15 Results for "

PDPK1

" in MedChemExpress (MCE) Product Catalog:
Products (15)

15 Results for "PDPK1" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-12063
CAS No.: 1191951-57-1
Purity:  98.09%
Target:  

Akt Apoptosis

Research Areas:  

Cancer

PHT-247 is an inhibitor of the pleckstrin homology (PH) domain of Akt, and it is also an inhibitor of PDPK1 with Kis of 2.7 µM and 5.2 µM and for Akt and PDPK1, respectively.
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1
1 Cited Publications
Cat. No.: HY-123467
CAS No.: 28957-08-6
Purity:  99.68%
Lasiokaurin is an anticancer agent. Lasiokaurin can be isolated from Rabdosia rubescens (Hemsl.) H. Hara. Lasiokaurin inhibits the function of the PDPK1-AKT axis, with a Kd value of 75.93 μM for PDPK1. Lasiokaurin inhibits mTOR, STAT3, MAPK and NF-κB. Lasiokaurin reduces the mRNA and protein expression levels of PLK1. Lasiokaurin decreases DNA synthesis levels, induces cell Apoptosis, and regulates Autophagy processes. Lasiokaurin inhibits tumor growth in xenograft models. Lasiokaurin can be used in research related to nasopharyngeal carcinoma, triple-negative breast cancer [1] .
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Cat. No.: HY-RS10287
Research Areas:  

Others

PDPK1 Human Pre-designed siRNA Set A contains three designed siRNAs for PDPK1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS17027
Research Areas:  

Others

Pdpk1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Pdpk1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS23470
Research Areas:  

Others

Pdpk1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Pdpk1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-N1022
CAS No.: 72458-85-6
Target:  

NF-κB

Research Areas:  

Inflammation/Immunology Cancer

11-Hydroxytephrosin is a potent NF-κB inhibitor with an IC50 of 0.19 μM or 4.21 μM. 11-Hydroxytephrosin is isolated from A. fruticosa. 11-Hydroxytephrosin inhibits the activation of NF-κB. 11-Hydroxytephrosin can be used in research related to cervical cancer and inflammatory diseases [1].
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Cat. No.: HY-108263B
CAS No.: 155848-20-7
Synonyms: (R)-CGP52421
Target:  

FLT3 Drug Metabolite

Research Areas:  

Cancer

(R)-3-Hydroxy Midostaurin ((R)-CGP52421) is a potent kinases inhibitor. (R)-3-Hydroxy Midostaurin is a major metabolite of midostaurin (PKC412; HY-10230) undergoing by the hepatic CYP3A4 enzyme. (R)-3-Hydroxy Midostaurin has the potential for acute myeloid leukemia (AML) [1].
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Cat. No.: HY-W719359
PHT-427-d4 is the deuterium labeled PHT-427 (HY-12063). PHT-247 is an inhibitor of the pleckstrin homology (PH) domain of Akt, and it is also an inhibitor of PDPK1 with Kis of 2.7 μM and 5.2 μM and for Akt and PDPK1, respectively.
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Cat. No.: HY-P701738
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: PDPK1; 3-phosphoinositide-dependent protein kinase 1; hPDK1
Species:  
Source:  
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Cat. No.: HY-P701739
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: PDPK1; 3-phosphoinositide-dependent protein kinase 1; hPDK1
Species:  
Source:  
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Cat. No.: HY-P86174
Synonyms: PDPK1; PDK1; 3-phosphoinositide-dependent protein kinase 1; hPDK1

Host:  

Rabbit

Application:  

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

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P86089
Synonyms: PDPK1; PDK1; 3-phosphoinositide-dependent protein kinase 1; hPDK1

Host:  

Rabbit

Application:  

WB, ICC/IF, IP, ELISA

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P81824
Synonyms: PDPK1; PDK1; 3-phosphoinositide-dependent protein kinase 1; hPDK1

Host:  

Rabbit

Application:  

WB

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P81824A
Synonyms: PDPK1; PDK1; 3-phosphoinositide-dependent protein kinase 1; hPDK1

Host:  

Rabbit

Application:  

WB

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-N11231
CAS No.: 7176-02-5
Fucoxanthinol, a carotenoid, is a deacetylated Fucoxanthin (HY-N2302) metabolite with oral activity, and inhibits rat pancreatic lipase with an IC50 of 764 nM. Fucoxanthinol reduces expression of Bcl-2, Bcl-xL, survivin, XIAP, cIAP2, cyclin D1, cyclin D2, cyclin E, CDK4, CDK6, β-catenin, JunD, PPARγ, and induces GADD45α expression. Fucoxanthinol activates caspase-3, caspase-8, caspase-9, Nrf2/Keap1/ARE pathway, and inhibits activation of Akt, NF-κB, AP-1, PDPK1, GSK3β phosphorylation. Fucoxanthinol induces apoptosis, G0/G1 cell cycle arrest, inhibits cancer cell viability, proliferation, migration, invasiveness, tumour growth, adipocyte differentiation, oxidative stress, neurotoxicity, triglyceride absorption, angiogenesis, and obesity-induced inflammation. Fucoxanthinol can be used for the research of osteosarcoma, leukemia, lymphoma, adult T-cell leukemia, prostate cancer, colon cancer, breast cancer, hypertriglyceridaemia, Alzheimer’s disease, Parkinson’s disease, obesity, insulin resistance, malignant melanoma, and type II diabetes [1] .
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