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Aurora Kinase

Aurora Kinase

Aurora kinases are serine/threonine kinases that are essential for cell proliferation. They are phosphotransferase enzymes that help the dividing cell dispense its genetic materials to its daughter cells. More specifically, Aurora kinases play a crucial role in cellular division by controlling chromatid segregation. Defects in this segregation can cause genetic instability, a condition which is highly associated with tumorigenesis.
TargetMol
1 2 3 4
Cat. No. Product Name CAS No. Purity Chemical Structure
T10412 Aurora inhibitor 1
化合物 T10412
2227019-45-4 98%
TargetMol Chemical Structure Aurora inhibitor 1
Aurora inhibitor 1 is a potent Aurora inhibitor (IC50: ≤ 4 nM and ≤13 nM for Aurora A and Aurora B kinase).
T78753 Aurora Kinases-IN-4
化合物 Aurora Kinases-IN-4
2877011-84-0 98%
TargetMol Chemical Structure Aurora Kinases-IN-4
Aurora Kinases-IN-4(Compound 11c)是共价ATP竞争型aurora kinaseA抑制剂,具有IC50为1.7 nM。该化合物对SJSA-1、MDA-MB-231、A549和HeLa细胞系的增殖抑制效果显著,其IC50分别为4.27、1.54、3.08和6.99 μM。Aurora Kina...
T82931 Aurora A inhibitor 3
化合物 Aurora A inhibitor 3
98%
TargetMol Chemical Structure Aurora A inhibitor 3
Aurora A inhibitor3 (Compound 5h) 是一种抑制Aurora-A激酶活性的化合物,IC50为0.78 μM。该化合物同时对MCF-7和MDA-MB-231细胞线表现出细胞毒性,其GI50值分别为0.12 μM和0.63 μM。
T83459 11α-O-Tigloyl-12β-O-acetyltenacigenin B
化合物 11α-O-Tigloyl-12β-O-acetyltenacigenin B
154022-51-2 98%
TargetMol Chemical Structure 11α-O-Tigloyl-12β-O-acetyltenacigenin B
11α-O-Tigloyl-12β-O-acetyltenacigenin B 是Tenacigenin B 的酯类衍生物,源自藤黄藤 (MTC)。该化合物具有调节Aurora-A活性,对淋巴瘤显示出潜在的抗肿瘤效果。
T11958 MBM-17
化合物 T11958
2083621-90-1 98%
TargetMol Chemical Structure MBM-17
MBM-17 is a potent inhibitor of NIMA-related kinase 2 (Nek2,IC50 of 3 nM). It effectively inhibits the proliferation of cancer cells by inducing cell cycle arres...
T6936 PF-03814735
化合物PF-03814735
942487-16-3 98%
TargetMol Chemical Structure PF-03814735
PF-03814735 是一种新型、有效和可逆的极光激酶 A 和 B 抑制剂,IC50值分别为0.8和5 nM。
T11959 MBM-17S
化合物 T11959
2083621-91-2 98%
TargetMol Chemical Structure MBM-17S
MBM-17S, a potent NIMA-related kinase 2 (Nek2) inhibitor with an IC50 of 3 nM, effectively inhibits cancer cell proliferation by inducing cell cycle arrest and a...
T16862 SCH-1473759
化合物 T16862
1094069-99-4 98%
TargetMol Chemical Structure SCH-1473759
SCH-1473759 is an inhibitor of the aurora (IC50s: 4 and 13 nM for Aurora A and B, respectively).
T8537 Tripolin A
化合物Tripolin A
1148118-92-6 98%
TargetMol Chemical Structure Tripolin A
Tripolin A 是一种特异性的非 ATP 竞争性 Aurora A 激酶抑制剂,对Aurora A 和Aurora B 的IC50分别为1.5 μM 和7 μM。
T12864 SCH-1473759 hydrochloride
化合物SCH-1473759 hydrochloride
1094067-13-6 98%
TargetMol Chemical Structure SCH-1473759 hydrochloride
SCH-1473759 hydrochloride 是一种多靶点极光激酶抑制剂,对极光激酶 A 和 B 的 IC50值分别为 4 和13 nM。
T11638 Ilorasertib hydrochloride
化合物 T11638
1847485-91-9 98%
TargetMol Chemical Structure Ilorasertib hydrochloride
Ilorasertib hydrochloride (ABT-348 hydrochloride) is an ATP-competitive multitargeted kinase inhibitor, which inhibits Aurora C, Aurora B, and Aurora A (IC50s: 1...
T15829 L 888607 Racemate
化合物 T15829
1030017-51-6 98%
TargetMol Chemical Structure L 888607 Racemate
L 888607 Racemate is a selective antagonist of prostaglandin D2 receptor subtype 1 (DP1) (Kis: 132 nM and 17 nM for DP1 and thromboxane A2 receptor (TP), respect...
T14926 Centrinone-B
化合物 T14926
1798871-31-4 98%
TargetMol Chemical Structure Centrinone-B
Centrinone-B (LCR-323) is a potent and highly selective inhibitor of PLK4 (Ki: 0.59 nM).
T23426 TC-A 2317 hydrochloride
化合物TC-A 2317 hydrochloride
1245907-03-2 98%
TargetMol Chemical Structure TC-A 2317 hydrochloride
TC-A 2317 hydrochloride 是 Aurora 激酶 A 的抑制剂,Ki 为 1.2 nM,而 Aurora 激酶 B 的 Ki 为 101 nM。 TC-A 2317 hydrochloride 显示出抗肿瘤活性。
T11960 MBM-55
化合物MBM-55
2083622-09-5 99.98%
TargetMol Chemical Structure MBM-55
MBM-55 是一种有效的中心体相关激酶 2 (NEK2) 抑制剂,IC50 为 1 nM。 MBM-55 通过诱导细胞周期停滞和凋亡有效抑制癌细胞的增殖。
T2509 Tozasertib
化合物Tozasertib
639089-54-6 99.96%
TargetMol Chemical Structure Tozasertib
Tozasertib (MK-0457) 是一种 Aurora A/B/C 激酶抑制剂,Ki 值分别为 0.6、18和4.6 nM。它显示出对 190 多种不同激酶的选择性。
T2617 SNS-314 Mesylate
化合物SNS-314 Mesylate
1146618-41-8 99.92%
TargetMol Chemical Structure SNS-314 Mesylate
SNS-314 Mesylate (SNS-314) 是一种有效且特异性的极光激酶抑制剂,对极光激酶 A、B、C 的 IC50值分别为 9,31 和 3 nM。
T2341 KW-2449
化合物KW2449
1000669-72-6 99.89%
TargetMol Chemical Structure KW-2449
KW-2449是一种多靶点激酶抑制剂,对FLT3,ABL,ABLT315I 和极光激酶的IC50值分别为6.6,14,4 和 48 nM。
T4428 CCT241736
化合物CCT241736
1402709-93-6 99.88%
TargetMol Chemical Structure CCT241736
CCT241736 是一种口服生物可利用的双重 FLT3/Aurora 激酶抑制剂,还抑制临床相关的 FLT3 耐药突变体,包括 FLT3-ITD 和 FLT3。它是 CCT137690 的高级类似物,是治疗人类恶性肿瘤的临床前开发候选物。
T2118 SC-514
化合物SC-514
354812-17-2 99.88%
TargetMol Chemical Structure SC-514
SC-514 (GK 01140) 是 IKK-2 的选择性抑制剂 (IC50=11.2 μM),不抑制其他 IKK 亚型或其他丝氨酸-苏氨酸和酪氨酸激酶。
Aurora inhibitor 1
T10412
Aurora inhibitor 1 is a potent Aurora inhibitor (IC50: ≤ 4 nM and ≤13 nM for Aurora A and Aurora B kinase).
Aurora Kinases-IN-4
T78753
Aurora Kinases-IN-4(Compound 11c)是共价ATP竞争型aurora kinaseA抑制剂,具有IC50为1.7 nM。该化合物对SJSA-1、MDA-MB-231、A549和HeLa细胞系的增殖抑制效果显著,其IC50分别为4.27、1.54、3.08和6.99 μM。Aurora Kina...
Aurora A inhibitor 3
T82931
Aurora A inhibitor3 (Compound 5h) 是一种抑制Aurora-A激酶活性的化合物,IC50为0.78 μM。该化合物同时对MCF-7和MDA-MB-231细胞线表现出细胞毒性,其GI50值分别为0.12 μM和0.63 μM。
11α-O-Tigloyl-12β-O-acetyltenacigenin B
T83459
11α-O-Tigloyl-12β-O-acetyltenacigenin B 是Tenacigenin B 的酯类衍生物,源自藤黄藤 (MTC)。该化合物具有调节Aurora-A活性,对淋巴瘤显示出潜在的抗肿瘤效果。
MBM-17
T11958
MBM-17 is a potent inhibitor of NIMA-related kinase 2 (Nek2,IC50 of 3 nM). It effectively inhibits the proliferation of cancer cells by inducing cell cycle arres...
PF-03814735
T6936
PF-03814735 是一种新型、有效和可逆的极光激酶 A 和 B 抑制剂,IC50值分别为0.8和5 nM。
MBM-17S
T11959
MBM-17S, a potent NIMA-related kinase 2 (Nek2) inhibitor with an IC50 of 3 nM, effectively inhibits cancer cell proliferation by inducing cell cycle arrest and a...
SCH-1473759
T16862
SCH-1473759 is an inhibitor of the aurora (IC50s: 4 and 13 nM for Aurora A and B, respectively).
Tripolin A
T8537
Tripolin A 是一种特异性的非 ATP 竞争性 Aurora A 激酶抑制剂,对Aurora A 和Aurora B 的IC50分别为1.5 μM 和7 μM。
SCH-1473759 hydrochloride
T12864
SCH-1473759 hydrochloride 是一种多靶点极光激酶抑制剂,对极光激酶 A 和 B 的 IC50值分别为 4 和13 nM。
Ilorasertib hydrochloride
T11638
Ilorasertib hydrochloride (ABT-348 hydrochloride) is an ATP-competitive multitargeted kinase inhibitor, which inhibits Aurora C, Aurora B, and Aurora A (IC50s: 1...
L 888607 Racemate
T15829
L 888607 Racemate is a selective antagonist of prostaglandin D2 receptor subtype 1 (DP1) (Kis: 132 nM and 17 nM for DP1 and thromboxane A2 receptor (TP), respect...
Centrinone-B
T14926
Centrinone-B (LCR-323) is a potent and highly selective inhibitor of PLK4 (Ki: 0.59 nM).
TC-A 2317 hydrochloride
T23426
TC-A 2317 hydrochloride 是 Aurora 激酶 A 的抑制剂,Ki 为 1.2 nM,而 Aurora 激酶 B 的 Ki 为 101 nM。 TC-A 2317 hydrochloride 显示出抗肿瘤活性。
MBM-55
T11960
MBM-55 是一种有效的中心体相关激酶 2 (NEK2) 抑制剂,IC50 为 1 nM。 MBM-55 通过诱导细胞周期停滞和凋亡有效抑制癌细胞的增殖。
Tozasertib
T2509
Tozasertib (MK-0457) 是一种 Aurora A/B/C 激酶抑制剂,Ki 值分别为 0.6、18和4.6 nM。它显示出对 190 多种不同激酶的选择性。
SNS-314 Mesylate
T2617
SNS-314 Mesylate (SNS-314) 是一种有效且特异性的极光激酶抑制剂,对极光激酶 A、B、C 的 IC50值分别为 9,31 和 3 nM。
KW-2449
T2341
KW-2449是一种多靶点激酶抑制剂,对FLT3,ABL,ABLT315I 和极光激酶的IC50值分别为6.6,14,4 和 48 nM。
CCT241736
T4428
CCT241736 是一种口服生物可利用的双重 FLT3/Aurora 激酶抑制剂,还抑制临床相关的 FLT3 耐药突变体,包括 FLT3-ITD 和 FLT3。它是 CCT137690 的高级类似物,是治疗人类恶性肿瘤的临床前开发候选物。
SC-514
T2118
SC-514 (GK 01140) 是 IKK-2 的选择性抑制剂 (IC50=11.2 μM),不抑制其他 IKK 亚型或其他丝氨酸-苏氨酸和酪氨酸激酶。
1 2 3 4
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