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SU11652 {[allProObj[0].p_purity_real_show]}

货号：A581825

SU11652 is a sunitinib analog with anti-tyrosine-kinase activity, also is identified as a potential inhibitor for Leishmania major (Lm) nucleoside diphosphate kinases NDK and structural studies indicated that this molecule binds to the active site of LmNDK in a similar conformation to nucleotides, mimicking natural substrates.

SU11652 化学结构
CAS号：326914-10-7

SU11652 3D分子结构
CAS号：326914-10-7

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SU11652 纯度/质量文件产品仅供科研

货号：A581825 标准纯度： {[allProObj[0].p_purity_real_show]} 产品说明书

批次查询：批次纯度: COA SDS NMR HPLC CNMR LC-MS

全球学术期刊中引用的产品: • JACS Au, 2024. Ambeed. [ A148168 ]; • JMC, 2024. Ambeed. [ A187643 ]; • JMC, 2024. Ambeed. [ A341145 , A633512 , A607865 , A167774 ]; • Biomacromolecules, 2024. Ambeed. [ A110759 ]; • Biomacromolecules, 2024. Ambeed. [ A203543 ]; 更多 >

VEGFR 亚型比较
c-Kit 亚型比较
PDGFR 亚型比较
FGFR 亚型比较

产品名称	VEGFR1 ↓ ↑	VEGFR2 ↓ ↑	VEGFR3 ↓ ↑	其他靶点	纯度
Motesanib Diphosphate	++++ VEGFR1, IC50: 2 nM	++++ VEGFR2/Flk1, IC50: 3 nM VEGFR2, 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	c-Kit,FGFR,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/Flk1, IC50: 270 nM VEGFR2/KDR, IC50: 37 nM	+ VEGFR3/FLT4, IC50: 660 nM	c-Kit,c-Fms	{[allProObj[0].p_purity_real_show]}
Axitinib	++++ VEGFR1/FLT1, IC50: 0.1 nM	++++ VEGFR2/Flk1, IC50: 0.18 nM VEGFR2/KDR, IC50: 0.2 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	+++ hVEGFR2, IC50: 9 nM mVEGF2, IC50: 165 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/Flk1, IC50: 90 nM VEGFR2, 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	FLT3,RET	{[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	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 (wt), IC50: 79 nM c-Kit (D816V), IC50: 37 nM	Src	{[allProObj[0].p_purity_real_show]}
Dasatinib	++ c-Kit (wt), IC50: 79 nM c-Kit (D816V), IC50: 37 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。

产品名称	PDGFR ↓ ↑	PDGFRα ↓ ↑	PDGFRβ ↓ ↑	其他靶点	纯度
Tyrphostin A9	+ PDGFR, IC50: 0.5 μM			EGFR	{[allProObj[0].p_purity_real_show]}
Tyrphostin AG1296					{[allProObj[0].p_purity_real_show]}
Motesanib Diphosphate	++ PDGFR, IC50: 84 nM				{[allProObj[0].p_purity_real_show]}
Pazopanib	++ PDGFR, IC50: 84 nM				{[allProObj[0].p_purity_real_show]}
Imatinib	+ PDGFR, IC50: 100 nM			c-Kit	{[allProObj[0].p_purity_real_show]}
Imatinib Mesylate	+ PDGFR, IC50: 100 nM			c-Kit	{[allProObj[0].p_purity_real_show]}
Sennoside B	✔				{[allProObj[0].p_purity_real_show]}
PP121	++++ PDGFR, IC50: 2 nM			mTOR,VEGFR	{[allProObj[0].p_purity_real_show]}
Crenolanib		++++ PDGFRα, Kd: 2.1 nM	++++ PDGFRβ, Kd: 3.2 nM		{[allProObj[0].p_purity_real_show]}
Masitinib		+ PDGFRα, IC50: 540 nM	+ PDGFRβ, IC50: 800 nM		{[allProObj[0].p_purity_real_show]}
Ki8751		++ PDGFRα, IC50: 67 nM		c-Kit	{[allProObj[0].p_purity_real_show]}
Tivozanib		++ PDGFRα, IC50: 40 nM	++ PDGFRβ, IC50: 49 nM		{[allProObj[0].p_purity_real_show]}
Ponatinib		++++ PDGFRα, IC50: 1.1 nM			{[allProObj[0].p_purity_real_show]}
Amuvatinib		++ PDGFRα (V561D), IC50: 40 nM			{[allProObj[0].p_purity_real_show]}
Axitinib		+++ PDGFRα, IC50: 5.0 nM	++++ PDGFRβ, IC50: 1.6 nM		{[allProObj[0].p_purity_real_show]}
CP-673451		+++ PDGFRα, IC50: 10 nM	++++ PDGFRβ, IC50: 1 nM		{[allProObj[0].p_purity_real_show]}
Telatinib		+++ PDGFRα, IC50: 15 nM		c-Kit	{[allProObj[0].p_purity_real_show]}
Nintedanib		++ PDGFRα, IC50: 59 nM	++ PDGFRβ, IC50: 65 nM		{[allProObj[0].p_purity_real_show]}
Avapritinib		++++ PDGFRα (D842V), IC50: 0.5 nM			{[allProObj[0].p_purity_real_show]}
MK-2461			+++ PDGFRβ, IC50: 22 nM		{[allProObj[0].p_purity_real_show]}
Lactate			+++ PDGFRβ, IC50: 27 nM	c-Kit,FLT3	{[allProObj[0].p_purity_real_show]}
Linifanib			++ PDGFRβ, IC50: 66 nM		{[allProObj[0].p_purity_real_show]}
AZD2932			+++ PDGFRβ, IC50: 4 nM	c-Kit	{[allProObj[0].p_purity_real_show]}
Dovitinib			+++ PDGFRβ, IC50: 27 nM	c-Kit,FLT3	{[allProObj[0].p_purity_real_show]}
Sorafenib			++ PDGFRβ, IC50: 57 nM mPDGFRβ, IC50: 57 nM		{[allProObj[0].p_purity_real_show]}
Sunitinib			++++ PDGFRβ , IC50: 2 nM	FLT3	{[allProObj[0].p_purity_real_show]}
Orantinib			+++ PDGFRβ, Ki: 8 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	FGFR ↓ ↑	FGFR1 ↓ ↑	FGFR2 ↓ ↑	FGFR3 ↓ ↑	FGFR4 ↓ ↑	其他靶点	纯度
Tyrphostin AG1296	+ FGFR (Swiss 3T3), IC50: 12.3 μM					PDGFR	{[allProObj[0].p_purity_real_show]}
Pazopanib	+ FGFR, IC50: 140 nM						{[allProObj[0].p_purity_real_show]}
Erdafitinib	✔					RET	{[allProObj[0].p_purity_real_show]}
Gambogenic acid	✔						{[allProObj[0].p_purity_real_show]}
Sulfatinib		+++ FGFR1, IC50: 15 nM					{[allProObj[0].p_purity_real_show]}
Nintedanib esylate		+ FGFR1, IC50: 69 nM	++ FGFR2, IC50: 37 nM	+ FGFR3, IC50: 108 nM			{[allProObj[0].p_purity_real_show]}
Zoligratinib		+++ FGFR1, IC50: 9.3 nM	+++ FGFR2, IC50: 7.6 nM	++ FGFR3, IC50: 22 nM	+ FGFR4, IC50: 290 nM		{[allProObj[0].p_purity_real_show]}
MK-2461		+ FGFR1, IC50: 65 nM	++ FGFR2, IC50: 39 nM	++ FGFR3, IC50: 50 nM			{[allProObj[0].p_purity_real_show]}
SU 5402		++ FGFR1, IC50: 30 nM					{[allProObj[0].p_purity_real_show]}
Brivanib		+ FGFR1, IC50: 148 nM					{[allProObj[0].p_purity_real_show]}
Lucitanib		++ FGFR1, IC50: 17.5 nM	+ FGFR2, IC50: 82.5 nM				{[allProObj[0].p_purity_real_show]}
Ponatinib		++++ FGFR1, IC50: 2.2 nM					{[allProObj[0].p_purity_real_show]}
PD-166866		+ FGFR1, IC50: 52.4 nM					{[allProObj[0].p_purity_real_show]}
Narazaciclib		++ FGFR1, IC50: 26 nM				RET	{[allProObj[0].p_purity_real_show]}
Lactate		+++ FGFR1, IC50: 8 nM		+++ FGFR3, IC50: 9 nM		c-Kit,FLT3	{[allProObj[0].p_purity_real_show]}
Lenvatinib mesylate		++ FGFR1, IC50: 46 nM				c-RET	{[allProObj[0].p_purity_real_show]}
LY2874455		++++ FGFR1, IC50: 2.8 nM	++++ FGFR2, IC50: 2.6 nM	+++ FGFR3, IC50: 6.4 nM	+++ FGFR4, IC50: 6 nM		{[allProObj[0].p_purity_real_show]}
FIIN-2		+++ FGFR1, IC50: 3.09 nM	+++ FGFR2, IC50: 4.3 nM	++ FGFR3, IC50: 27 nM	++ FGFR4, IC50: 45.3 nM		{[allProObj[0].p_purity_real_show]}
FIIN-3		+++ FGFR1, IC50: 13.1 nM	++ FGFR2, IC50: 21 nM	++ FGFR3, IC50: 31.4 nM	++ FGFR4, IC50: 35.3 nM		{[allProObj[0].p_purity_real_show]}
Infigratinib		++++ FGFR1, IC50: 0.9 nM	++++ FGFR2, IC50: 1.4 nM	++++ FGFR3, IC50: 1.0 nM FGFR3 (K650E), IC50: 4.9 nM	+ FGFR4, IC50: 60 nM		{[allProObj[0].p_purity_real_show]}
Danusertib		++ FGFR1, IC50: 47 nM				RET	{[allProObj[0].p_purity_real_show]}
R1530		++ FGFR1, IC50: 28 nM					{[allProObj[0].p_purity_real_show]}
ENMD-2076		+ FGFR1, IC50: 92.7 nM	+ FGFR2, IC50: 70.8 nM			FLT3,RET	{[allProObj[0].p_purity_real_show]}
Dovitinib		+++ FGFR1, IC50: 8 nM		+++ FGFR3, IC50: 9 nM		c-Kit,FLT3	{[allProObj[0].p_purity_real_show]}
Sorafenib		+ FGFR1, IC50: 580 nM					{[allProObj[0].p_purity_real_show]}
SSR128129E		+ FGFR1, IC50: 1.9 μM					{[allProObj[0].p_purity_real_show]}
AZD-4547		++++ FGFR1, IC50: 0.2 nM	++++ FGFR2, IC50: 2.5 nM	++++ FGFR3, IC50: 1.8 nM			{[allProObj[0].p_purity_real_show]}
Lenvatinib		++ FGFR1, IC50: 46 nM				RET	{[allProObj[0].p_purity_real_show]}
PD173074		++ FGFR1, IC50: ~25 nM					{[allProObj[0].p_purity_real_show]}
S49076		++ FGFR1, IC50: 18 nM	+++ FGFR2, IC50: 17 nM	+++ FGFR3, IC50: 15 nM			{[allProObj[0].p_purity_real_show]}
Futibatinib		++++ FGFR1, IC50: 1.8 nM	++++ FGFR2, IC50: 1.4 nM	++++ FGFR3, IC50: 1.6 nM	+++ FGFR4, IC50: 3.7 nM		{[allProObj[0].p_purity_real_show]}
Ferulic Acid		+ FGFR1, IC50: 3.78 μM	+ FGFR2, IC50: 12.5 μM				{[allProObj[0].p_purity_real_show]}
Nintedanib		+ FGFR1, IC50: 69 nM	++ FGFR2, IC50: 37 nM	+ FGFR3, IC50: 108 nM	+ FGFR4, IC50: 610 nM		{[allProObj[0].p_purity_real_show]}
ASP5878		++++ FGFR1, IC50: 0.47 nM	++++ FGFR2, IC50: 0.6 nM	++++ FGFR3, IC50: 0.74 nM	+++ FGFR4, IC50: 3.5 nM		{[allProObj[0].p_purity_real_show]}
PRN1371		++++ FGFR1, IC50: 0.6 nM	++++ FGFR2, IC50: 1.3 nM	+++ FGFR3, IC50: 4.1 nM	++ FGFR4, IC50: 19.3 nM		{[allProObj[0].p_purity_real_show]}
Derazantinib		+++ FGFR1, IC50: 4.5 nM	++++ FGFR2, IC50: 1.8 nM	+++ FGFR3, IC50: 4.5 nM	++ FGFR4, IC50: 34 nM	RET	{[allProObj[0].p_purity_real_show]}
ODM-203		+++ FGFR1, IC50: 11 nM	+++ FGFR2, IC50: 16 nM	+++ FGFR3, IC50: 6 nM	++ FGFR4, IC50: 35 nM		{[allProObj[0].p_purity_real_show]}
Pemigatinib		++++ FGFR1, IC50: 0.4 nM	++++ FGFR2, IC50: 0.5 nM	++++ FGFR3, IC50: 1.2 nM	++ FGFR4, IC50: 30 nM		{[allProObj[0].p_purity_real_show]}
SKLB 610			✔			PDGFR	{[allProObj[0].p_purity_real_show]}
Alofanib			✔				{[allProObj[0].p_purity_real_show]}
Lirafugratinib			✔				{[allProObj[0].p_purity_real_show]}
Masitinib mesylate				✔		FAK	{[allProObj[0].p_purity_real_show]}
BLU9931				+ FGFR3, IC50: 150 nM	+++ FGFR4, IC50: 3 nM		{[allProObj[0].p_purity_real_show]}
BO-264				✔			{[allProObj[0].p_purity_real_show]}
Fisogatinib					+++ FGFR4, IC50: 5 nM		{[allProObj[0].p_purity_real_show]}
H3B-6527					++++ FGFR4, IC50: <1.2 nM		{[allProObj[0].p_purity_real_show]}
Roblitinib					++++ FGFR4, IC50: 1.9 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。

SU11652 生物活性

描述

SU11652 is a sunitinib analog with anti-tyrosine-kinase activity, also is identified as a potential inhibitor for Leishmania major (Lm) nucleoside diphosphate kinases NDK and structural studies indicated that this molecule binds to the active site of LmNDK in a similar conformation to nucleotides, mimicking natural substrates.

SU11652 参考文献

[1]Ellegaard AM, Groth-Pedersen L, et al. Sunitinib and SU11652 inhibit acid sphingomyelinase, destabilize lysosomes, and inhibit multidrug resistance. Mol Cancer Ther. 2013 Oct;12(10):2018-30.

[2]Guo Y, Chen Y, et al. SU11652 Inhibits tyrosine kinase activity of FLT3 and growth of MV-4-11 cells. J Hematol Oncol. 2012 Dec 6;5:72.

SU11652 实验方案

计算器

存储液制备

1mg

5mg

10mg

1 mM

5 mM

10 mM

2.41mL

0.48mL

0.24mL

12.05mL

2.41mL

1.21mL

24.10mL

4.82mL

2.41mL

SU11652 技术信息

CAS号	326914-10-7
分子式	C₂₂H₂₇ClN₄O₂
分子量	414.928

别名
运输	蓝冰

存储条件

粉末

液体 -20°C:3-6个月-80°C:12个月

溶解度

DMSO: 9 mg/mL(21.69 mM)，配合低频超声，并水浴加热至45℃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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最近浏览的产品

大规格询价

摩尔计算器

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总药量计算器

工作液计算器

细胞研究

临床研究

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