G Protein (Small)

Small G proteins (small GTPases) are homologous to Gα proteins and are often referred to as the Ras proto-oncogene superfamily. Small GTPases regulate a wide variety of processes in the cell, including growth, differentiation, movement and lipid vesicle transport.

Products for G Protein (Small)

  1. Cat.No. Product Name Information/Activity
  2. BCC5581 CCG-1423 CCG-1423 is a novel inhibitor of RhoA/C-mediated gene transcription that is capable of inhibiting invasion of PC-3 prostate cancer cells in a Matrigel model of metastasis. CCG-1423 chemical structure
  3. BCC6075 EHT 1864 EHT 1864 is an inhibitor of Rac family small GTPases. EHT 1864 directly binds and impairs the ability of this small GTPase to engage critical downstream effectors required for growth transformation. The Kd values are 40, 50, 60, and 230 nM for Rac1, Rac1b, Rac2 and Rac3, respectively. EHT 1864 also potently inhibits other Rac-dependent transformation processes, Tiam1- and Ras-mediated growth transformation. EHT 1864 prevents Aβ 40 and Aβ 42 production in vivo. EHT 1864 chemical structure
  4. BCC6529 GNF-7 GNF-7 inhibits Bcr-Abl WT and Bcr-Abl T315I with IC50 of 133 nM and 61 nM, respectively. GNF-7 chemical structure
  5. BCC4373 Golgicide A Golgicide A is a potent, highly specific, and reversible inhibitor of the cis-Golgi ADP-ribosylation factor guanine nucleotide exchange factors (ArfGEF), GBF1. Golgicide A drastically reduced replication of coxsackievirus B3 (CVB3) and other human enterovirus species. Golgicide A chemical structure
  6. BCC6302 HJC 0350 HJC0350 is a potent and specific EPAC2 antagonist with an IC50 of 0.3 µM. HJC 0350 chemical structure
  7. BCC6066 ITX3 ITX3 is a specific and nontoxic inhibitor of the TrioN (N-terminal GEF domain of the multidomain Trio protein) with IC50 of 76 uM; inhibits TrioN-stimulated RhoG exchange in vitro. ITX3 chemical structure
  8. BCC8092 ML 141 ML141 (CID-2950007) is a potent, allosteric,selective and reversible non-competitive inhibitor of Cdc42 GTPase. ML141 inhibits Cdc42 wild type and Cdc42 Q61L mutant with EC50s of 2.1 and 2.6 μM, respectively. ML141 shows low micromolar potency and selectivity against other members of the Rho family of GTPases (Rac1, Rab2, Rab7). ML141 do not show cytotoxicity in multiple cell lines. ML 141 chemical structure
  9. BCC1149 NSC 23766 NSC 23766 trihydrochloride is an inhibitor of Rac1 activation. NSC 23766 chemical structure
  10. BCC7648 QS 11 ARFGAP1 inhibitor; modulates Wnt signaling pathway,QS11 is a GTPase activating protein of ADP-ribosylation factor 1 (ARFGAP1) inhibitor. QS 11 chemical structure
  11. BCC5887 Rac1 Inhibitor F56, control peptide 1315378-77-8 Rac1 Inhibitor F56, control peptide chemical structure

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