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 |
M7019 | NBD 556 | NBD 556 is a cD4 mimetic; blocks HIV-1 cell entry. |
M7018 | NAV 26 | NAV 26 is a selective Na v1.7 channel blocker. |
M7017 | NAS-181 | NAS-181 is a selective r5-HT 1B antagonist. Active in vivo. |
M7014 | Naltrindole hydrochloride | Naltrindole hydrochloride is a selective non-peptide δ antagonist. |
M7013 | Naltriben mesylate | Naltriben mesylate is a standard δ 2 selective antagonist. |
M7011 | NADA | NADA is a endogenous CB 1 agonist. Also vanilloid agonist and inhibitor of FAAH and AMT. |
M7010 | N20C hydrochloride | N20C hydrochloride is a non-competitive NMDA receptor open-channel blocker. |
M7009 | Muristerone A | Muristerone A is a stimulates Bcl-XL mRNA transcription; antiapoptotic. |
M7006 | MSOP | MSOP is a specific group III mGlu antagonist. |
M7005 | MS 245 oxalate | MS 245 oxalate is a high affinity 5-HT 6 antagonist. |
M7004 | MS 21570 | MS 21570 is a gPR171 antagonist. |
M7003 | MRS 2500 tetraammonium salt | MRS 2500 tetraammonium salt is a extremely potent and selective P2Y 1 antagonist. |
M7002 | MRS 2279 | MRS 2279 is a selective, high affinity P2Y 1 antagonist. |
M7001 | MRS 2219 | MRS 2219 is a potentiates P2X 1-mediated responses. |
M6997 | MRS 1220 | MRS 1220 is a highly potent, selective hA 3 antagonist. |
M6996 | MRK 560 | MRK 560 is a γ-secretase inhibitor; attenuates amyloid plaque deposition. |
M6994 | MR 16728 hydrochloride | MR 16728 hydrochloride is a stimulates ACh release. |
M6993 | Mps BAY 2a | Mps BAY 2a is a potent and selective Mps1 kinase inhibitor. |
M6990 | MNI-caged-NMDA | MNI-caged-NMDA is a caged NMDA. |
M6989 | MNI-caged-D-aspartate | MNI-caged-D-aspartate is a caged D-aspartate; NMDA agonist. |
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