| Cat.No. | Name | Information |
|---|---|---|
| M40502 | MccC7 | MccC7 is a small molecule 7 peptide encoded by an E. coli plasmid with inhibitory activity against microorganisms such as Klebsiella pneumoniae, Salmonella spp. and Yersinia spp. |
| M40500 | Epidermin | Epidermin is an antimicrobial peptide isolated from Staphylococcus epidermidis. |
| M40498 | Enviomycin | Enviomycin is a cyclic peptide antibiotic with antimicrobial activity that can be used in studies related to tuberculosis. |
| M40497 | Viomycin | Viomycin, a cyclic peptide antibiotic produced by the actinomycete Streptomyces violetus, blocks translocations on bacterial ribosomes and can be used in tuberculosis-related studies. |
| M40493 | RES-701-2 | RES-701-2 is a cyclic peptide and an antagonist of the endothelin receptor ETB. |
| M39833 | L-Selenocystine | L-Selenocystine is a diselenide-bridged amino acid. L-Selenocystine induces an unfolded protein response, ER stress, and large cytoplasmic vacuolization in HeLa cells and has cytostatic effects in a range of cancer cell types. |
| M39832 | Boc-Glu(OBzl)-OH | Boc-Glu(OBzl)-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
| M39831 | H-Phe(3,5-DiF)-OH | H-Phe(3,5-DiF)-OH is a difluorophenylalanines in the L-configuration [L-(F2)Phe]. H-Phe(3,5-DiF)-OH can be incorporated into the thrombin receptor-tethered ligand peptide SFLLRNP to identify the phenyl hydrogens of the Phe-2 residue involved in the CH/π receptor interaction. |
| M39830 | Ethyl 2-(benzylamino)acetate | Ethyl 2-(benzylamino)acetate is an important chemical, pesticide and pharmaceutical intermediate with a wide range of applications in the synthesis of chemical products. |
| M39829 | 5-Amino-2-((tert-butoxycarbonyl)amino)-5-oxopentanoic acid | 5-Amino-2-((tert-butoxycarbonyl)amino)-5-oxopentanoic acid is a glutamine derivative. |
| M39828 | (R)-4-Amino-2-((tert-butoxycarbonyl)amino)-4-oxobutanoic acid | (R)-4-Amino-2-((tert-butoxycarbonyl)amino)-4-oxobutanoic acid is an asparagine derivative. |
| M31383 | CLP-002 | CLP-002 is a low molecular weight anti-PD-L1 short peptide inhibitor, which can act by blocking the interaction between pd-1 and pd-l1, and thus can be used in tumor related studies. Sequence: WHRSYYTWNLNT |
| M31364 | Dolcanatide | Dolcanatide is an orally active uridine analog that is also a guanylate cyclase C (GC-C) agonist with anti-inflammatory activity and may be used in studies related to inflammatory bowel disease. |
| M31363 | YH14618 | YH14618 is a synthetic peptide that is also a TGF-β1 modulator and can be used in studies related to disc degenerative diseases. |
| M31362 | SR-0379 | SR-0379 is a synthetic peptide that enhances the proliferation of human dermal fibroblasts (NHDFs) via integrin-mediated interactions via the PI3K-Akt-mTOR pathway. Possesses antimicrobial activity. Can be wound repair related studies. |
| M31351 | Dirucotide | Dirucotide (MBP8298) is a 17 amino acid synthetic peptide with a sequence identical to that of some human myelin basic proteins, and an MBP modulator. It can be used in the study of autoimmune diseases of the central nervous system such as multiple sclerosis (MS). |
| M31346 | Ularitide | Ularitide is a synthetic natriuretic peptide that increases glomerular filtration rate by acting on the glomerulus and inducing pre-glomerular vasodilation and post-glomerular vasoconstriction, and can be used in heart failure studies. |
| M31343 | Surotomycin | Surotomycin is a novel cyclic lipopeptide antibiotic that can be used in studies related to Clostridium difficile infection (CDI). |
| M31342 | Iseganan | Iseganan is a protein integrin as well as an anti-microbial peptide that is active against both Gram-positive and Gram-negative bacteria as well as fungi, and kills bacteria and fungi by attaching to and disrupting the integrity of lipid cell membranes. It can be used in studies related to oral mucositis. |
| M31339 | Trebananib | Trebananib (AMG 386) is a first-in-class (first-in-class) peptide that inhibits the interaction of Ang1 and Ang2 with their receptor Tie2, as well as an inhibitor of the non-VEGF-dependent angiogenic pathway. |
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