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 prevent 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. |
M9331 | 10-Hydroxy-trans-2-decenoic acid | 10-hydroxy-2-decenoic acid (10-H2DA) is the principal lipid component in royal jelly which is the food for queen and larvae honeybees. |
M8017 | PTACH | HDAC inhibitor; more potent than the majority of HDAC inhibitors except for SAHA (gold standard). |
M8016 | PD-118057 | PD-118057 is an activator of ether-a-go-go-related (hERG) potassium channel. |
M8012 | Papaverine hydrochloride | Smooth muscle relaxant and cerebral vasodilator; phosphodiesterase inhibitor. |
M8011 | Ponasterone A | Ponasterone A is an insect hormone, involved in regulating metamorphosis. |
M8010 | Phloridzin dihydrate | Competitive inhibitor of SGLT1 and SGLT2. |
M8009 | Pipamperone dihydrochloride | D2 dopamine receptor antagonist; 5-HT2 serotonin receptor antagonist; antipsychotic. |
M8006 | PD 404,182 | Potential antibiotic of gram negative bacteria. |
M8005 | PD 168,077 maleate salt | Selective D4 dopamine receptor agonist. |
M8003 | (+)-PD 128,907 hydrochloride | Selective D3 dopamine receptor agonist. |
M8000 | Pirenperone | 5-HT2 serotonin receptor antagonist. |
M7999 | 8-PIP-cAMP | Selective cAMP-dependent protein kinase (PKA) activator. |
M7998 | PET-cGMP | cGMP-dependent protein kinase (PKG I and PKG II) activator. |
M7996 | PRL-3 Inhibitor I | PRL-3 Inhibitor I is a rhodanine derivative with an IC50 value of 0. |
M7995 | Pranlukast hemihydrate | Pranlukast is a subtype specific CysLT1 receptor antagonist. |
M7993 | PalGly | PalGly is an endogenous signaling lipid that modulates calcium influx and nitric oxide production. |
M7990 | Pyocyanin | Pyocyanin, a blue-green pigment belonging to phenazine pigments, is a redox-active phenazine. |
M7989 | PS48 | PS48 is a PDK1 (phosphoinositide-depende |
M7988 | 5Z-7-Oxozeaenol | 5Z-7-oxozeaenol is a potent ATP-competitive irreversible inhibitor of ERK2 (IC50 = 80 nM), TAK1 (MEKK7), MKK7, and MEK1, which all contain a common cysteine residue in the ATP-binding site. |
M7986 | OM137 | OM137 is an inhibitor of aurora kinases; inhibitor of spindle checkpoint. |
M7985 | Olprinone hydrochloride | Selective phosphodiesterase 3 (PDE3) inhibitor. |
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