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. 2015 Apr 30;5:9802. doi: 10.1038/srep09802

Table 1. List of studies using SMIFH2 (as of September, 2014).

Year Study Concentration used Treatment duration Purpose of use
2009 Rizvi et al., 200939 5 - 30 µM 30 minutes up to 72 hours Characterization of SMIFH2 in Fission yeast, NIH3T3 mouse fibroblasts and A549 human lung adenocarcinoma epithelial cells
2011 Poincloux et al., 201149 25 µM up to 4 hours To study Formin-dependent invasive capacities of MDA-MB-231 human breast carcinoma cells
Li et al., 201143 100 nM not specified To study the relationship between Formin function and melanoblast motility
2012 Tang and Brieher, 201253 not specified 30 minutes To study the contribution of Formins during actin recovery in apical junctions of polarized MDCK cells after Latrunculin B treatment
Wyse et al., 201256 10 µM ~63 minutes To study the role of mDia Formins in CXCL12-induced bleb formation in MDA-MB-231 human breast carcinoma cells
Oakes et al., 201247 10 – 15 µM >4 hours To confirm a previous study that formation of radial stress fibres formation in U2OS cells is Formin Dia1-dependent
Miklavc et al., 201245 25 µM not specified To show that actin coat formation on lamellar bodies in alveolar type II cells are Formin-dependent
Chin et al., 201260 10 µM 4 hours To study the role of Formin-mediated cytoskeletal signaling in Chlamydia bacterial inclusion and extrusion from host cells (HeLa cells)
Rosero et al., 201251 5 - 30 µM 72 hours To study the plant cell growth and morphogenesis of Arabidopsis plants
2013 Sandbo et al., 201352 3 - 30 µM 30 minutes To study myofibroblast differentation in human lung fibroblast cells
Fritzsche et al., 201365 40 µM 30 minutes To analyse the contribution of Formin-mediated actin polymerization on actin cortex homeostasis
Goldspink et al., 201340 10 µM 40 minutes To show that microtubule reorganization of EB-2 depleted ARPE-19 cells are restored to normal upon Formin inhibition
Wilson et al., 201355 40 µM up to 490 seconds To study the contribution of Formin-mediated actin polymerization at the leading edge of polarized HL60 neutrophil-like cells during 3D migration
Rao et al., 201350 30 µM 3 hours As a negative control that activation of endogenous Diaphanous-related Formins by photoactivatable-DAD construct is indeed Formin dependent
Aragona et al., 201358 5, 15 or 30 µM 24 hours To study the link between actin dynamics and Formin activity related to YAP/TAZ activity
Yu et al., 201357 50 µM up to ~49 minutes To study the requirement of Formin activity for podosome formation in RPTPalpha++ mouse embryonic fibroblasts
Iskratsch et al., 201341 5 - 10 µM up to 40 minutes To confirm the contribution of FHOD1 on cell spreading and adhesion maturation
Luo et al., 201344 20 - 40 uM 24 hours To study the formation of actin nodes that mediate the formation of actin network within HeLa cells
Murk et al., 201346 75 µM 2 hours To study the contribution of Formin on transition of stellate astrocytes to polygonal cells during Arp2/3 complex inhibition
Buvall et al., 201359 10 µM 90 minutes To examine the Formin-dependency of stress fibre formation in podocytes
2014 Jennings et al., 201442 10 µM pretreatment not specified To show that priming or degranulation of neutrophil is suppressed by Formins downstream of RhoA
Pettee et al., 201448 10 µM 48 hours To confirm that organized ovarian spheroid formation of ES-2 cells is dependent on mDia2
Tien and Chang, 201454 10 - 100 µM 4 hours To show the correlation between Dia1 inhibition and regulation of ERK activity in MDCK cells
Beckham et al., 201461 10 µM 4 hours To show the mechanism of formation of lamellipodia in MCF10A cells
Harris et al., 201462 40 µM 1 hour To assess the mechanism controlling establishment of tissue-level tension in MDCK-II cell monolayers
Kajita et al., 201463 25 µM 12-24 hours To assess apical extrusion of ts-Src- or RasV12-MDCK cells
Lechuga et al., 201464 50 µM 24 hours To assess (epithelial to myofibroblast transition) EMyT induction in A549 cells