| 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 |
| M6517 | BMS 299897 | BMS 299897 is a potent γ-secretase inhibitor. |
| M6516 | BMS 195614 | BMS 195614 is a selective RARα antagonist. |
| M6515 | BMS 182874 hydrochloride | BMS 182874 hydrochloride is a highly selective, orally active non-peptide ET A antagonist. |
| M6514 | BML 111 | BML 111 is a fPR2 (lipoxin A 4 receptor) agonist. |
| M6513 | BL 1249 | BL 1249 is a putative K 2P2.1 (TREK-1) channel opener. |
| M6510 | Bisindolylmaleimide II | Bisindolylmaleimide II is a potent PKC inhibitor and nicotinic receptor antagonist. |
| M6507 | BIMU 8 | BIMU 8 is a potent 5-HT 4 receptor full agonist. |
| M6500 | BHPI | BHPI is a eRα antagonist; also activates unfolded protein response; active in vivo. |
| M6497 | BDY TR-X, SE | BDY TR-X, SE is a orange/red fluorescent dye for the labeling of amines; supplied as NHS ester. |
| M6493 | BC 11-38 | BC 11-38 is a selective PDE11 inhibitor. |
| M6492 | BAY-X 1005 | BAY-X 1005 is a orally active 5-lipoxygenase activating protein (FLAP) inhibitor. |
| M6488 | Bay 36-7620 | Bay 36-7620 is a non-competitive mGlu 1 antagonist with inverse agonist activity. |
| M6486 | Bax channel blocker | Bax channel blocker is a inhibits Bax-mediated mitochondrial cytochrome c release. |
| M6484 | AZM 475271 | AZM 475271 is a src tyrosine kinase inhibitor. |
| M6483 | AZD 9272 | AZD 9272 is a potent and selective mGlu 5 antagonist; brain penetrant. |
| M6481 | AZD 2066 | AZD 2066 is a mGlu 5 antagonist; orally bioavailable and brain penetrant. |
| M6478 | AZ Dyrk1B 33 | AZ Dyrk1B 33 is a potent and selective Dyrk1B kinase inhibitor. |
| M6476 | AZ 12216052 | AZ 12216052 is a positive allosteric modulator at mGlu 8. |
| M6472 | ATC 0175 hydrochloride | ATC 0175 hydrochloride is a mCH 1 antagonist; also 5-HT 2B antagonist and 5-HT 1A partial agonist. |
| M6464 | AR-R 17779 hydrochloride | AR-R 17779 hydrochloride is a α7-selective agonist. |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2024 AbMole BioScience. All Rights Reserved.
