118 Results for "

RAC1

" in MedChemExpress (MCE) Product Catalog:
Products (118)

118 Results for "RAC1" in MCE Product Catalog:

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Cat. No.: HY-106381A
Purity:  ≥98.0%
Target:  

PKC TrxR NF-κB

Research Areas:  

Inflammation/Immunology Cancer

Aurothiomalate tetramer sodium is the tetrameric form of Aurothiomalate sodium (HY-106381). Aurothiomalate sodium acts as an inhibitor of PKCI and TrxR1. Aurothiomalate sodium disrupts the PKCI-Par6-Rac1 signaling pathway, and also inhibits TrxR1 activity, TNFα-induced NF-κB activation, and the expression of pro-inflammatory genes. Aurothiomalate sodium blocks Kras-mediated BASC expansion and lung tumor growth, inhibits anchorage-independent growth and tumorigenicity of lung cancer cells, and suppresses neutrophil chemotaxis, phagocytosis, and leukocyte extravasation. Aurothiomalate sodium can be used in research related to rheumatoid arthritis and non-small cell lung cancer [1] .
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Cat. No.: HY-P1382
CAS No.: 1095179-01-3
Target:  

Ras

Research Areas:  

Cancer

Rac1 Inhibitor W56 is a peptide containing residues 45-60 of Rac1. Rac1 Inhibitor W56 inhibits Rac1 interaction with guanine nucleotide exchange factors TrioN, GEF-H1, and Tiam [1].
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Cat. No.: HY-P10038A
Synonyms: Myr-FEEERA-OH TFA
Target:  

Integrin

Research Areas:  

Infection

mP6 (Myr-FEEERA-OH) TFA is a myristoylated peptide. mP6 TFA inhibits the interaction of Gα13 with integrin β3 without disrupting talin-dependent integrin function. mP6 TFA can block the GTP usage of Rac1, Rap1, and Rab7, effectively inhibiting the infection of CHO-A24 cells [1].
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Cat. No.: HY-144624
CAS No.: 3033401-47-4
Target:  

PROTACs TAM Receptor Ras

Research Areas:  

Cancer

PROTAC Axl Degrader 1 is an orally active PROTAC degrader targeting the AXL receptor tyrosine kinase, with an IC50 of 0.92 μM against human targets. PROTAC Axl Degrader 1 induces cytoplasmic vacuolization, methuosis (macropinocytosis-induced cell death), excessive macropinosome production, and Rac1 activation. PROTAC Axl Degrader 1 inhibits the proliferation and migration of cancer cells. PROTAC Axl Degrader 1 can be used in breast cancer-related research [1].
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Cat. No.: HY-P1383A
Target:  

Ras

Research Areas:  

Others

Rac1 Inhibitor F56, control peptide TFA is a peptide containing residues 45-60 of Rac1. Rac1 Inhibitor F56, control peptide TFA contains a Trp 56 to Phe 56 mutation. Rac1 Inhibitor F56, control peptide TFA has no effect on Rac1 interaction with its guanine nucleotide exchange factors (GEFs) [1].
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Cat. No.: HY-RS16742
Research Areas:  

Others

Rac1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Rac1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-W127391
CAS No.: 17598-94-6
Synonyms: (RAC)-1,2-Didodecanoylglycerol
1,2-Dilaurin is a diacylglycerol containing lauric acid at the sn-1 and sn-2 positions. It has been used as an internal standard for the quantification of diglycerides in rat desheathed sciatic nerves. [1] Monomolecular films containing 1,2-dilauroyl-rac-glycerol have been used as substrates to measure surface pressure and the effect of pancreatic procolipase and colipase on porcine pancreatic lipase activity. [2] References: [1]. Zhu, X. and Eichberg, J. 1,2-Diacylglycerol content and its arachidonyl-containing molecular species are reduced in the sciatic nerve of streptozotocin-induced diabetic rats. J. Neurochemistry. 55(3), 1087-1090 (1990).[2]. Wieloch, T., Borgstr m, B., Piéroni, G. et al. Porcine trypsinogen and its trypsin-activated form: lipid binding and lipase activation on monomolecular membranes. FEBS Express. 128(2), 217-220 (1981).
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Cat. No.: HY-N0710R
CAS No.: 473-08-5
Synonyms: α-Cyperone (Standard); (+)-α-Cyperone (Standard)
alpha-Cyperone (Standard) is the analytical standard of alpha-Cyperone. This product is intended for research and analytical applications. alpha-Cyperone (α-Cyperone) is associated with the down-regulation of COX-2, IL-6, Nck-2, Cdc42 and Rac1, resulting in reduction of inflammation, which would be highly beneficial for treatment of inflammatory diseases such as AD.
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Cat. No.: HY-115507
CAS No.: 1332290-68-2
NMac1 is an orally active Nm23/NDPK activator. NMac1 directly binds to Nm23-H1 and activates the NDPK activity of recombinant Nm23-H1 with an EC50 of 10.7 uM. NMac1 induces AMPK activation and inhibits mTOR and ERK, leading to mitochondrial OXPHOS dysregulation and suppressing mitochondrial ROS production, which in turn induces mitochondrial dysfunction in MDA-MB-231 cells. NMac1 inhibits Complex I activity and suppresses changes in morphology and actin cytoskeleton organization following Rac1 activation in MDA-MB-231 cells. NMac1 inhibits tumor invasion, migration and metastasis. NMac1 is useful for studying metastatic tumors, such as breast cancer. NMac1 can be isolated from the ginger cassumunar Roxb [1] .
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Cat. No.: HY-P1383
CAS No.: 1315378-77-8
Target:  

Inhibitory Antibodies

Research Areas:  

Others

Rac1 Inhibitor F56, control peptide is a peptide containing residues 45-60 of Rac1. Rac1 Inhibitor F56, control peptide contains a Trp 56 to Phe 56 mutation. Rac1 Inhibitor F56, control peptide has no effect on Rac1 interaction with its guanine nucleotide exchange factors (GEFs) [1].
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Cat. No.: HY-RS23179
Research Areas:  

Others

Rac1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Rac1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-W127363
CAS No.: 13071-60-8
1,2-O-Dihexadecyl-rac-glycerol is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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Cat. No.: HY-50733
CAS No.: 1009821-06-0
Research Areas:  

Cancer

CX-5011 free base is a potent CK2 inhibitor. CX-5011 free base also is a Rac-1 activator. CX-5011 free base induces methuosis and promotes macropinocytosis. CX-5011 free base induces apoptosis. CX-5011 free base decreases the expression of rpS6 phosphorylation [1] .
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Cat. No.: HY-W010270A
CAS No.: 74916-57-7
Target:  

PKC NF-κB TrxR

Research Areas:  

Inflammation/Immunology Cancer

Aurothiomalate disodium acts as an inhibitor of PKCI and TrxR1. Aurothiomalate disodium disrupts the PKCI-Par6-Rac1 signaling pathway, and also inhibits TrxR1 activity, TNFα-induced NF-κB activation, and the expression of pro-inflammatory genes. Aurothiomalate disodium blocks Kras-mediated BASC expansion and lung tumor growth, inhibits anchorage-independent growth and tumorigenicity of lung cancer cells, and suppresses neutrophil chemotaxis, phagocytosis, and leukocyte extravasation. Aurothiomalate disodium can be used in research related to rheumatoid arthritis and non-small cell lung cancer [1] .
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Cat. No.: HY-N8960A
CAS No.: 124898-71-1
(Rac)-1-Hydroxybisabola-2,10-dien-4-one (Compound 24) is a Bisabolene (HY-121262) derivative. (Rac)-1-Hydroxybisabola-2,10-dien-4-one can be isolated from the aerial parts of C. peckii [1].
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Cat. No.: HY-W013060
CAS No.: 2190-15-0
(Rac)-1,2-Dilinoleoyl-3-palmitoyl-glycerol is a kind of biochemical reagent.
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Cat. No.: HY-W127356
CAS No.: 1246818-85-8
rac-1,2-Distearoyl-3-chloropropanediol-d5 is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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Cat. No.: HY-15723AR
CAS No.: 1177865-17-6
Target:  

Ras Apoptosis

Research Areas:  

Cancer

NSC 23766 (trihydrochloride) (Standard) is the analytical standard of NSC 23766 (trihydrochloride). This product is intended for research and analytical applications. NSC 23766 trihydrochloride is an inhibitor of Rac1 activation.
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Cat. No.: HY-122687
CAS No.: 627042-19-7
Target:  

Ras

Research Areas:  

Cancer

Rac1-IN-1 is a potent Rac1 inhibitor with an IC50 of 95 nM and a Ki of 6.8 μM. Rac1-IN-1 blocks the binding of Rac1 to downstream PAK1 by targeting the nucleotide-binding site of Rac1, thereby specifically inhibiting Rac1 activation without affecting Cdc42/RhoA. Rac1-IN-1 can be used for research on pancreatic cancer [1].
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Cat. No.: HY-P10107
Target:  

Ras

Research Areas:  

Others

TAT-PAK18 R192A is an inactive Tat-Pak peptide. TAT-PAK18 R192A does not have any effect in the translocation of Rac1 triggered by any of the interrogated proteins [1].
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