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 |
M53714 | Thymus peptide C | Thymus peptide C is a hormonal agent derived from the thymus glands of young calves, which works as a substitute for the physiological functions of the thymus. |
M53712 | Boc-Lys-OH | Boc-Lys-OH is a lysine derivative of azocyclic and anthraquinone. |
M53711 | N-Stearoylglycine | N-stearoylglycine is a lipid and has a small ionizable polar headgroup whose charge is pH dependent and whose amide moiety can form H-bonded network between adjacent molecules in ordered films. |
M53697 | pGlu-Pro-Arg-MNA monoacetate | pGlu-Pro-Arg-MNA monoacetate is a chromogenic substrate. |
M53696 | Goralatide TFA | Goralatide TFA is an inhibitor of cell cycle progression. |
M53695 | H-Gly-Gly-Pro-OH | H-Gly-Gly-Pro-OH is a peptide with 3 amino acid. |
M53694 | Bac5(1-25) | Bac5(1-25) is an N-terminal fragment of the bovine proline-rich antimicrobial peptide Bac5. |
M53692 | SBP1 peptide | SBP1 peptide is a chemically synthesized 23-mer peptide fragment of the ACE2 PD α1 helix. |
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). |
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