23 Results for "

55684

" in MedChemExpress (MCE) Product Catalog:
Products (23)

23 Results for "55684" in MCE Product Catalog:

5
5 Cited Publications
製品番号: HY-16585
CAS 番号: 1246560-33-7
別名: SB2343
Target:  

PI3K mTOR

研究分野:  

Cancer

VS-5584 is a pan-PI3K/mTOR kinase inhibitor with IC50s of 16 nM, 68 nM, 42 nM, 25 nM, and 37 nM for PI3Kα, PI3Kβ, PI3Kδ, PI3Kγ and mTOR, respectively. VS-5584 simultaneously blocks mTORC2 as well as mTORC1.
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3
3 Cited Publications
製品番号: HY-19910
CAS 番号: 1266084-51-8
別名: SCYX-7158; AN5568
Target:  

Parasite

研究分野:  

Infection

Acoziborole (SCYX-7158) is an effective, safe and orally active antiprotozoal agent for the research of human african trypanosomiasis (HAT). In the T. b. brucei S427 strain, the MIC value for SCYX-7158 is 0.6 μg/mL .
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製品番号: HY-156628
CAS 番号: 2231294-96-3
純度:  99.51%
別名: MK-5684; ODM-208
Target:  

Cytochrome P450

研究分野:  

Cancer

Opevesostat (MK-5684; ODM-208) is an orally active and selective CYP11A1 inhibitor. Opevesostat has the potential for the research of metastatic castration-resistant prostate cancer (mCRPC) .
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製品番号: HY-161116
CAS 番号: 2306525-79-9
研究分野:  

Cancer

AD-5584 is an ACSS2 inhibitor with blood-brain permeability. AD-5584 can significantly reduce lipid storage, reduce colony formation, and increase cell death. AD-5584 has antitumor activity .
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製品番号: HY-114873
CAS 番号: 107889-31-6
別名: LY25684
LY256548 (LY25648) is an orally available anti-ischemic and anti-inflammatory compound with central nervous system activity. LY256548 is an inhibitor of phospholipase A2, 5-lipoxygenase (5-LOX), and COX, and inhibits A23187 (HY-N6687)-stimulated leukotriene B4 production. LY256548 inhibits bone damage and paw swelling in the rat Freund's complete adjuvant-induced arthritis (FCA) model .
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製品番号: HY-R01763
Target:  

MicroRNA

研究分野:  

Cancer

hsa-miR-5684 mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.
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製品番号: HY-101776A
純度:  98.63%
別名: Desmethyl-SB2343 hydrochloride
Target:  

PI3K mTOR

研究分野:  

Cancer

Desmethyl-VS-5584 hydrochloride is a dimethyl analog of VS-5584, a potent and selective mTOR/< with a pyridine[2,3-d]pyrimidine structure. b>PI3KDual inhibitor .
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製品番号: HY-101776
CAS 番号: 1246535-95-4
別名: Desmethyl-SB2343
Target:  

mTOR PI3K

研究分野:  

Cancer

Desmethyl-VS-5584 is a dimethyl analog of VS-5584 which is an potent and selective mTOR/PI3K dual inhibitor with pyrido [2,3-d] pyrimidine structure .
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製品番号: HY-R01734
Target:  

MicroRNA

研究分野:  

Cancer

hsa-miR-5584-3p mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.
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製品番号: HY-R01735
Target:  

MicroRNA

研究分野:  

Cancer

hsa-miR-5584-5p mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.
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製品番号: HY-RI01734A
Target:  

MicroRNA

研究分野:  

Cancer

hsa-miR-5584-3p antagomirs are chemically-modified oligonucleotides that hybridize with mature miRNAs. The miRNA antagomirs have 2 phosphorothioates at the 5' end, 4 phosphorothioates at the 3' end, 1 cholesterol group at the 3' end, and full-length nucleotide 2'-methoxy modification. The miRNA antagomirs strongly compete with mature miRNAs to prevent the complementary pairing of miRNAs and their target genes, thereby inhibiting miRNAs from functioning. Stability of miRNA antagomirs appears to be significantly higher than miRNA inhibitors, they exhibits enhanced cellular uptake, stability and regulatory activity in vivo.
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製品番号: HY-R01763A
Target:  

MicroRNA

研究分野:  

Cancer

hsa-miR-5684 agomirs are chemically-modified double-strand miRNA mimics with modified mature miRNA strand: 2 phosphorothioates at the 5' end, 4 phosphorothioates at the 3' end, 3' end cholesterol group, and full-length nucleotide 2'-methoxy modification. They are designed to mimic endogenous miRNAs and recommended for miRNA functional studies. Compared with miRNA mimics, they exhibits enhanced cellular uptake, stability and regulatory activity in vivo.
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製品番号: HY-RI01763
Target:  

MicroRNA

研究分野:  

Cancer

hsa-miR-5684 inhibitors are chemically-modified oligonucleotides that hybridize with mature miRNAs. The miRNA inhibitors have full-length nucleotide 2'-methoxy modification. The miRNA inhibitors strongly compete with mature miRNAs to prevent the complementary pairing of miRNAs and their target genes, thereby inhibiting miRNAs from functioning.
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製品番号: HY-RI01763A
Target:  

MicroRNA

研究分野:  

Cancer

hsa-miR-5684 antagomirs are chemically-modified oligonucleotides that hybridize with mature miRNAs. The miRNA antagomirs have 2 phosphorothioates at the 5' end, 4 phosphorothioates at the 3' end, 1 cholesterol group at the 3' end, and full-length nucleotide 2'-methoxy modification. The miRNA antagomirs strongly compete with mature miRNAs to prevent the complementary pairing of miRNAs and their target genes, thereby inhibiting miRNAs from functioning. Stability of miRNA antagomirs appears to be significantly higher than miRNA inhibitors, they exhibits enhanced cellular uptake, stability and regulatory activity in vivo.
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製品番号: HY-P85992

Host:  

Mouse

Application:  

IHC-P, ELISA

Reactivity:  

Human, Mouse, Rat

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製品番号: HY-P85876

Host:  

Mouse

Application:  

WB, ICC/IF, ELISA

Reactivity:  

Human

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製品番号: HY-R01734A
Target:  

MicroRNA

研究分野:  

Cancer

hsa-miR-5584-3p agomirs are chemically-modified double-strand miRNA mimics with modified mature miRNA strand: 2 phosphorothioates at the 5' end, 4 phosphorothioates at the 3' end, 3' end cholesterol group, and full-length nucleotide 2'-methoxy modification. They are designed to mimic endogenous miRNAs and recommended for miRNA functional studies. Compared with miRNA mimics, they exhibits enhanced cellular uptake, stability and regulatory activity in vivo.
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製品番号: HY-R01735A
Target:  

MicroRNA

研究分野:  

Cancer

hsa-miR-5584-5p agomirs are chemically-modified double-strand miRNA mimics with modified mature miRNA strand: 2 phosphorothioates at the 5' end, 4 phosphorothioates at the 3' end, 3' end cholesterol group, and full-length nucleotide 2'-methoxy modification. They are designed to mimic endogenous miRNAs and recommended for miRNA functional studies. Compared with miRNA mimics, they exhibits enhanced cellular uptake, stability and regulatory activity in vivo.
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製品番号: HY-RI01734
Target:  

MicroRNA

研究分野:  

Cancer

hsa-miR-5584-3p inhibitors are chemically-modified oligonucleotides that hybridize with mature miRNAs. The miRNA inhibitors have full-length nucleotide 2'-methoxy modification. The miRNA inhibitors strongly compete with mature miRNAs to prevent the complementary pairing of miRNAs and their target genes, thereby inhibiting miRNAs from functioning.
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製品番号: HY-RI01735
Target:  

MicroRNA

研究分野:  

Cancer

hsa-miR-5584-5p inhibitors are chemically-modified oligonucleotides that hybridize with mature miRNAs. The miRNA inhibitors have full-length nucleotide 2'-methoxy modification. The miRNA inhibitors strongly compete with mature miRNAs to prevent the complementary pairing of miRNAs and their target genes, thereby inhibiting miRNAs from functioning.
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