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Chemical Structure| 1430208-73-3 Chemical Structure| 1430208-73-3

Structure of 1A-116
CAS No.: 1430208-73-3

Chemical Structure| 1430208-73-3

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1A-116 is a specific Rac1 inhibitor.

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Product Details of 1A-116

CAS No. :1430208-73-3
Formula : C16H16F3N3
M.W : 307.31
SMILES Code : N=C(NC1=CC=CC=C1C(F)(F)F)NC2=CC(C)=CC(C)=C2
MDL No. :MFCD31619254
InChI Key :DVIJFJSZZNOTLP-UHFFFAOYSA-N
Pubchem ID :71543346

Safety of 1A-116

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P280-P305+P351+P338

Related Pathways of 1A-116

GPCR

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
Neonatal rat cardiac fibroblasts (NRCFs) 30 μM 24 h Inhibition of P-Rex1 activity, reduction of AngII-induced collagen1, CTGF, and α-SMA expression Cardiovasc Drugs Ther. 2024 Oct;38(5):861-872
Neonatal rat cardiac fibroblasts (NRCFs) 30 μM 30 min Inhibition of P-Rex1 activity, reduction of AngII-induced Rac1-GTP activation Cardiovasc Drugs Ther. 2024 Oct;38(5):861-872
COS-1 cells 50 μM 24 h To evaluate the inhibitory effect of 1A-116 on Rac1 activity Front Cell Dev Biol. 2020 Apr 15;8:240
Ker-CT cells 100 nM 11 days To evaluate the inhibitory effect of 1A-116 on Rac1 signaling pathway in a 3D skin model Front Cell Dev Biol. 2020 Apr 15;8:240
LN229 human glioblastoma cells 20 μM 6 h To assess the pro-apoptotic effect of 1A-116, showing stronger induction at 10 HPS Pharmaceutics. 2021 Jul 16;13(7):1091
LN229 human glioblastoma cells 10 μM 16 h To evaluate the inhibitory effect of 1A-116 on cell migration, showing significant inhibition at 10 HPS Pharmaceutics. 2021 Jul 16;13(7):1091
LN229E1 cells (BMAL1 knockdown) 20 μM 72 h To assess the effect of 1A-116 on proliferation in BMAL1 knockdown cells, showing no circadian dependency Pharmaceutics. 2021 Jul 16;13(7):1091
LN229 human glioblastoma cells 20 μM 72 h To evaluate the inhibitory effect of 1A-116 on cell proliferation, showing the strongest inhibition at 10 HPS Pharmaceutics. 2021 Jul 16;13(7):1091
HT295FUR cells 20 µM 36 h To evaluate the effect of 1A-116 on restoring sensitivity to 5-FU in resistant cells, results showed that 1A-116 reversed morphological changes associated with 5-FU resistance and restored sensitivity to 5-FU. Cells. 2024 Oct 26;13(21):1776
HCT1165FUR cells 20 µM 36 h To evaluate the effect of 1A-116 on restoring sensitivity to 5-FU in resistant cells, results showed that 1A-116 reversed morphological changes associated with 5-FU resistance and restored sensitivity to 5-FU. Cells. 2024 Oct 26;13(21):1776
CT265FUR cells 20 µM 36 h To evaluate the effect of 1A-116 on restoring sensitivity to 5-FU in resistant cells, results showed that 1A-116 reversed morphological changes associated with 5-FU resistance and restored sensitivity to 5-FU. Cells. 2024 Oct 26;13(21):1776

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
C57BL/6 mice AngII-induced cardiac fibrosis model Intraperitoneal injection 5 mg/kg Once daily for 4 weeks Inhibition of P-Rex1 activity, amelioration of AngII-induced abnormalities in heart structure and function Cardiovasc Drugs Ther. 2024 Oct;38(5):861-872
BALB/c mice CT265FUR subcutaneous tumor model Intraperitoneal injection 5 mg/kg BW/day Once daily until the end of the experiment To evaluate the effect of 1A-116 on tumor growth inhibition and metastasis prevention in 5-FU-resistant tumors, results showed that 1A-116 significantly inhibited tumor growth and reduced metastasis. Cells. 2024 Oct 26;13(21):1776

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.25mL

0.65mL

0.33mL

16.27mL

3.25mL

1.63mL

32.54mL

6.51mL

3.25mL

References

 

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