21 Results for "

55565

" in MedChemExpress (MCE) Product Catalog:
Products (21)

21 Results for "55565" in MCE Product Catalog:

7
7 Publications Verification
Cat. No.: HY-19635
CAS No.: 1648863-90-4
Target:  

PAK

Research Areas:  

Cancer

G-5555 is a potent p21-activated kinase 1 (PAK1) inhibitor with Kis of 3.7 nM and 11 nM for PAK1 and PAK2, respectively.
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7
7 Publications Verification
Cat. No.: HY-19635A
CAS No.: 2319590-15-1
Target:  

PAK

Research Areas:  

Cancer

G-5555 hydrochloride is a potent and selective p21-activated kinase 1 (PAK1) inhibitor with a Ki of 3.7 nM.
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6
6 Cited Publications
Cat. No.: HY-12650
CAS No.: 1138245-13-2
Purity:  99.31%
Synonyms: DS5565
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

Mirogabalin (DS-5565) is a novel, preferentially selective α2δ-1 ligand characterized by high potency and selectivity to the α2δ-1 subunit of voltage-sensitive calcium channel complexes in the CNS.
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6
6 Cited Publications
Cat. No.: HY-108006
CAS No.: 1138245-21-2
Purity:  99.57%
Synonyms: DS 5565 besylate
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

Mirogabalin besylate is a selective and orally available ligand for the α2δ subunit of voltage-gated calcium channels, with Kds of 13.5 nM, 22.7 nM, 27 nM, and 47.6 nM for human α2δ-1, human α2δ-2, rat α2δ-1, and rat α2δ-2, respectively.
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4
4 Cited Publications
Cat. No.: HY-50867
CAS No.: 111358-88-4
Synonyms: CEP-701; KT-5555
Research Areas:  

Cancer

Lestaurtinib (CEP-701) is an orally active and selective RPTKs (receptor protein tyrosine kinase) inhibitor, competitively inhibits ATP binding to the TrkA/B/C domain. Lestaurtinib inhibits RPTKs phosphorylation, with IC50s of 2, 25 and 0.9 nM for FLT3, TrkA and JAK2, respectively. Lestaurtinib induces apoptosis and cycle arrest, also can inhibit growth of tumor .
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Cat. No.: HY-18200
CAS No.: 751475-53-3
Synonyms: E5555; ER-172594-00
Atopaxar (E5555) is a potent, orally active, selective and reversible thrombin receptor protease-activated receptor-1 (PAR-1) antagonist. Atopaxar, an antiplatelet agent, interferes with platelet signaling. Atopaxar can be used for the research of atherothrombotic disease .
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Cat. No.: HY-W010869
CAS No.: 172854-55-6
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

GR 55562 hydrochloride is a selective 5-HT1B receptor antagonist. GR 55562 hydrochloride can be used for the research of nerve disease .
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Cat. No.: HY-P4325
CAS No.: 109528-50-9
Target:  

Thrombin

Research Areas:  

Others

Hirudin (55-65) (sulfated) is a fragment of Hirudin with anticoagulant effects. Hirudin is a thrombin inhibitor with blood anticoagulant property.
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Cat. No.: HY-12650S1
Synonyms: DS5565-d4
Mirogabalin-d4 (DS5565-d4) is a deuterated compound of Mirogabalin (HY-12650), a ligand that selectively targets the voltage-sensitive calcium channel complex α2δ-1 .
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Cat. No.: HY-101367
CAS No.: 159533-26-3
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

GR 55562 is a selective 5-HT1B receptor antagonist. GR 55562 can be used for the research of nerve disease .
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Cat. No.: HY-18200B
CAS No.: 474550-69-1
Synonyms: E5555 hydrobromide; ER 172594-06
Atopaxar (E5555) hydrobromide is a potent, orally active, selective and reversible thrombin receptor protease-activated receptor-1 (PAR-1) antagonist. Atopaxar hydrobromide, an antiplatelet agent, interferes with platelet signaling. Atopaxar hydrobromide can be used for the research of atherothrombotic disease .
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Cat. No.: HY-12650S
Synonyms: DS5565-13C2,d1 (Mixture of Diastereomers)
Mirogabalin- 13C2,d1 (Mixture of Diastereomers) is a 13C and deuterium labeled Mirogabalin. Mirogabalin (DS-5565) is a preferentially selective α2δ-1 ligand characterized by high potency and selectivity to the α2δ-1 subunit of voltage-sensitive calcium channel complexes in the CNS .
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Cat. No.: HY-101367A
CAS No.: 159533-25-2
Purity:  ≥99.0%
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

GR 55562 dihydrochloride is a selective 5-HT1B receptor antagonist. GR 55562 dihydrochloride can be used for the research of nerve disease .
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Cat. No.: HY-12650A
CAS No.: 1138244-97-9
Synonyms: (rel)-DS5565
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

(rel)-Mirogabalin ((rel)-DS5565) is a voltage-dependent calcium channel inhibitor that acts on the α2δ-1 subunit .
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Cat. No.: HY-12650R
CAS No.: 1138245-13-2
Synonyms: DS5565 (Standard)
Research Areas:  

Neurological Disease

Mirogabalin (Standard) is the analytical standard of Mirogabalin. This product is intended for research and analytical applications. Mirogabalin (DS-5565) is a novel, preferentially selective α2δ-1 ligand characterized by high potency and selectivity to the α2δ-1 subunit of voltage-sensitive calcium channel complexes in the CNS.
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Cat. No.: HY-P4795
CAS No.: 125441-01-2
Target:  

Thrombin

Research Areas:  

Others

Acetyl-Hirudin (55-65) (sulfated) is a Acetyl-fragment of Hirudin. Hirudin is a thrombin inhibitor with blood anticoagulant property .
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Cat. No.: HY-18200A
CAS No.: 474544-83-7
Synonyms: E5555 hydrochloride; ER-172594-00 hydrochloride
Atopaxar hydrochloride (E5555 hydrochloride) is the hydrochloride salt form of Atopaxar (HY-18200). Atopaxar hydrochloride is an orally active, selective and reversible antagonist for thrombin receptor protease-activated receptor-1 (PAR-1). Atopaxar hydrochloride is the inhibitor for Janus kinase 1 (JAK1) and JAK2, which inhibits the JAK-STAT with EC50 of 5.90 μM in A549. Atopaxar hydrochloride inhibits the cell viability of A549 (IC50=7.02 μM), arrests the cell cycle at G1 phase and induces apoptosis. Atopaxar hydrochloride exhibits antiplatelet and antitumor activities. Atopaxar hydrochloride can be used for the research of atherothrombotic disease .
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Cat. No.: HY-108006R
CAS No.: 1138245-21-2
Synonyms: DS 5565 besylate (Standard)
Research Areas:  

Neurological Disease

Mirogabalin besylate (Standard) is the analytical standard of Mirogabalin besylate (HY-108006). This product is intended for research and analytical applications. Mirogabalin besylate is a selective and orally available ligand for the α2δ subunit of voltage-gated calcium channels, with Kds of 13.5 nM, 22.7 nM, 27 nM, and 47.6 nM for human α2δ-1, human α2δ-2, rat α2δ-1, and rat α2δ-2, respectively.
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Cat. No.: HY-P85864
Synonyms: LIM domain kinase 1; LIMK-1;

Host:  

Mouse

Application:  

WB, ICC/IF, ELISA

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P85863
Synonyms: Sodium/potassium-transporting ATPase subunit alpha-1; Na; +; /K; +; ATPase alpha-1 subunit; Sodium pump subunit alpha-1;

Host:  

Mouse

Application:  

IHC-P, ICC/IF, ELISA

Reactivity:  

Human, Mouse, Rat

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