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Cat. No. Product Name Target Signaling Pathways
T12010 Aurora B inhibitor 1

Aurora Kinase Cell Cycle/Checkpoint; Chromatin/Epigenetic
Aurora B inhibitor 1 是一种 Aurora B (Aurora-1) 抑制剂(Ki <0.010 uM),具有潜在的抗癌活性,可用于研究癌症。
T35570 Chiauranib

CS2164,西奥罗尼

c-Fms; VEGFR; FLT; PDGFR; c-Kit; Aurora Kinase Angiogenesis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Tyrosine Kinase/Adaptors
Chiauranib 是一种针对肿瘤血管生成的多靶点抑制剂,具有强大的抗癌作用。 Chiauranib 有效抑制血管生成相关激酶(VEGFR1、VEGFR2、VEGFR3、PDGFRα 和 c-Kit)、有丝分裂相关激酶 Aurora B 和慢性炎症相关激酶 CSF1R,IC50 值范围为 1-9 nM。
T6435 CCT129202

2-[4-[6-氯-2-(4-二甲基氨基苯基)-3H-咪唑并[4,5-B]吡啶-7-基]哌嗪-1-基]-N-(噻唑-2-基)乙酰胺

Aurora Kinase Cell Cycle/Checkpoint; Chromatin/Epigenetic
CCT129202 是一种 ATP 竞争性泛极光激酶抑制剂,作用于 Aurora A、Aurora BAurora C,IC50 分别为 0.042 μM、0.198 μM 和 0.227 μM。
T11638 Ilorasertib hydrochloride

ABT-348 hydrochloride

Aurora Kinase Cell Cycle/Checkpoint; Chromatin/Epigenetic
Ilorasertib hydrochloride (ABT-348 hydrochloride) is an ATP-competitive multitargeted kinase inhibitor, which inhibits Aurora C, Aurora B, and Aurora A (IC50s: 1 nM, 7 nM, 120 nM). It also suppresses RET tyrosine kinase, PDGFRβ, and Flt1 (IC50s: 7 nM, 3 nM, and 32 nM).
TQ0059 Ilorasertib

ABT-348

VEGFR; FLT; c-RET; PDGFR; Aurora Kinase Angiogenesis; Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Tyrosine Kinase/Adaptors
Ilorasertib (ABT-348) 是一种 ATP 竞争性多靶点激酶抑制剂,可抑制 Aurora A、Aurora BAurora C,IC50值为120 nM、7 nM 和1 nM。它还抑制 RET 酪氨酸激酶、PDGFRβ 和 Flt1,IC50为7 nM、3 nM 和 32 nM。
T6380 AMG 900

AMG900,AMG-900,莪术醇.姜黄醇

p38 MAPK; Tyrosine Kinases; Aurora Kinase Cell Cycle/Checkpoint; Chromatin/Epigenetic; MAPK; Tyrosine Kinase/Adaptors
AMG 900 是一种有效且高度选择性的泛极光激酶抑制剂,对Aurora A、B 和C 的IC50分别为 5 nM、4 nM 和 1 nM。
T3068 AT9283

J-504568

Apoptosis; FLT; JAK; Bcr-Abl; Aurora Kinase; Autophagy Angiogenesis; Apoptosis; Autophagy; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors
AT9283 (J-504568) 是一种多靶点激酶抑制剂,抑制多种实体瘤在体内外的生长和存活,有效抑制Aurora A/B,JAK2/3,Abl (T315I),和Flt3,IC50值范围为 1-30 nM。
T6129 GSK-1070916

GSK-1070916A,GSK1070916

Apoptosis; Tie-2; FLT; AMPK; Aurora Kinase Angiogenesis; Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
GSK-1070916 (GSK-1070916A) 是一种选择性,ATP 竞争型的极光激酶B/C 抑制剂,Ki 值分别为0.38和1.5 nM。
T6039 TAK-285

TAK285,TAK 285

EGFR; MEK; HER; Aurora Kinase Angiogenesis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; JAK/STAT signaling; MAPK; Tyrosine Kinase/Adaptors
TAK-285 是一种新型 HER2 和 EGFR(HER1) 双重抑制剂,IC50 分别为 17 和 23 nM。它可穿过血脑屏障,有抗肿瘤活性,对 HER1/2 的选择性是 HER4 的 10 倍以上。
T6458 CYC-116

噻氯匹定

VEGFR; FLT; CDK; S6 Kinase; Aurora Kinase Angiogenesis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; MAPK; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
CYC116是一种有效的极光激酶 A 和 B 的抑制剂,Ki 值分别为8和9 nM。
T10412 Aurora inhibitor 1

Aurora Kinase Cell Cycle/Checkpoint; Chromatin/Epigenetic
Aurora inhibitor 1 is a potent Aurora inhibitor (IC50: ≤ 4 nM and ≤13 nM for Aurora A and Aurora B kinase).
T71169 XMD-12

XMD-12, also known as DUN57447, Aurora inhibitor (compound 1) or Aurora-IN-1, is an Auroro inhibitor, which targets Aurora A/B/C. (5.6/18.4/24.6 nM).
T71112 SAR156497

SAR156497 is an exquisitely selective Aurora A, B, and C inhibitor with in vitro and in vivo efficacy with IC50 = 0.5 nM (Aurora A); 1 nM (Aurora B / incenp); 3 nM (Aurora C / incenp) respectively SAR156497 combines high in vitro potency with satisfactory metabolic stability and limited CYP 3A4 and PDE3 inhibition. In vitro, SAR156497 displayed high antiproliferative activity on a large panel of tumor cell lines without correlation with any particular genetic signature or Aurora kinases expressi...
T6936 PF-03814735

FAK; VEGFR; FLT; Trk receptor; Aurora Kinase Angiogenesis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors
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。
T61527 GSK2646264

GSK2646264 (Compound 44) is a highly effective and specific inhibitor of spleen tyrosine kinase (SYK) with a pIC50 of 7.1. In addition to targeting SYK, GSK2646264 also inhibits several other kinases, including LCK, LRRK2, GSK3β, JAK2, VEGFR2, Aurora B, and Aurora A, with pIC50 values of 5.4, 5.4, 5.3, 5, 4.5, <4.6 and <4.3, respectively. Notably, GSK2646264 demonstrates skin penetrability, reaching both the epidermis and dermis [1].
T36199 AZD 1152 (hydrochloride)

AZD 1152 is an orally bioavailable prodrug of AZD 1152-HQPA, a selective inhibitor of Aurora kinase B (IC50= 0.36 nM).1AZD 1152 is converted to AZD 1152-HQPA in plasma. Inhibition of Aurora B results in disruption of spindle checkpoint functions and chromosome alignment, resulting in inhibition of cytokinesis followed by apoptosis.2,3AZD 1152 inhibits tumor xenograft growthin vivo.4,5 1.Mortlock, A.A., Foote, K.M., Heron, N.M., et al.Discovery, synthesis, and in vivo activity of a new class of p...
T61061 JH295 hydrate

JH295 hydrate 通过 Cys22 烷基化从而抑制细胞Nek2,它是有效的,不可逆和选择性的NIMA 相关激酶 2 (Nek2)抑制剂 (IC50 = 770 nM)。JH295 hydrate 对有丝分裂激酶 Cdk1Aurora B 或 Plk1 不具有活性,不干扰双极纺锤体组件或纺锤体组件检查点。

化合物

Aurora B inhibitor 1
Cat.No: T12010
Synonym:
Target: Aurora Kinase
Chiauranib
Cat.No: T35570
Synonym: CS2164,西奥罗尼
Target: c-Fms, VEGFR, FLT, PDGFR, c-Kit, Aurora Kinase
CCT129202
Cat.No: T6435
Synonym: 2-[4-[6-氯-2-(4-二甲基氨基苯基)-3H-咪唑并[4,5-B]吡啶-7-基]哌嗪-1-基]-N-(噻唑-2-基)乙酰胺
Target: Aurora Kinase
Ilorasertib hydrochloride
Cat.No: T11638
Synonym: ABT-348 hydrochloride
Target: Aurora Kinase
Ilorasertib
Cat.No: TQ0059
Synonym: ABT-348
Target: VEGFR, FLT, c-RET, PDGFR, Aurora Kinase
AMG 900
Cat.No: T6380
Synonym: AMG900,AMG-900,莪术醇.姜黄醇
Target: p38 MAPK, Tyrosine Kinases, Aurora Kinase
AT9283
Cat.No: T3068
Synonym: J-504568
Target: Apoptosis, FLT, JAK, Bcr-Abl, Aurora Kinase, Autophagy
GSK-1070916
Cat.No: T6129
Synonym: GSK-1070916A,GSK1070916
Target: Apoptosis, Tie-2, FLT, AMPK, Aurora Kinase
TAK-285
Cat.No: T6039
Synonym: TAK285,TAK 285
Target: EGFR, MEK, HER, Aurora Kinase
CYC-116
Cat.No: T6458
Synonym: 噻氯匹定
Target: VEGFR, FLT, CDK, S6 Kinase, Aurora Kinase
Aurora inhibitor 1
Cat.No: T10412
Synonym:
Target: Aurora Kinase
XMD-12
Cat.No: T71169
Synonym:
Target:
SAR156497
Cat.No: T71112
Synonym:
Target:
PF-03814735
Cat.No: T6936
Synonym:
Target: FAK, VEGFR, FLT, Trk receptor, Aurora Kinase
GSK2646264
Cat.No: T61527
Synonym:
Target:
AZD 1152 (hydrochloride)
Cat.No: T36199
Synonym:
Target:
JH295 hydrate
Cat.No: T61061
Synonym:
Target:
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