| 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 |
| M8457 | NID-1 | NID-1 (Novel Inducer of Death-1) is a cell permeable and potent inducer of energy-dependent non-apoptotic cell death in mammalian cell lines. |
| M8456 | Thiophene-4 | Thiophene-4 (TP4) is an inhibitor of polyketide synthase 13 (Pks13), which plays a critical role in the biosynthesis of mycolic acid, an essential component of the cell wall in M. |
| M8455 | Noopept | Noopept is a nootropic and neuroprotective compound that normalizes the balance of the pro- and antioxidant systems. |
| M8454 | VU0071063 | VU0071063 is a potent activator of Kir6. |
| M8453 | ML138 | ML138 (CID 44601470) is a highly selective agonist at kappa opioid receptors (KOR) that potently activate G protein coupling but weakly interact with β arrestin2. |
| M8451 | SW155246 | SW155246 is a potent and selective DNMT1 (DNA methyltransferase 1) inhibitor that demethylates cytosines in vivo in a cell-based assay without affecting protein levels or generating reactive oxygen species. |
| M8450 | HUP30 | HUP30 is a potent vasodilating agent that stimulates soluble guanylyl cyclase, activate K+ channels, and blocks extracellular Ca2+ influx. |
| M8449 | PDP-EA | 3-N-Pentadecylphenolethan |
| M8448 | Thiophene-2 | Thiophene-2 (TP2) is an inhibitor of polyketide synthase 13 (Pks13), which plays a critical role in the biosynthesis of mycolic acid, an essential component of the cell wall in M. |
| M8447 | PQ-10 | PQ-10 is a potent and selective inhibitor of phosphodiesterase 10A (PDE10). |
| M8445 | S 24795 | S 24795 is a selective partial agonist for the α7-subtype of nicotinic acetylcholine receptor (nAChR). |
| M8444 | Adaphostin | Adaphostin is a p210bcr/abl tyrosine kinase inhibitor displaying anti-proliferative activity in leukemia models, human prostate cancer cell line PC-3 and other cancer cell lines. |
| M8443 | UCF-101 | UCF-101 is a selective inhibitor of the pro-apoptotic mitochondrial serine protease Omi/HtrA2, involved in the cellular response to thermal and oxidative stress. |
| M8442 | NQTrp | NQTrp is a potent inhibitor of amyloid aggregation (AD). |
| M8441 | BC8-15 | BC8-15 is a potent PDE4/8 inhibitor that elevates steroidogenesis in mouse Leydig cells. |
| M8440 | PKI-166 | PKI-166 is a potent, selective and orally available EGF-R tyrosine kinase inhibitor. |
| M8439 | SMI481 | SMI481 is a selective small-molecule inhibitor (SMI) of the yeast phosphatidylinositol transfer protein (PITP) Sec14, a key regulator of phosphoinositide signaling, regulating membrane trafficking through the trans-Golgi network and endosomal systems. |
| M8437 | BMS-195614 | BMS-195614 (BMS614) is a potent neutral retinoic acid receptor RARα selective antagonist with an IC50 of 2. |
| M8435 | 4-Bromo-Resveratrol | 4-Bromo-Resveratrol is a resveratrol analog that potently inhibits Sirt1 and Sirt3. |
| M8433 | SR-58611A | SR58611A is a potent, specific b3 adrenergic receptor agonist. |
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