About 13 results found for searched term "79-06-1" (0.056 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M11469 | Acrylamide | Western Blot |
| Acrylamide is a neurotoxic monomer with a wide range of industrial uses. It is a precursor compound of polyacrylamide. | ||
| M5334 | PF-431396 | FAK |
| PF-431396 is a dual PYK2/FAK inhibitor with IC50 of 11 nM and 2 nM, respectively. | ||
| M7130 | PHCCC | GluR |
| PHCCC is a potent group I mGlu antagonist. | ||
| M16367 | 3α-Cinnamoyloxypterokaurene L3 | Diterpenoids |
| 3α-Cinnamoyloxypterokaurene L3 | ||
| M16371 | 3α-Angeloyloxypterokaurene L3 | Diterpenoids |
| 3α-Angeloyloxypterokaurene L3 | ||
| M20810 | PBD-150 | Amyloid |
| PBD-150 is a potent human glutaminyl cyclase (hQC) Y115E-Y117E variant inhibitor with Ki of 60 nM. | ||
| M28867 | VH032-PEG5-C6-Cl | PROTAC |
| HaloPROTAC 2 | ||
| VH032-PEG5-C6-Cl (HaloPROTAC 2) is a conjugate of ligands for E3 and 21-atom-length linker. The connector of linker is Halogen group. VH032-PEG5-C6-Cl incorporates the VH032 based VHL ligand and 5-unit PEG linker. VH032-PEG5-C6-Cl is capable of inducing the degradation of GFP-HaloTag7 in cell-based assays. | ||
| M30618 | TASIN-1 | Others |
| TASIN-1 is a selective inhibitor of truncated APC gene (adenomatous polyposis coli gene) and exerts cytotoxic effects through inhibition of cholesterol biosynthesis. TASIN-1 represents a potential therapeutic strategy for prevention and intervention in CRC with mutant APC. | ||
| M38905 | Boc-L-Alaninol | Others |
| Boc-L-Alaninol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||
| M39194 | (-)-Corynoxidine | AChR/AChE |
| (-)-Corynoxidine is an acetylcholinesterase inhibitor with an IC50 value of 89.0 μM, isolated from the aerial parts of Corydalis speciosa. (-)-Corynoxidine exhibits antibacterial activities against Staphylococcus aureus and methicillin-resistant S. aureus strains in different degrees. | ||
| M41086 | Urease-IN-8 | Antibiotic |
| Urease-IN-8 is a competitive Urease inhibitor (IC50: 3.51 μM, Ki: 3.11 μM). | ||
| M45288 | Casein Kinase inhibitor A86 | Casein Kinase |
| Casein Kinase inhibitor A86 is a potent and orally active casein kinase 1α (CK1α) inhibitor that also inhibits CDK7 (TFIIH) and CDK9 (P-TEFb). In addition, Casein Kinase inhibitor A86 induces apoptosis in leukemia cells and may be used in leukemia-related studies. | ||
| M50716 | H-Glu-Val-OH | Others |
| H-Glu-Val-OH is a polypeptide that can be found by peptide screening. | ||
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