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TG003

CAT: 0931-T60367-01Size: 1 mgDry Ice: NoHazardous: No
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CAT#:0931-T60367-01Size:1 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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CAS Number
719277-26-6
Target
CDK
Related Pathways
Cell Cycle/Checkpoint
Purity
0.9946
Bioactivity
TG003 is a potent Clk1/Sty inhibitor that inhibits Clk1 and Clk4, inhibits cancer cell growth and induces apoptosis, and can be used in the study of Duchenne muscular dystrophy.
Smiles
C(C)N\1C=2C(S/C1=C\C(C)=O)=CC=C(OC)C2
Molecular Formula
C13H15NO2S
Molecular Weight
249.33
Shipping Conditions
Ice Packs
Storage Temperature
-20°C

Chemical Information

TG-003

TG003 is a pharmacological inhibitor known to target Cdc2 like kinases (CLKs) and dual-specificity tyrosine-regulated kinases (DYRKs). These kinases play a role in pre-mRNA splicing regulation and other cellular processes.

CAS Number719277-26-6
PubChem CID1893668
IUPAC Name(1Z)-1-(3-ethyl-5-methoxy-1,3-benzothiazol-2-ylidene)propan-2-one
Molecular FormulaC13H15NO2S
Molecular Weight249.33
XLogP2.6
Topological Polar Surface Area54.8
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count4
Rotatable Bond Count3
Heavy Atom Count17
Formal Charge0
Complexity329
SMILES
CCN\1C2=C(C=CC(=C2)OC)S/C1=C\C(=O)C
InChI
InChI=1S/C13H15NO2S/c1-4-14-11-8-10(16-3)5-6-12(11)17-13(14)7-9(2)15/h5-8H,4H2,1-3H3/b13-7-
InChIKey
BGVLELSCIHASRV-QPEQYQDCSA-N
Chemical Structure
2D Structure
2D structure of TG-003
CAS: 719277-26-6
CID: 1893668
Formula: C13H15NO2S
MW: 249.33
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight249.33
XLogP32.6
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count4
Rotatable Bond Count3
Exact Mass249.08234989
Monoisotopic Mass249.08234989
Topological Polar Surface Area54.8 Ų
Heavy Atom Count17
Formal Charge0
Complexity329
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

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