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Homopravastatin is an impurity of Pravastatin. Form: Pale Yellow Solid Melting Point: 163-165 degrees C Solubility: Methanol, Water
Homopravastatin derivative, an impurity of Pravastatin. Form: Yellow Oil Solubility: Dichloromethane, Ethyl Acetate
Homoharringtonine (HHT) combined with some botanical drugs could induce cancer cells to resemble normal cells. HHT was prepared by a semi-synthetic method...
Homogeneous nonionic detergent with bile acid hydrophobic group. Useful in solubilization of functional opiate receptor. Form: White to Off-White Solid...
HOMER3, also known as homer protein homolog 3, is a member of the HOMER family of postsynaptic density scaffolding proteins that share a similar domain...
Homatropine methylbromide or Methylhomatropine bromide is a quaternary ammonium salt of methylhomatropine. Methylhomatropine is a peripherally acting...
Homatropine is an anticholinergic agent. Homatropine acts as an inhibitor of the muscarinic acetylcholine receptors. Homatropine is used in eye drops as a...
Histone deacetylase inhibitor. A cell-permeable, relatively non-toxic HDAC inhibitor that facilitates transcriptional activation (TGFb/Smad4) in both stable...
Histone deacetylase inhibitor. A cell-permeable, aromatic sulfonamide derivative with a hydroxamic acid group that potently inhibits mammalian HDAC by...
Histone deacetylase inhibitor. A cell-permeable inhibitor of HDAC1 and HDAC3. Shown to suppresses the growth of proliferating keratinocytes and squamous cell...
Histone deacetylase inhibitor III. A cell-permeable amide analog of Trichostatin A that potently inhibits HDACs.
Histone deacetylase inhibitor II. A cell-permeable second generation hybrid polar agent that inhibits HDAC activity. Inhibition is believed to arise as a...
Hippurate analog. Inhibitor of peptidylglycine a-hydroxylating monooxygenase (PHM). Pesticide. Form: Pale Yellow Solid Solubility: Methanol
Hippurate analog. Inhibitor of peptidylglycine a-hydroxylating monooxygenase (PHM). Pesticide. Form: Pale Yellow Solid Solubility: Methanol
Highly selective, reversible and cell permeable MEK (MAP kinase kinase) inhibitor. Blocks the phosphorylation and activation of the MAP kinase pathway. T...
Highly selective, reversible and cell permeable MEK (MAP kinase kinase) inhibitor. Blocks the phosphorylation and activation of the MAP kinase pathway. T...
Highly selective and potent non-peptide delta-opioid receptor agonist. Mediates downregulation of the delta-opioid receptor. Shows antidepressant-like...
Highly reactive, thiol-specific spin-label. Specific conformational probe of thiol site structure by its minimal rotational freedom and distance from the...
Highly reactive species. Form: White Solid Solubility: Dichloromethane, Chloroform, Ethanol, Ethyl Acetate, Methanol
Highly potent and selective Scr family tyrosine kinase inhibitor. Shows anti-Ras cancer potential by blocking Ras-induced activation of PAK1. Antitumor...
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