30 Results for "

63948

" in MedChemExpress (MCE) Product Catalog:
Products (30)

30 Results for "63948" in MCE Product Catalog:

Cat. No.: HY-19048
CAS No.: 101189-47-3
Target:  

Histamine Receptor

Research Areas:  

Endocrinology

CP-66948 is a histamine H2-receptor antagonist with gastric antisecretory activity and mucosal protective properties.
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Cat. No.: HY-47599
CAS No.: 643042-43-7
Target:  

Drug Derivative

Research Areas:  

Others

WAY-639418 is an active molecule for the study of amyloid diseases and synucleinopathies.
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Cat. No.: HY-162821
CAS No.: 3024591-38-3
Target:  

IPK Superfamily

Research Areas:  

Neurological Disease

IP6K-IN-2 (compound 29c) is an orally bioavailable and blood-brain barrier permeable IP6K inhibitor (IC50: 15.8 nM) that can be used in the study of central nervous system diseases .
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Cat. No.: HY-106027
CAS No.: 109543-76-2
Synonyms: RO 31-3948
Target:  

PPAR

Romazarit (RO 31-3948) is an anti-inflammatory agent with antirheumatic effect. Romazarit exhibits PPARα agonist activity. Romazarit (30 mg/kg) inhibits the development of hindpaw inflammation in an adjuvant arthritis model .
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Cat. No.: HY-R03354
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-6348 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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Cat. No.: HY-R03401
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-6394 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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Cat. No.: HY-R03621
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-6948-3p 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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Cat. No.: HY-R03622
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-6948-5p 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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Cat. No.: HY-RI03621
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-6948-3p 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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Cat. No.: HY-R03354A
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-6348 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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Cat. No.: HY-R03401A
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-6394 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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Cat. No.: HY-R03405
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-6398 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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Cat. No.: HY-R03405A
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-6398 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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Cat. No.: HY-RI03354
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-6348 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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Cat. No.: HY-RI03354A
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-6348 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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Cat. No.: HY-RI03401
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-6394 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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Cat. No.: HY-RI03401A
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-6394 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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Cat. No.: HY-RI03405
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-6398 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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Cat. No.: HY-RI03405A
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-6398 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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Cat. No.: HY-R03621A
Target:  

MicroRNA

Research Areas:  

Cancer

mmu-miR-6948-3p 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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