| 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 |
| M53950 | c-Myc Peptide TFA | c-Myc Peptide (TFA) is a synthetic peptide corresponding to the C-terminal amino acids (410-419) of human c-myc protein, and participates in regulation of growth-related gene transcription. |
| M53949 | His-Pro hydrochloride | His-Pro hydrochloride is a dipeptide consisting of histidyl and proline. |
| M53948 | Neuropeptide W-23 (human) | Neuropeptide W-23 (human) (NPW-23), the active form of Neuropeptide W, is an endogenous agonist of NPBW1 (GPR7) and NPBW2 (GPR8). |
| M53947 | D-JBD19 | D-JBD19 is a non-permeable peptide. |
| M53941 | LAH5 | LAH5 is an amphipathic cell-penetrating peptide. |
| M53936 | Vitronectin (367-378) | Vitronectin (367-378) is a peptide corresponding to residues 367-378 of Vitronectin. |
| M53935 | Suc-Ala-Phe-Lys-AMC | Suc-Ala-Phe-Lys-AMC is a highly sensitive fluorogenic substrate for plasmin. |
| M53924 | Amylin (8-37), rat | Amylin (8-37), rat is a truncated analog of native Amylin that selectively inhibits insulin-related glucose uptake and glycogen deposition in muscle tissue. |
| M53921 | Hexa-His | Hexa-His is a peptide consisting of 6 His residues, used as a metal binding site for the recombinant protein and mainly used for separation and purification of corresponding proteins. |
| M53920 | Calcitonin (8-32), salmon | Calcitonin (8-32), salmon is a highly selective amylin receptor antagonist. |
| M53914 | Platelet Factor 4 (58-70), human | Platelet Factor 4 (58-70), human is a peptide based on the amino acid sequence corresponding to residues 58-70 of platelet factor-4 (PF-4), contains the major heparin-binding domain. |
| M53913 | Smcy HY Peptide (738-746) | Smcy HY Peptide (738-746) is a H2-Db-restricted peptide corresponding to amino acids 738-746 of Smcy protein. |
| M53912 | Pam3-Cys-OH | Pam3-Cys-OH is a synthetic bacterial lipoprotein. |
| M53902 | MR 409 | MR 409 is a selected growth hormone-releasing hormone (GHRH) agonist. |
| M53894 | Adrenocorticotropic Hormone (ACTH) (18-39), human TFA | Adrenocorticotropic Hormone (ACTH) (18-39), human TFA is a corticotropinlike intermediate lobe peptide, which is is produced in the melanotrophs of the intermediate lobe of the pituitary. |
| M53893 | DfTat | DfTat is a dimer of the prototypical cell-penetrating peptide TAT. |
| M53892 | bFGF (119-126) | bFGF (119-126) is a biological active peptide. |
| M53891 | Semax acetate | Semax acetate is a nootropic neuroprotective peptide. |
| M53874 | Cys-Penetratin | Cys-Penetratin is a cell-penetrating peptide (CPP) with sequence of CRQIKIWFQNRRMKWKK. |
| M53872 | Amylin, amide, rat | Amylin, amide, rat is a potent and high affinity ligand of Amylin receptor AMY1 and AMY3 receptors and variably of AMY2 receptors; binding studies are generally used for the latter receptor. |
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