12 Results for "

Thienopyridine

" in MedChemExpress (MCE) Product Catalog:
Products (12)

12 Results for "Thienopyridine" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-15284
CAS No.: 150322-43-3
Purity:  99.75%
Synonyms: PCR 4099
Target:  

P2Y Receptor

Research Areas:  

Cardiovascular Disease

Prasugrel (PCR 4099), a thienopyridine and proagent, inhibits platelet function. Prasugrel is an orally active and potent P2Y12 receptor antagonist, and inhibits ADP-induced platelet aggregation .
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1
1 Cited Publications
Cat. No.: HY-15284A
CAS No.: 389574-19-0
Purity:  98.49%
Synonyms: PCR 4099 hydrochloride
Target:  

P2Y Receptor

Research Areas:  

Cardiovascular Disease

Prasugrel hydrochloride (PCR 4099 hydrochloride), a thienopyridine and proagent, inhibits platelet function. Prasugrel hydrochloride is an orally active and potent P2Y12 receptor antagonist, and inhibits ADP-induced platelet aggregation .
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Cat. No.: HY-15284S2
CAS No.: 1189919-49-0
Synonyms: PCR 4099-d4
Prasugrel-d4 is the deuterium labeled Prasugrel . Prasugrel (PCR 4099), a thienopyridine and proagent, inhibits platelet function. Prasugrel is an orally active and potent P2Y12 receptor antagonist, and inhibits ADP-induced platelet aggregation .
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Cat. No.: HY-110367A
CAS No.: 1228102-01-9
Target:  

Src

Research Areas:  

Others

LCB 03-0110, a thienopyridine derivative, is a potent pan-discoidin domain receptor/c-Src family tyrosine kinase inhibitor. LCB 03-0110 suppresses scar formation by inhibiting fibroblast and macrophage activation .
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Cat. No.: HY-15284B
CAS No.: 389574-20-3
Synonyms: PCR 4099 (Maleic acid)
Target:  

P2Y Receptor

Research Areas:  

Cardiovascular Disease

Prasugrel (PCR 4099) Maleic acid is a thienopyridine and proagent, inhibits platelet function. Prasugrel Maleic acid is an orally active and potent P2Y12 receptor antagonist, and inhibits ADP-induced platelet aggregation .
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Cat. No.: HY-15284S1
CAS No.: 1127253-02-4
Purity:  98.58%
Synonyms: PCR 4099-d3
Prasugrel-d3 is the deuterium labeled Prasugrel. Prasugrel (PCR 4099), a thienopyridine and proagent, inhibits platelet function. Prasugrel is an orally active and potent P2Y12 receptor antagonist, and inhibits ADP-induced platelet aggregation .
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Cat. No.: HY-15284S
CAS No.: 1127252-92-9
Synonyms: PCR 4099-d5
Prasugrel-d5 is deuterium labeled Prasugrel. Prasugrel (PCR 4099), a thienopyridine and prodrug, inhibits platelet function. Prasugrel is an orally active and potent P2Y12 receptor antagonist, and inhibits ADP-induced platelet aggregation .
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Cat. No.: HY-15284AR
CAS No.: 389574-19-0
Synonyms: PCR 4099 hydrochloride (Standard)
Research Areas:  

Cardiovascular Disease

Prasugrel (hydrochloride) (Standard) is the analytical standard of Prasugrel (hydrochloride). This product is intended for research and analytical applications. Prasugrel hydrochloride (PCR 4099 hydrochloride), a thienopyridine and proagent, inhibits platelet function. Prasugrel hydrochloride is an orally active and potent P2Y12 receptor antagonist, and inhibits ADP-induced platelet aggregation .
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Cat. No.: HY-15284R
CAS No.: 150322-43-3
Synonyms: PCR 4099 (Standard)
Research Areas:  

Cardiovascular Disease

Prasugrel (Standard) is the analytical standard of Prasugrel. This product is intended for research and analytical applications. Prasugrel (PCR 4099), a thienopyridine and proagent, inhibits platelet function. Prasugrel is an orally active and potent P2Y12 receptor antagonist, and inhibits ADP-induced platelet aggregation .
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Cat. No.: HY-15284S3
CAS No.: 1261394-83-5
Synonyms: PCR 4099-13C6
Prasugrel-13C6 is a deuterated labeled Prasugrel . Prasugrel (PCR 4099), a thienopyridine and proagent, inhibits platelet function. Prasugrel is an orally active and potent P2Y12 receptor antagonist, and inhibits ADP-induced platelet aggregation .
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Cat. No.: HY-180793
CAS No.: 3056612-67-7
Target:  

PROTACs Deubiquitinase

Research Areas:  

Cancer

PROTAC USP7 Degrader-2 (Compound D16) is an efficient and selective USP7 PROTAC degrader with a DC50 of 1.91 μM (in TE-12 cells). PROTAC USP7 Degrader-2 inhibits the migration of upper gastrointestinal tract (UGI) cancer cells and shows relatively weak anti-proliferative activity. PROTAC USP7 Degrader-2 can be used in the research of metastatic upper gastrointestinal cancer.
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Cat. No.: HY-170924
Research Areas:  

Cancer

Tubulin polymerization-IN-76 (compound 20b) is a potent and orally active Tubulin polymerization inhibitor. Tubulin polymerization-IN-76 inhibits Tubulin polymerization with an IC50 of 2.505 μM by acting on the colchicine binding site, thereby disrupting intracellular Microtubule networks and interfering with cell mitosis. Tubulin polymerization-IN-76 demonstrates exceptional efficacy against MGC-803 and HGC-27 cells with IC50s of 1.61 and 1.82 nM, respectively. Tubulin polymerization-IN-76 effectively inhibits the colony formation and cell migration activities, and induces G2/M phase cycle arrest and Apoptosis in MGC-803 and HGC-27 cells.Tubulin polymerization-IN-76 shows a broad-spectrum antiproliferative activity .
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