| 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. |
| 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. |
| M56962 | Dehydroindapamide | Dehydroindapamide is the indole form of Indapamide. |
| M56961 | Diiodoacetic acid | Diiodoacetic acid is a disinfection by-product (DBP) formed during water disinfection. |
| M56959 | NR2F2-IN-1 | NR2F6 modulator-2 (CIA1) is a potent and selective orphan nuclear receptor COUP-TFII (NR2F2) inhibitor. |
| M56958 | Uricosuric agent-1 | Uricosuric agent-1 (KT-433) is an uricosuric agent. |
| M56957 | Bumadizone calcium | Bumadizone calcium is the calcium salt of Bumadizone. |
| M56956 | Biocytin hydrazide | Biocytin hydrazide is a selective label for sialic acids, galactose, and other sugars in glycoconjugates using avidin-biotin technology. |
| M56955 | Silvestrol aglycone | Silvestrol aglycone is a Silvestrol analogue, inhibits protein translation initiation in cancer cells, with EC50s of 10 and 200 nM for myc-LUC and tub-LUC luciferase reporter protein translation, respectively. |
| M56954 | Antitumor agent-119 | Antitumor agent-119 is a 2-benzoxazolyl hydrazone derivative with anticancer activities. |
| M56952 | Palmitoyl sulfatide | Palmitoyl sulfatide is an ester product. |
| M56951 | FAM alkyne, 6-isomer | FAM alkyne, 6-isomer is a click chemistry regent that can be used in 1,3-dipolar cycloaddition with azido-labeled compound. |
| M56950 | γ-Linolenyl alcohol | γ-Linolenyl alcohol (6(Z),9(Z),12(Z)-Octadecatrienol) is an ester product. |
| M56949 | Carcainium chloride | Carcainium chloride (QX 572) is a quaternary derivative of Lidocaine. |
| M56948 | NR2F2-IN-1 free base | NR2F2-IN-1 (free base) is a potent and selective orphan nuclear receptor COUP-TFII (NR2F2) inhibitor. |
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