| 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 |
| M42925 | Cy-FBP/SBPase-IN-1 | Cy-FBP/SBPase-IN-1 is a Cy-FBP/SBPase inhibitor, which is an important regulatory enzyme in cyanobacterial photosynthesis. |
| M42924 | XY-52 | XY-52 is a Stimulation-2 (ST2) inhibitor, with an IC50 value of 5.68 μM in AlphaLISA assay, and 4.59 μM in HEK-Blue assay. |
| M42923 | AST 7062601 | AST 7062601 (AST070) is a Ucp1 inducer that strongly induces endogenous Ucp1 expression in primary mouse brown adipocytes. |
| M42922 | Z-Nle-Lys-Arg-AMC | Z-Nle-Lys-Arg-AMC is a fluorogenic peptide substrate that specifically monitors cathepsin B activity over a broad pH range. |
| M42921 | TP-5801 TFA | TP-5801 TFA is an orally active TNK1 (non-receptor tyrosine kinase) inhibitor (IC50=1.40 nM), and shows anti-tumor activity. |
| M42920 | GPR52 receptor modulator 1 | GPR52 receptor modulator 1 (Procedure 1) is a GPR52 receptor modulator with the potential to study neuropsychiatric diseases. |
| M42919 | Thozalinone | Thozalinone also known as 5phenyl-2-dimethylamino-2-oxazolin-4-one, is an antidepressant with activity against Tetrabenazine. |
| M42918 | 11alpha-Hydroxyprogesterone | 11alpha-Hydroxyprogesterone is the inactive analogue of 11beta-Hydroxyprogesterone, and can be used as an experimental control. |
| M42916 | L-γ-Glutamyl-L-glutamic acid | L-γ-Glutamyl-L-glutamic acid is the inactive isomer of D-γ-Glutamyl-D-glutamic acid, and can be used as an experimental control. |
| M42915 | Methyltetrazine-amine hydrochloride | Methyltetrazine-Amine, a tetrazine compound, is used for the site-specific dual functionalization of the resulting bioconjugates. |
| M42914 | WRN inhibitor 5 | WRN inhibitor 5, a cyclic vinyl sulfone compound, is a Wemer Syndrome ATP dependent helicase enzyme (WRN) inhibitor. |
| M42912 | WRN inhibitor 3 | WRN inhibitor 3, a cyclic vinyl sulfone compound, is a Wemer Syndrome ATP dependent helicase enzyme (WRN) inhibitor. |
| M42911 | Fluocinolone | Fluocinolone is a corticosteroid that is used to relieve redness, itching, swelling, or other discomfort caused by skin conditions. |
| M42910 | PDCD4-IN-1 | PDCD4-IN-1is a PDCD4 inhibitor with a Kd value of 350 nM, which can promote the expression of BDNF in hippocampal neuron cell HT-22. |
| M42909 | Thiotraniliprole | Thiotraniliprole is an ortho formamidobenzamide insecticide that can be used for the synthesis of insecticidal combinations. |
| M42908 | Bistrifluron | Bistrifluron has insecticidal effects on the larval stage, and also has an effect on adult longevity, reproduction, and hatchability. |
| M42907 | Anhydroleucovorin | Anhydroleucovorin is a form of tetrahydrofolate and is a substrate for cyclohydrolase, which converts it to 10-formyltetrahydrofolate. |
| M42906 | HDAC-IN-55 | HDAC-IN-55(8j) is a small molecular compound that can increase the expression of E-cadherin and inhibit the proliferation of cancer cells. |
| M42905 | Cathepsin Inhibitor 3 | Cathepsin Inhibitor 3 is a non-radioactive intermediate in compound [18F] 2k radioactive synthesis, which has selectivity for cathepsin S. |
| M42904 | Cyclohexanoyl coenzyme A | Cyclohexanoyl coenzyme A is the active form of cyclohexane carboxylic acid (CHC) from anaerobic degradation in Rhodopseudomonas palustris. |
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