CAS 845272-21-1|Varlitinib
Introduction：Basic information about CAS 845272-21-1|Varlitinib, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | Varlitinib | ||
|---|---|---|---|
| CAS Number | 845272-21-1 | Molecular Weight | 466.943 |
| Density | 1.5±0.1 g/cm3 | Boiling Point | 637.1±65.0 °C at 760 mmHg |
| Molecular Formula | C22H19ClN6O2S | Melting Point | / |
| MSDS | / | Flash Point | 339.1±34.3 °C |
Names
| Name | 4-N-[3-chloro-4-(1,3-thiazol-2-ylmethoxy)phenyl]-6-N-[(4R)-4-methyl-4,5-dihydro-1,3-oxazol-2-yl]quinazoline-4,6-diamine |
|---|---|
| Synonym | More Synonyms |
Varlitinib BiologicalActivity
| Description | Varlitinib (ARRY-334543; ASLAN001) is a potent, reversible, small molecule pan-EGFR inhibitor with IC50s of 7, 2, 4 nM for HER1, HER2 and HER4, respectively. |
|---|---|
| Related Catalog | Research Areas >>Cancer |
| Target | HER1:7 nM (IC50) HER2:2 nM (IC50) HER4:4 nM (IC50) |
| In Vitro | In cell-based assays using tumor cells that over-express EGFR (A431) or ErbB-2 (BT474), Varlitinib (ARRY-334543) potently inhibits substrate phosphorylation. Varlitinib is shown to be highly selective for EGFR/ErbB-2, and does not show any significant activity when screened against a panel of 104 kinases[2]. |
| In Vivo | Varlitinib treatment potently inhibits tumor growth with complete tumor regression observed at dosing of 100 mg/kg twice a day. After five days of Varlitinib treatment, phosphorylation of HER1-3, RAS/RAF/MEK/MAPK, p70S6K, S6 ribosomal, 4EBP1, Cdk-2, Cdc-2 and retinoblastoma are strongly inhibited. Varlitinib treatment results in a significant reduction in survivin and a concomittant increase in Caspase 3 cleavage products[1]. In murine xenograft models, Varlitinib (ARRY-334543) demonstrates significant dose-related (25, 50, 100 mg/kg) tumor growth inhibition in A431-derived tumors when administered orally, twice a day, for 21 days[2]. |
| Animal Admin | Mice: The effects of Varlitinib is tested in patient-derived HCC xenograft in SCID mice (HCC29-0909A) with co-expression of HER1, HER2 and HER3 recepors. Mice are treated with Varlitinib when the tumors reach the size of approximately 100-150 mm3. Tumor size measurements are performed twice a week and tumor volumes are calculated[1]. |
| References | [1]. Hsieh C, et al. Varlitinib to demonstrate anti-tumour efficacy in patient-derived hepatocellular carcinoma xenograft models. Journal of Clinical Oncology 34, no. 15_suppl [2]. Miknis G, et al. ARRY-334543, A potent, orally active small molecule inhibitor of EGFR and ErbB-2.Proc Amer Assoc Cancer Res, Volume 46, 2005 |
Chemical & Physical Properties
| Density | 1.5±0.1 g/cm3 |
|---|---|
| Boiling Point | 637.1±65.0 °C at 760 mmHg |
| Molecular Formula | C22H19ClN6O2S |
| Molecular Weight | 466.943 |
| Flash Point | 339.1±34.3 °C |
| Exact Mass | 466.097870 |
| PSA | 121.79000 |
| LogP | 3.51 |
| Vapour Pressure | 0.0±1.9 mmHg at 25°C |
| Index of Refraction | 1.742 |
| InChIKey | UWXSAYUXVSFDBQ-CYBMUJFWSA-N |
| SMILES | CC1COC(Nc2ccc3ncnc(Nc4ccc(OCc5nccs5)c(Cl)c4)c3c2)=N1 |
| Storage condition | -20℃ |
Synonyms
| 4,6-Quinazolinediamine, N-[3-chloro-4-(2-thiazolylmethoxy)phenyl]-N-[(4R)-4,5-dihydro-4-methyl-2-oxazolyl]- |
| ARRY-543 |
| N-[3-Chloro-4-(1,3-thiazol-2-ylmethoxy)phenyl]-N-[(4R)-4-methyl-4,5-dihydro-1,3-oxazol-2-yl]-4,6-quinazolinediamine |
| Varlitinib (USAN/INN) |
| Varlitinib |
