| 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. |
| M7048 | NS 2028 | NS 2028 is a potent soluble guanylyl cyclase (sGC) 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. |
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