10862 Results for "

active oxygen method

" in MedChemExpress (MCE) Product Catalog:
Products (10862)

10862 Results for "active oxygen method" in MCE Product Catalog:

26
26 Cited Publications
Cat. No.: HY-10158
CAS No.: 380843-75-4
Pureté:  99.89%
Synonyms: SKI-606
Target:  

Src Bcr-Abl Autophagy

Bosutinib is an orally active Src/Abl tyrosine kinase inhibitor with IC50 of 1.2 nM and 1 nM, respectively .
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26
26 Cited Publications
Cat. No.: HY-N1362
CAS No.: 121521-90-2
Synonyms: Lithospermic acid B
Salvianolic acid B is an active ingredient of Salvia miltiorrhiza, which has been widely applied in China for the management of various microcirculation-related disorders, such as cardiovascular disease, cerebrovascular disease, and diabetic vascular complication.
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26
26 Cited Publications
Cat. No.: HY-13848
CAS No.: 911715-90-7
Pureté:  99.54%
Synonyms: AZD8797; KAND567
Target:  

CX3CR1 CXCR

Domaines de recherche:  

Inflammation/Immunology Endocrinology Cancer

AZD8797 (KAND567) is an allosteric non-competitive and orally active antagonist of the human CX3CR1 receptor; antagonizes CX3CR1 and CXCR2 with Kis of 3.9 and 2800 nM, respectively .
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25
25 Cited Publications
Cat. No.: HY-126793
CAS No.: 2044-85-1
Pureté:  98.95%
Synonyms: DCFH2-DA
2′,7′-Dichlorofluorescein diacetate (DCFH2-DA) is a cell-permeable fluorescent probe. 2′,7′-Dichlorofluorescein diacetate can be used to detect the generation of reactive oxygen intermediates and for assessing the overall oxidative stress in toxicological phenomenon .
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25
25 Cited Publications
Cat. No.: HY-101474A
CAS No.: 1691249-45-2
Pureté:  99.71%
Synonyms: BGB-3111
Target:  

Btk

Domaines de recherche:  

Cancer

Zanubrutinib (BGB-3111) is a selective and orally active Bruton tyrosine kinase (Btk) inhibitor (IC50: 0.3 nM) .
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25
25 Cited Publications
Cat. No.: HY-12216
CAS No.: 920509-32-6
Pureté:  99.90%
Synonyms: MGL-3196; VIA-3196
Domaines de recherche:  

Cardiovascular Disease Endocrinology

Resmetirom (MGL-3196) is a highly selective and orally active thyroid hormone receptor β (THR-β) agonist with an EC50 value of 0.21 μM. Resmetirom can be used for the study of noncirrhotic nonalcoholic steatohepatitis .
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25
25 Cited Publications
Cat. No.: HY-132167
CAS No.: 2589531-76-8
Pureté:  99.76%
Synonyms: AZD5305
Target:  

PARP

Domaines de recherche:  

Cancer

Saruparib (AZD5305) is a potent, orally active and selective PARP inhibitor and trapper with IC50 values of 3 nM and 1400 nM for PARP1 and PARP2, respectively. Saruparib has anti-proliferative activity and inhibits growth in cells with deficiencies in DNA repair .
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25
25 Cited Publications
Cat. No.: HY-N0289
CAS No.: 2188-68-3
Lycorine hydrochloride is the main active ingredient of the herbal medicine derived from Lycoris radiata (L’Her.) Herb. and is also a melanoma vasculogenic inhibitor and has anti-tumor activity . Lycorine hydrochloride effectively inhibits mitotic proliferation of Hey1B cells (IC50 of 1.2 μM) .
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24
24 Cited Publications
Cat. No.: HY-50295
CAS No.: 212631-79-3
Synonyms: PD 184352
Target:  

MEK Apoptosis

Domaines de recherche:  

Cancer

CI-1040 (PD 184352) is an orally active, highly specific, small-molecule inhibitor of MEK with an IC50 of 17 nM for MEK1.
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24
24 Cited Publications
Cat. No.: HY-N0751
CAS No.: 27740-01-8
Scutellarin, an active flavone isolated from Scutellaria baicalensis, can down-regulates the STAT3/Girdin/Akt signaling in HCC cells, and inhibits RANKL-mediated MAPK and NF-κB signaling pathway in osteoclasts. Scutellarin is active against HIV-1IIIB, HIV-1(74V) and HIV-1KM018 with EC50s of 26 μM, 253 μM and 136 μM, respectively.
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24
24 Cited Publications
Cat. No.: HY-109099
CAS No.: 1513857-77-6
Pureté:  99.84%
Synonyms: INCB054828
Target:  

FGFR

Domaines de recherche:  

Cancer

Pemigatinib (INCB054828) is an orally active, selective FGFR inhibitor with IC50s of 0.4 nM, 0.5 nM, 1.2 nM, 30 nM for FGFR1, FGFR2, FGFR3, FGFR4, respectively. Pemigatinib has the potential for cholangiocarcinoma .
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24
24 Cited Publications
Cat. No.: HY-19615B
CAS No.: 1992047-64-9
Domaines de recherche:  

Cancer

MS023 dihydrochloride is a potent, selective, and cell-active inhibitor of human type I protein arginine methyltransferases (PRMTs) inhibitor, with IC50s of 30, 119, 83, 4 and 5 nM for PRMT1, PRMT3, PRMT4, PRMT6, and PRMT8, respectively .
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24
24 Cited Publications
Cat. No.: HY-10343
CAS No.: 425637-18-9
Pureté:  99.79%
Synonyms: AEB071
Target:  

MARCKS PKC

Domaines de recherche:  

Inflammation/Immunology Cancer

Sotrastaurin (AEB071) is a potent and orally-active pan-PKC inhibitor, with Kis of 0.22 nM, 0.64 nM, 0.95 nM, 1.8 nM, 2.1 nM and 3.2 nM for PKCθ, PKCβ, PKCα, PKCη, PKCδ and PKCε, respectively .
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24
24 Cited Publications
Cat. No.: HY-19615
CAS No.: 1831110-54-3
Domaines de recherche:  

Cancer

MS023, a chemical probe, is a potent, selective, and cell-active inhibitor of human type I protein arginine methyltransferases (PRMTs) inhibitor, with IC50s of 30, 119, 83, 4 and 5 nM for PRMT1, PRMT3, PRMT4, PRMT6, and PRMT8, respectively .
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23
23 Cited Publications
Cat. No.: HY-B2130
CAS No.: 69-93-2
Uric acid is an orally active oxygen free radical scavenger that helps maintain stable blood pressure and combat oxidative stress. Uric acid can scavenge ROS, such as singlet oxygen and peroxynitrite, and inhibit lipid peroxidation. Uric acid can be used as a modeling agent in research on hyperuricemia-induced hypertension models .
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23
23 Cited Publications
Cat. No.: HY-B2130A
CAS No.: 1198-77-2
Synonyms: Monosodium urate
Uric acid sodium is an orally active oxygen free radical scavenger that helps maintain stable blood pressure and combat oxidative stress. Uric acid sodium can scavenge ROS, such as singlet oxygen and peroxynitrite, and inhibit lipid peroxidation. Uric acid sodium can be used as a modeling agent in research on hyperuricemia-induced hypertension models .
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23
23 Cited Publications
Cat. No.: HY-101894
CAS No.: 109244-58-8
Pureté:  99.83%
Synonyms: DHR 123
Target:  

Fluorescent Dye

Domaines de recherche:  

Others

Dihydrorhodamine 123 (DHR 123) is a non-fluorescent reactive oxygen species (ROS) indicator. Dihydrorhodamine 123 is oxidized to fluorescent Rhodamine 123 (HY-D0816) within cells in the presence of reactive oxygen species and it localizes in mitochondria (Ex/Em = 515/536 nm).
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23
23 Cited Publications
Cat. No.: HY-113324
CAS No.: 53-57-6
Pureté:  99.49%
NADPH is a coenzyme of glutathione reductase (GR), thioredoxin reductase (TrxR) and NADPH oxidase (NOX), and participates in redox reactions as a hydrogen donor. NADPH has the characteristic of selectively participating in the regulation of cellular redox homeostasis. NADPH exerts antioxidant activity and resists reactive oxygen species (ROS) damage by providing reducing equivalents for the regeneration of glutathione (GSH) and thioredoxin (Trx); at the same time, it acts as a substrate of NOX to generate superoxide anions, mediating oxidative stress and immune response. NADPH participates in maintaining the intracellular reducing environment, biosynthesis and regulating gene expression (such as the Nrf2 pathway), and is mainly used in the study of oxidative stress-related diseases (such as cardiovascular diseases, neurodegenerative diseases, cancer) and immune regulation mechanisms .
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23
23 Cited Publications
Cat. No.: HY-W353258
CAS No.: 192927-63-2
Synonyms: BAY 12-8039 monohydrate
Moxifloxacin (BAY 12-8039) hydrochloride monohydrate is an orally active bacterial inhibitor that is effective against Streptococcus pneumoniae. Moxifloxacin hydrochloride monohydrate can be used in tuberculosis research .
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23
23 Cited Publications
Cat. No.: HY-66011A
CAS No.: 151096-09-2
Synonyms: BAY 12-8039 free base
Target:  

Bacterial Antibiotic

Domaines de recherche:  

Infection Cancer

Moxifloxacin is an orally active 8-methoxyquinolone antimicrobial for use in the treatment of acute bacterial sinusitis, acute bacterial exacerbations of chronic bronchitis, and community-acquired pneumonia .
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