1218 Results for "

generation

" in MedChemExpress (MCE) Product Catalog:
Products (1218)

1218 Results for "generation" in MCE Product Catalog:

12
12 Cited Publications
Cat. No.: HY-13257
CAS No.: 1226056-71-8
Purity:  99.57%
Target:  

ROCK

Research Areas:  

Cancer

Thiazovivin is a potent ROCK inhibitor, which can protect human embryonic stem cells. Thiazovivin improves the efficiency of iPSC generation.
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12
12 Cited Publications
Cat. No.: HY-15229
CAS No.: 929904-85-8
Purity:  98.04%
Synonyms: SGI-110 sodium; S-110 sodium
Target:  

DNA Methyltransferase

Research Areas:  

Cancer

Guadecitabine sodium (SGI-110 sodium) is a second-generation DNA methyltransferases (DNMT) inhibitor for research of acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS) .
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12
12 Cited Publications
Cat. No.: HY-P0286
CAS No.: 92915-79-2
Target:  

Inhibitory Antibodies

Research Areas:  

Inflammation/Immunology

OVA Peptide (323-339) represents a T and B cell epitope of Ovalbumin (Ova), which is important in the generation and development of immediate hypersensitivity responses in BALB/c mice.
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12
12 Cited Publications
Cat. No.: HY-16488
CAS No.: 122341-38-2
Synonyms: m-THPC; KW2345
Research Areas:  

Cancer

Temoporfin (m-THPC), a reduced porphyrin, is a potent second-generation photosensitizer. Temoporfin can be used in the research of photodynamic therapy (PDT) for head and neck cancers .
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12
12 Cited Publications
Cat. No.: HY-113424A
CAS No.: 4235-95-4
Purity:  98.11%
Synonyms: DOPC
1,2-Dioleoyl-sn-glycero-3-phosphocholine (DOPC) is a phospholipid and is commonly used alone, or with other components, in the generation of micelles, liposomes, and other types of artificial membranes.
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12
12 Cited Publications
Cat. No.: HY-N2515
CAS No.: 494753-69-4
Ginsenoside Rk1 is a unique component created by processing the ginseng plant (mainly Sung Ginseng, SG) at high temperatures . Ginsenoside Rk1 has anti-inflammatory effect, suppresses the activation of Jak2/Stat3 signaling pathway and NF-κB . Ginsenoside Rk1 has anti-tumor effect, antiplatelet aggregation activities, anti-insulin resistance, nephroprotective effect, antimicrobial effect, cognitive function enhancement, lipid accumulation reduction and prevents osteoporosis . Ginsenoside Rk1 induces cell apoptosis by triggering intracellular reactive oxygen species (ROS) generation and blocking PI3K/Akt pathway .
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11
11 Cited Publications
Cat. No.: HY-P0019
CAS No.: 66216-78-2
Research Areas:  

Cardiovascular Disease

Z-Gly-Gly-Arg-AMC is a thrombin-specific fluorogenic substrate for testing of thrombin generation in PRP and platelet-poor plasma (PPP) (Ex/Em = 390/480 nm) .
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11
11 Cited Publications
Cat. No.: HY-P0019A
CAS No.: 2070009-61-7
Research Areas:  

Others

Z-Gly-Gly-Arg-AMC acetate is a thrombin-specific fluorogenic substrate for testing of thrombin generation in PRP and platelet-poor plasma (PPP) (Ex/Em = 390/480 nm) .
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11
11 Cited Publications
Cat. No.: HY-B1256
CAS No.: 56238-63-2
Research Areas:  

Infection Cancer

Cefuroxime sodium is an orally active second-generation cephalosporin antibiotic with increased stability to β-lactamase. Cefuroxime sodium has a broad spectrum activity against Gram-positive and Gram-negative bacteria .
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11
11 Cited Publications
Cat. No.: HY-B1256A
CAS No.: 55268-75-2
Synonyms: Kefurox
Research Areas:  

Infection Cancer

Cefuroxime is an orally active second-generation cephalosporin antibiotic with increased stability to β-lactamase. Cefuroxime has a broad spectrum activity against Gram-positive and Gram-negative bacteria .
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11
11 Cited Publications
Cat. No.: HY-76200
CAS No.: 137234-62-9
Synonyms: UK-109496
Target:  

Fungal Bacterial

Research Areas:  

Infection Neurological Disease Cancer

Voriconazole (UK-109496) is a second-generation, broad-spectrum triazole antifungal agent that inhibits fungal ergosterol biosynthesis. Voriconazole exerts its antifungal activity by inhibition of 14-α-lanosterol demethylation, which is mediated by fungal cytochrome P450 enzymes. Voriconazole can penetrate the blood brain barrier (BBB) .
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11
11 Cited Publications
Cat. No.: HY-B1077
CAS No.: 26864-56-2
Synonyms: R-16341
Penfluridol (R-16341) is a potent, long-acting, first-generation, oral diphenylbutylpiperidine antipsychotic agent by targeting D2-like dopamine receptor. Penfluridol effectively inhibits TNFα-induced NF-κB activation and alleviates the severity of arthritis and colitis in vivo. Penfluridol is a Ca2+-calmodulin inhibitor. Penfluridol induces apoptosis and autophagy. Penfluridol is used for chronic schizophrenia, acute psychosis, Tourette syndrome and autoimmune diseases. Penfluridol inhibites the growth of E. faecalis planktonic cells with the MIC of 7.81 μg/ml .
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10
10 Cited Publications
Cat. No.: HY-B1381
CAS No.: 79350-37-1
Synonyms: FR-17027; FK-027; CL-284635
Target:  

Antibiotic Bacterial

Research Areas:  

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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10
10 Cited Publications
Cat. No.: HY-B1381A
CAS No.: 125110-14-7
Synonyms: FR-17027 trihydrate; FK-027 trihydrate; CL-284635 trihydrate
Target:  

Antibiotic Bacterial

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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10
10 Cited Publications
Cat. No.: HY-19619
CAS No.: 200933-14-8
Target:  

Phospholipase Apoptosis

Research Areas:  

Cancer

m-3M3FBS is a potent phospholipase C (PLC) activator. m-3M3FBS stimulates superoxide generation in human neutrophils, upregulates intracellular calcium concentration, and stimulates inositol phosphate generation in various cell lines. m-3M3FBS induces monocytic leukemia cell apoptosis .
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10
10 Cited Publications
Cat. No.: HY-13065
CAS No.: 20784-50-3
Purity:  99.01%
Synonyms: Corylifolinin; Isobacachalcone
Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity .
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10
10 Cited Publications
Cat. No.: HY-N0621
CAS No.: 480-16-0
Morin is an orally active plant-derived flavonoid. Morin inhibits ROS generation. Morin induces Apoptosis. Morin inhibits PTP1B (IC50 of 15 μM) and activates the insulin receptor. Morin has a detoxifying effect. Morin can be used in diabetes, leukemia, colon cancer, cervical cancer, Parkinson's disease and hypertension research .
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10
10 Cited Publications
Cat. No.: HY-112823
CAS No.: 1899921-05-1
Purity:  99.83%
Synonyms: HS-10296
Target:  

EGFR

Research Areas:  

Cancer

Almonertinib (HS-10296) is an orally available, irreversible, third-generation EGFR tyrosine kinase inhibitor with high selectivity for EGFR-sensitizing and T790M resistance mutations. Almonertinib shows great inhibitory activity against T790M, T790M/L858R and T790M/Del19 (IC50: 0.37, 0.29 and 0.21 nM, respectively), and is less effective against wild type (3.39 nM). Almonertinib is used for the research of the non-small cell lung cancer .
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10
10 Cited Publications
Cat. No.: HY-112823A
CAS No.: 2134096-06-1
Purity:  99.67%
Synonyms: HS-10296 mesylate
Target:  

EGFR

Research Areas:  

Cancer

Almonertinib (HS-10296) mesylate is an orally available, irreversible, third-generation EGFR tyrosine kinase inhibitor with high selectivity for EGFR-sensitizing and T790M resistance mutations. Almonertinib mesylate shows great inhibitory activity against T790M, T790M/L858R and T790M/Del19 (IC50: 0.37, 0.29 and 0.21 nM, respectively), and is less effective against wild type (3.39 nM). Almonertinib mesylate is used for the research of the non-small cell lung cancer .
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10
10 Cited Publications
Cat. No.: HY-112823B
CAS No.: 2134096-03-8
Purity:  99.77%
Synonyms: HS-10296 hydrochloride
Target:  

EGFR

Research Areas:  

Cancer

Almonertinib (HS-10296) hydrochloride is an orally available, irreversible, third-generation EGFR tyrosine kinase inhibitor with high selectivity for EGFR-sensitizing and T790M resistance mutations. Almonertinib hydrochloride shows great inhibitory activity against T790M, T790M/L858R and T790M/Del19 (IC50: 0.37, 0.29 and 0.21 nM, respectively), and is less effective against wild type (3.39 nM). Almonertinib hydrochloride is used for the research of the non-small cell lung cancer .
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