| 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 |
| 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. |
| M56974 | Thermospermine | Thermospermine, a structural isomer of Spermine, is synthesized by a thermospermine synthase designated ACAULIS5 (ACL5). |
| 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. |
| M56969 | Glycidyl oleate | Glycidyl oleate (Oleic acid glycidyl ester) is an ester product. |
| M56968 | 8-Azanebularine | 8-Azanebularine, a compound with hydrogen in place of the C6 amino group, inhibits the ADAR2 reaction at high concentrations (IC50=15 mM). |
| M56967 | C12-Sphingosine | C12-Sphingosine is a short-chain Sphingosine homologue. |
| M56966 | GOT1 inhibitor-1 | GOT1 inhibitor-1, a tryptamine-based derivative, acts as a novel, potent and non-covalent inhibitor of glutamate oxaloacetate transaminase 1 (GOT1) with an IC50 of 8.2 uM. |
| M56965 | JTV-519 fumarate | JTV-519 fumarate (K201 fumarate) is a Ca2+-dependent blocker of sarcoplasmic reticulum Ca2+-stimulated ATPase (SERCA) and a partial agonist of ryanodine receptors in striated muscle. |
| M56964 | FFN 102 mesylate | FFN 102 mesylate is a synthetic biogenic neurotransmitter analogue with PH-dependent fluorescence and electrical activity. |
| M56963 | DMNB-caged-Serine | DMNB-caged-Serine is a photocaged amino acid. |
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