TYRPHOSTIN B46
- Product Name
- TYRPHOSTIN B46
- CAS No.
- 133550-34-2
- Chemical Name
- TYRPHOSTIN B46
- Synonyms
- AG 555;AG 555, >98%;TYRPHOSTIN B46;TYRPHOSTIN AG 555;TyrphostinB46 AG 555;TyrphostinB46 A 555;AG555(Tyrphostin B46);TYRPHOSTIN AG 555, >98%;AG 555 (Tyrphostin AG 555);TYRPHOSTIN AG 555;TYRPHOSTIN AG-555;TYRPHOSTIN AG555
- CBNumber
- CB5469835
- Molecular Formula
- C19H18N2O3
- Formula Weight
- 322.36
- MOL File
- 133550-34-2.mol
TYRPHOSTIN B46 Property
- Boiling point:
- 621.1±55.0 °C(Predicted)
- Density
- 1.273±0.06 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Store in freezer, under -20°C
- solubility
- DMSO or ethanol: soluble
- pka
- 8.82±0.10(Predicted)
- form
- Powder
- color
- Light yellow to yellow
Safety
- Safety Statements
- 22-24/25
- WGK Germany
- 3
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
- Precautionary statements
-
P280Wear protective gloves/protective clothing/eye protection/face protection.
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
- J61704
- Product name
- Tyrphostin B46, 98+%
- Packaging
- 10mg
- Price
- $152.65
- Updated
- 2024/03/01
- Product number
- J61704
- Product name
- Tyrphostin B46, 98+%
- Packaging
- 50mg
- Price
- $644
- Updated
- 2021/12/16
- Product number
- 23247
- Product name
- AG-555
- Purity
- ≥95%
- Packaging
- 5mg
- Price
- $48
- Updated
- 2024/03/01
- Product number
- 23247
- Product name
- AG-555
- Purity
- ≥95%
- Packaging
- 10mg
- Price
- $85
- Updated
- 2024/03/01
- Product number
- 23247
- Product name
- AG-555
- Purity
- ≥95%
- Packaging
- 25mg
- Price
- $198
- Updated
- 2024/03/01
TYRPHOSTIN B46 Chemical Properties,Usage,Production
Description
AG-555 is a tyrphostin inhibitor of the EGF receptor (EGFR; IC50 = 0.7 μM). It selectively inhibits EFGR over ErbB2 (IC50 = 35 μM). AG-555 inhibits EGF-dependent growth of HER 14 cells (IC50 = 2.5 μM) as well as the growth of psoriatic keratinocytes isolated from patients with psoriasis when used at concentrations ranging from 1 to 50 μM. It also inhibits Moloney murine leukemia virus (Mo-MuLV) reverse transcriptase activity (IC50 = 10.8 μM) without affecting Mo-MuLV-infected NIH3T3 cell growth (IC50 = 210 μM).
Uses
Inhibitor of EGF receptor kinase activity
Biological Activity
Potent epidermal growth factor receptor (EGFR) kinase inhibitor (IC 50 = 0.7 μ M) that displays 50-fold and >140-fold selectivity over ErbB2 and insulin receptor kinase respectively. Induce G 1 growth arrest selectively in transformed cells (IC 50 values are 6.4 and 9.4 μ M in HPV16-immortalized and normal keratinocytes respectively).
References
[1]. ben-bassat h, rosenbaum-mitrani s, hartzstark z, et al. inhibitors of epidermal growth factor receptor kinase and of cyclin-dependent kinase 2 activation induce growth arrest, differentiation, and apoptosis of human papilloma virus 16-immortalized human keratinocytes. cancer res, 1997, 57(17): 3741-3750.
[2]. kleinberger-doron n, shelah n, capone r, et al. inhibition of cdk2 activation by selected tyrphostins causes cell cycle arrest at late g1 and s phase. exp cell res, 1998, 241(2): 340-351.
[3]. sion-vardy n, vardy d, rodeck u, et al. antiproliferative effects of tyrosine kinase inhibitors (tyrphostins) on human bladder and renal carcinoma cells. j surg res, 1995, 59(6): 675-680.
[4]. seri i, aflalo e, gazit a, et al. tyrphostin ag-555 inhibits early and late stages of moloney murine leukemia virus replication cycle. int j oncol, 1997, 10(6): 1185-1189.
TYRPHOSTIN B46 Preparation Products And Raw materials
Raw materials
Preparation Products
TYRPHOSTIN B46 Suppliers
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