLR1). Mirvetuximab soravtansine has an anti-proliferative effect via growth arrest and augmented DNA damage .
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2
2 Cited Publications
Art. -Nr.: HY-100303A
CAS. Nr.: 204067-52-7
Reinheit:  98.76%
Forschungsgebiete:  

Metabolic Disease

FR194738 is a squalene epoxidase inhibitor. FR194738 inhibits squalene epoxidase activity in HepG2 cell homogenates with an IC50 of 9.8 nM.
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2
2 Cited Publications
Art. -Nr.: HY-P990587

Target:  

CD28

Forschungsgebiete:  

Inflammation/Immunology

FR104 is a humanized antibody expressed in CHO cells that targets CD28. FR104 comprises a huIgG2 heavy chain and a huκ light chain, with a predicted molecular weight (MW) of 145.08 kDa. The isotype control for FR104 can be referenced as Human IgG2 kappa, Isotype Control (HY-P99002).
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2
2 Cited Publications
Art. -Nr.: HY-100303
CAS. Nr.: 204067-45-8
Reinheit:  99.84%
Forschungsgebiete:  

Metabolic Disease

FR194738 free base is a squalene epoxidase inhibitor. FR194738 inhibits squalene epoxidase activity in HepG2 cell homogenates with an IC50 of 9.8 nM.
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2
2 Cited Publications
Art. -Nr.: HY-112853
CAS. Nr.: 66508-37-0
Reinheit:  99.72%
Synonyms: FR-31564
Target:  

Bacterial Antibiotic

Forschungsgebiete:  

Infection

Fosmidomycin sodium salt is a phosphonic acid antibiotic and a antimalarial agent, which is active against both Gram-negative and Gram-positive bacteria.
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2
2 Cited Publications
Art. -Nr.: HY-101128
CAS. Nr.: 37134-40-0
Reinheit:  99.76%
Synonyms: FR2054
Target:  

Bacterial Antibiotic

Forschungsgebiete:  

Infection

Bicyclomycin benzoate is an antibiotic exhibiting activity against a broad spectrum of Gram-negative bacteria and against the Gram-positive bacterium.
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2
2 Cited Publications
Art. -Nr.: HY-P99225
CAS. Nr.: 1453084-36-0
Synonyms: M9346A

Forschungsgebiete:  

Cancer

Mirvetuximab (M9346A) is an anti-FOLR1 (folate receptor 1) monoclonal antibody. Mirvetuximab is the antibody moiety of folate receptor alpha (FRα)-targeting ADC (Mirvetuximab soravtansine). Mirvetuximab soravtansine can be used in ovarian and other FRα-positive cancer research .
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2
2 Cited Publications
Art. -Nr.: HY-P99225A
CAS. Nr.: 1453084-36-0
Synonyms: M9346A (powder)

Forschungsgebiete:  

Cancer

Mirvetuximab (M9346A) (powder) is an anti-FOLR1 (folate receptor 1) monoclonal antibody. Mirvetuximab (powder) is the antibody moiety of folate receptor alpha (FRα)-targeting ADC (Mirvetuximab soravtansine). Mirvetuximab soravtansine can be used in ovarian and other FRα-positive cancer research .
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