Products for Research Use Only

HS-276

CAT: 1410-M35623-07Size: 200 mgDry Ice: NoHazardous: No
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CAT#:1410-M35623-07Size:200 mg
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Description
HS-276 is a highly selective, orally active inhibitor of TAK1 (Ki: 2.5 nM) . HS-276 significantly inhibits TAK1 (IC50: 8.25 nM), CLK2 (IC50: 29 nM), GCK (IC50: 22 nM), ULK2 (IC50: 63 nM), MAP4K5 (IC50. HS-276 can be used to study rheumatoid arthritis (RA) .
CAS Number
2767422-72-8
Stability
≥ 2 years
Purity
>98% (HPLC)
Weight
419.52
Molecular Formula
C24H29N5O2
Notes
Research use only, not for human use.
Receptor
MAPK

Chemical Information

N-(6-(Piperidin-1-ylmethyl)-1-propyl-1H-benzo[d]imidazol-2-yl)isophthalamide
CAS Number2767422-72-8
PubChem CID164517032
IUPAC Name3-N-[6-(piperidin-1-ylmethyl)-1-propylbenzimidazol-2-yl]benzene-1,3-dicarboxamide
Molecular FormulaC24H29N5O2
Molecular Weight419.5
XLogP3
Topological Polar Surface Area93.3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count7
Heavy Atom Count31
Formal Charge0
Complexity623
SMILES
CCCN1C2=C(C=CC(=C2)CN3CCCCC3)N=C1NC(=O)C4=CC=CC(=C4)C(=O)N
InChI
InChI=1S/C24H29N5O2/c1-2-11-29-21-14-17(16-28-12-4-3-5-13-28)9-10-20(21)26-24(29)27-23(31)19-8-6-7-18(15-19)22(25)30/h6-10,14-15H,2-5,11-13,16H2,1H3,(H2,25,30)(H,26,27,31)
InChIKey
NPEMHKSMWPZEOV-UHFFFAOYSA-N
Chemical Structure
2D Structure
2D structure of N-(6-(Piperidin-1-ylmethyl)-1-propyl-1H-benzo[d]imidazol-2-yl)isophthalamide
CAS: 2767422-72-8
CID: 164517032
Formula: C24H29N5O2
MW: 419.5
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight419.5
XLogP33
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count7
Exact Mass419.23212518
Monoisotopic Mass419.23212518
Topological Polar Surface Area93.3 Ų
Heavy Atom Count31
Formal Charge0
Complexity623
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes