| 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 |
| M7687 | CGS-12066 maleate salt | 5-HT1B serotonin receptor agonist. |
| M7686 | cDPCP | cDPCP is a tumor cell permeable, potent platinum-based antineoplastic agent. |
| M7682 | III-31-C | III-31-C is a (hydroxyethyl)urea γ-secretase inhibitor that binds to γ-secretase at the substrate docking site. |
| M7679 | Acetylethylcholine mustard hydrochloride | Acetylethylcholine mustard is a precursor for ethylcholine mustard aziridinium ion (AF-64A); irreversible ligand for the high affinity choline transport system; specific presynaptic long action cholinotoxin; inhibitor of choline acetyl-transferase. |
| M7678 | BMS-764459 | BMS-764459 is a pyrazinone-containing antagonist that targets corticotropin-releasing factor/hormone (CRF or CRH) receptor 1 (CRF1, CRF-R1, CRFR-1, CRH-R1, CRHR-1) with high affinity (IC50 = 0. |
| M7677 | BMS-665053 | BMS-665053 is a pyrazinone-containing antagonist that targets corticotropin-releasing factor/hormone (CRF or CRH) receptor 1 (CRF1, CRF-R1, CRFR-1, CRH-R1, CRHR-1) with high affinity (IC50 |
| M7676 | BMS-763534 | BMS-763534 is a pyrazinone-containing antagonist that targets corticotropin-releasing factor/hormone (CRF or CRH) receptor 1 (CRF1, CRF-R1, CRFR-1, CRH-R1, CRHR-1) with high affinity (IC50 = 0. |
| M7675 | BMS-248360 | BMS-248360 is an orally active dual antagonist of angiotensin II subtype 1 (AT1) and endothelin subtype A (ETA) receptors. |
| M7673 | BMS-870145 | BMS-870145 is an orally available, potent and selective P2Y1 purinergic receptor antagonist. |
| M7672 | BMS-986034 | BMS-986034 is a GPR119 agonist. |
| M7666 | BMS-199264 hydrochloride | BMS-199624 is a potent inhibitor of the ATP hydrolase activity of mitochondrial F1F0 ATP synthase. |
| M7665 | BMS-207940 | BMS-207940 is a very potent and selective ETA endothelin receptor antagonist. |
| M7664 | BMS-191095 hydrochloride | BMS-191095 is a potent and selective mitochondrial ATP-sensitive K1 channel (KATP) channel opener devoid of peripheral vasodilating activity. |
| M7663 | Razaxaban hydrochloride | Razaxaban is an orally available, potent and specific coagulation factor Xa inhibitor that reduces thrombus and fibrin formation. |
| M7662 | Ifetroban sodium | Ifetroban (BMS-180291) is a potent and selective thromboxane receptor antagonist. |
| M7659 | BMS-341400 methanesulfonate | BMS-341400 is a selective and potent phosphodiesterase 5 (PDE 5) inhibitor. |
| M7658 | BTA-1 | BTA-1 is a probe for β-amyloid aggregates; fluorescent thioflavin-T derivative; exhibits high affinity for amyloid deposits; displays 50-fold higher affinity than thioflavin-T; selectively stains cerebral plaques and cerebrovascular amyloid deposits in the brains of PS1/APP transgenic mice, as well as Aβ fibrils in postmortem brain tissue obtained from AD patients; crosses the blood brain barrier. |
| M7657 | Bay u9773 | Subtype-selective cysteinyl-leukotriene (Cys-Lt) antagonist. |
| M7656 | BP897 | Partially selective D3 dopamine receptor agonist. |
| M7655 | BW A868C | BW A868C is a potent, selective DP prostanoid receptor antagonist. |
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