11 Results for "

rta 408 bus schedule

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "rta 408 bus schedule" in MCE Product Catalog:

26
26 Cited Publications
Cat. No.: HY-12212
CAS No.: 1474034-05-3
Purity:  99.38%
Synonyms: rta 408
Target:  

Keap1-Nrf2 STING Apoptosis

Research Areas:  

Inflammation/Immunology Cancer

Omaveloxolone (RTA 408) is an antioxidant inflammation modulator (AIM), which activates Nrf2 and suppresses nitric oxide (NO). Omaveloxolone attenuates osteoclastogenesis by inhibiting STING dependent NF-κb signaling.
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Cat. No.: HY-138253
CAS No.: 114248-23-6
Purity:  99.87%
Synonyms: dFdU; 2',2'-Difluoro-2'-deoxyuridine
Research Areas:  

Cancer

2’,2’-Difluorodeoxyuridine (dFdU) is the main metabolite of Gemcitabine (HY-17026). 2’,2’-Difluorodeoxyuridine causes a concentration- and schedule- dependent radiosensitising effect in vitro. 2’,2’-Difluorodeoxyuridine arrests cell cycle at the early S phase and induces apoptosis in cancer cells .
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Cat. No.: HY-173447
CAS No.: 344402-39-7
Target:  

NTPDase CD73

Research Areas:  

Cancer

8-BuS-AMP is a NTPDase1 inhibitor and a CD73/CD39 inhibitor, with an IC50 of 35 μM and a Ki value of 0.292 μM against human NTPDase1; its Ki values against human CD73 and CD39 are 1.19 μM and 0.847 μM, respectively. 8-BuS-AMP binds to the substrate-binding pockets of NTPDase1 and CD73 to effectively block the conversion of ATP and AMP to adenosine, thereby enhancing the activation and proliferation of human peripheral T lymphocytes. 8-BuS-AMP possesses excellent enzymatic hydrolysis resistance and metabolic stability, resists hydrolysis by multiple NTPDase subtypes, and shows no activity against P2Y1 and P2Y12 receptors. 8-BuS-AMP can be used in purinergic signaling pathway and cancer-related studies .
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Cat. No.: HY-138253R
CAS No.: 114248-23-6
Synonyms: dFdU (Standard); 2',2'-Difluoro-2'-deoxyuridine (Standard)
Research Areas:  

Cancer

2′,2′-Difluorodeoxyuridine (Standard) is the analytical standard of 2′,2′-Difluorodeoxyuridine. This product is intended for research and analytical applications. 2’,2’-Difluorodeoxyuridine (dFdU) is the main metabolite of Gemcitabine (HY-17026). 2’,2’-Difluorodeoxyuridine causes a concentration- and schedule- dependent radiosensitising effect in vitro. 2’,2’-Difluorodeoxyuridine arrests cell cycle at the early S phase and induces apoptosis in cancer cells.
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Cat. No.: HY-138253S
CAS No.: 1233921-75-9
Synonyms: dFdU-13C,15N2; 2',2'-Difluoro-2'-deoxyuridine-13C,15N2
2′,2′-Difluorodeoxyuridine- 13C, 15N2 (dFdU- 13C, 15N2) is a 13C- and 15N-labeled compound. 2’,2’-Difluorodeoxyuridine (dFdU) is the main metabolite of Gemcitabine (HY-17026). 2’,2’-Difluorodeoxyuridine causes a concentration- and schedule- dependent radiosensitising effect in vitro. 2’,2’-Difluorodeoxyuridine arrests cell cycle at the early S phase and induces apoptosis in cancer cells .
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Cat. No.: HY-130394
CAS No.: 178557-21-6
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

2C-B-FLY hydrochloride is the dihydrodifuran analog of the Schedule I hallucinogen 4-bromo-2,5-dimethoxyphenethylamine (2C-B).
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Cat. No.: HY-157623
CAS No.: 143077-66-1
Synonyms: 1-Palmitoyl-2-hydroxy-sn-glycero-3-phospho-L-serine sodium
Research Areas:  

Others

16:0 Lyso PS (1-Palmitoyl-2-hydroxy-sn-glycero-3-phospho-L-serine sodium) is a lysophospholipid. 16:0 Lyso PS serves as a standard for preparing standard curves .
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Cat. No.: HY-12212R
CAS No.: 1474034-05-3
Synonyms: rta 408 (Standard)
Omaveloxolone (Standard) is the analytical standard of Omaveloxolone (HY-12212). This product is intended for research and analytical applications. Omaveloxolone (RTA 408) is an antioxidant inflammation modulator (AIM), which activates Nrf2 and suppresses nitric oxide (NO). Omaveloxolone attenuates osteoclastogenesis by inhibiting STING dependent NF-κb signaling.
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Cat. No.: HY-W756829
Synonyms: rta 408-d3
Omaveloxolone-d3 (RTA 408-d3) is the deuterated-labeled Omaveloxolone (HY-12212). Omaveloxolone (RTA 408) is an antioxidant inflammation modulator (AIM), which activates Nrf2 and suppresses nitric oxide (NO). Omaveloxolone attenuates osteoclastogenesis by inhibiting STING dependent NF-κb signaling.
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Cat. No.: HY-156031
Target:  

Cholinesterase (ChE)

Research Areas:  

Neurological Disease

BChE-IN-19 (Compound 7b) is a para-substituted derivative of indone (7b) with inhibitory activity of butyryl cholinesterase (BChE) (IC50=0.04 μM). BChE-IN-19 improves cholinergic scheduling in the nervous system. BChE-IN-19 can be used against Alzheimer's disease .
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Cat. No.: HY-187739
CAS No.: 67049-84-7
Target:  

Cholinesterase (ChE)

Research Areas:  

Others

Aminostigmine hydrochloride is a Cholinesterase (ChE) inhibitor. Aminostigmine hydrochloride is a carbamate nerve agent precursor with a Kd of 6.6 mM for BSA. Aminostigmine hydrochloride exerts toxicity through carbamoylation of the enzyme active site and binds to serum albumin to reduce free toxicity. Aminostigmine hydrochloride is useful for studying atomic-level binding interactions between toxic compounds and carrier proteins .
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