19 Results for "

PAK3

" in MedChemExpress (MCE) Product Catalog:
Products (19)

19 Results for "PAK3" in MCE Product Catalog:

  • Isoforms Recommended:
  • Targets Recommended:
10
10 Cited Publications
Cat. No.: HY-15542B
CAS No.: 1232030-35-1
Purity:  98.01%
Target:  

PAK

Research Areas:  

Cancer

FRAX486 is a p21-activated kinase (PAK) inhibitor with IC50s of 14, 33 and 39 nM for PAK1, PAK2 and PAK3, respectively.
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Cat. No.: HY-RS00964
Research Areas:  

Others

ARHGEF7 Human Pre-designed siRNA Set A contains three designed siRNAs for ARHGEF7 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS09991
Research Areas:  

Others

Pak3 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Pak3 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS09990
Research Areas:  

Others

PAK3 Human Pre-designed siRNA Set A contains three designed siRNAs for PAK3 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS09992
Research Areas:  

Others

Pak3 Rat Pre-designed siRNA Set A contains three designed siRNAs for Pak3 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-146786
CAS No.: 2415295-37-1
Target:  

PAK Apoptosis

Research Areas:  

Cancer

ZMF-10 is a highly potent PAK1 inhibitor, with IC50s of 174 nM, 1.038 μM and 1.372 μM for PAK1, PAK2 and PAK3, respectively. ZMF-10 can inhibit PAK1 activity to affect PAK1-regulated apoptosis, ER-Stress and migration in MDA-MB-231 cells. ZMF-10 can be used for researching anticancer .
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Cat. No.: HY-123739
CAS No.: 337500-87-5
Target:  

PAK

Research Areas:  

Cancer

LDN-0028574 is a PAK3 inhibitor. LDN-0028574 can be used in the research of p53-deficient cancers .
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Cat. No.: HY-P81622
Synonyms: PAK3; OPHN3; Serine/threonine-protein kinase PAK 3; Beta-PAK; Oligophrenin-3; p21-activated kinase 3; PAK-3

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, IP

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-178812
CAS No.: 2098649-83-1
Target:  

PI3K PAK mTOR PERK Apoptosis

Research Areas:  

Cancer

PI3Kα-IN-27 (Compound 50b) is an orally active PI3K-α inhibitor, with an IC50 of 40 nM. PI3Kα-IN-27 effectively inhibits PAK3, p110α, phospho-mTOR and phospho-ERK1/2. PI3Kα-IN-27 induces early Apoptosis. PI3Kα-IN-27 shows anticancer activity against pancreatic cancer, lung cancer, breast cancer .
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Cat. No.: HY-P81785
Synonyms: PAK3; OPHN3; Serine/threonine-protein kinase PAK 3; Beta-PAK; Oligophrenin-3; p21-activated kinase 3; PAK-3

Host:  

Rabbit

Application:  

WB, IHC-F, IHC-P, ICC/IF, IP

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P81785A
Synonyms: PAK3; OPHN3; Serine/threonine-protein kinase PAK 3; Beta-PAK; Oligophrenin-3; p21-activated kinase 3; PAK-3

Host:  

Rabbit

Application:  

WB, IHC-F, IHC-P, ICC/IF, IP

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-184447
CAS No.: 3091508-49-2
Target:  

PAK

Research Areas:  

Others

RN193 is a type II kinase inhibitor with a human PAK1 IC50 of 4.28 μM. RN193 functionally inhibits kinase activity of PAK1, PAK2, and PAK3, and engages with their kinase domains in live cells. RN193 induces thermal shifts in CLK1, GSK3B, ULK1, MELK, MAPK13, BRAF, and STK10, indicating binding and stabilization of these proteins. RN193 induces formation of PAK3:PAK2 heterodimers and displaces PAK2 homodimers in live cells. RN193 acts as a tool compound for studying group I PAK conformational states .
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Cat. No.: HY-P83870
Synonyms: ARA; bPAK; MRX30; MRX47; OPHN3; PAK-3; PAK3beta; beta-PAK

Host:  

Mouse

Application:  

WB, ELISA

Reactivity:  

Human, Monkey

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Cat. No.: HY-P83870A
Synonyms: ARA; bPAK; MRX30; MRX47; OPHN3; PAK-3; PAK3beta; beta-PAK

Host:  

Mouse

Application:  

WB, ELISA

Reactivity:  

Human, Monkey

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Cat. No.: HY-P74654
Purity:  ≥ 80%, as determined by reducing SDS-PAGE.
Synonyms: PAK3; HPAK3; Prev. MRX30; PAK-3; Prev. MRX47; Adriamycin Resistance-Associated; BPAK; Mental Retardation, X-Linked 47; P21 Protein (Cdc42/Rac)-Activated Kinase 3; P21-Activated Kinase 3; Serine/Threonine-Protein Kinase PAK 3; PAK3beta; P21 (CDKN1A)-Activa
Species:  
Source:  
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Cat. No.: HY-P702746
Purity:  ≥ 80%, as determined by reducing SDS-PAGE.
Synonyms: PAK3; HPAK3; Prev. MRX30; PAK-3; Prev. MRX47; Adriamycin Resistance-Associated; BPAK; Mental Retardation, X-Linked 47; P21 Protein (Cdc42/Rac)-Activated Kinase 3; P21-Activated Kinase 3; Serine/Threonine-Protein Kinase PAK 3; PAK3beta; P21 (CDKN1A)-Activa
Species:  
Source:  
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Cat. No.: HY-P705853
Purity:  ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: PAK3; HPAK3; Prev. MRX30; PAK-3; Prev. MRX47; Adriamycin Resistance-Associated; BPAK; Mental Retardation, X-Linked 47; P21 Protein (Cdc42/Rac)-Activated Kinase 3; P21-Activated Kinase 3; Serine/Threonine-Protein Kinase PAK 3; PAK3beta; P21 (CDKN1A)-Activa
Species:  
Source:  
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Cat. No.: HY-118606
CAS No.: 296246-47-4
Target:  

PAK Parasite

Research Areas:  

Infection Cancer

LDN-0044878 is a PAK3 inhibitor. LDN-0044878 inhibits the proliferation or induces the death of p53-deficient cells. LDN-0044878 exhibits moderate trypanocidal activity against Trypanosoma brucei, but does not directly inhibit the core target Rhodesain. LDN-0044878 can be used in studies related to cervical adenocarcinoma and Trypanosoma brucei infection.
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Cat. No.: HY-P703253
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: ARHGEF7; PAK3; Rho Guanine Nucleotide Exchange Factor 7; P50; P85SPR; Rho Guanine Nucleotide Exchange Factor (GEF) 7; COOL1; SH3 Domain-Containing Proline-Rich Protein; PIXB; DKFZp686C12170; P85; DKFZp761K1021; PAK-Interacting Exchange Factor Beta; COOL-1
Species:  
Source:  
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