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About This Item
Empirical Formula (Hill Notation):
C23H19NO3
CAS Number:
Molecular Weight:
357.40
UNSPSC Code:
12352202
PubChem Substance ID:
MDL number:
Assay:
≥95% (HPLC)
Form:
solid
assay
≥95% (HPLC)
form
solid
solubility
DMSO: 40 mg/mL
SMILES string
COc1ccc(cc1)\C(c2ccc(OC)cc2)=C3\C(=O)Nc4ccccc34
InChI
1S/C23H19NO3/c1-26-17-11-7-15(8-12-17)21(16-9-13-18(27-2)14-10-16)22-19-5-3-4-6-20(19)24-23(22)25/h3-14H,1-2H3,(H,24,25)
InChI key
KUEYYIJXBRWZIB-UHFFFAOYSA-N
Biochem/physiol Actions
Inhibitor of migration and proliferation in vascular smooth muscle cells; inhibitor of restenosis.
TAS-301 is known to block intimal thickening post balloon injury in rat carotid arteries. It inhibits intimal thickening by blocking Ca2+/calmodulin-dependent protein kinase II (CaM kinase II) and cytoskeletal depolymerization. Moreover, TAS 301 can also inhibit receptor-regulated influx of calcium in rat vascular smooth muscle cells (VSMCs).
Preparation Note
TAS-301 is soluble in DMSO at 40 mg/ml.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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E Sasaki et al.
Pharmacology, 63(1), 17-27 (2001-06-16)
We previously demonstrated that a recently synthesized drug, TAS-301 [3-bis(4-methoxyphenyl)methylene-2-indolinone], inhibited neointimal thickening after single-balloon injury to the rat common carotid artery by inhibiting both the migration and proliferation processes of vascular smooth muscle cells (VSMCs). The purpose of this
E Sasaki et al.
Japanese journal of pharmacology, 84(3), 252-258 (2001-01-04)
The purpose of this study was to determine the effect of a recently synthesized drug, TAS-301 [3-bis(4-methoxyphenyl)methylene-2-indolinone], on vascular smooth muscle cell (VSMC) proliferation and the intracellular signal transduction pathways involved in VSMC proliferation. In an in vitro assay, TAS-301
Y Muranaka et al.
The Journal of pharmacology and experimental therapeutics, 285(3), 1280-1286 (1998-06-17)
The purpose of this study was to determine the efficacy and the possible mechanism of action of a recently synthesized drug, TAS-301 [3-bis (4-methoxyphenyl)methylene-2-indolinone], on intimal formation in comparison with those of tranilast, the clinical efficacy of which was reported
Related Content
Product Information Sheet
Global Trade Item Number
| SKU | GTIN |
|---|---|
| T9324-10MG | 04061833632567 |
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