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CAS No.: 1177865-17-6
Synonyms: NSC 23766 (hydrochloride);NSC23766 3HCl salt;NSC23766 hydrochloride
NSC23766 is identified to fit into a surface groove of Rac1 known to be critical for GEF specification.
生物活性
靶点 | Rac IC50:~50μM |
实验方案
技术信息
CAS号 | 1177865-17-6 | 储存条件 |
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分子式 | C24H38Cl3N7 | 运输 | 蓝冰 | |||||
分子量 | 530.96 | 别名 | NSC 23766 (hydrochloride);NSC23766 3HCl salt;NSC23766 hydrochloride | |||||
溶解度 |
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动物实验配方 |
Cell Lines | Concentration | Assay Type | Time | Activity Description | Data Sources |
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A172MG | 50 mM | Cell Viability Assay | 144 h | exhibits synergistic antiproliferative effects combined treatment with erlotinib | 23832120 |
A172MG | 50 mM | Function Assay | 24 h | enhances the antimigratory effect of erlotinib | 23832120 |
A431 | 100 μM | Growth Inhibition Assay | 24/48/72 h | inhibits cell growth in a time dependent manner | 25109327 |
A431 | 100 μM | Function Assay | 24 h | induces cell cycle arrest in the G1 phase | 25109327 |
IEC-6 | 120 µM | Function Assay | 4/6/8 h | prevents the increased activation of FAK at 6 and 8 h | 20448461 |
Ki-67+ CLL | 50 µM | Growth Inhibition Assay | 5 d | decreases the number of Ki-67+ CLL cells | 24501217 |
MCF7 | 0-100 μM | Cytotoxicity Assay | 48 h | decreases cell viability in a dose dependent manner | 20515940 |
MCF7 | 100 μM | Function Assay | 48 h | increases the cell number in G1 phase and decreases the cell number in S and G2-M phases | 20515940 |
MDA-MB-231 | 0-100 μM | Cytotoxicity Assay | 48 h | decreases cell viability in a dose dependent manner | 20515940 |
MDA-MB-231 | 0-100 μM | Function Assay | 24 h | selectively inhibits Rac1 activation without interfering with the activity of the closely related small GTPase Cdc42 | 20515940 |
MDA-MB-231 | 100 μM | Function Assay | 48 h | increases the cell number in G1 phase and decreases the cell number in S and G2-M phases | 20515940 |
MDA-MB-231 | 50/100 μM | Function Assay | 24 h | increases phosphorylation of JNK in a dose dependent manner | 20515940 |
MDA-MB-231 | 50/100 μM | Function Assay | 48 h | induces a dose-dependent decrease in phosphorylation of p65 subunit | 20515940 |
MDA-MB-468 | 0-100 μM | Cytotoxicity Assay | 48 h | decreases cell viability in a dose dependent manner | 20515940 |
MDA-MB-468 | 50/100 μM | Apoptosis Assay | 24 h | induces apoptosis | 20515940 |
MDA-MB-468 | 100 μM | Function Assay | 24 h | inhibits caspase-3 activation | 20515940 |
MDA-MB-468 | 50/100 μM | Function Assay | 24 h | increases phosphorylation of JNK in a dose dependent manner | 20515940 |
MDA-MB-468 | 50/100 μM | Function Assay | 48 h | induces a dose-dependent decrease in phosphorylation of p65 subunit | 20515940 |
NCI-H1703 | 0-500 μM | Growth Inhibition Assay | 24 h | inhibits cell growth in a dose dependent manner | 22549160 |
NCI-H1703 | 100 μg/ml | Function Assay | 24 h | slows progression through the G1 phase of the cell cycle | 22549160 |
NCI-H1703 | 0-500 μM | Function Assay | 24 h | diminishes basal NF-κB activity dose dependently | 22549160 |
NIH3T3 | 100 μM | Growth Inhibition Assay | 24 h | has no significant impact on cell viability | 25037060 |
PC38 | 50 mM | Cell Viability Assay | 144 h | exhibits synergistic antiproliferative effects combined treatment with erlotinib | 23832120 |
PC40 | 50 mM | Cell Viability Assay | 144 h | exhibits synergistic antiproliferative effects combined treatment with erlotinib | 23832120 |
RA1 | 50 μM | Function Assay | 24 h | inhibits Matrigel invasion | 17622308 |
RA2 | 50 μM | Function Assay | 24 h | inhibits Matrigel invasion | 17622308 |
RA3 | 50 μM | Function Assay | 24 h | inhibits Matrigel invasion | 17622308 |
RA4 | 50 μM | Function Assay | 24 h | inhibits Matrigel invasion | 17622308 |
RA-FLS (RA2) | 25/50 μM | Growth Inhibition Assay | 1-9 d | inhibits cell growth in both dose and time dependent manner | 17622308 |
RBMECs | 100 μM | Function Assay | 30 min | blockes 6Bnz-cAMP-mediated activation of Rac1 in EMAP-II-treated RBMECs | 26358039 |
SKBR3 | 50 μM | Function Assay | 24 h | inhibits Rac1 activation | 21943825 |
SKBR3-pMKO.1 | 50 μM | Function Assay | 24 h | inhibits Rac1 activation | 21943825 |
SW480 | 100 μM | Growth Inhibition Assay | 24/48/72 h | inhibits cell growth in a time dependent manner | 25109327 |
SW480 | 100 μM | Function Assay | 24 h | induces cell cycle arrest in the G1 phase | 25109327 |
T47D | 0-100 μM | Cytotoxicity Assay | 48 h | decreases cell viability in a dose dependent manner | 20515940 |
T47D | 100 μM | Function Assay | 48 h | increases the cell number in G1 phase and decreases the cell number in S and G2-M phases | 20515940 |
T98MG | 50 mM | Cell Viability Assay | 144 h | exhibits synergistic antiproliferative effects combined treatment with erlotinib | 23832120 |
T98MG | 50 mM | Function Assay | 24 h | enhances the antimigratory effect of erlotinib | 23832120 |
U2-OS | 100 μM | Growth Inhibition Assay | 24/48/72 h | inhibits cell growth in a time dependent manner | 25109327 |
U2-OS | 100 μM | Function Assay | 24 h | induces cell cycle arrest in the G1 phase | 25109327 |
U87MG | 50 mM | Cell Viability Assay | 144 h | exhibits synergistic antiproliferative effects combined treatment with erlotinib | 23832120 |
U87MG | 50 mM | Function Assay | 24 h | enhances the antimigratory effect of erlotinib | 23832120 |
靶点 | Description | IC50 |
---|---|---|
Rac | IC50:~50μM |
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