| Cat.No. | Name | Information |
|---|---|---|
| M40760 | Human β-defensin-3 | Human β-defensin-3 is an antimicrobial peptide produced by epithelial cells that reduces inflammatory cytokine responses, as well as inhibits microbial growth, and has immunomodulatory activity with IC90 values ranging from 6-25 μg/ml. |
| 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. |
| M40670 | Theopalauamide | Theopalauamide is a bicyclic peptide from the genus Theonella of sponges, constructed via a histidine alanine bridge. |
| M40669 | Theonellamide | Theonellamide is a bicyclic peptide from the sponge genus Theonella, constructed via a histidine alanine bridge. It has antifungal activity and cytotoxic activity. |
| M40588 | Efinopegdutide | Efinopegdutide is a dual agonist of GCGR and GLP-1R and may be used in studies related to non-alcoholic fatty liver disease (NAFLD). |
| M40586 | YH14617 | YH14617 is a synthetic peptide that is also an inhibitor of LAG3 and TIM3 and can be used in studies related to Parkinson's (PD) and diabetes. |
| M40579 | MAR701 | MAR701 is a synthetic peptide that acts on GLP-1R as well as GIPR and can be used in studies related to type 2 diabetes. |
| M40574 | AC2592 | AC2592 is a synthetic peptide that acts on the GLP-1 receptor and can be used in studies related to cardiovascular disease and diabetes. |
| M40569 | (D-His2,D-Trp6)-LHRH | (D-His2,D-Trp6)-LHRH is a peptide that can be discovered by peptide screening. Peptide screening is a research tool that assembles active peptides primarily by immunoassay. It can be used for protein interactions, functional analysis, antigenic epitope screening, and the development and study of active molecules. |
| M40539 | Dolastatin 15 | Dolastatin 15, a heptasubunit condensed peptide derived from Dolabella auricularia, is also a potent antimitotic agent and microtubule destabilizer that inhibits mitosis by blocking microtubule assembly. In addition, Dolastatin 15 induces cell cycle arrest and apoptosis in multiple myeloma cells. It can also be used as an ADC cytotoxin for ADC development studies. |
| M40535 | LIP1 (human) | LIP1 (human) is a polypeptide produced from the anterior region of nerve growth factor (NGF) containing 29 amino acids that induces F-actin rearrangement, phosphorylates TrkA and Akt, and has antiproliferative as well as neuroprotective activities. Sequence: ARSAPAAAIAARVAGQTRNITVDPRLFKK |
| M40503 | Lugdunin | Lugdunin is a class of non-ribosomal peptides (NRPs) with good antimicrobial activity and inhibits methicillin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant enterococci (VRE) and Listeria monocytogenes. |
| 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. |
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