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(E/Z)-AG490 {[allProObj[0].p_purity_real_show]}

货号:A603326 同义名: Tyrphostin B 42;(E/Z)-Tyrphostin AG490 Ambeed 开学季,买赠积分,赢豪礼

(E/Z)-AG490是 AG490 的消旋体,其中 (E)-AG490 是一种酪氨酸激酶抑制剂,能够抑制 EGFRStat-3 及 JAK2/3 信号通路。该化合物在癌症研究中展示出显著的抑制肿瘤增殖和转移的潜力。

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Type HazMat fee for 500 gram (Estimated)
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Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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(E/Z)-AG490 化学结构 CAS号:134036-52-5
(E/Z)-AG490 化学结构
CAS号:134036-52-5
(E/Z)-AG490 3D分子结构
CAS号:134036-52-5
(E/Z)-AG490 化学结构 CAS号:134036-52-5
(E/Z)-AG490 3D分子结构 CAS号:134036-52-5
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(E/Z)-AG490 纯度/质量文件 产品仅供科研

货号:A603326 标准纯度: {[allProObj[0].p_purity_real_show]}
批次查询: 批次纯度:

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产品名称 EGFR/ErbB1 ErbB3 ErbB4 HER2/ErbB2 mutant EGFR 其他靶点 纯度
WZ-3146 ++++

EGFR (E746_A750/T790M), IC50: 14 nM

EGFR (E746_A750), IC50: 2 nM

{[allProObj[0].p_purity_real_show]}
Daphnetin +

EGFR, IC50: 7.67 μM

PKC,PKA {[allProObj[0].p_purity_real_show]}
Lifirafenib ++

EGFR, IC50: 29 nM

+

EGFR(T790M/L858R), IC50: 495 nM

{[allProObj[0].p_purity_real_show]}
PD168393 ++++

EGFR, IC50: 0.70 nM

{[allProObj[0].p_purity_real_show]}
Nazartinib ++

mutant EGFR, Ki: 0.031 μM

++

mutant EGFR, Ki: 0.031 μM

{[allProObj[0].p_purity_real_show]}
Norcantharidin {[allProObj[0].p_purity_real_show]}
CL-387785 ++++

EGFR, IC50: 370 pM

{[allProObj[0].p_purity_real_show]}
WHI-P154 +++

EGFR, IC50: 4 nM

Src,VEGFR {[allProObj[0].p_purity_real_show]}
Tyrphostin A9 +

EGFR, IC50: 460 μM

PDGFR {[allProObj[0].p_purity_real_show]}
AG 555 +

EGFR, IC50: 0.7 μM

{[allProObj[0].p_purity_real_show]}
AG 494 +

EGFR, IC50: 1.2 μM

{[allProObj[0].p_purity_real_show]}
AG-556 +

EGFR, IC50: 5 μM

{[allProObj[0].p_purity_real_show]}
RG13022 +

EGFR, IC50: 4 μM

{[allProObj[0].p_purity_real_show]}
Tyrphostin RG 14620 {[allProObj[0].p_purity_real_show]}
Vandetanib +

EGFR, IC50: 500 nM

{[allProObj[0].p_purity_real_show]}
CNX-2006 ++

mutant EGFR, IC50: <20 nM

++

mutant EGFR, IC50: <20 nM

{[allProObj[0].p_purity_real_show]}
AZD3759 ++++

EGFR (L858R), IC50: 0.2 nM

EGFR (WT), IC50: 0.3 nM

{[allProObj[0].p_purity_real_show]}
Erlotinib ++++

EGFR, IC50: 2 nM

{[allProObj[0].p_purity_real_show]}
Saracatinib +++

EGFR, IC50: 5 nM

EGFR (L861Q), IC50: 4 nM

{[allProObj[0].p_purity_real_show]}
AG1557 {[allProObj[0].p_purity_real_show]}
Rociletinib ++

EGFR (L858R/T790M), Ki: 21.5 nM

EGFR (wt), Ki: 303.3 nM

{[allProObj[0].p_purity_real_show]}
AG490 +

EGFR, IC50: 0.1 μM

{[allProObj[0].p_purity_real_show]}
Cetuximab ++++

EGFR, Kd: 0.39 nM

{[allProObj[0].p_purity_real_show]}
Osimertinib ++

L858R/T790M EGFR, IC50: 11.44 nM

WT EGFR, IC50: 12.92 nM

{[allProObj[0].p_purity_real_show]}
Osimertinib mesylate {[allProObj[0].p_purity_real_show]}
Chrysophanol mTOR {[allProObj[0].p_purity_real_show]}
PD153035 ++++

EGFR, Ki: 5.2 pM

{[allProObj[0].p_purity_real_show]}
Olmutinib BTK {[allProObj[0].p_purity_real_show]}
WZ4002 ++++

EGFR (L858R), IC50: 2 nM

EGFR (L858R/T790M), IC50: 8 nM

{[allProObj[0].p_purity_real_show]}
Icotinib +++

EGFR, IC50: 5 nM

{[allProObj[0].p_purity_real_show]}
Desmethyl Erlotinib HCl ++++

EGFR, IC50: 2 nM

{[allProObj[0].p_purity_real_show]}
Cyasterone {[allProObj[0].p_purity_real_show]}
PP 3 +

EGFR tyrosine kinase, IC50: 2.7 μM

{[allProObj[0].p_purity_real_show]}
WZ8040 {[allProObj[0].p_purity_real_show]}
(-)-Epigallocatechin Gallate {[allProObj[0].p_purity_real_show]}
AG 18 +

EGFR, IC50: 35 μM

{[allProObj[0].p_purity_real_show]}
O-Desmethyl gefitinib ++

EGFR, IC50: 36 nM

{[allProObj[0].p_purity_real_show]}
Falnidamol {[allProObj[0].p_purity_real_show]}
AZ-5104 ++++

EGFR (L858R), IC50: 6 nM

EGFR (L861Q) , IC50: <1 nM

+++

ErbB4, IC50: 7 nM

BRK {[allProObj[0].p_purity_real_show]}
Butein {[allProObj[0].p_purity_real_show]}
Genistein {[allProObj[0].p_purity_real_show]}
SU5214 +

EGFR, IC50: 36.7 μM

{[allProObj[0].p_purity_real_show]}
Naquotinib {[allProObj[0].p_purity_real_show]}
Gefitinib ++

EGFR, IC50: 15.5 nM

+

EGFR (858R/T790M), IC50: 823.3 nM

{[allProObj[0].p_purity_real_show]}
Theliatinib +++

WT EGFR, IC50: 3 nM

++

EGFR T790M/L858R, IC50: 22 nM

{[allProObj[0].p_purity_real_show]}
Lazertinib ++++

L858R/T790M EGFR, IC50: 2 nM

WT EGFR, IC50: 76 nM

++++

Del19/T790M, IC50: 1.7 nM

{[allProObj[0].p_purity_real_show]}
Gefitinib-based PROTAC 3 ++

EGFR, DC50: 22.3 nM

{[allProObj[0].p_purity_real_show]}
MTX-211 PI3K {[allProObj[0].p_purity_real_show]}
(E)-AG 99 {[allProObj[0].p_purity_real_show]}
Licochalcone D Caspase,PARP {[allProObj[0].p_purity_real_show]}
Zipalertinib +++

EGFR WT, IC50: 8 nM

EGFR (L861Q), IC50: 4.1 nM

+++

HER4, IC50: 4 nM

++++

EGFR(d746-750), IC50: 1.4 nM

EGFR L858R, IC50: 2 nM

{[allProObj[0].p_purity_real_show]}
JND3229 +++

EGFR WT, IC50: 6.8 nM

++

EGFR L858R/T790M, IC50: 30.5 nM

{[allProObj[0].p_purity_real_show]}
Firmonertinib mesylate {[allProObj[0].p_purity_real_show]}
Tyrphostin AG30 {[allProObj[0].p_purity_real_show]}
EGFR-IN-12 ++

EGFR, IC50: 21 nM

{[allProObj[0].p_purity_real_show]}
Mobocertinib {[allProObj[0].p_purity_real_show]}
(Rac)-JBJ-04-125-02 {[allProObj[0].p_purity_real_show]}
(S)-Sunvozertinib {[allProObj[0].p_purity_real_show]}
BLU-945 {[allProObj[0].p_purity_real_show]}
Poziotinib +++

HER1, IC50: 3.2 nM

++

HER4, IC50: 23.5 nM

+++

HER2, IC50: 5.3 nM

{[allProObj[0].p_purity_real_show]}
TAK-285 ++

EGFR/HER1, IC50: 23 nM

+

HER4, IC50: 260 nM

++

HER2, IC50: 17 nM

{[allProObj[0].p_purity_real_show]}
ARRY-380 analog {[allProObj[0].p_purity_real_show]}
Canertinib ++++

EGFR, IC50: 1.5 nM

+++

ErbB2, IC50: 9.0 nM

{[allProObj[0].p_purity_real_show]}
Dacomitinib +++

EGFR, IC50: 6.0 nM

+

ErbB4, IC50: 73.7 nM

+

ErbB2, IC50: 45.7 nM

{[allProObj[0].p_purity_real_show]}
EGFR/ErbB-2/ErbB-4 inhibitor-2 +

ErbB4, IC50: 1.91 μM

+

ErbB2, IC50: 0.08 μM

{[allProObj[0].p_purity_real_show]}
(E/Z)-CP-724714 ++

HER2/ErbB2, IC50: 10 nM

{[allProObj[0].p_purity_real_show]}
Lapatinib ++

EGFR, IC50: 10.8 nM

+

ErbB4, IC50: 367 nM

+++

ErbB2, IC50: 9.2 nM

{[allProObj[0].p_purity_real_show]}
AEE788 ++++

EGFR, IC50: 2 nM

+

HER4/ErbB4, IC50: 160 nM

+++

HER2/ErbB2, IC50: 6 nM

c-Fms {[allProObj[0].p_purity_real_show]}
AV-412 free base ++++

EGFR, IC50: 0.75 nM

++

ErbB2, IC50: 19 nM

++++

EGFRT790M, IC50: 0.79 nM

EGFRL858R/T790M, IC50: 0.51 nM

{[allProObj[0].p_purity_real_show]}
Neratinib +

EGFR, IC50: 92 nM

+

HER2, IC50: 59 nM

Src {[allProObj[0].p_purity_real_show]}
BMS-599626 ++

HER1, IC50: 20 nM

+

HER4, IC50: 190 nM

++

HER2, IC50: 30 nM

{[allProObj[0].p_purity_real_show]}
Tucatinib +++

ErbB2, IC50: 8 nM

{[allProObj[0].p_purity_real_show]}
Allitinib ++++

EGFR, IC50: 0.5 nM

++++

ErbB4, IC50: 0.8 nM

+++

ErbB2, IC50: 3.0 nM

{[allProObj[0].p_purity_real_show]}
Pelitinib +

EGFR, IC50: 38.5 nM

+

ErbB2, IC50: 1.255 μM

Src,Raf {[allProObj[0].p_purity_real_show]}
Sapitinib +++

EGFR, IC50: 4 nM

+++

ErbB3, IC50: 4 nM

+++

ErbB2, IC50: 3 nM

{[allProObj[0].p_purity_real_show]}
CUDC-101 +++

EGFR, IC50: 2.4 nM

++

HER2, IC50: 15.7 nM

HDAC {[allProObj[0].p_purity_real_show]}
Varlitinib +++

ErbB1, IC50: 7 nM

++++

ErbB2, IC50: 2 nM

{[allProObj[0].p_purity_real_show]}
Afatinib dimaleate ++++

EGFR (wt), IC50: 0.5 nM

EGFR (L858R/T790M), IC50: 0.4 nM

++

HER2, IC50: 14 nM

{[allProObj[0].p_purity_real_show]}
Canertinib dihydrochloride +++

EGFR, IC50: 7.4 nM

+++

ErbB2, IC50: 9 nM

{[allProObj[0].p_purity_real_show]}
Allitinib tosylate ++++

EGFR (T790M/L858R), IC50: 12 nM

EGFR, IC50: 0.5 nM

++++

ErbB4, IC50: 0.8 nM

+++

ErbB2, IC50: 3.0 nM

{[allProObj[0].p_purity_real_show]}
Tyrphostin AG 528 +

EGFR, IC50: 4.9 μM

+

HER2, IC50: 2.1 μM

{[allProObj[0].p_purity_real_show]}
Afatinib ++++

EGFR (wt), IC50: 0.5 nM

EGFR (L858R), IC50: 10 nM

++++

ErbB4, IC50: 1 nM

++

HER2, IC50: 14 nM

{[allProObj[0].p_purity_real_show]}
Pyrotinib dimaleate ++

EGFR, IC50: 0.013 μM

++

HER2, IC50: 0.038 μM

{[allProObj[0].p_purity_real_show]}
Epertinib HCl ++++

EGFR, IC50: 1.48 nM

+++

HER4, IC50: 2.49 nM

+++

HER2, IC50: 7.15 nM

{[allProObj[0].p_purity_real_show]}
Tuxobertinib ++++

EGFR, Kd: 0.2 nM

++++

HER2, Kd: 0.76 nM

{[allProObj[0].p_purity_real_show]}
ALK-IN-1 ++

EGFR(C797S/del19), IC50: 138.6 nM

EGFR(del19), IC50: 36.8 nM

ALK {[allProObj[0].p_purity_real_show]}
Brigatinib +

EGFR(C797S/T790M/del19), IC50: 67.2 nM

EGFR(del19), IC50: 39.9 nM

ALK,FLT3 {[allProObj[0].p_purity_real_show]}
Avitinib ++++

EGFR L858R/T790M, IC50: 0.18 nM

BTK {[allProObj[0].p_purity_real_show]}
EAI045 {[allProObj[0].p_purity_real_show]}
Almonertinib {[allProObj[0].p_purity_real_show]}
BI-4020 ++++

EGFRdel19 T790M C797S, IC50: 0.2 nM

{[allProObj[0].p_purity_real_show]}
EGFR-IN-7 ++++

EGFRd746-750/T790M/C797S, IC50: 0.26 nM

EGFRL858R/T790M, IC50: 0.19 nM

{[allProObj[0].p_purity_real_show]}
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。
产品名称 STAT1 STAT3 STAT5 其他靶点 纯度
Nifuroxazide {[allProObj[0].p_purity_real_show]}
Fludarabine {[allProObj[0].p_purity_real_show]}
Artesunate {[allProObj[0].p_purity_real_show]}
BP-1-102 +++

STAT3, Kd: 504 nM

{[allProObj[0].p_purity_real_show]}
Niclosamide ++

STAT3, IC50: 0.7 μM

{[allProObj[0].p_purity_real_show]}
Napabucasin {[allProObj[0].p_purity_real_show]}
Cryptotanshinone ++

STAT3, IC50: 4.6 μM

{[allProObj[0].p_purity_real_show]}
Stattic +

STAT3, IC50: 5.1 μM

{[allProObj[0].p_purity_real_show]}
NSC 74859 +

STAT3, IC50: 86 μM

{[allProObj[0].p_purity_real_show]}
Ochromycinone {[allProObj[0].p_purity_real_show]}
HO-3867 {[allProObj[0].p_purity_real_show]}
C188-9 ++++

STAT3, Kd: 4.7 nM

{[allProObj[0].p_purity_real_show]}
HJC0152 {[allProObj[0].p_purity_real_show]}
SH5-07 {[allProObj[0].p_purity_real_show]}
SH-4-54 ++++

STAT3, Kd: 300 nM

+++

STAT5, Kd: 464 nM

{[allProObj[0].p_purity_real_show]}
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。
产品名称 JAK1 JAK2 JAK3 Tyk2 其他靶点 纯度
Decernotinib +++

JAK1, IC50: 11 nM

JAK1, Ki: 11 nM

+++

JAK2, Ki: 13 nM

++++

JAK3, Ki: 2.5 nM

+++

TYK2, Ki: 13 nM

{[allProObj[0].p_purity_real_show]}
ZM39923 HCl +

JAK1, pIC50: 4.4

+

JAK3, pIC50: 7.1

EGFR {[allProObj[0].p_purity_real_show]}
Cerdulatinib +++

JAK1, IC50: 12 nM

+++

JAK2, IC50: 6 nM

+++

JAK3, IC50: 8 nM

++++

TYK2, IC50: 0.5 nM

{[allProObj[0].p_purity_real_show]}
Momelotinib +++

JAK1, IC50: 11 nM

++

JAK2, IC50: 18 nM

+

JAK3, IC50: 155 nM

{[allProObj[0].p_purity_real_show]}
XL019 +

JAK1, IC50: 134.3 nM

++++

JAK2, IC50: 2.2 nM

+

JAK3, IC50: 214.2 nM

FLT3 {[allProObj[0].p_purity_real_show]}
Ruxolitinib +++

JAK1, IC50: 3.3 nM

++++

JAK2, IC50: 2.8 nM

{[allProObj[0].p_purity_real_show]}
Tofacitinib +

JAK1, IC50: 112 nM

++

JAK2, IC50: 20 nM

++++

JAK3, IC50: 1 nM

{[allProObj[0].p_purity_real_show]}
Ruxolitinib (S enantiomer) +++

JAK1, IC50: 3.3 nM

++++

JAK2, IC50: 2.8 nM

++

TYK2, IC50: 19 nM

{[allProObj[0].p_purity_real_show]}
Filgotinib +++

JAK1, IC50: 10 nM

++

JAK2, IC50: 28 nM

+

JAK3, IC50: 810 nM

+

TYK2, IC50: 116 nM

{[allProObj[0].p_purity_real_show]}
Baricitinib +++

JAK1, IC50: 5.9 nM

+++

JAK2, IC50: 5.7 nM

++

TYK2, IC50: 53 nM

{[allProObj[0].p_purity_real_show]}
Gandotinib ++

JAK1, IC50: 19.8 nM

++++

JAK2, IC50: 0.288 nM

JAK2 (V617F), Ki: 0.245 nM

++

JAK3, IC50: 48.0 nM

++

TYK2, IC50: 44 nM

FLT3 {[allProObj[0].p_purity_real_show]}
Oclacitinib maleate +++

JAK1, IC50: 10nM

++

JAK2, IC50: 18nM

+

JAK3, IC50: 99nM

+

TYK2, IC50: 84nM

{[allProObj[0].p_purity_real_show]}
NVP-BSK805 2HCl ++

JAK1, IC50: 31.63 nM

++++

JAK2, IC50: ~0.5 nM

++

JAK3, IC50: 18.68 nM

+++

TYK2, IC50: 10.76 nM

{[allProObj[0].p_purity_real_show]}
Peficitinib {[allProObj[0].p_purity_real_show]}
Go6976 FLT3 {[allProObj[0].p_purity_real_show]}
AZD-1480 ++++

JAK2, IC50: 0.26 nM

{[allProObj[0].p_purity_real_show]}
Fedratinib +++

JAK2, IC50: 3 nM

JAK2 (V617F), IC50: 3 nM

RET,FLT3 {[allProObj[0].p_purity_real_show]}
WP1066 +

JAK2, IC50: 2.3 μM

{[allProObj[0].p_purity_real_show]}
Curcumol {[allProObj[0].p_purity_real_show]}
AZ960 ++++

JAK2, IC50: <3 nM

JAK2, Ki: 0.45 nM

{[allProObj[0].p_purity_real_show]}
GLPG0634 analog {[allProObj[0].p_purity_real_show]}
CEP-33779 ++++

JAK2, IC50: 1.8 nM

{[allProObj[0].p_purity_real_show]}
FLLL32 +

JAK2, IC50: <5 μM

{[allProObj[0].p_purity_real_show]}
WHI-P154 +

JAK3, IC50: 1.8 μM

Src,VEGFR,EGFR {[allProObj[0].p_purity_real_show]}
BMS-911543 ++++

JAK2, IC50: 1.1 nM

+

JAK3, IC50: 75 nM

++

TYK2, IC50: 66 nM

{[allProObj[0].p_purity_real_show]}
TG101209 +++

JAK2, IC50: 6 nM

+

JAK3, IC50: 169 nM

RET,FLT3 {[allProObj[0].p_purity_real_show]}
AT9283 ++++

JAK2, IC50: 1.2 nM

++++

JAK3, IC50: 1.1 nM

{[allProObj[0].p_purity_real_show]}
Pacritinib ++

JAK2, IC50: 23 nM

JAK2 (V617F), IC50: 19 nM

+

JAK3, IC50: 520 nM

++

TYK2, IC50: 50 nM

FLT3 {[allProObj[0].p_purity_real_show]}
Tofacitinib citrate ++

JAK2, IC50: 20 nM

++++

JAK3, IC50: 1 nM

{[allProObj[0].p_purity_real_show]}
FM-381 ++++

JAK3, IC50: 127 pM

{[allProObj[0].p_purity_real_show]}
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

(E/Z)-AG490 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.40mL

0.68mL

0.34mL

16.99mL

3.40mL

1.70mL

33.98mL

6.80mL

3.40mL

(E/Z)-AG490 技术信息

CAS号134036-52-5
分子式C17H14N2O3
分子量 294.305
别名 Tyrphostin B 42;(E/Z)-Tyrphostin AG490;(E/Z)-Tyrphostin B42
运输蓝冰
存储条件

粉末 Keep in dark place,Inert atmosphere,Store in freezer, under -20°C

液体 -20°C:3-6个月-80°C:12个月

溶解度

DMSO: 105 mg/mL(356.77 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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