| 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 |
| M7119 | PF 06281355 | PF 06281355 is a selective myeloperoxidase (MPO) inhibitor. |
| M7100 | PAF (C16) | PAF (C16) is a platelet-activating factor and ligand for PAF G-protein-coupled receptor (PAFR). C16-PAF exhibits anti-apoptotic effect and inhibits caspase-dependent death by activating the PAFR. C16-PAF is a potent MAPK and MEK/ERK activator. C16-PAF induces increased vascular permeability. |
| M7085 | OR-486 | OR-486 is a catechol O-methyltransferase inhibitor. |
| M7084 | OPC 21268 | OPC 21268 is a orally active vasopressin V1 antagonist. |
| M7073 | O4I2 | O4I2 is a oct3/4 inducer; induces expression of pluripotent-associated genes. |
| M7072 | O4I1 | O4I1 is a oct3/4 inducer. |
| M7066 | NVP 231 | NVP 231 is a potent, selective and reversible CerK inhibitor. |
| M7046 | NS-1643 | NS-1643 is a kV11.1 (hERG) channel activator; antiarrhythmic. |
| M7044 | NQ 301 | NQ 301 is a selective CD45 inhibitor. |
| M7021 | NBQX | NBQX (FG9202) is a potent and selective AMPA receptor antagonist. NBQX has neuroprotective and anticonvulsant activity. It is more selective than CNQX. |
| M7020 | NBMPR | NBMPR is a equilibrative nucleoside transporter 1 (ENT1) inhibitor. |
| M7015 | Nanchangmycin | Nanchangmycin is an antiviral compound; Has a positive effect on Zika, West Nile and Dengue. |
| M6980 | ML 349 | ML 349 is a selective and reversible lysophospholipase 2 (LYPLA2) inhibitor. |
| M6966 | MKT 077 | MKT 077 is a binds mot-2; selectively cytotoxic in cancer cells. |
| M6965 | MK-571 sodium salt | MK-571 sodium salt is a selective, orally active CysLT1 receptor antagonist. MK-571 sodium is also a inhibitor of multidrug resistance-associated protein MRP4 (ABCC4) and ABCC1 (MRP1). |
| M6959 | Tetradecyltrimethylammonium bromide | Tetradecyltrimethylammonium bromide is a dynamin inhibitor. |
| M6942 | MDA 19 | MDA 19 is a cB 2 agonist. |
| M6939 | M62812 | M62812 is a tLR-4 inhibitor. |
| M6899 | L-Cysteinesulfinic acid | L-Cysteinesulfinic acid is a nMDA and mGlu agonist. |
| M6892 | LAP | LAP (Lithium phenyl-2,4,6-trimethylbenzoylphosphinate) is a water soluble, cytocompatible, Type I photoinitiator for use in the polymerization of hydrogels or other polymeric materials. This photoinitator is preferred over Irgacure 2959 for biological applications due to its increased water solubility, increased polymerization rates with 365 nm light, and absorbance at 400 nm allowing for polymerization with visible light. |
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