| 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. |
| M56990 | Fenquizone | Fenquizone (MG-13054), a thiazide-like diuretic, exhibits chronic antihypertensive effect. |
| M56989 | Lactyl-CoA | Lactyl-CoA is an acyl-CoA formally condensed from the sulfhydryl group of CoA and the carboxyl group of lactic acid, also known as lactyl-CoA. |
| M56988 | FATP1-IN-1 | FATP1-IN-1 is a fatty acid transport protein 1 (FATP1) inhibitor. |
| M56987 | LDN-193188 | LDN 193188 is a phosphatidylcholine transfer protein (PC-TP) inhibitor. |
| M56986 | Draflazine | Draflazine (R-75231) is a ENT1 inhibitor. |
| M56985 | Heptamidine | Heptamidine (SBi4211) is a potent Pentamidine-related inhibitor of the calcium-binding protein S100B (Kd=6.9 μM), selectively kills melanoma cells with S100B over those without S100B. |
| M56984 | SaRI 59-801 | SaRI 59-801 is an orally effective hypoglycemic compound. |
| M56983 | ASN04421891 | ASN04421891 is a potent GPR17 receptor modulator, with an EC50 of 3.67 nM in [35S]GTPγS binding assay. |
| M56982 | Phytosterols | Phytosterols are anticancer agents. |
| M56981 | Hexaflumuron | Hexazinone is a nonselective herbicide from the triazine family. |
| M56980 | Methsuximide | Methsuximide is an anticonvulsant agent. |
| M56979 | Seletracetam | Seletracetam (Ucb 44212), as an analog of the antiepileptic agent Levetiracetam, is a SV2A modulator for the research of epilepsy. |
| M56978 | NCGC00262650 | NCGC00262650 is a potent apical membrane antigen 1-rhoptry neck protein 2 (AMA1-RON2) interaction inhibitor. |
| M56977 | Chlophedianol | Chlophedianol (Clofedanol) is an orally active and potent antitussive agent. |
| M56976 | Lobeglitazone | Lobeglitazone is a new type of thiazolidinedione. |
| M56975 | Enitociclib | Enitociclib (VIP152; BAY-1251152) is a selective CDK9 inhibitor. |
| M56973 | Testololactone | Testololactone is an aromatase inhibitor. |
| M56972 | SBI-477 analog | SBI-477 analog inhibits intracellular lipid accumulation, increase celluar glucose uptake. |
| M56971 | Oxyphenisatine | Oxyphenisatine (Oxyphenisatin) is a laxative. |
| M56970 | AHL modulator-1 | AHL modulator-1 is a modulator of N-acylated L-homoserine lactone (AHL), with the agonism and antagonism of 21% and 42% in cellulase activity and 5% and 32% in potato macerationa, respectively. |
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