| Cat.No. | Name | Information |
|---|---|---|
| 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 |
| M7791 | Exo-1 | Exo1 is a reversible inhibitor of exocytosis, also a Golgi ARF 1 (ADP-Ribosylation Factor) GTPase activator. |
| M53368 | N, O-Didansyl-L-tyrosine cyclohexylammonium | N,O-Didansyl-L-tyrosine cyclohexylammonium is a potent selective thymidylate synthase (TS) inhibitor, acts on TS of Escherichia coli, Lactobacillus casei and human with the IC50 values of 5.0, 3.4 and 119 μM, respectively. |
| M53346 | Phallacidin | Phallacidin is a member of the phallotoxin family of mushroom toxins. |
| M53344 | Larazotide | Larazotideis a peptide which is an orally active zonulin antagonist. |
| M53343 | Peptide5 | Peptide5, a connexin 43 mimetic peptide, reduce animals swelling, astrogliosis, and neuronal cell death after spinal cord injury. |
| M53342 | Gap19 | Gap19, a peptide derived from nine amino acids of the Cx43 cytoplasmic loop (CL), is a potent and selective connexin 43 (Cx43) hemichannel blocker. |
| M53279 | Acetyl-Amylin (8-37) (human) | Acetyl-Amylin (8-37) (human) is a specific amylin antagonist. |
| M53278 | Amylin (1-37) (human) | Amylin (1-37) (human) (hIAPP (1-37)) is a peptide hormone, present in pancreatic betacell secretory granules. |
| M53277 | Amylin (8-37) (human) | Amylin (8-37) (human) (hIAPP (8-37)) is a 8-37 fragment of human islet amyloid polypeptide (IAPP). |
| M53276 | Amylin (IAPP), feline | Amylin (IAPP), feline is a 37-amino acid polypeptide from feline. |
| M53275 | Amylin (8-37), human | Amylin (8-37), human is a fragment of human Amylin. |
| M53274 | AC 187 | AC 187 is a potent and orally active amylin receptor antagonist with an IC50 of 0.48 nM and a Ki of 0.275 nM. |
| M53260 | NH2-c[X-R-L-S-X]-K-G-P-(D-2Nal) | NH2-c[X-R-L-S-X]-K-G-P-(D-2Nal), a macrocyclic analogue of Ape13, is a potent APJ agonist (Ki=5.7 nM). |
| M53232 | Gamma-Glu-Abu | Gamma-Glu-Abu is a potent calcium sensing receptor (CaSR) agonist. |
| M53223 | Chemerin-9, mouse | Chemerin-9, mouse (Chemerin148-156, mouse) is a C-terminal nonapeptide of chemerin. |
| M53182 | PEN (rat) | PEN (rat), one of the most abundant hypothalamic neuropeptide and derived from the proprotein ProSAAS, is an endogenous ligand of GPR83. |
| M53181 | Corazonin | Corazonin is a highly conserved neuropeptide hormone of wide-spread occurrence in insects, serves a central regulator of caste identity and behavior in social insects. |
| M53180 | GRK2i | GRK2i is a Gβγ-inhibitory peptide that selectively prevents Gβγ-mediated signaling. |
| M53106 | Apelin-17(human, bovine) | Apelin-17(human, bovine) is an endogenous orphan G protein-coupled receptor APJ agonist. |
| M53105 | Kisspeptin-10, rat | Kisspeptin-10, rat is a potent vasoconstrictor and inhibitor of angiogenesis. |
| M53104 | TAK-448 | TAK-448 (MVT-602) is a potent and full KISS1R agonist with an IC50 of 460 pM and an EC50 of 632 pM. |
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