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AT-13148

Product Name
AT-13148
CAS No.
1056901-62-2
Chemical Name
AT-13148
Synonyms
CS-1252;AT-13148;AT13148 HCl;AT13148, >=98%;AT-13148;AT 13148;AT-13148 USP/EP/BP;AT13148 hydrochloride;AT 13148 dihydrochloride;AT-13148; AT 13148; AT13148; AT13148 HYDROCHLORIDE; AT13148 HCL;(S)-1-(4-(1H-pyrazol-4-yl)phenyl)-2-amino-1-(4-chlorophenyl)ethanol
CBNumber
CB22627346
Molecular Formula
C17H16ClN3O
Formula Weight
313.78
MOL File
1056901-62-2.mol
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AT-13148 Property

Boiling point:
595.9±50.0 °C(Predicted)
Density 
1.328±0.06 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
Soluble in DMSO
form 
Powder
pka
10.92±0.50(Predicted)
color 
White to off-white
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
21597
Product name
AT-13148
Purity
≥98%
Packaging
1mg
Price
$37
Updated
2024/03/01
Cayman Chemical
Product number
21597
Product name
AT-13148
Purity
≥98%
Packaging
5mg
Price
$134
Updated
2024/03/01
Cayman Chemical
Product number
21597
Product name
AT-13148
Purity
≥98%
Packaging
10mg
Price
$213
Updated
2024/03/01
Cayman Chemical
Product number
21597
Product name
AT-13148
Purity
≥98%
Packaging
25mg
Price
$310
Updated
2024/03/01
TRC
Product number
A790350
Product name
AT-13148
Packaging
10mg
Price
$4150
Updated
2021/12/16
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AT-13148 Chemical Properties,Usage,Production

Uses

AT13148 is an oral, ATP-competitive, multi-AGC kinase inhibitor.

Biological Activity

at13148 is a novel, oral and atp-competitive inhibitor of multi-agc kinase with ic50 values of 38nm, 8nm, 3nm, 63nm and 4nm for akt, p70s6 kinase, pka, sgk and rho kinase, respectively [1].

in vitro

studies, at13148 has been reported to inhibit activity of agc kinases which including akt, p70s6 kinase, pka, sgk and rho kinase with the ic50 values of 38nm, 8nm, 3nm, 63nm and 4nm, respectively. in addition, at13148 has been revealed to inhibit proliferation with gi50 values of 1.54μm, 1.59μm, 1.82μm, 2.65μm and 3.77μm in mes-sa, bt474, hct-116, a549 and sk-ov-3 cell lines, respectively.

in vivo

studies, at13148 has shown the antitumor activity in multiple human tumor xenograft models including pten-deficient mes-sa human uterine sarcoma, her2-positive, pik3ca-mutant bt474 human breast cancer xenografts [1].

References

[1] yap ta1, walton mi, grimshaw km, te poele rh, eve pd, valenti mr, de haven brandon ak, martins v, zetterlund a, heaton sp, heinzmann k, jones ps, feltell re, reule m, woodhead sj, davies tg, lyons jf, raynaud fi, eccles sa, workman p, thompson nt, garrett md. at13148 is a novel, oral multi-agc kinase inhibitor with potent pharmacodynamic and antitumor activity. clin cancer res. 2012 jul 15;18(14):3912-23.

AT-13148 Preparation Products And Raw materials

Raw materials

Preparation Products

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AT-13148 Suppliers

Axon Medchem BV
Tel
--
Fax
--
Email
info@axonmedchem.com
Country
The Netherlands
ProdList
477
Advantage
30

1056901-62-2, AT-13148Related Search:


  • AT-13148
  • (+)-(S)-2-Amino-1-(4-chlorophenyl)-1-[4-(1H-pyrazol-4-yl)phenyl]ethanol
  • AT13148 HCl
  • AT13148 hydrochloride
  • AT-13148; AT 13148; AT13148; AT13148 HYDROCHLORIDE; AT13148 HCL
  • AT-13148;AT 13148
  • CS-1252
  • (alphaS)-alpha-(Aminomethyl)-alpha-(4-chlorophenyl)-4-(1H-pyrazol-4-yl)benzenemethanol
  • (S)-1-(4-(1H-pyrazol-4-yl)phenyl)-2-amino-1-(4-chlorophenyl)ethanol
  • (+)-(S)-2-Amino-1-(4-chlorophenyl)-1-[4-(1H-pyrazol-4-yl)phenyl]ethanol AT13148
  • AT13148, >=98%
  • AT 13148 dihydrochloride
  • (1S)-2-Amino-1-(4-chlorophenyl)-1-[4-(1H-pyrazol-4-yl)phenyl]ethanol
  • Benzenemethanol, α-(aminomethyl)-α-(4-chlorophenyl)-4-(1H-pyrazol-4-yl)-, (αS)-
  • AT-13148 USP/EP/BP
  • inhibit,AT 13148,Protein kinase B,S6K,AT13148,PKB,AT-13148,ROK,Protein kinase A,Rho-associated protein kinase,Akt,PKA,Rho-associated kinase,Ribosomal S6 Kinase (RSK),Rho-kinase,ROCK,Inhibitor
  • 1056901-62-2
  • Inhibitors