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Cat. No. Product Name Target Signaling Pathways
T11997 MELK-IN-1

Nintedanib Impurity L,MELK inhibitor 17,尼达尼布杂质L

MELK PI3K/Akt/mTOR signaling
MELK-IN-1 (MELK inhibitor 17)是一种母体胚胎亮氨酸拉链激酶的有效抑制剂,IC50=3 nM,Ki=0.39 nM。
T11996 MELK-8a hydrochloride

MELK PI3K/Akt/mTOR signaling
MELK-8a hydrochloride 是一种有效的母体胚胎亮氨酸拉链激酶抑制剂,IC50 为 2 nM。
T1759 OTSSP167

MELK inhibitor,OTS167

MELK PI3K/Akt/mTOR signaling
OTSSP167 (OTS167) 是一种高效的,ATP 竞争性的 MELK 抑制剂,其 IC50=0.41 nM。
T35342 MELK-8a Dihydrochloride

MELK PI3K/Akt/mTOR signaling
MELK-8a Dihydrochloride 是一种新型的母体胚胎亮氨酸拉链激酶(MELK)抑制剂,其 IC50值为2 nM。
T11725 JNJ-47117096 hydrochloride

MELK-T1 hydrochloride

Others Others
JNJ-47117096 hydrochloride is potent and selective MELK inhibitor, with an IC50 of 23 nM, also effectively inhibits Flt3, with an IC50 of 18 nM.
T62417 MELK-8a

MELK-8a (NVS-MELK8a) 是一种高效的、选择性的母体胚胎亮氨酸拉链激酶 (MELK) 抑制剂 (IC50: 2 nM)。MELK-8a 也能够抑制 Flt3 (ITD) (IC50: 0.18 μM)、Haspin (IC50: 0.19 μM)、PDGFRα (IC50: 0.42 μM)。其中 MELK 在调节癌细胞的细胞有丝分裂中具有重要作用。
T21559 OTSSP167 hydrochloride

OTSSP 167 盐酸盐

MELK PI3K/Akt/mTOR signaling
OTSSP167 hydrochloride 是一种高效的,ATP 竞争性的MELK 抑制剂,其 IC50=0.41 nM。
T4327 Prexasertib dihydrochloride

LY2606368 (dihydrochloride),Prexasertib HCl,LY2606368

Apoptosis; Chk; S6 Kinase Apoptosis; Cell Cycle/Checkpoint; MAPK; PI3K/Akt/mTOR signaling
Prexasertib dihydrochloride (LY2606368) 是一种选择性的,ATP 竞争性的细胞周期检测点激酶 1 抑制剂,Ki 为 0.9 nM,IC50为 <1 nM。它抑制 CHK2(IC50=8 nM) 和 RSK1 (IC50=9 nM)。它引起双链 DNA 断裂和复制突变,导致细胞凋亡,有抗肿瘤活性。
T4310 Prexasertib

5-[[5-[2-(3-氨基丙氧基)-6-甲氧基苯基]-1H-吡唑-3-基]氨基]-2-吡嗪甲腈,LY2606368

Apoptosis; Chk Apoptosis; Cell Cycle/Checkpoint
Prexasertib (LY2606368) 是一种具有潜在抗肿瘤活性的检查点激酶 1 抑制剂。它可引起双链 DNA 断裂和复制突变,导致细胞凋亡。
T24152 HTH-01-091

HTH-01091,HTH01-091,HTH 01-091,HTH 01091

Serine/threonin kinase; Pim; MELK; DYRK; CDK; RIP kinase Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; JAK/STAT signaling; Metabolism; NF-κB; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
HTH-01-091 是一种强效且选择性的 maternal embryonic leucine zipper kinase (MELK) 抑制剂(IC50 :10.5 nM)。HTH-01-091 对PIM1/2/3、RIPK2、DYRK3、smMLCK 和 CLK2有抑制作用。HTH-01-091 可用于研究乳腺癌。
T71197 JW-7-25-1

JW-7-25-1 is a potent multi-target inhibitor, acting on MELK, PIK3CA, mTOR, GSK3A and CDK7.
T79582 Antitumor agent-116

MELK PI3K/Akt/mTOR signaling
Antitumor agent-116 (compound 6C) 是一种显示出对MELK受体具有结合亲和力的抗肿瘤剂,它具有抗增殖活性并能诱导细胞凋亡(apoptosis)。
T73867 HTH-01-091 TFA

HTH-01-091 TFA 是一种强效且选择性的maternal embryonic leucine zipper kinase (MELK)抑制剂,其IC50为 10.5 nM。HTH-01-091 TFA 还能抑制PIM1/2/3、RIPK2、DYRK3、smMLCK 和CLK2。HTH-01-091 TFA 可用于乳腺癌研究。
T12237 NMS-P715

Casein Kinase; Kinesin; MELK; MAPK Cytoskeletal Signaling; MAPK; Metabolism; PI3K/Akt/mTOR signaling; Stem Cells
NMS-P715 是一种 ATP 竞争性MPS1选择性抑制剂,IC50值为 182 nM。
T82385 FMF-06-098-1

PROTACs PROTAC
FMF-06-098-1是一种多靶点蛋白降解剂。通过专一性降解作用,FMF-06-098-1针对多种激酶,能够有效降解AAK1, ABL2, AURKA, AURKB, BUB1B, CDC7, CDK1, CDK12, CDK13, CDK2, CDK4, CDK6, CDK7, CDK9, CHEK1, CSNK1D, EPHA1, PER, FGFR1, GAK, IRAK4, ITK, LIMK2, MAP4K2, MAP4K3, MAPK6, MAPK7, MARK4, MELK, PKN3, PLK4, PRKAA1, PTK2, PTK6, RPS6KA4, S1K2, STK35, TNK2, UHMK1, ULK1及WEE1等关键蛋白。
T16142 MRT199665

Others Others
MRT199665 is an effective and ATP-competitive, selective MARK/SIK/AMPK inhibitor (IC50s of 2/2/3/2 nM, 10/10 nM, and 110/12/43 nM for MARK1/MARK2/MARK3/MARK14, AMPKα1/AMPKα2, and SIK1/SIK2/SIK3, respectively). MRT199665 suppresses the phosphorylation of S

化合物

MELK-IN-1
Cat.No: T11997
Synonym: Nintedanib Impurity L,MELK inhibitor 17,尼达尼布杂质L
Target: MELK
MELK-8a hydrochloride
Cat.No: T11996
Synonym:
Target: MELK
OTSSP167
Cat.No: T1759
Synonym: MELK inhibitor,OTS167
Target: MELK
MELK-8a Dihydrochloride
Cat.No: T35342
Synonym:
Target: MELK
JNJ-47117096 hydrochloride
Cat.No: T11725
Synonym: MELK-T1 hydrochloride
Target: Others
MELK-8a
Cat.No: T62417
Synonym:
Target:
OTSSP167 hydrochloride
Cat.No: T21559
Synonym: OTSSP 167 盐酸盐
Target: MELK
Prexasertib dihydrochloride
Cat.No: T4327
Synonym: LY2606368 (dihydrochloride),Prexasertib HCl,LY2606368
Target: Apoptosis, Chk, S6 Kinase
Prexasertib
Cat.No: T4310
Synonym: 5-[[5-[2-(3-氨基丙氧基)-6-甲氧基苯基]-1H-吡唑-3-基]氨基]-2-吡嗪甲腈,LY2606368
Target: Apoptosis, Chk
HTH-01-091
Cat.No: T24152
Synonym: HTH-01091,HTH01-091,HTH 01-091,HTH 01091
Target: Serine/threonin kinase, Pim, MELK, DYRK, CDK, RIP kinase
JW-7-25-1
Cat.No: T71197
Synonym:
Target:
Antitumor agent-116
Cat.No: T79582
Synonym:
Target: MELK
HTH-01-091 TFA
Cat.No: T73867
Synonym:
Target:
NMS-P715
Cat.No: T12237
Synonym:
Target: Casein Kinase, Kinesin, MELK, MAPK
FMF-06-098-1
Cat.No: T82385
Synonym:
Target: PROTACs
MRT199665
Cat.No: T16142
Synonym:
Target: Others
TargetMol Loading
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