Cat.No. | Name | Information |
---|---|---|
M43612 | H-γ-Glu-Gln-OH | H-γ-Glu-Gln-OH is a hydrophilic peptide and can be conjugated to drugs. |
M42109 | 8-Epixanthatin | 8-Epixanthatin is a potential colchicine binding site inhibitor isolated from Xanthium chinese Mill. |
M41127 | Quinine sulfate hydrate | Quinine sulfate hydrate (2:1:4) is an orally active potassium channel inhibitor that inhibits voltage pulse-induced currents in MT mSlo3 (KCa5.1) channels +100 mV with an IC50 of 169 μM.In addition, Quinine sulfate hydrate binds to PfPNP with low nanomolar affinity. In addition, Quinine sulfatehydrate binds to purine nucleoside phosphorylase (PfPNP) with low nanomolar affinity. |
M40865 | Peplomycin | Peplomycin is a peptide polyene compound derived from Streptomyces and a Bleomycin analog with high antitumor activity. In addition, Peplomycin induces a variety of skin abnormalities and induces apoptosis in oral squamous carcinoma SSCKN cells and lung fibrosis. |
M40864 | Isepamicin | Isepamicin is an aminoglycoside antibiotic derived from actinomycetes with an antimicrobial spectrum that includes Enterobacteriaceae and Staphylococcus spp. and has been shown to have improved activity against strains producing type I 6'-acetyltransferase. |
M40863 | Carumonam | Carumonam (AMA-1080) is a sulfonated monocyclic β-lactam antibiotic from Chromobacterium purpureum that targets penicillin-binding proteins (PBPs), is active against aerobic Gram-negative bacteria and is resistant to β-lactamase-mediated hydrolysis. |
M40862 | Plaunotol | Plaunotol is an acyclic diterpenoid extracted from the stems and leaves of the Croton plant and can be used in studies related to gastric ulcers. |
M40858 | Miocamycin | Miocamycin is a macrolide antibiotic of Streptomyces origin that inhibits protein synthesis by binding to the bacterial 70S ribosome and is effective against a wide range of Gram-positive and Gram-negative microorganisms. |
M40838 | Boromycin | Boromycin is a compound isolated from Streptomyces antibioticus and a boron-containing macrolide antibiotic with potent activity against a number of viruses, gram-positive bacteria and protozoan parasites. It can be used to induce a mouse model of pulmonary fibrosis and can be used in malaria-related studies. |
M40727 | Teixobactin | Teixobactin, a cyclic condensed peptide antibiotic isolated from the soil bacterium Eleftheria terrae, inhibits the synthesis of both peptidoglycan and teichoic acid, and exhibits antimicrobial activity against Gram-positive bacteria and Mycobacterium. |
M40568 | Apicularen B | Apicularen B is a cytotoxic macrolide produced by Archangium gephyra and is also a specific V-ATPase inhibitor. Its IC50 values range from 0.2 to 1.2 μg/mL and it exhibits weak activity against some Gram-positive bacteria. |
M40567 | Apicularen A | Apicularen A is a macrolide isolated from the mucoid bacterium Chondrosporium spp. It is also a highly selective inhibitor of vesicular ATPase. |
M40514 | Humimycin A | Humimycin A is a compound derived from Rhodococcus equi that resensitizes bacteria and eliminates bacterial resistance to beta-lactams. |
M40513 | Thiocillin | Thiocillin (high-sulfur penicillin) is a natural product antibiotic derived from a ribosome-encoded peptide. |
M40512 | Commendamide | Commendamide is an N-acylamide natural product isolated from Bacteroides vulgatus and also a GPCR G2A/GPR132 agonist with an EC50 value of 11.8 μM. |
M40511 | Lactocillin | Lactocillin is an antibiotic found in the human microbiota that inhibits the growth of gram-positive bacteria and exhibits antimicrobial activity at the nanomolar level against the pathogenic bacteria Staphylococcus aureus and Enterococcus faecalis. |
M40509 | Ovalicin | Ovalicin is a sesquiterpenoid from a fungus that is also an inhibitor of angiogenesis. |
M40501 | Salivaricin B | Salivaricin B is a compound produced by Streptococcus salivarius and exhibits inhibitory activity against common human microorganisms such as Streptococcus salivarius, Streptococcus pyogenes, Streptococcus lighteri, and Micrococcus garciniae. |
M40478 | Scopolamine hydrochloride | Scopolamine hydrochloride is a non-selective and high affinity (≤1 nM) muscarinic antagonist that is used for the prevention of post-operative nausea and vomiting. Scopolamine readily passes the blood brain barrier. Scopolamine also reversibly inhibits 5-HT3 receptor-responses with an IC50 of 2.09 μM. |
M40477 | Z-GMCA | GMCA is a natural product isolated from Matricaria chamomilla. |
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