CAS 303727-31-3|L-779450
Introduction：Basic information about CAS 303727-31-3|L-779450, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | L-779450 | ||
|---|---|---|---|
| CAS Number | 303727-31-3 | Molecular Weight | 347.79800 |
| Density | 1.335g/cm3 | Boiling Point | 579.783ºC at 760 mmHg |
| Molecular Formula | C20H14ClN3O | Melting Point | / |
| MSDS | ChineseUSA | Flash Point | 304.442ºC |
| Symbol | GHS06 | Signal Word | Danger |
Names
| Name | 2-chloro-5-(2-phenyl-5-pyridin-4-yl-1H-imidazol-4-yl)phenol |
|---|---|
| Synonym | More Synonyms |
L-779450 BiologicalActivity
| Description | L-779450 is a potent and selective B-Raf kinase inhibitor with a Kd of 2.4 nM. |
|---|---|
| Related Catalog | Signaling Pathways >>Autophagy >>AutophagyResearch Areas >>Cancer |
| Target | B-Raf:2.4 nM (Kd) |
| In Vitro | L-779450 (L-779,450) shows a high degree of specificity towards Raf. The only other tested kinase inhibited is p38MAPK, which has a kinase domain structurally related to Raf. L-779450 inhibits anchorage-independent growth of human tumor lines at doses ranging from 0.3 to 2 μM[2]. The effects of L-779450 (L-779,450) on TRAIL sensitivity are investigated here in melanoma cell lines with high TRAIL sensitivity (A-375 and SK-Mel-147), moderate sensitivity (Mel-HO, SK-Mel-13, and SK-Mel-28), and permanent resistance (MeWo, Mel-2a, and SK-Mel-103), as well as in TRAIL-selected cell lines with acquired resistance (A-375-TS and Mel-HO-TS). Despite only moderate direct effects of L-779450 on apoptosis, it strongly enhances TRAIL-induced apoptosis in sensitive melanoma cells and overrules TRAIL resistance in Mel-2a, SK-Mel-103, A-375-TS, and Mel-HO-TS. At 24 hours, 16-35% apoptosis induction is obtained[3]. |
| Cell Assay | For induction of apoptosis, TRAIL (20 ng/mL), the pan-RAF inhibitor L-779450 (0.1-50 μM), the MEK inhibitor U0126 (20 μM), and the selective BRAF(V600E) inhibitor Vemurafenib/PLX4032 are used. For continuous monitoring cell growth, the xCELLigence system is applied. Relative cell indices correspond to attached cell numbers. Cell cycle analyses are performed for quantification of apoptosis and cell cycle arrest. Cells harvested by trypsinization are stained for 1 hour with propidium iodide (200 mg/mL), and sub-G1 fractions, corresponding to cells with fragmented DNA, are quantified by flow cytometry[3]. |
| References | [1]. Takle AK, et al. The identification of potent, selective and CNS penetrant furan-based inhibitors of B-Raf kinase. Bioorg Med Chem Lett. 2008 Aug 1;18(15):4373-6. [2]. Shelton JG, et al. Differential effects of kinase cascade inhibitors on neoplastic and cytokine-mediated cell proliferation. Leukemia. 2003 Sep;17(9):1765-82. [3]. Berger A, et al. RAF inhibition overcomes resistance to TRAIL-induced apoptosis in melanoma cells. J Invest Dermatol. 2014 Feb;134(2):430-440. |
Chemical & Physical Properties
| Density | 1.335g/cm3 |
|---|---|
| Boiling Point | 579.783ºC at 760 mmHg |
| Molecular Formula | C20H14ClN3O |
| Molecular Weight | 347.79800 |
| Flash Point | 304.442ºC |
| Exact Mass | 347.08300 |
| PSA | 61.80000 |
| LogP | 5.16470 |
| Index of Refraction | 1.671 |
| InChIKey | WXJLXRNWMLWVFB-UHFFFAOYSA-N |
| SMILES | Oc1cc(-c2nc(-c3ccccc3)[nH]c2-c2ccncc2)ccc1Cl |
| Storage condition | Store at +4°C |
Safety Information
| Symbol | GHS06 |
|---|---|
| Signal Word | Danger |
| Hazard Statements | H301-H315-H319-H335 |
| Precautionary Statements | P280-P301 + P310 + P330-P304 + P340 + P312-P305 + P351 + P338-P337 + P313 |
| RIDADR | UN 2811 6.1 / PGIII |
| HS Code | 2933990090 |
Customs
| HS Code | 2933990090 |
|---|---|
| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Synonyms
| Chlormethiazole hydrochloride |
| L-779450 |
| 2-(Phenyl)-4-(3-hydroxy-4-chlorophenyl)-5-(4-pyridyl)-1H-imidazole |
