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SIS3 HCl
Cat. No.:
OB0225WX-2721
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, and HPLC.
Size:
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Product Overview
Description:
SIS3 acts as a novel and specific inhibitor of Smad3 that suppresses TGF-beta and activin signaling by blocking Smad3 phosphorylation, while remaining inactive against MAPK/p38, ERK, or PI3-kinase pathways.
Synonym:
SIS3; 521984-48-5; Sis3 HCl; SIS3 hydrochloride; (E)-SIS3; MFCD09265258; (2E)-1-(6,7-Dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl)-3-(1-methyl-2-phenyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-propenone hydrochloride; SIS 3; (E)-1-(6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl)-3-(1-methyl-2-phenylpyrrolo[2,3-b]pyridin-3-yl)prop-2-en-1-one;hydrochloride; 2-Propen-1-one, 1-(3,4-dihydro-6,7-dimethoxy-2(1H)-isoquinolinyl)-3-(1-methyl-2-phenyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-, hydrochloride (1:1), (2E)-; Caneritinib; 1,2,3,4-Tetrahydro-6,7-dimethoxy-2-[(2E)-3-(1-methyl-2-phenyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-1-oxo-2-propenyl]-isoquinoline Monohydrochloride; SIS 3 Hydrochloride; SIS3(HCl); SIS-3; Specific Inhibitor of Smad3; (2E)-1-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)-3-(1-methyl-2-phenyl-1H-pyrrolo[2,3-b]pyridin-3-yl)prop-2-en-1-one hydrochloride; (E)-1-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)-3-(1-methyl-2-phenyl-1H-pyrrolo[2,3-b]pyridin-3-yl)prop-2-en-1-one HCl; (E)-1-(6,7-Dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)-3-(1-methyl-2-phenyl-1H-pyrrolo[2,3-b]pyridin-3-yl)prop-2-en-1-one hydrochloride; isoquinoline, 1,2,3,4-tetrahydro-6,7-dimethoxy-2-[(2E)-3-(1-methyl-2-phenyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-1-oxo-2-propenyl]-, monohydrochloride
CAS No.:
521984-48-5
Compound CID:
16079005
Formula:
C28H27N3O3·HCl
Formula Weight:
489.99
Specification
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
SIS3 HCl is employed in fibrotic disease research as a potent and selective inhibitor of Smad3 phosphorylation to investigate the disruption of TGF-beta1-induced myofibroblast differentiation and extracellular matrix production.
Library Information
Target:
Smad pathway activator
Receptor:
Smad3
Pathways:
TGF-beta/Smad
Plate Number:
L6700-09
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
97 mg/mL; 197.96 mM
ALogP:
5.076
HBA_Count:
4
HBD_Count:
0
Rotatable Bond:
5





