| 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 |
| M6659 | D-CPP-ene | D-CPP-ene is a potent, competitive NMDA antagonist. |
| M6658 | DCG IV | DCG IV is a very potent, selective group II mGlu agonist. Also NMDA agonist. |
| M6657 | DCEBIO | DCEBIO is a activates Cl- conductance and hKCa3.1 channels. |
| M6655 | DAU 5884 hydrochloride | DAU 5884 hydrochloride is a m 3 receptor antagonist. |
| M6653 | D-AP4 | D-AP4 is a broad spectrum EAA antagonist. |
| M6651 | Damnacanthal | Damnacanthal is a potent, selective p56 lck inhibitor; also LIMK1/2 inhibitor. |
| M6645 | CyPPA | CyPPA is a activator of K Ca2.2 and K Ca2.3 channels. |
| M6641 | Cyclothiazide | Cyclothiazide is a aMPA selective desensitization inhibitor. |
| 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. |
| M6638 | Cyanine 7, SE | Cyanine 7, SE is a near-infrared fluorescent dye for labeling of amines; supplied as NHS ester. |
| M6637 | CU CPT 4a | CU CPT 4a is a selective TLR3 inhibitor. |
| 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. |
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