48 Results for "

Pim2

" in MedChemExpress (MCE) Product Catalog:
Products (48)

48 Results for "Pim2" in MCE Product Catalog:

  • Isoforms Recommended:
  • Targets Recommended:
  • Recombinant Proteins Recommended:
Cat. No.: HY-115590
CAS No.: 1902983-63-4
Research Areas:  

Cancer

JP-11646 is a pan-PIM inhibitor with increased potency against PIM2 (IC50 = 0.5 nM). JP11646 is freely reversible and ATP non-competitive. JP-11646 results in a decrease of PIM1, 2, and 3 mRNA. JP-11646 can effectively inhibit cell viability in small cell lung cancer (SCLC) and large cell neuroendocrine carcinomas of the lung (LCNEC). JP-11646 can cause a decrease in p-4EBP-1 protein, increasing the cleavage of caspases while decreasing caspase-3. JP-11646 induces apoptosis or necroptosis in cells. JP-11646 leads to reductions in MYC paralogs. JP-11646 can be used for the study of SCLC, LCNEC, human acute leukemia (AML), multiple myeloma (MM), and triple-negative breast cancer (TNBC) [2] .
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Cat. No.: HY-RS10551
Research Areas:  

Others

Pim2 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Pim2 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-101783
CAS No.: 1527523-39-2
Target:  

Pim

Research Areas:  

Cancer

GNE-955 is a potent and orally active pan Pim kinase inhibitor with Kis of 0.018, 0.11, 0.08 nM for Pim1, Pim2, Pim3, respectively.
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Cat. No.: HY-124638
CAS No.: 1889336-59-7
Purity:  99.38%
Target:  

MNK

Research Areas:  

Cancer

MNK inhibitor 9 is a potent and selective inhibitor of MNK1/2 with IC50 values of 0.003 µM and 0.003 µM for MNK1 and MNK2 respectively. MNK inhibitor 9 has good cell permeability. MNK inhibitor 9 can be used in tumor related research .
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Cat. No.: HY-164460
CAS No.: 1204181-93-0
Target:  

Pim

Research Areas:  

Cancer

AZD1897 is a PIM1, PIM2, and PIM3 inhibitor with IC50 values of less than 3 nM for these three PIM kinases. AZD1897 exhibits anticancer activity and synergistically inhibits the activity of acute myeloid leukemia (AML) cells in combination with Capivasertib (HY-15431). This synergistic inhibitory effect is achieved through the inhibition of the mTOR and MCL1 pathways [2].
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Cat. No.: HY-RS10550
Research Areas:  

Others

PIM2 Human Pre-designed siRNA Set A contains three designed siRNAs for PIM2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS10552
Research Areas:  

Others

Pim2 Rat Pre-designed siRNA Set A contains three designed siRNAs for Pim2 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-15901
CAS No.: 1210417-75-6
Target:  

mTOR

Research Areas:  

Cancer

LGB321 is an inhibitor of PIM2-dependent multiple myeloma cell lines, effectively inhibiting proliferation and key signaling pathways such as mTOR-C1 and phosphorylation of BAD .
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Cat. No.: HY-13287A
CAS No.: 1173928-26-1
Target:  

Pim Apoptosis Autophagy

Research Areas:  

Inflammation/Immunology Cancer

SGI-1776 is an inhibitor of Pim kinases, with IC50s of 7 nM, 363 nM, and 69 nM for Pim-1, Pim-2 and Pim-3, respectively [2] .
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Cat. No.: HY-126379
CAS No.: 1883650-96-1
Purity:  98.07%
Target:  

Apoptosis

Research Areas:  

Cancer

CDDO-2P-Im is an analogue of CDDO-Imidazolide with chemopreventive effect. CDDO-2P-Im can reduce the size and the severity of the lung tumors in mouse lung cancer model .
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Cat. No.: HY-157404
CAS No.: 2918764-16-4
Target:  

Pim

Research Areas:  

Cancer

Pim-1/2 kinase inhibitor 2 (compound 5b) is a competitive PIM-1 and PIM-2 kinase inhibitor with IC50s of 1.31 μM and 0.67 μM, respectively. Pim-1/2 kinase inhibitor 2 shows in-vitro low cytotoxicity against normal human lung fibroblast Wi-38 cell line and potent in-vitro anticancer activity against myeloid leukaemia (NFS-60), liver (HepG-2), prostate (PC-3), and colon (Caco-2) cancer cell lines .
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Cat. No.: HY-P701746
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Pim2; Pim-2h; Pim-2 Proto-Oncogene, Serine/Threonine Kinase; Proto-Oncogene Pim-2 (Serine Threonine Kinase); Serine/Threonine-Protein Kinase Pim-2; Non-Specific Serine/Threonine Protein Kinase; Pim-2 Oncogene
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P701747
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Pim2; Pim-2h; Pim-2 Proto-Oncogene, Serine/Threonine Kinase; Proto-Oncogene Pim-2 (Serine Threonine Kinase); Serine/Threonine-Protein Kinase Pim-2; Non-Specific Serine/Threonine Protein Kinase; Pim-2 Oncogene
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P706086
Purity:  ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: Pim2; Pim-2h; Pim-2 Proto-Oncogene, Serine/Threonine Kinase; Proto-Oncogene Pim-2 (Serine Threonine Kinase); Serine/Threonine-Protein Kinase Pim-2; Non-Specific Serine/Threonine Protein Kinase; Pim-2 Oncogene
Species:  
Human
Source:  
Sf9 insect cells
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Cat. No.: HY-160006
CAS No.: 1006699-45-1
Target:  

Pim

Research Areas:  

Cancer

PIM-IN-2 (Pim-2) is a Pim kinases inhibitor (IC50 = 25 nM). PIM-IN-2 promotes cell survival, is antiapoptotic, and has exhibited an elevated level of expression in a variety of human tumors .
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Cat. No.: HY-P83005
Synonyms: Pim2; Serine/threonine-protein kinase Pim-2; Pim-2h

Host:  

Rabbit

Application:  

WB, ICC/IF, IP

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-168479
Target:  

Pim

Research Areas:  

Infection Cancer

VB1080 (compound 12) is a potent PIM inhibitor with IC50 values of 69.5, 4996, 9.88 µM for PIM1, PIM2, PIM3, respectively. VB1080 shows cytotoxicity. VB1080 shows anthelmintic activity .
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Cat. No.: HY-163442A
Target:  

Pim

Research Areas:  

Cancer

PIM3-IN-1 hydrochloride (Compound 19a) is an inhibitor of (PIM2/3), with the highest inhibition level being against PIM3, having an IC50 value in the nanomolar range. PIM3-IN-1 hydrochloride can be used in cancer research .
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Cat. No.: HY-19322C
Synonyms: (1S,3R,5R)-LGH447 dihydrochloride
Target:  

Pim

Research Areas:  

Cancer

(1S,3R,5R)-PIM447 (dihydrochloride) an PIM inhibitor extracted from patent US 20100056576 A1, compound example 72, has IC50 values of 0.095 μM for Pim1, 0.522 μM for Pim2 and 0.369 μM for Pim3.
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Cat. No.: HY-184811
CAS No.: 2698319-19-4
Target:  

Pim

Research Areas:  

Cancer

PIM-IN-6 is an inhibitor of PIM1 and PIM2, with an IC50 of 254 nM against PIM1 and an IC50 of 1.78 μM against PIM2. PIM-IN-6 can be used for the research of acute myeloid leukemia .
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