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CAS RN: 153437-55-9 | Product Number: W0021
WHI-P180 Hydrochloride
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Purity: >97.0%(T)(HPLC)
Synonyms:
- 3-[(6,7-Dimethoxy-4-quinazolinyl)amino]phenol Hydrochloride
- 3-[(6,7-Dimethoxyquinazolin-4-yl)amino]phenol Hydrochloride
Product Documents:
| Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time |
Shipping Information
|
|---|---|---|---|---|---|
| 25MG |
$126.00
|
18 | 0 | It can be shipped in about 2 weeks after ordering |
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* The storage conditions are subject to change without notice.
| Product Number | W0021 |
Purity / Analysis Method 
|
>97.0%(T)(HPLC) |
| Molecular Formula / Molecular Weight | C__1__6H__1__5N__3O__3·HCl = 333.77 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature
|
Room Temperature (Recommended in a cool and dark place, <15°C) |
| Store Under Inert Gas | Store under inert gas |
| Condition to Avoid | Air Sensitive,Hygroscopic |
| CAS RN | 153437-55-9 |
| Reaxys Registry Number | 8592187 |
| PubChem Substance ID | 468593126 |
| MDL Number | MFCD09026915 |
Specifications
| Appearance | White to Light gray to Light yellow powder to crystal |
| Purity(HPLC) | min. 97.0 area% |
| Water | max. 2.0 % |
| NMR | confirm to structure |
Properties (reference)
GHS
Related Laws:
Transport Information:
| H.S.code* | 2933.59-000 |
Application
WHI-P180 Hydrochloride: A Multi-Kinase Inhibitor
WHI-P180 (hydrochloride) is a multi-kinase inhibitor. There are reports that it inhibits rearranged during transfection (RET) kinase and kinase insert domain receptor (KDR), respectively.1) It also inhibits epidermal growth factor receptor (EGFR) as well as Janus Kinase 3 (JAK3).2,3) It inhibits IgE/antigen-induced vascular hyper-permeability,4) and cyclin-dependent kinase 2 (CDK2).5) In addition, it binds to tau-tubulin kinase 1 (TTBK1).6) (The product is for research purpose only.)
References
- 1) The discovery of 2-substituted phenol quinazolines as potent RET kinase inhibitors with improved KDR selectivity
- 2) 4-[(3-Bromo-4-hydroxyphenyl)amino]-6,7-dimethoxyquinazolin-1-ium chloride methanol solvate and 4-[(3-hydroxyphenyl)amino]-6,7-dimethoxy-1-quinazolinium chloride
- 3) Treatment of post-bone marrow transplant acute graft-versus-host disease with a rationally designed JAK3 inhibitor
- 4) Pharmacokinetics and biologic activity of the novel mast cell inhibitor, 4-(3'-hydroxyphenyl)-amino-6,7-dimethoxyquinazoline in mice
- 5) Binding mode of the 4-anilinoquinazoline class of protein kinase inhibitor: X-ray crystallographic studies of 4-anilinoquinazolines bound to cyclin-dependent kinase 2 and p38 kinase
- 6) X-ray structural analysis of tau-tubulin kinase 1 and its interactions with small molecular inhibitors
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