| 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. |
| M9665 | N-(2-amino-2-oxoethyl)acrylamide | N-(2-Amino-2-oxoethyl)acrylamide |
| M6583 | CGP 36216 hydrochloride | CGP 36216 hydrochloride is a gABA B antagonist; displays activity at presynaptic receptors. |
| M6582 | CGP 12177 hydrochloride | CGP 12177 hydrochloride is a β 3 partial agonist. β 1/β 2 antagonist. |
| M6581 | CGH 2466 dihydrochloride | CGH 2466 dihydrochloride is a a 1, A 2B and A 3 antagonist and inhibitor of p38 MAPK and PDE4. |
| M6579 | Cerestat | Cerestat (also known as Aptiganel, CNS-1102) is a potent and noncompetitive NMDA receptor antagonist. |
| M6578 | Ceranib 1 | Ceranib 1 is a ceramidase inhibitor; antiproliferative. |
| M6575 | CE3F4 | CE3F4 is a noncompetitive Epac1 inhibitor. |
| M6574 | CDP 840 hydrochloride | CDP 840 hydrochloride is a potent and selective PDE4 inhibitor. |
| M6572 | CD 2314 | CD 2314 is a selective RARβ agonist. |
| M6570 | CCMQ | CCMQ is a used to characterize NR2B-containing NMDA receptors. |
| M6569 | CCG 63802 | CCG 63802 is a inhibitor of regulator of G-protein signaling 4 (RGS4) protein. |
| M6568 | CCG 2046 | CCG 2046 is a inhibitor of regulator of G-protein signaling 4 (RGS4). |
| M6565 | CBiPES hydrochloride | CBiPES hydrochloride is a positive allosteric modulator of mGlu 2. |
| M6564 | CB 65 | CB 65 is a high affinity, selective CB 2 agonist. |
| M6563 | Cardionogen 1 | Cardionogen 1 is a inhibitor of Wnt/β-catenin signaling. |
| M6556 | cAMPS-Sp, triethylammonium salt | cAMPS-Sp, triethylammonium salt is a cell-permeable cAMP analog. |
| M6551 | Bz 423 | Bz 423 is a aTP synthase inhibitor (IC50 ~5 μM). Bz 423 binds the oligomycin sensitivity conferring protein (OSCP) component of mitochondrial F1F0-ATPase in vitro resulting in generation of superoxide and apoptosis. Bz 423 kills primary B and T cell in mice in vivo. Bz 423 suppresses autoimmunity and prolongs survival in mouse lupus model. |
| M6550 | BYK 49187 | BYK 49187 is a pARP-1 and PARP-2 inhibitor. |
| M6548 | BYK 191023 dihydrochloride | BYK 191023 dihydrochloride is a potent and selective inhibitor of iNOS. |
| M6545 | BW-B 70C | BW-B 70C is a 5-Lipoxygenase inhibitor. |
| M6543 | BW 373U86 | BW 373U86 is a potent, selective non-peptide δ agonist. |
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