Description
WHI-P180 is a multi-kinase inhibitor. It inhibits human proto-oncogene receptor tyrosine kinase RET (Rearranged during Transfection) and kinase insert domain receptor (KDR) with IC₅₀ values of 4.5 nM and 66 nM respectively. It inhibits epidermal growth factor receptor (EGFR) kinase with an IC₅₀ of 4.0 μM and also inhibits Janus kinase 3 (JAK3). It exhibits potent anti-graft-versus-host disease activity and IgE-mediated mast cell responses in vitro and in vivo.
WHI-P180 is a multi-kinase inhibitor. It inhibits human proto-oncogene receptor tyrosine kinase RET (Rearranged during Transfection) and kinase insert domain receptor (KDR) with IC₅₀ values of 4.5 nM and 66 nM respectively. It inhibits epidermal growth factor receptor (EGFR) kinase with an IC₅₀ of 4.0 μM and also inhibits Janus kinase 3 (JAK3). It exhibits potent anti-graft-versus-host disease activity and IgE-mediated mast cell responses in vitro and in vivo.
Alternate Name/Synonyms: 3-[(6,7-dimethoxyquinazolin-4-yl)amino]phenol; 4-[3-Hydroxyanilino]-6,7-Dimethoxyquinazoline; Janex3; 4-(3'-hydroxyphenyl)-amino-6,7-dimethoxyquinazoline
Appearance: A crystalline solid
Formulation:
CAS Number: 211555-08-7
Structure Available?: True
Peptide sequence:
Salt Form: false
Molecular Formula: C₁₆H₁₅N₃O₃
Molecular Weight: 297.31
Cell-Permeable?: True
Purity: >98%
Solubilities: ~15 mg/ml in in DMSO, ~25 mg/ml in DMF in 0
Handling: Do not take internally. Wear gloves and mask when handling the product! Avoid contact by all modes of exposure.
Country of Origin: USA
Tag Line: A multi-kinase inhibitor
MDL Number:
PubChem CID: 5687
SMILES: COC1=C(C=C2C(=C1)C(=NC=N2)NC3=CC(=CC=C3)O)OC
InChi: InChI=1S/C16H15N3O3/c1-21-14-7-12-13(8-15(14)22-2)17-9-18-16(12)19-10-4-3-5-11(20)6-10/h3-9,20H,1-2H3,(H,17,18,19)
InChi Key:
Additional Information
Storage Condition: |
-20ºC |
Shipping Condition: |
RT |
Shelf Life: |
36 months |