| Cat.No. | Name | Information |
|---|---|---|
| M9075 | Etomoxir sodium salt | Etomoxir((R)-(+)-Etomoxir) sodium salt is an irreversible inhibitor of carnitine palmitoyltransferase 1a (CPT-1a), inhibits fatty acid oxidation (FAO) through CPT-1a and inhibits palmitate β-oxidation in human, rat and guinea pig. |
| M10566 | Valepotriate | Valepotriate has anti-epileptic and anti-cancer activities, it isolated from Valeriana jatamansi Jones. |
| M7755 | Dehydroleucodine | Dehydroleucodine is a sesquiterpene lactone isolated from Artemisia douglasiana Besser; mast cell stabilizers. |
| M38844 | Glyphosate | Glyphosate is an herbicidal derivative of the amino acid glycine. Glyphosate targets and blocks a plant metabolic pathway not found in animals, the shikimate pathway, required for the synthesis of aromatic amino acids in plants. |
| M2763 | Ibandronate sodium | Ibandronate sodium is a potent nitrogen-containing bisphosphonate that can be used in studies related to osteoporosis. |
| M2557 | Ezatiostat | Ezatiostat (TER199, TLK199) is a glutathione analog inhibitor of glutathione S-transferase (GST) P1-1. Ezatiostat leads to JNK activation by inhibiting GSTP1. Ezatiostat stimulates both lymphocyte production and bone marrow progenitor proliferation. |
| M2375 | Aloperine | Aloperine is exhibits anti-inflammatory, antibacterial, antiviral, and anti-tumor properties. |
| M1955 | 23-Hydroxybetulinic acid | 23-Hydroxybetulinic acid is a novel anticancer substance. |
| M58358 | DB2115 tertahydrochloride | DB2115 tertahydrochloride is a potent inhibitor of myeloid master regulator PU.1. DB2115 tertahydrochloride has the potential for researching cancers, including hematologic cancers. |
| M58200 | 14-3-3η Protein inhibitor 1 | 14-3-3η Protein inhibitor 1 is a 14-3-3η protein inhibitor with a KD of 35 µM. |
| M55877 | SEC | SEC induces activation of ANXA7 GTPase via the AMPK/mTORC1/STAT3 signaling pathway. |
| M55876 | Ap4A | Ap4A (P1,P4-Di-(adenosine-5')-tetraphosphate) is a conserved second messenger in organisms ranging from bacteria to humans. |
| M55874 | YM281 | YM281 is a potent EZH2 inhibitor. |
| M55873 | DB1976 | DB1976 is a selenophene analog of DB270 and a potent and cell-permeable fully efficacious transcription factor PU.1 inhibitor. |
| M55871 | STM3006 | STM3006 is a highly potent, selective and orally active METTL3 inhibitor. |
| M55870 | LYG-202 | LYG-202, a flavonoid, has potent anti-angiogenic and antitumor activity. |
| M55869 | nor-NOHA | nor-NOHA is a selective and reversible arginase inhibitor. |
| M55868 | Benidipine | Benidipine is a potent and orally active calcium channel antagonist. |
| M55867 | Oxythiamine | Oxythiamine (Hydroxythiamin), an analogue of anti-metabolite, can suppress the non-oxidative synthesis of ribose and induce cell apoptosis. |
| M55866 | Imifoplatin | Imifoplatin (PT-112) is a platinum-based agent belonging to the phosphaplatin family. |
| M55865 | Sparfosic acid | Sparfosic acid, a DNA antimetabolite agent, is a potent inhibitor of aspartate transcarbamoyl transferase, the enzyme catalyzing the second step of de novo pyrimidine biosynthesis. |
| M55864 | Flurochloridone | Flurochloridone (R-40244) is a selective preemergence and persistent herbicide. |
| M55863 | Ap4A tetraammonium | Ap4A tetraammonium (P1,P4-Di-(adenosine-5')-tetraphosphate tetraammonium) is a conserved second messenger in organisms ranging from bacteria to humans. |
| M55862 | Oxythiamine chloride | Oxythiamine (Hydroxythiamine) chloride, an analogue of anti-metabolite, can suppress the non-oxidative synthesis of ribose and induce cell apoptosis. |
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