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 |
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. |
M6542 | BVT 948 | BVT 948 is a non-competitive protein tyrosine phosphatase inhibitor; enhances insulin signaling. |
M6541 | Butabindide oxalate | Butabindide oxalate is a cCK-inactivating serine protease inhibitor. |
M6539 | BU 226 hydrochloride | BU 226 hydrochloride is a potent, highly selective I 2 ligand. |
M6537 | BTS 54-505 hydrochloride | BTS 54-505 hydrochloride is a potent SNRI; active metabolite of sibutramine. |
M6536 | BTC | BTC is a selective estrogen receptor modulator (SERM). |
M6531 | BRL 15572 hydrochloride | BRL 15572 hydrochloride is a selective h5-HT 1D antagonist. |
M6530 | Bretazenil | Bretazenil is a benzodiazepine partial agonist. |
M6527 | BPIPP | BPIPP is a non-competitive GC inhibitor. Also AC inhibitor. |
M6526 | Borrelidin | Borrelidin is an antiangiogenic compound; Inhibit threonyl-TrNA synthase. |
M6525 | BNTX maleate | BNTX maleate is a standard δ 1 selective antagonist. |
M6524 | BMY 45778 | BMY 45778 is a non-prostanoid prostacyclin IP receptor partial agonist. |
M6523 | BMS 961 | BMS 961 is a selective RARγ agonist. |
M6522 | BMS 795311 | BMS 795311 is a potent cholesteryl ester transfer protein (CETP) inhibitor. |
M6520 | BMS 605541 | BMS 605541 is a potent VEGFR-2 inhibitor. |
M6519 | BMS 509744 | BMS 509744 is a potent and selective ITK inhibitor. |
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