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VEGFR-IN-1 {[allProObj[0].p_purity_real_show]}

货号:A204345 同义名: VEGFR Tyrosine Kinase Inhibitor II;Vascular Endothelial Growth Factor Tyrosine Kinase Inhibitor II Ambeed 开学季,买赠积分,赢豪礼

VEGFR-IN-1是一种高效的血管生成抑制剂,能够抑制 KDR、Flt-1、c-Kit、EGF-R 和 c-Src,IC50 分别为 0.02、0.18、0.24、7.3 和 7 µM,适用于与血管生成相关的癌症及其他疾病的研究。

VEGFR-IN-1 化学结构 CAS号:269390-69-4
VEGFR-IN-1 化学结构
CAS号:269390-69-4
VEGFR-IN-1 3D分子结构
CAS号:269390-69-4
VEGFR-IN-1 化学结构 CAS号:269390-69-4
VEGFR-IN-1 3D分子结构 CAS号:269390-69-4
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VEGFR-IN-1 纯度/质量文件 产品仅供科研

货号:A204345 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 VEGFR1 VEGFR2 VEGFR3 其他靶点 纯度
Motesanib Diphosphate ++++

VEGFR1, IC50: 2 nM

++++

VEGFR2, IC50: 3 nM

VEGFR2/Flk1, IC50: 3 nM

+++

VEGFR3, IC50: 6 nM

RET,PDGFR {[allProObj[0].p_purity_real_show]}
Tivozanib ++

VEGFR1, IC50: 30 nM

+++

VEGFR2, IC50: 6.5 nM

++

VEGFR3, IC50: 15 nM

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

VEGFR1, IC50: 380 nM

++

VEGFR2, IC50: 25 nM

Flk1, IC50: 25 nM

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

VEGFR1, IC50: 13 nM

+++

VEGFR2, IC50: 4.2 nM

+

VEGFR3, IC50: 46 nM

RET {[allProObj[0].p_purity_real_show]}
Pazopanib +++

VEGFR1, IC50: 10 nM

++

VEGFR2, IC50: 30 nM

+

VEGFR3, IC50: 47 nM

FGFR,c-Kit,PDGFR {[allProObj[0].p_purity_real_show]}
Sitravatinib +++

VEGFR1 (FLT1), IC50: 6 nM

+++

VEGFR2 (KDR), IC50: 5 nM

++++

VEGFR3 (FLT4), IC50: 2 nM

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

VEGFR1/FLT1, IC50: 6.8 nM

++++

KDR, IC50: 0.86 nM

++++

VEGFR3/FLT4, IC50: 2.8 nM

Tie-2 {[allProObj[0].p_purity_real_show]}
MGCD-265 analog ++++

VEGFR1, IC50: 3 nM

++++

VEGFR2, IC50: 3 nM

++++

VEGFR3, IC50: 4 nM

Tie-2 {[allProObj[0].p_purity_real_show]}
Lactate +++

VEGFR1/FLT1, IC50: 10 nM

+++

VEGFR2/Flk1, IC50: 13 nM

+++

VEGFR3/FLT4, IC50: 8 nM

c-Kit,FLT3 {[allProObj[0].p_purity_real_show]}
AEE788 +

FLT1, IC50: 59 nM

+

KDR, IC50: 77 nM

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

VEGFR1/FLT1, IC50: 3 nM

++++

VEGFR2/KDR, IC50: 4 nM

+

VEGFR3/FLT4, IC50: 190 nM

FLT3 {[allProObj[0].p_purity_real_show]}
Vatalanib 2HCl +

VEGFR1/FLT1, IC50: 77 nM

++

VEGFR2/KDR, IC50: 37 nM

VEGFR2/Flk1, IC50: 270 nM

+

VEGFR3/FLT4, IC50: 660 nM

c-Kit,c-Fms {[allProObj[0].p_purity_real_show]}
Axitinib ++++

VEGFR1/FLT1, IC50: 0.1 nM

++++

VEGFR2/KDR, IC50: 0.2 nM

VEGFR2/Flk1, IC50: 0.18 nM

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

VEGFR1/FLT1, IC50: 10 nM

+++

VEGFR2/Flk1, IC50: 13 nM

+++

VEGFR3/FLT4, IC50: 8 nM

c-Kit,FLT3 {[allProObj[0].p_purity_real_show]}
ZM 306416 +

VEGFR1, IC50: 0.33 μM

Src {[allProObj[0].p_purity_real_show]}
KRN-633 +

VEGFR1, IC50: 170 nM

+

VEGFR2, IC50: 160 nM

+

VEGFR3, IC50: 125 nM

c-Kit,BTK {[allProObj[0].p_purity_real_show]}
OSI-930 +++

FLT1, IC50: 8 nM

+++

KDR, IC50: 9 nM

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

VEGFR1/FLT1, IC50: 22 nM

++++

VEGFR2/KDR, IC50: 4.0 nM

+++

VEGFR3/FLT4, IC50: 5.2 nM

{[allProObj[0].p_purity_real_show]}
NVP-BAW2881 +

hVEGFR1, IC50: 820 nM

+++

mVEGF2, IC50: 165 nM

hVEGFR2, IC50: 9 nM

+

hVEGFR3, IC50: 420 nM

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

VEGFR1/FLT1, IC50: 5 nM

++++

VEGFR2/KDR, IC50: 0.5 nM

c-Kit {[allProObj[0].p_purity_real_show]}
Nintedanib ++

VEGFR1, IC50: 34 nM

+++

VEGFR2, IC50: 13 nM

+++

VEGFR3, IC50: 13 nM

FLT3 {[allProObj[0].p_purity_real_show]}
BMS-794833 ++

VEGFR2, IC50: 15 nM

{[allProObj[0].p_purity_real_show]}
SKLB1002 ++

VEGFR2, IC50: 32 nM

{[allProObj[0].p_purity_real_show]}
Cabozantinib S-malate ++++

VEGFR2/KDR, IC50: 0.035 nM

{[allProObj[0].p_purity_real_show]}
Ki8751 ++++

VEGFR2, IC50: 0.9 nM

c-Kit {[allProObj[0].p_purity_real_show]}
SU 5402 ++

VEGFR2, IC50: 20 nM

{[allProObj[0].p_purity_real_show]}
Rivoceranib Mesylate ++++

VEGFR2, IC50: 1 nM

RET {[allProObj[0].p_purity_real_show]}
Ponatinib ++++

VEGFR2, IC50: 1.5 nM

{[allProObj[0].p_purity_real_show]}
LY2874455 +++

VEGFR2, IC50: 7 nM

{[allProObj[0].p_purity_real_show]}
ZM323881 HCl ++++

VEGFR2, IC50: <2 nM

{[allProObj[0].p_purity_real_show]}
AZD2932 +++

VEGFR-2, IC50: 8 nM

c-Kit {[allProObj[0].p_purity_real_show]}
Cabozantinib ++++

VEGFR2/KDR, IC50: 0.035 nM

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

VEGFR2, IC50: 90 nM

VEGFR2/Flk1, IC50: 90 nM

{[allProObj[0].p_purity_real_show]}
CYC-116 ++

VEGFR2, Ki: 44 nM

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

VEGFR2, IC50: 16 nM

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

VEGFR2 , IC50: 80 nM

FLT3 {[allProObj[0].p_purity_real_show]}
RAF265 ++

VEGFR2, EC50: 30 nM

{[allProObj[0].p_purity_real_show]}
PD173074 {[allProObj[0].p_purity_real_show]}
BFH772 ++++

VEGFR2, IC50: 3 nM

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

VEGFR2/Flk1, IC50: 1.23 μM

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

VEGFR2, IC50: 40 nM

+

VEGFR3, IC50: 110 nM

EGFR {[allProObj[0].p_purity_real_show]}
SAR131675 ++

VEGFR3, IC50: 23 nM

{[allProObj[0].p_purity_real_show]}
ENMD-2076 +

VEGFR2/KDR, IC50: 58.2 nM

++

VEGFR3/FLT4, IC50: 15.9 nM

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

VEGFR2, IC50: 6 nM

++++

VEGFR3, IC50: 4 nM

c-Kit {[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 EGFR/ErbB1 ErbB3 ErbB4 HER2/ErbB2 mutant EGFR 其他靶点 纯度
WZ-3146 ++++

EGFR (E746_A750), IC50: 2 nM

EGFR (E746_A750/T790M), IC50: 14 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 (L861Q), IC50: 4 nM

EGFR, IC50: 5 nM

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

EGFR (wt), Ki: 303.3 nM

EGFR (L858R/T790M), Ki: 21.5 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 ++

WT EGFR, IC50: 12.92 nM

L858R/T790M EGFR, IC50: 11.44 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 ++++

WT EGFR, IC50: 76 nM

L858R/T790M EGFR, IC50: 2 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 L858R, IC50: 2 nM

EGFR(d746-750), IC50: 1.4 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

Raf,Src {[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 (L858R/T790M), IC50: 0.4 nM

EGFR (wt), IC50: 0.5 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, IC50: 0.5 nM

EGFR (T790M/L858R), IC50: 12 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 (L858R), IC50: 10 nM

EGFR (wt), IC50: 0.5 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(del19), IC50: 36.8 nM

EGFR(C797S/del19), IC50: 138.6 nM

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

EGFR(del19), IC50: 39.9 nM

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

EGFRL858R/T790M, IC50: 0.19 nM

EGFRd746-750/T790M/C797S, IC50: 0.26 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 c-Kit 其他靶点 纯度
Tyrphostin AG1296 +

c-Kit (Swiss 3T3), IC50: 1.8 μM

PDGFR {[allProObj[0].p_purity_real_show]}
Masitinib +

Kit, IC50: 200 nM

{[allProObj[0].p_purity_real_show]}
Motesanib Diphosphate +++

Kit, IC50: 8 nM

{[allProObj[0].p_purity_real_show]}
Ki8751 ++

c-Kit, IC50: 40 nM

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

c-Kit, IC50: 78 nM

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

c-Kit, IC50: 140 nM

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

Kit, IC50: 6 nM

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

Kit, IC50: 10 nM

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

c-Kit, IC50: 2 nM

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

c-Kit (D816H), IC50: 10 nM

{[allProObj[0].p_purity_real_show]}
Imatinib Mesylate +

c-Kit, IC50: 100 nM

PDGFR {[allProObj[0].p_purity_real_show]}
AZD2932 +++

c-Kit, IC50: 9 nM

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

Kit, IC50: 1.7 nM

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

c-Kit, IC50: 2 nM

FLT3 {[allProObj[0].p_purity_real_show]}
Sunitinib FLT3 {[allProObj[0].p_purity_real_show]}
OSI-930 +

Kit, IC50: 80 nM

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

c-Kit, IC50: 1 nM

{[allProObj[0].p_purity_real_show]}
Dasatinib monohydrate ++

c-Kit (D816V), IC50: 37 nM

c-Kit (wt), IC50: 79 nM

Src {[allProObj[0].p_purity_real_show]}
Dasatinib ++

c-Kit (D816V), IC50: 37 nM

c-Kit (wt), IC50: 79 nM

Src {[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。

VEGFR-IN-1 生物活性

描述 VEGFR-IN-1 acts as a strong inhibitor of angiogenesis, exhibiting IC50 values of 0.02 µM for KDR, 0.18 µM for Flt-1, 0.24 µM for c-Kit, 7.3 µM for EGF-R, and 7 µM for c-Src, respectively[1].

VEGFR-IN-1 参考文献

[1]Furet P, et al. Identification of a new chemical class of potent angiogenesis inhibitors based on conformational considerations and database searching. Bioorg Med Chem Lett. 2003;13(18):2967-2971.

VEGFR-IN-1 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.96mL

0.59mL

0.30mL

14.80mL

2.96mL

1.48mL

29.60mL

5.92mL

2.96mL

VEGFR-IN-1 技术信息

CAS号269390-69-4
分子式C19H16ClN3O
分子量 337.803
别名 VEGFR Tyrosine Kinase Inhibitor II;Vascular Endothelial Growth Factor Tyrosine Kinase Inhibitor II
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: 120 mg/mL(355.24 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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