10 results for "Rho GTPase Inhibitors" in Products

Rho GTPase Inhibitors

Rho GTPases regulate many aspects of actin dynamics and are involved in processes that are dependent on changes to cell morphology and movement, including phagocytosis, mitosis and wound healing. To enable cells to respond to external cues, these processes require rapidly activated and spatio-temporally regulated signaling networks, of which Rho GTPases are a key component.

Three Rho GTPases have been widely studied: Cdc42, Rac1 and RhoA. For these enzymes, over 60 targets have been identified including Rho-Kinases (ROCKs), phospholipases and ion channels. As with other small GTPases, the activity of Rho GTPases is regulated by GEFs and GAPs. Inactive Rho GTPases are sequestered to the cytosol by Rho-specific guanine nucleotide dissociation inhibitors (GDIs), preventing their membrane association. Of the 20 Rho family members, 10 have been identified as being constitutively bound to GTP and so are constitutively active and have alternative regulation mechanisms.

Neuronal dendrite spine growth is dependent on Rho GTPases. This process is key to synaptic plasticity and long-term potentiation/depression, which underly learning and memory. RhoA and Cdc42 are activated by CaMKII, which is activated by the influx of Ca2+ through NMDA receptors upon glutamate binding.

Selective inhibitor of Rac1-GEF interaction; antioncogenic

Chemical Name: N6-[2-[[4-(Diethylamino)-1-methylbutyl]amino]-6-methyl-4-pyrimidinyl]-2-methyl-4,6-quinolinediamine trihydrochloride
Purity: ≥98%
Selective inhibitor of Rac1-GEF interaction; antioncogenic
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Potent Rac family inhibitor

Chemical Name: 5-(5-(7-(Trifluoromethyl)quinolin-4-ylthio)pentyloxy)-2-(morpholinomethyl)-4H-pyran-4-one dihydrochloride
Purity: ≥98%
Potent Rac family inhibitor
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Selective Cdc42 Rho family inhibitor

Alternate Names: CID 2950007
Chemical Name: 4-[4,5-Dihydro-5-(4-methoxyphenyl)-3-phenyl-1H-pyrazol-1-yl]benzenesulfonamide
Purity: ≥98%
Selective Cdc42 Rho family inhibitor
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DOCK2-Rac1 interaction inhibitor

Chemical Name: 4-[3-(2-Chlorophenyl)-2-propen-1-ylidene]-1-phenyl-3,5-pyrazolidinedione
Purity: ≥98%
DOCK2-Rac1 interaction inhibitor
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Rho inhibitor

Chemical Name: D-Tryptophan (2E)-2-(6-quinoxalinylmethylene)hydrazide hydrochloride
Purity: ≥98%
Rho inhibitor
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Cdc42 inhibitor

Chemical Name: 2-[(2,3,4,9-Tetrahydro-6-phenyl-1H-carbazol-1-yl)amino]ethanol
Purity: ≥98%
Cdc42 inhibitor
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Promotes mitochondrial Rho GTPase 1 (Miro1) degradation

Chemical Name: N-(3-Fluorophenyl)-N'-[4-[[6-(1H-imidazol-1-yl)-4-pyrimidinyl]amino]phenyl]urea hydrochloride
Purity: ≥98%
Promotes mitochondrial Rho GTPase 1 (Miro1) degradation
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Rac inhibitor

Chemical Name: N4-(9-Ethyl-9H-carbazol-3-yl)-N2-[3-(4-morpholinyl)propyl]-2,4-pyrimidinediamine
Purity: ≥98%
Rac inhibitor
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Rac1 inhibitor; blocks Rac1-P-Rex1 interaction

Chemical Name: N-(3,5-Dimethylphenyl)-N'-[2-(trifluoromethyl)phenyl]guanidine
Purity: ≥98%
Rac1 inhibitor; blocks Rac1-P-Rex1 interaction
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Geranylgeranyltransferase-I (GGTase-I) inhibitor

Chemical Name: (2R)-3,3,3-Trifluoro-2-methoxy-1-[(7R)-7-(2-methoxyphenyl)-3,9-diazaspiro[5.5]undec-3-yl]-2-phenyl-1-propanone hydrochloride
Purity: ≥98%
Geranylgeranyltransferase-I (GGTase-1) inhibitor
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