| Cat.No. | Name | Information |
|---|---|---|
| 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 |
| M7791 | Exo-1 | Exo1 is a reversible inhibitor of exocytosis, also a Golgi ARF 1 (ADP-Ribosylation Factor) GTPase activator. |
| M6640 | Cyclofenil | Cyclofenil is a selective estrogen receptor modulator (SERM). |
| M6639 | Cyanopindolol hemifumarate | Cyanopindolol hemifumarate is a 5-HT 1A/1B antagonist. Also β-adrenergic antagonist. |
| M6633 | CPPHA | CPPHA is a positive allosteric modulator at mGlu 1 and mGlu 5. |
| M6631 | CPCCOEt | CPCCOEt is a selective non-competitive mGlu 1 receptor antagonist. |
| M6630 | CP 99994 dihydrochloride | CP 99994 dihydrochloride is a high affinity NK 1 antagonist. |
| M6629 | CP 93129 dihydrochloride | CP 93129 dihydrochloride is a 5-HT 1B agonist. |
| M6627 | CP 775146 | CP 775146 is a selective, high affinity PPARα agonist. |
| M6626 | CP 55,940 | CP 55,940 is a potent, non-selective cannabinoid receptor agonist. |
| M6624 | CP 135807 | CP 135807 is a selective 5-HT 1D agonist. |
| M6621 | Conantokin-R | Conantokin-R is a potent, non-competitive NMDA receptor peptide antagonist with an IC50 of 93 nM.Conantokin-R is also NR2 subunit selective. It inhibits the inward current induced by NMDA in CNS neurons (IC50 = 350 nM). In addition, Conantokin R bound to Zn2+ and Mg2+ with Kd of 0.15 μM and 6.5 μM, respectively. |
| M6620 | CNQX disodium salt | CNQX disodium salt is a potent AMPA/kainate antagonist. More water soluble form of CNQX. |
| M6618 | CMPDA | CMPDA is a positive allosteric modulator of GluR2 receptors. |
| M6617 | CMPD101 | CMPD101 is a potent and selective GRK2/3 inhibitor. |
| M6616 | Cl-HIBO | Cl-HIBO is a subtype-selective AMPA agonist (GluR1 and GluR2). |
| M6608 | Cirazoline hydrochloride | Cirazoline hydrochloride is a selective α 1 agonist. |
| M6607 | Cinnabarinic acid | Cinnabarinic acid is a selective mGlu 4 agonist. |
| M6606 | Cinalukast | Cinalukast is a potent, selective CysLT 1 (LTD 4) antagonist; orally active. |
| M6600 | CID 2858522 | CID 2858522 is a selectively inhibits PKC-induced NF-κB activation. |
| M6599 | CI 976 | CI 976 is a selective ACAT inhibitor. |
| M6598 | CHPG | CHPG is a mGlu 5 selective agonist. |
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