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Results for "

SL 0101-1

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Antibiotic (4) Bacterial (3) Fungal (4) MicroRNA (4) Ribosomal S6 Kinase (RSK) (1) Small Interfering RNA (siRNA) (1)
By Research Areas:	Cancer (5) Infection (4) Inflammation/Immunology (2)

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Isotope-Labeled Compounds

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-15237

SL 0101-1 4 Publications Verification SL0101	Ribosomal S6 Kinase (RSK)	Cancer
SL 0101-1 (SL0101), a kaempferol glycoside, isolated from the tropical plant F. refracta, is a cell-permeable, selective, reversible, ATP-competitive p90 Ribosomal S6 Kinase (RSK) inhibitor, with an IC₅₀ of 89 nM . SL 0101-1 (SL0101) is a selective RSK1/2 inhibitor, with a K_i of 1 μM .

HY-B0101

Fluconazole Maximum Cited Publications 10 Publications Verification UK-49858	Fungal Antibiotic Bacterial	Infection Cancer
Fluconazole (UK-49858) is a triazole antifungal agent with excellent activities against a broad range of fungi, especially against Candida albicans. Fluconazole inhibits C. albicans and Candida kefyr with IC₉₉s range from 0.20 μg/mL to 0.39 μg/mL .

HY-N0101

Neohesperidin 5 Publications Verification Hesperetin 7-O-neohesperidoside	Others	Inflammation/Immunology
Neohesperidin is a flavonoid compound found in high amounts in citrus fruits with anti-oxidant and anti-inflammatory effects.

HY-B0101A

Fluconazole hydrate UK 49858 hydrate	Fungal Antibiotic Bacterial	Infection Cancer
Fluconazole (hydrate) is a triazole antifungal drug used in the treatment and prevention of superficial and systemic fungal infections.

HY-B0101B

Fluconazole mesylate UK 49858 mesylate	Fungal Antibiotic Bacterial	Infection Cancer
Fluconazole (mesylate) is a triazole antifungal drug used in the treatment and prevention of superficial and systemic fungal infections.

HY-B0101S

Fluconazole-d4 UK-49858-d₄	Fungal Antibiotic	Infection
Fluconazole-d₄ is the deuterium labeled Fluconazole. Fluconazole (UK-49858) is a triazole antifungal agent with excellent activities against a broad range of fungi, especially against Candida albicans. Fluconazole inhibits C. albicans and Candida kefyr with IC99s range from 0.20 μg/mL to 0.39 μg/mL[1].

HY-R01011

hsa-miR-4327 mimic	MicroRNA	Cancer
hsa-miR-4327 mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.

hsa-miR-4327 mimic hsa-miR-4327 mimic

HY-R01011A

hsa-miR-4327 agomir	MicroRNA
hsa-miR-4327 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.

hsa-miR-4327 agomir hsa-miR-4327 agomir

HY-RI01011

hsa-miR-4327 inhibitor	MicroRNA
hsa-miR-4327 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.

hsa-miR-4327 inhibitor hsa-miR-4327 inhibitor

HY-RI01011A

hsa-miR-4327 antagomir	MicroRNA
hsa-miR-4327 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.

hsa-miR-4327 antagomir hsa-miR-4327 antagomir

HY-N0101R

Neohesperidin (Standard) Hesperetin 7-O-neohesperidoside (Standard)	Others	Inflammation/Immunology
Neohesperidin (Standard) is the analytical standard of Neohesperidin. This product is intended for research and analytical applications. Neohesperidin is a flavonoid compound found in high amounts in citrus fruits with anti-oxidant and anti-inflammatory effects.

HY-RS01011

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

ARNT Human Pre-designed siRNA Set A ARNT Human Pre-designed siRNA Set A

FCH Group Screening Library	2,244,487 compounds
FCH Group Screening Library Collection contains about 2,244,487 lead-like compounds for biological screening. This brand new collection comprises polar molecules with pharmacologically important groups such as free carboxylic and amino groups.

Palmitoyl dipeptide-5 diaminohydroxybutyrate	Peptides	Others
Palmitoyl dipeptide-5 diaminohydroxybutyrate is a bioactive peptide with anti-aging effect and has been reported used as a cosmetic ingredient .

Cat. No.	Product Name	Category	Target	Chemical Structure