86 Results for "

PI 3-kinase

" in MedChemExpress (MCE) Product Catalog:
Products (86)

86 Results for "PI 3-kinase" in MCE Product Catalog:

13
13 Publications Verification
Cat. No.: HY-13246
CAS No.: 1032754-93-0
Purity:  99.29%
Synonyms: GDC-0980; GNE 390; RG 7422
Target:  

PI3K mTOR Apoptosis

Research Areas:  

Cancer

Apitolisib (GDC-0980; GNE 390; RG 7422) is a selective, potent, orally bioavailable Class I PI3 kinase and mTOR kinase (TORC1/2) inhibitor with IC50s of 5 nM/27 nM/7 nM/14 nM for PI3Kα/PI3Kβ/PI3Kδ/PI3Kγ, and with a?Ki?of 17 nM for mTOR.
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8
8 Cited Publications
Cat. No.: HY-P80846
Synonyms: PIK3R1; GRB1; Phosphatidylinositol 3-kinase regulatory subunit alpha; PI3-kinase regulatory subunit alpha; PI3K regulatory subunit alpha; PtdIns-3-kinase regulatory subunit alpha; Phosphatidylinositol 3-kinase 85 kDa regulatory subunit alpha; PI3-kinase s

Host:  

Rabbit

Application:  

WB, IHC-F, IHC-P, ICC/IF, ELISA

Reactivity:  

Human, Mouse, Rat

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7
7 Cited Publications
Cat. No.: HY-P81211
Synonyms: PI3-kinase p110 subunit beta; p-PI3Kβ(Ser1070); PI 3-kinase C2β; p110 BETA; p110Beta; Phosphatidylinositol 3 kinase catalytic beta polypeptide; Phosphatidylinositol 4 5 bisphosphate 3 kinase 110 kDa catalytic subunit beta; Phosphatidylinositol 4 5 bisphosphate 3 kinase catalytic subunit beta isoform; Phosphatidylinositol-4; Phosphoinositide 3 kinase catalytic beta polypeptide; PI3 kinase p110 subunit beta; PI3-kinase subunit beta; PI3K; PI3K beta; PI3K-beta; PI3Kbeta; PI3KCB; PIK3C1; PIk3cb; PK3CB_HUMAN; PtdIns 3 kinase p110; PtdIns-3-kinase subunit beta; PtdIns-3-kinase subunit p110-beta; 5-bisphosphate 3-kinase 110 kDa catalytic subunit beta; 5-bisphosphate 3-kinase catalytic subunit beta isoform.

Host:  

Rabbit

Application:  

WB, IHC-P, IHC-F, ICC/IF

Reactivity:  

Human, Mouse, Rat

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6
6 Cited Publications
Cat. No.: HY-12037A
CAS No.: 592542-59-1
Purity:  99.01%
Synonyms: ON-01910
Research Areas:  

Cancer

Rigosertib (ON-01910) is a multi-kinase inhibitor and a selective anti-cancer agent, which induces apoptosis by inhibition the PI3 kinase/Akt pathway, promots the phosphorylation of histone H2AX and induces G2/M arrest in cell cycle . Rigosertib is a selective and non-ATP-competitive inhibitor of PLK1 with an IC50 of 9 nM .
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4
4 Cited Publications
Cat. No.: HY-N2081
CAS No.: 83-95-4
Skimmianine is an orally active furoquiniline alkaloid present mainly in the Rutaceae family. Skimmianine has analgesic, antispastic, sedative, and anti-inflammatory properties. Skimmianine inhibits acetylcholinesterase (AChE) (IC50 = 8.6 μg/mL). Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity. Skimmianine has antioxidant and anti-inflammatory effects on ischemia-reperfusion (IR) injury. Skimmianine exerts anti-inflammatory effects through activation of the phosphatidylinositol-3-kinase (PI3K)-protein kinase B (AKT) pathway. Skimmianine is neuroprotective by targeting the NF-κB activation pathway to prevent neuroinflammation. Skimmianine inhibits the release of histamine, intracellular Ca 2+ signaling and protein kinase C signaling .
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4
4 Cited Publications
Cat. No.: HY-15290
CAS No.: 873305-35-2
Purity:  99.95%
Target:  

Ack1

Research Areas:  

Cancer

AIM-100 is a potent and selective Ack1 inhibitor with an IC50 of 21.58 nM. AIM-100 also inhibits Tyr 267 phosphorylation. AIM-100 does not inhibits other kinases including PI3-kinase and AKT subfamily members. AIM-100 has an anticancer effect .
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4
4 Cited Publications
Cat. No.: HY-P80867
Synonyms: PIK3R1; GRB1; Phosphatidylinositol 3-kinase regulatory subunit alpha; PI3-kinase regulatory subunit alpha; PI3K regulatory subunit alpha; PtdIns-3-kinase regulatory subunit alpha; Phosphatidylinositol 3-kinase 85 kDa regulatory subunit alpha; PI3-kinase s

Host:  

Mouse

Application:  

WB, IHC-P

Reactivity:  

Human, Mouse, Rat

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3
3 Cited Publications
Cat. No.: HY-10811
CAS No.: 1033735-94-2
Purity:  99.81%
Target:  

PI3K mTOR

Research Areas:  

Cancer

GNE-493 is a potent, selective, and orally available dual pan-PI3-kinase/mTOR inhibitor with IC50s of 3.4 nM, 12 nM, 16 nM, 16 nM and 32 nM for PI3Kα, PI3Kβ, PI3Kδ, PI3Kγ and mTOR.
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2
2 Cited Publications
Cat. No.: HY-110193
CAS No.: 1357349-91-7
Purity:  99.71%
Target:  

RET

Research Areas:  

Cancer

SPP-86 is a potent and selective cell permeable inhibitor of RET tyrosine kinase, with an IC50 of 8 nM. SPP-86 inhibits RET-induced phosphatidylinositide 3-kinases (PI3K)/Akt and MAPK signaling, also inhibits RET-induced estrogen receptorα (ERα) phosphorylation in MCF7 cells . SPP-86 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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1
1 Cited Publications
Cat. No.: HY-P703580
Purity:  ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: PIK3CA; Phosphatidylinositol-4,5-Bisphosphate 3-kinase; Phosphatidylinositol-4,5-Bisphosphate 3-kinase Catalytic Subunit Alpha; PI3-kinase P110 Subunit Alpha; Phosphatidylinositol 4,5-Bisphosphate 3-kinase Catalytic Subunit Alpha Isoform; PtdIns-3-kinase
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-P701744
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: PIK3R3; PI3-kinase Regulatory Subunit Gamma; Phosphoinositide-3-kinase Regulatory Subunit 3; PI3K Regulatory Subunit Gamma; Phosphatidylinositol 3-kinase 55 KDa Regulatory Subunit Gamma; PI3-kinase Subunit P55-Gamma; Phosphatidylinositol 3-kinase Regulato
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-P80866
Synonyms: GRB1; P85A; PI3-kinase p85-alpha subunit; PI3K; PI3K p85-alpha; P55G; PI3-kinase p85-gamma subunit; PI3K p85-gamma

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF

Reactivity:  

Human, Mouse, Rat

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1
1 Cited Publications
Cat. No.: HY-P86116

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, IP, ELISA

Reactivity:  

Human, Mouse, Rat

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1
1 Cited Publications
Cat. No.: HY-P80865
Synonyms: PI3K; PIK3; PI3CG; PI3Kgamma; p110gamma; p120-PI3K

Host:  

Mouse

Application:  

WB

Reactivity:  

Human

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Cat. No.: HY-147419
CAS No.: 2390105-79-8
Purity:  99.60%
Target:  

PI3K

Research Areas:  

Cancer

Vulolisib is a potent and orally active phosphatidylinositol 3-kinase (PI3K) inhibitor, with IC50 values of 0.2 nM, 168 nM, 90 nM and 49 nM for PI3Kα, PI3Kβ, PI3Kγ and PI3Kδ, respectively. Antiproliferative and antineoplastic activity .
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Cat. No.: HY-153120A
CAS No.: 2361009-23-4
Purity:  98.13%
Target:  

PI3K mTOR

Research Areas:  

Cancer

PI3K/mTOR Inhibitor-13 sodium is an orally active dual inhibitor of phosphoinositol 3-kinase (PI3K) and mTOR kinase. PI3K/mTOR Inhibitor-13 sodium has potential applications in sexual diseases, solid tumor and idiopathic pulmonary fibrosis (IPF) .
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Cat. No.: HY-15268
CAS No.: 1092787-12-6
Research Areas:  

Cancer

PP487 is a selective dual inhibitor of Tyrosine kinase/PI3-K, with IC50 values of 0.017 μM, 0.072 μM, 0.004 μM, 0.01 μM, 0.55 μM, 0.22 μM, and < 0.01 μM against DNA-PK, mTOR, Hck, Src, EGFR, EphB4, and PDGFR, respectively. PP487 can be used in cancer research .
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Cat. No.: HY-153120
CAS No.: 1621718-37-3
Target:  

PI3K mTOR

Research Areas:  

Cancer

PI3K/mTOR Inhibitor-13 is an orally active dual inhibitor of phosphoinositol 3-kinase (PI3K) and mTOR kinase. PI3K/mTOR Inhibitor-13 has potential applications in sexual diseases, solid tumor and idiopathic pulmonary fibrosis (IPF) .
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Cat. No.: HY-161366
CAS No.: 3033806-03-7
Target:  

PI3K

Research Areas:  

Cancer

OMS14 is exhibits inhibitory activity for phosphoinositide 3-kinase γ (PI3Kγ) and PIK3CD/PIK3R1, which inhibits 19% PI3Kγ and 65% PIK3CD/PIK3R1 activity at 100 μM. OMS14 exhibits anticancer efficacy in various cancer cells .
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Cat. No.: HY-109029
CAS No.: 1262440-25-4
Synonyms: INCB040093
Target:  

PI3K

Research Areas:  

Cancer

Dezapelisib (NCB040093) is a potent inhibitor of phosphatidylinositol 3-kinase δ (PI3Kδ). Dezapelisib is a promising research strategy for select R/R B-cell lymphomas .
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