MedChem Express
Hymenoxin (compound 7) is a dual inhibitor of iNOS and NF-κB with IC50 of 42.7 μM and 85.5 μM respectively. Hymenoxin can inhibit 16% of oxidative stress at a concentration of 125 μg/mL[1].
More Information
Supplier Page
MedChem Express
HYOU1 Human Pre-designed siRNA Set A contains three designed siRNAs for HYOU1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
HYOU1-IN-1 (Compound 33) is an inhibitor of hypoxia-upregulated protein 1 (HYOU1) with anti-inflammatory activity. HYOU1-IN-1 can be used in research on the regulation of fibroblast activation, chronic inflammation, and fibrotic diseases[1].
More Information
Supplier Page
MedChem Express
HYPK Human Pre-designed siRNA Set A contains three designed siRNAs for HYPK gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
MedChem Express
MedChem Express
I-As-1 is a potent inhibitor of Bruton’s tyrosine kinase (BTK), with the IC50 of 2.35 nM. I-As-1 shows antiproliferative activities among Ramos cells and OCI-LY10 cells with IC50s of 0.52 μM and 0.11 μM, respectively[1].
More Information
Supplier Page
MedChem Express
I-BOP is an agonist for thromboxane A2 receptor (TP) with a KD of 0.61 nM. I-BOP promotes proliferation through activation of PI3K pathway in vascular smooth muscle[1]. I-BOP dose-dependently biphasicly affects the excitatory postsynaptic potential (e.p.s.p.) in hippocampal neurons[2].
More Information
Supplier Page
MedChem Express
I-XW-053 is an inhibitor of HIV-1 capsid protein that can suppress the replication of HIV-189BZ167 with an IC50 value of 164.2 μM. I-XW-053 exhibits antiviral activity and can block the interface between capsid protein (CA) N-terminal domains (NTD-NTD interface) with micromolar affinity[1].
More Information
Supplier Page
MedChem Express
I-XW-053 is an inhibitor of HIV-1 capsid protein that can suppress the replication of HIV-189BZ167 with an IC50 value of 164.2 μM. I-XW-053 exhibits antiviral activity and can block the interface between capsid protein (CA) N-terminal domains (NTD-NTD interface) with micromolar affinity[1].
More Information
Supplier Page
MedChem Express
I-XW-053 is an inhibitor of HIV-1 capsid protein that can suppress the replication of HIV-189BZ167 with an IC50 value of 164.2 μM. I-XW-053 exhibits antiviral activity and can block the interface between capsid protein (CA) N-terminal domains (NTD-NTD interface) with micromolar affinity[1].
More Information
Supplier Page
MedChem Express
IAA/BSA is one of protein/peptide and small molecule drug conjugates (PDCs), consisting of IAA () and BSA. PCDs are promising targeted therapeutics with better cell permeability and drug selectivity than antibody-drug conjugates (ADCs). PDCs have been widely used in research on cancer, COVID-19, and metabolic diseases[1].
More Information
Supplier Page
MedChem Express
IAH1 Human Pre-designed siRNA Set A contains three designed siRNAs for IAH1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
IAPP Human Pre-designed siRNA Set A contains three designed siRNAs for IAPP gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
IARS2 Human Pre-designed siRNA Set A contains three designed siRNAs for IARS2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
IAV-IN-2 (Compound MC-22) inhibits for Influenza A Virus (IAV) through blocking the entry of IAV into host cell via clathrin-mediated endocytosis (CME)[1].
More Information
Supplier Page
MedChem Express
IB-96212 (compound 5) is a member of oligomycin class which can be extracted ftom the marine Micromonospora sp. L-25-ES25-008 ref. IB-96212 is an antitumor antibiotic against P-388, it also exhibits antimicrobial activity against Micrococcus luteus[1].
More Information
Supplier Page
MedChem Express
IBA57 Human Pre-designed siRNA Set A contains three designed siRNAs for IBA57 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
Iberverin (-Methylthiopropyl isothiocyanate) is a sulforaphane homolog. Iberverin has anticancer activity. Iberverin inhibits cell proliferation and migration. Iberverin induces mitochondrial-related apoptosis and intracellular reactive oxygen species[1].
More Information
Supplier Page
MedChem Express
Iberverin (-Methylthiopropyl isothiocyanate) is a sulforaphane homolog. Iberverin has anticancer activity. Iberverin inhibits cell proliferation and migration. Iberverin induces mitochondrial-related apoptosis and intracellular reactive oxygen species[1].
More Information
Supplier Page
MedChem Express
IBG3 is a dual-JQ1-containing BET degrader that targets protein degradation via intramolecular bivalent glues. IBG3 is a BRD2 and BRD4 bifunctional degrader with DC50 values of 8.6 pM and 6.7 pM, respectively[1].
More Information
Supplier Page
MedChem Express
Ibrexafungerp (MK 3118) is an orally active β-1,3-glucan synthesis inhibitor, with potential antifungal activity. Ibrexafungerp can be used for research of Candida and Aspergillus infections[1].
More Information
Supplier Page
MedChem Express
IBSP Human Pre-designed siRNA Set A contains three designed siRNAs for IBSP gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
IBTK Human Pre-designed siRNA Set A contains three designed siRNAs for IBTK gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
Ibutilide (fumarate) (Standard) is the analytical standard of Ibutilide (fumarate). This product is intended for research and analytical applications. Ibutilide (U70226E) fumarate, an action potential-prolonging antiarrhythmic, is a potent blocker of the rapidly activating delayed rectifier K+ current (IKr) in AT-1 cells[1].
More Information
Supplier Page
MedChem Express
ICA1 Human Pre-designed siRNA Set A contains three designed siRNAs for ICA1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
ICAM1 Human Pre-designed siRNA Set A contains three designed siRNAs for ICAM1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
ICAM2 Human Pre-designed siRNA Set A contains three designed siRNAs for ICAM2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
ICAM3 Human Pre-designed siRNA Set A contains three designed siRNAs for ICAM3 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
ICAM4 Human Pre-designed siRNA Set A contains three designed siRNAs for ICAM4 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
ICAM5 Human Pre-designed siRNA Set A contains three designed siRNAs for ICAM5 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
ICE1 Human Pre-designed siRNA Set A contains three designed siRNAs for ICE1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
ICE2 Human Pre-designed siRNA Set A contains three designed siRNAs for ICE2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
ICI-63197 is a phosphodiesterase 3 (PDE3) and PDE4 inhibitor with Ki values of 9 µM and 10 µM, respectively. ICI-63197 is selectivity against PDE1 and PDE2. ICI-63197 has antidepressant effects[1][2].
More Information
Supplier Page
MedChem Express
ICL-CCIC-0019 is an inhibitor of choline kinase α (CHKα). ICL-CCIC-0019 induces G1 block, endoplasmic reticulum stress apoptosis in cancer cell lines[1].
More Information
Supplier Page
MedChem Express
ICMT Human Pre-designed siRNA Set A contains three designed siRNAs for ICMT gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
Icopezil is a selective acetylcholinesterase (AchE) inhibitor. Icopezil can be used in Alzheimer’s disease research[1].
More Information
Supplier Page
MedChem Express
ICOS Human Pre-designed siRNA Set A contains three designed siRNAs for ICOS gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
ICOSLG Human Pre-designed siRNA Set A contains three designed siRNAs for ICOSLG gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
ID1 Human Pre-designed siRNA Set A contains three designed siRNAs for ID1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
ID2 Human Pre-designed siRNA Set A contains three designed siRNAs for ID2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
ID3 Human Pre-designed siRNA Set A contains three designed siRNAs for ID3 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
ID4 Human Pre-designed siRNA Set A contains three designed siRNAs for ID4 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
More Information
Supplier Page
MedChem Express
IDD-8E is an effective anti-pseudomonal agent (MIC =4.4 µM ) with no cytotoxicity. IDD-8E shows significant pseudomonal killing and disruption of pseudomonal biofilm. IDD-8E binds to the ATP-binding pocket of WaaP and also inhibits other ESKAPE pathogens. [1]
More Information
Supplier Page