| 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. |
| M55676 | Calcium Levofolinate EP Impurity I | Arfolitixorin is an antifolate modulator. |
| M55673 | VJDT | VJDT is a TREM1 inhibitor, it effectively blocks TREM1 signaling. VJDT inhibits tumor growth and has potential for study in cancer research. |
| M55406 | Pegfilgrastim | Pegfilgrastim is a sustained-duration form of filgrastim, a recombinant methionyl form of human granulocyte colony-stimulating factor (G-CSF), to which a 20 kDa polyethylene glycol molecule is covalently bound to the N-terminal methionine residue. Similar to filgrastim, pegfilgrastim increases the proliferation and differentiation of neutrophils from committed progenitor cells, induces maturation, and enhances the survival and function of mature neutrophils, resulting in dose-dependent increases in neutrophils. |
| M55405 | Adenophostin A | Adenophostin A is a potent agonist of inositol 1,4,5-trisphosphate receptors (IP(3) R). Adenophostin A possesses the highest known affinity for the inositol 1,4,5-trisphosphate (Ins(1,4,5)P3) receptor (InsP3R). In high concentrations, adenophostin A released Ca2+ from Ins(1,4, 5)P3-sensitive stores and stimulated a Cl- current that depended upon the presence of extracellular Ca2+. |
| M55377 | 2-Bromo-2'-methoxyacetophenone | 2-Bromo-2'-methoxyacetophenone |
| M55045 | Izeltabart | Izeltabart is a high-affinity humanized antibody targeting ADAM9. Izeltabart can be used as ADC Antibody for site-specific conjugation with Maytansinoid-based DM21-C to synthesize IMGC936, an Antibody-drug Conjugate with strong anti-cancer activity. IMGC936 exhibits cytotoxicity against ADAM9-positive human tumor cell lines and potent antitumor activity in xenograft tumor models. |
| M55032 | M3554 (anti-GD2 ADC) | M3554 is a novel anti-GD2 ADC designed based on humanized ch14.18 anti-GD2 antibody. M3554 has anti-tumor activity. |
| M54834 | 6-Aminopyridine-3-boronic acid | 6-Aminopyridine-3-boronic acid is a boronic acid derivative. Boronic acid derivatives are widely used in organic synthesis for carbon-carbon bond formation. In Suzuki coupling, aryl halides and boronic acid aryl or vinyl esters or boronic acid are coupled using Pd(PPh3)4. It can be used as a pharmaceutical intermediate. |
| M54796 | Linderene acetate | Linderene acetate is a prolyl endopeptidase inhibitor, which can be isolated from the root of Lindera strychnifolia. |
| M54779 | Pralmorelin | Pralmorelin (also known as KP-102, GPA-748, GHRP-2, and Growth Hormone Releasing Peptide-2) is a potent growth hormone secretagogue that acts on the pituitary gland and the hypothalamus to stimulate and amplify pulsatile growth hormone release. It acts as signal molecules that are involved in the control of cell growth and differentiation. |
| M54734 | SLK/STK10-IN-1 | SLK/STK10-IN-1 is a potent and selective inhibitor of SLK and STK10 with nanomolar potency. |
| M54713 | ZH8667 | ZH8667 is a trace amine-associated receptor 1 (TAAR1)–Gs agonist. |
| M54688 | Pegtibatinase | Pegtibatinase is a cystathionine beta synthase (CBS) regulator that can be used in studies related to homocystinuria. |
| M54656 | NJH-2-056 | NJH-2-056 is a deubiquitinase-targeting chimera (DUBTAC) linking EN523, a recruitment factor for OTUB1, to lumacaftor, a CFTR chaperone protein.NJH-2-056 can be used in cystic fibrosis-related studies. |
| M54642 | Scalaradial | Scalaradial is a marine-derived natural product that modulates protein tyrosine kinase receptor-mediated signaling pathways. |
| M54638 | Aspulvinone O | Aspulvinone O is a natural inhibitor of aspartate aminotransferase 1 (GOT1) and inhibits the growth of pancreatic ductal adenocarcinoma cells by interfering with glutamine metabolism. |
| M54566 | Efanesoctocog alfa | Efanesoctocog alfa is a novel fusion protein consisting of a single-chain factor VIII (FVIII) with a deletion in the B structural domain linked to the D'D3 structural domain of vascular hemophilic factor (VWF). It can be used for research related to hemophilia A. |
| M54559 | Zilebesiran | Zilebesiran is a small interfering RNA covalently linked to the N-acetylgalactosamine ligand that binds with high affinity to the hepatic asialoglycoprotein receptor.Zilebesiran specifically reduces hepatic angiotensinogen messenger RNA, thereby decreasing angiotensinogen synthesis. |
| M54552 | Anselamimab | Anselamimab is a human IgG1κ anti-amyloidogenic fibrillar antibody targeting serum amyloid A1 (SAA1) for studies related to AL-type amyloidosis. |
| M54549 | AZD3152 | AZD3152 is a monoclonal antibody targeting SARS-CoV-2. |
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