ChemicalBook > CAS DataBase List > TYRPHOSTIN B46
TYRPHOSTIN B46
TYRPHOSTIN B46
- CAS No.133550-34-2
- Chemical Name:TYRPHOSTIN B46
- 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
- form Powder
- pka 8.82±0.10(Predicted)
- color Light yellow to yellow
Safety
- Safety Statements :22-24/25
- WGK Germany :3
-
Symbol(GHS)
- Signal wordWarning
- Hazard statements H302
- Precautionary statements P280-P305+P351+P338
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).
- IC 50 EGFR
-
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
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133550-34-2, TYRPHOSTIN B46Related Search:
- Intracellular Signaling
- Protein Kinase
- 抑制剂
- 药靶配体
- Receptor Tyrosine Kinase Inhibitors
- Epidermal Growth Factor Receptor (EGFR)
- Kinase/Phosphatase Biology
- Cell Signaling and Neuroscience
- Cell Biology
- BioChemical
- 化合物AG 555,10 MM DMSO 溶液
- AG 555 (TYRPHOSTIN B46),EGFR-TYROSINE KINASE抑制剂
- AG 555(TYRPHOSTIN B46),抑制剂
- 化合物AG 555
- (E)-2-氰基-3-(3,4-二羟基苯基)-N-(3-苯基丙基)丙烯酰胺
- 133550-34-2
- AG 555, 10 mM in DMSO
- AG 555 (Tyrphostin B46), EGFR-tyrosine kinase inhibitor
- TyrphostinB46 A 555
- TyrphostinB46 AG 555
- Tyrphostin AG-555,EGFR,Reverse Transcriptase,Bovine,Tyrphostin AG555,HER1,BPV,ErbB-1,Inhibitor,AG 555,Epidermal growth factor receptor,AG-555,AG555,inhibit,antiretroviral,Papillomavirus
- (E)-2-Cyano-3-(3,4-dihydroxyphenyl)-N-(3-phenylpropyl)acrylamide
- AG555(Tyrphostin B46)
- TYRPHOSTIN AG 555, >98%
- AG 555, >98%
- TYRPHOSTIN AG 555;TYRPHOSTIN AG-555;TYRPHOSTIN AG555
- 2-Propenamide,2-cyano-3-(3,4-dihydroxyphenyl)-N-(3-phenylpropyl)-, (2E)-
- AG 555 (Tyrphostin AG 555)
- Tyrphostin B46, N-(3μ-Phenylpropyl)-3,4-dihydroxybenzylidenecyanoacetamide
- ALPHA-CYANO-(3,4-DIHYDROXY)-N-(3-PHENYLPROPYL)CINNAMIDE
- AG 555
- (E)-2-CYANO-3-(3,4-DIHYDROXYPHENYL)-N-(3-PHENYLPROPYL)-2-PROPENAMIDE
- TYRPHOSTIN B46
- TYRPHOSTIN AG 555
- N-(3'-PHENYLPROPYL)-3,4-DIHYDROXYBENZYLIDENECYANOACETAMIDE
- N-(3-PHENYLPROPYL)-3,4-DIHYDROXY-ALPHA CYANOCINNAMIDE