ERK5-IN-2
- Product Name
- ERK5-IN-2
- CAS No.
- 1888305-96-1
- Chemical Name
- ERK5-IN-2
- Synonyms
- ERK5-IN-2;ERK5 inhibitor 2;ERK5-IN-2 ,S6786;ERK5-IN-2, 10 mM in DMSO;ERK5-IN 2; ERK5 IN-2; ERK5-IN-2;1H-Pyrrole-2-carboxamide, 4-(2-bromo-6-fluorobenzoyl)-N-3-pyridinyl-;4-(2-Bromo-6-fluorobenzoyl)-N-(pyridin-3-yl)-1H-pyrrole-2-carboxamide;Inhibitor,ERK5 IN 2,Extracellular signal regulated kinases,inhibit,ERK,ERK-5-IN-2,ERK5IN2
- CBNumber
- CB95430841
- Molecular Formula
- C17H11BrFN3O2
- Formula Weight
- 388.19
- MOL File
- 1888305-96-1.mol
ERK5-IN-2 Property
- Boiling point:
- 525.1±50.0 °C(Predicted)
- Density
- 1.628±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- solubility
- DMSO: 250 mg/mL (644.01 mM)
- pka
- 12.92±0.50(Predicted)
- form
- Solid
- color
- White to off-white
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- CS-0099026
- Product name
- ERK5-IN-2
- Purity
- 98.67%
- Packaging
- 5mg
- Price
- $150
- Updated
- 2021/12/16
- Product number
- CS-0099026
- Product name
- ERK5-IN-2
- Purity
- 98.67%
- Packaging
- 10mg
- Price
- $250
- Updated
- 2021/12/16
- Product number
- CS-0099026
- Product name
- ERK5-IN-2
- Purity
- 98.67%
- Packaging
- 25mg
- Price
- $500
- Updated
- 2021/12/16
- Product number
- CS-0099026
- Product name
- ERK5-IN-2
- Purity
- 98.67%
- Packaging
- 50mg
- Price
- $850
- Updated
- 2021/12/16
- Product number
- orb611948
- Product name
- ERK5-IN-2
- Purity
- >98%
- Packaging
- 100mg
- Price
- $912.9
- Updated
- 2021/12/16
ERK5-IN-2 Chemical Properties,Usage,Production
Uses
ERK5-IN-2 is an orally active, sub-micromolar, selective ERK5 inhibitor with IC50s of 0.82 μM, 3 μM for ERK5 and ERK5 MEF2D, respectively. ERK5-IN-2 does not interact with the BRD4 bromodomain. ERK5-IN-2 suppresses both tumor xenograft growth and basic fibroblast growth factor (bFGF) driven Matrigel plug angiogenesis[1].
in vivo
ERK5-IN-2 (compound 46) (p.o.; 100 mg/kg; CD1 mice for 7 days and CD1 nude (nu/nu) mice for 10 days) has an anti-angiogenic effect and low concentrations of haemoglobin[1].
ERK5-IN-2 (i.v. or p.o.; 10 mg/kg for 0.083-24 hours) exhibits low intrinsic clearance and has high flux and a low efflux ratio (ER) in a caco-2 cell permeability assay in both human and mouse[1].
| Animal Model: | Female CD1 mice (8-10 weeks old) with Matrigel inoculation and female CD1 nude (nu/nu) mice (8-10 weeks old) bearing A2780 human ovarian carcinoma xenografts[1] |
| Dosage: | 100?mg/kg |
| Administration: | P.o.; twice-daily; CD1 mice for 7 days and CD1 nude (nu/nu) mice for 10 days |
| Result: | Tumor volumes were significantly reduced. |
| Animal Model: | Female CD1 mice at 8-10 weeks of age[1] |
| Dosage: | 10 mg/kg |
| Administration: | I.v. or p.o.; 0.083-24?hours |
| Result: | The terminal plasma half-life was 38?min, with a plasma clearance of 27?mL/min/kg, and oral bioavailability of 68%. |
IC 50
ERK5: 0.82 μM (IC50); ERK5 MEF2D: 3 μM (IC50)
References
[1] Myers SM, et al. Identification of a novel orally bioavailable ERK5 inhibitor with selectivity over p38α and BRD4. Eur J Med Chem. 2019 May 25;178:530-543. DOI:10.1016/j.ejmech.2019.05.057
ERK5-IN-2 Preparation Products And Raw materials
Raw materials
Preparation Products
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