| Cat.No. | Name | Information |
|---|---|---|
| M2206 | TH-302 (Evofosfamide) | TH-302 is a highly potent and selective hypoxia-activated procompound targeting hypoxic regions of solid tumors with IC50 of 19 nM. |
| M6098 | Baicalein | Baicalein is a CYP2C9 and prolyl endopeptidase inhibitor, IC50 value of 3.12 mM. |
| M9325 | EGTA | EGTA is a specific calcium chelator with a Kd of 60.5 nM at physiological pH (7.4) and a high specificity for Ca2+ than for Mg2+.EGTA significantly inhibits the substrate adhesion capacity of inflammatory macrophages. |
| M9330 | Brij-35 | Brij-35 (Polidocanol) is a high HLB, ethoxylated, nonionic ether of lauryl alcohol with broad pH stability. |
| M6154 | 2-PMPA tetrasodium | 2-PMPA (PMPA tetrasodium salt) is a potent and selective inhibitor of glutamate carboxypeptidase II (GCPII) with an IC50 of 300 pM. |
| M2250 | Pamidronate disodium | Pamidronate disodium is a nitrogen containing bisphosphonate, used to the research of preventing osteoporosis. |
| M9916 | DPPH | DPPH (2,2-Diphenyl-1-picrylhydrazyl) is a stable free radical that measures the free radical scavenging activity of antioxidants. |
| M9194 | Insulin (human) | Insulin (human) is a polypeptide hormone that regulates the level of sugar (glucose) in the blood and is produced by beta cells of islets. |
| M3409 | Formestane | Formestane is a second generation selective aromatase inhibitor with an IC50 of 80 nM. |
| M9665 | N-(2-amino-2-oxoethyl)acrylamide | N-(2-Amino-2-oxoethyl)acrylamide |
| M50456 | LL-21 | LL-21 (LL-37 LLG) is a polypeptide that can be found by peptide screening. |
| M50455 | LyP-1 | LyP-1 is a cyclic 9‐amino‐acids tumor homing peptide and selectively bind to p32 receptors overexpressed in various tumor-associated cells. |
| M50454 | MAP17 | MAP17 (Cell-penetrating peptide MAP17) is a synthetic secondary amphipathic cell-penetrating peptides, with sequence of QLALQLALQALQAALQLA. |
| M50453 | SN50M | SN50M, a mutant peptide of SN50, is a cell membrane-permeable inactive control peptide. |
| M50452 | SynB1 | SynB1 is a cell penetrating polypeptide, internalized by, or is associated with lipid vesicle (LV). |
| M50451 | YIGSR | YIGSR is a peptide that can inhibit the tumour growth and metastasis of leukaemic cells. |
| M50450 | CADY | CADY is a cell-penetrating peptide (CPPs) peptide with a sequence of GLWRALWRLLRSLWRLLWRA. |
| M50449 | CPP2 | CPP2 is a cell-penetrating peptide, with a high intracellular translocation efficiency. |
| M50448 | DT-2 | DT-2 is a potent and selective inhibitor of the cGMP-dependent protein kinase (PKG). |
| M50447 | GE11 | GE11 is a active peptide and combines with colloidal drug delivery systems as smart carriers for antitumor drugs and can be used for cancer study. |
| M50446 | HN-1 | HN-1 is a 12-mer peptide with specific activity to head and neck squamous cell cancer (HNSCC) cells. |
| M50445 | Hs-1 | Hs-1 is an antimicrobial peptide displays 80% protection against the dengue-2 virus . |
| M50444 | INF7 | INF7 is a derivative of the N-terminal domain of the HA2 protein that can be used to enhance the endosomal escape of polyplexes or liposome-encapsulated proteins. |
| M50443 | Iα52 | Iα52 is a naturally processed peptide encompassed the residues 52-68 of the murine I-Eα chain and may contribute to selection of immature T cells. |
| M50442 | L17E | L17E, an endosomolytic peptide, is a cationic amphiphilic peptide with specific membrane lytic activity for late endosomes (LEs). |
| M50441 | RGDT | RGDT is a synthetic peptide. |
| M50440 | RGDV | RGDV is a platelet aggregation inhibitor. |
| M50439 | SDGR | SDGR is a Ser-Asp-Gly-Arg tetrapeptide sequence that effectively inhibits fibronectin-mediated cell attachment. |
| M50438 | CRT | CRT, an iron peptide mimic, can bind to apo-transferrin (apo-Tf). |
| M50437 | HR1 | HR1 is a mastoid protease. |
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