| 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 |
| M56841 | 3-Chloro-6-methylpyridazine | 3-Chloro-6-methylpyridazine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
| M56840 | 2,4-Dichloro-5-nitropyridine | 2,4-Dichloro-5-nitropyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
| M56839 | Oleoyl Coenzyme A triammonium | Oleoyl coenzyme A triammonium is the salt form of Oleoyl coenzyme A, which exhibits an inhibitory effects for neutral lipase. |
| M56838 | DAB | 3,3'-Diaminobenzidine, also known as 3,3',4,4'-tetraaminobiphenyl, consists of a biphenyl backbone, with each of the four carbon atoms at the para-position of the two benzene rings linked with Amino. |
| M56837 | 1-Hexadecylglycero-3-phosphate | 1-Hexadecyl lysophosphatidic acid is an ether analog of lysophosphatidic acid (LPA) containing a hexadecyl group in the sn-1 position. |
| M56835 | Decyltrimethylammonium chloride | N,N,N-Trimethyldecan-1-aminium chloride is a compound belonging to the class of quaternary ammonium compounds. |
| M56834 | Adenosine 3'-phosphate 5'-phosphosulfate lithium | Adenosine 3'-phosphate 5'-phosphosulfate lithium is a co-substrate used for the sulfonation of glycans. |
| M56833 | 3′-Phosphoadenosine 5′-phosphosulfate tetralithium salt | 3′-Phosphoadenosine 5′-phosphosulfate tetralithium salt (PAPS tetralithium salt) is the cosubstrate and the source of sulfonic acid groups in sulfation reactions. |
| M56822 | NAG-thiazoline | NAG-thiazoline is a O-GlcNAcase inhibitor with a Ki of 180 nM. |
| M56792 | 3FAx-Neu5Ac | 3FAx-Neu5Ac, a Sialic acid peracetylated analog, is a sialyltransferase inhibitor. |
| M56778 | Y-29794 | Y-29794 is a selective, orally active inhibitor for non-peptide prolyl endopeptidase (PREP), with an IC50 of 3 nM and a Ki of 0.95 nM. |
| M56777 | Y-29794 tosylate | Y-29794 tosylate is a selective, orally active inhibitor for non-peptide prolyl endopeptidase (PREP), with an IC50 of 3 nM and a Ki of 0.95 nM. |
| M56729 | 4-(6-Bromo-2-benzothiazolyl)benzenamine | 4-(6-Bromo-2-benzothiazolyl)benzenamine is a β-amyloid PET (positron emission tomography) tracer that can be used in the diagnosis of neurological diseases, such as Alzheimer's and Down's syndrome. |
| M56728 | Candoxatril | Candoxatril is a neutral endopeptidase (NEP) inhibitor. |
| M56705 | Galloflavin potassium | Galloflavin potassium is a novel lactate dehydrogenase inhibitor that can be used for the research of cancer. |
| M56692 | SSM3 tetraTFA | SSM3 tetraTFA is a potent synthetic furin inhibitor with an EC50 and a Ki of 54 nM and 12 nM, respectively. |
| M56609 | Indoluidin E | Indoluidin E selectively inhibits DHODH and suppresses cancer cell growth. |
| M56603 | Nitecapone | Nitecapone (OR-462) is an orally active and short-acting catechol-O-methyltransferase (COMT) inhibitor with gastroprotective and antioxidant properties. |
| M56602 | SACLAC | SACLAC, a Ceramide analog, is a potent and covalent acid ceramidase (ASAH1; AC) inhibitor with a Ki of 97.1 nM. |
| M56601 | Acid Ceramidase-IN-1 | Acid Ceramidase-IN-1 is a potent and oral bioavailable acid ceramidase (AC, ASAH-1) inhibitor (hAC IC50=0.166 μM). |
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