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PI3K

PI3K

Phosphoinositide 3-kinases (PI3Ks), also called phosphatidylinositol 3-kinases, are a family of enzymes involved in cellular functions such as cell growth, proliferation, differentiation, motility, survival and intracellular trafficking, which in turn are involved in cancer.PI3Ks are a family of related intracellular signal transducer enzymes capable of phosphorylating the 3 position hydroxyl group of the inositol ring of phosphatidylinositol (PtdIns). The pathway, with oncogene PIK3CA and tumor suppressor PTEN, is implicated in the sensitivity of cancer tumors to insulin and IGF1, and in calorie restriction.
TargetMol
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Cat. No. Product Name CAS No. Purity Chemical Structure
TQ0003L 740 Y-P(TFA)(1236188-16-1 free base)
化合物740 Y-P(TFA)
TQ0003L 98%
TargetMol Chemical Structure 740 Y-P(TFA)(1236188-16-1 free base)
740 Y-P(TFA)(1236188-16-1 free base) (740YPDGFR(TFA)) 是一种有效的细胞渗透性 PI3K 激活剂。
T72374 PI3K/mTOR Inhibitor-12
化合物 PI3K/mTOR Inhibitor-12
2891692-83-2 98%
TargetMol Chemical Structure PI3K/mTOR Inhibitor-12
PI3K/mTOR Inhibitor-12为口服有效且选择性的PI3K/mTOR抑制剂,对PI3Kα和mTOR的IC50分别为0.06 nM及3.12 nM,表现出抗肿瘤活性且肝毒性较低。
T72713 PI3K/VEGFR2-IN-1
化合物 PI3K/VEGFR2-IN-1
2851067-08-6 98%
TargetMol Chemical Structure PI3K/VEGFR2-IN-1
PI3K/VEGFR2-IN-1是一种具有双重抑制效应的化合物,对PI3K和VEGFR2的IC50分别为2.21 μM和68 μM,能够诱导细胞凋亡(apoptosis),在癌症研究中应用。
T12467 PI4KIII beta inhibitor 3
化合物 T12467
1245319-54-3 98%
TargetMol Chemical Structure PI4KIII beta inhibitor 3
PI4KIII beta inhibitor 3 is a novel and high effective inhibitor of PI4KIIIβ (IC50 of 5.7 nM).
T74782 CXJ-2
化合物 CXJ-2
2919976-92-2 98%
TargetMol Chemical Structure CXJ-2
CXJ-2,一种环状肽,对EDP(弹性蛋白衍生肽)具中等亲和力。该化合物有效抑制PI3K/ERK通路,减少肝星状细胞的增殖与迁移,展现出显著的抗纤维化能力。
T11610 Idelalisib D5
化合物 T11610
1830330-31-8 98%
TargetMol Chemical Structure Idelalisib D5
Idelalisib D5 is a deuterium-labeled Idelalisib. Idelalisib is a highly selective and orally bioavailable p110δ inhibitor.
TN5201 Uncarinic acid E
化合物 TN5201
277751-61-8 98%
TargetMol Chemical Structure Uncarinic acid E
Uncarinic acid E has anti-cancer activity, it induces apoptosis in HepG2 cells via accumulation of p53, alters the Bax/Bcl-2 ratio, and activates caspases, resul...
T16908 Sonolisib
化合物 T16908
502632-66-8 98%
TargetMol Chemical Structure Sonolisib
Sonolisib is an irreversible and pan-isoform inhibitor of PI3K (IC50=0.1 nM (p110α), 1.0 nM (p120γ), 2.9 nM (p110δ)).
T12458 PI3K-IN-9
化合物 T12458
2360875-63-2 98%
TargetMol Chemical Structure PI3K-IN-9
PI3K-IN-9 is a potent and selective inhibitor of PI3Kδ(IC50 of 8.9 nM).
T17066 Umbralisib hydrochloride
化合物 T17066
1532533-78-0 98%
TargetMol Chemical Structure Umbralisib hydrochloride
Umbralisib hydrochloride is a novel PI3Kδ inhibitor (IC50 and EC50 of 22.2 nM and 24.3 nM, respectively). Umbralisib hydrochloride is also active against CK1ε (E...
TN5050 Sprengerinin C
化合物 TN5050
88861-91-0 98%
TargetMol Chemical Structure Sprengerinin C
Sprengerinin C exerts anti-tumorigenic effects in hepatocellular carcinoma via inhibition of proliferation and angiogenesis and induction of apoptosis, it can st...
T10660L2 CAL-130 Racemate
化合物 T10660L2
474012-90-3 98%
TargetMol Chemical Structure CAL-130 Racemate
CAL-130 Racemate is the racemate of CAL-130. CAL-130 is a PI3Kδ and PI3Kγ inhibitor (IC50s: 1.3 and 6.1 nM).
T77629 FD274
化合物FD274
2641899-38-7 98%
TargetMol Chemical Structure FD274
FD274 是一种高效的 PI3K/mTOR 双重抑制剂,对 PI3Kα/β/γ/δ 和 mTOR 具有抑制作用, IC50 分别为 0.65 nM、1.57 nM、0.65 nM、0.42 nM 和 2.03 nM。 FD274 在 AML 细胞系抗增殖实验中显示出显着的抗增殖活性。 FD274 在 HL-60 异种移...
T15800 LY117018
化合物 T15800
63676-25-5 98%
TargetMol Chemical Structure LY117018
LY117018 shows antiproliferative effects on breast cancer cell lines. LY117018 is a Raloxifene analog and is a selective estrogen receptor modulator.
T11818 LAS191954
化合物 T11818
1403947-26-1 98%
TargetMol Chemical Structure LAS191954
LAS191954 is a selective, potent and orally active PI3Kδ inhibitor for inflammatory diseases treatment(IC50 : 2.6 nM).
TN4213 Hirsutenone
化合物 TN4213
41137-87-5 98%
TargetMol Chemical Structure Hirsutenone
Hirsutenone has potent antioxidant activity, it shows significant free radical scavenging activity and exhibits inhibition effect on the mitochondrial lipid pero...
T3229 Cytochalasin D
细胞松弛素D
22144-77-0 98%
TargetMol Chemical Structure Cytochalasin D
Cytochalasin D is an actin inhibitor, the removal of actin stress fibers is crucial for the chondrogenic differentiation. It may be an inhibitor of some fertiliz...
TN3323 Monomethyl lithospermate
紫草酸单甲酯
933054-33-2 98%
TargetMol Chemical Structure Monomethyl lithospermate
Monomethyl lithospermate (Lithospermic acid monomethyl ester) 具有潜在的抗病毒活性,通过激活PI5K/Akt信号传导,减轻体内大脑中动脉闭塞小鼠缺血性中风损伤,并在体外保护氧葡萄糖剥夺/复氧诱导的SHSY-3Y细胞。Monomethyl lithosperma...
TN3753 Dalbergioidin
化合物 TN3753
30368-42-4 98%
TargetMol Chemical Structure Dalbergioidin
Dalbergioidin exhibits tyrosinase inhibitory activity with an IC50 of 20 mM. It shows a melanin biosynthesis inhibition zone in the culture plate of Streptomyces...
TN1367 Alismol
化合物Alismol
87827-55-2 98%
TargetMol Chemical Structure Alismol
Alismol has antihypertensive action, it decreases cardiac output, heart rate and left ventricular pressure, but it increases coronary flow, it has been used for ...
740 Y-P(TFA)(1236188-16-1 free base)
TQ0003L
740 Y-P(TFA)(1236188-16-1 free base) (740YPDGFR(TFA)) 是一种有效的细胞渗透性 PI3K 激活剂。
PI3K/mTOR Inhibitor-12
T72374
PI3K/mTOR Inhibitor-12为口服有效且选择性的PI3K/mTOR抑制剂,对PI3Kα和mTOR的IC50分别为0.06 nM及3.12 nM,表现出抗肿瘤活性且肝毒性较低。
PI3K/VEGFR2-IN-1
T72713
PI3K/VEGFR2-IN-1是一种具有双重抑制效应的化合物,对PI3K和VEGFR2的IC50分别为2.21 μM和68 μM,能够诱导细胞凋亡(apoptosis),在癌症研究中应用。
PI4KIII beta inhibitor 3
T12467
PI4KIII beta inhibitor 3 is a novel and high effective inhibitor of PI4KIIIβ (IC50 of 5.7 nM).
CXJ-2
T74782
CXJ-2,一种环状肽,对EDP(弹性蛋白衍生肽)具中等亲和力。该化合物有效抑制PI3K/ERK通路,减少肝星状细胞的增殖与迁移,展现出显著的抗纤维化能力。
Idelalisib D5
T11610
Idelalisib D5 is a deuterium-labeled Idelalisib. Idelalisib is a highly selective and orally bioavailable p110δ inhibitor.
Uncarinic acid E
TN5201
Uncarinic acid E has anti-cancer activity, it induces apoptosis in HepG2 cells via accumulation of p53, alters the Bax/Bcl-2 ratio, and activates caspases, resul...
Sonolisib
T16908
Sonolisib is an irreversible and pan-isoform inhibitor of PI3K (IC50=0.1 nM (p110α), 1.0 nM (p120γ), 2.9 nM (p110δ)).
PI3K-IN-9
T12458
PI3K-IN-9 is a potent and selective inhibitor of PI3Kδ(IC50 of 8.9 nM).
Umbralisib hydrochloride
T17066
Umbralisib hydrochloride is a novel PI3Kδ inhibitor (IC50 and EC50 of 22.2 nM and 24.3 nM, respectively). Umbralisib hydrochloride is also active against CK1ε (E...
Sprengerinin C
TN5050
Sprengerinin C exerts anti-tumorigenic effects in hepatocellular carcinoma via inhibition of proliferation and angiogenesis and induction of apoptosis, it can st...
CAL-130 Racemate
T10660L2
CAL-130 Racemate is the racemate of CAL-130. CAL-130 is a PI3Kδ and PI3Kγ inhibitor (IC50s: 1.3 and 6.1 nM).
FD274
T77629
FD274 是一种高效的 PI3K/mTOR 双重抑制剂,对 PI3Kα/β/γ/δ 和 mTOR 具有抑制作用, IC50 分别为 0.65 nM、1.57 nM、0.65 nM、0.42 nM 和 2.03 nM。 FD274 在 AML 细胞系抗增殖实验中显示出显着的抗增殖活性。 FD274 在 HL-60 异种移...
LY117018
T15800
LY117018 shows antiproliferative effects on breast cancer cell lines. LY117018 is a Raloxifene analog and is a selective estrogen receptor modulator.
LAS191954
T11818
LAS191954 is a selective, potent and orally active PI3Kδ inhibitor for inflammatory diseases treatment(IC50 : 2.6 nM).
Hirsutenone
TN4213
Hirsutenone has potent antioxidant activity, it shows significant free radical scavenging activity and exhibits inhibition effect on the mitochondrial lipid pero...
Cytochalasin D
T3229
Cytochalasin D is an actin inhibitor, the removal of actin stress fibers is crucial for the chondrogenic differentiation. It may be an inhibitor of some fertiliz...
Monomethyl lithospermate
TN3323
Monomethyl lithospermate (Lithospermic acid monomethyl ester) 具有潜在的抗病毒活性,通过激活PI5K/Akt信号传导,减轻体内大脑中动脉闭塞小鼠缺血性中风损伤,并在体外保护氧葡萄糖剥夺/复氧诱导的SHSY-3Y细胞。Monomethyl lithosperma...
Dalbergioidin
TN3753
Dalbergioidin exhibits tyrosinase inhibitory activity with an IC50 of 20 mM. It shows a melanin biosynthesis inhibition zone in the culture plate of Streptomyces...
Alismol
TN1367
Alismol has antihypertensive action, it decreases cardiac output, heart rate and left ventricular pressure, but it increases coronary flow, it has been used for ...
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