All ProductsDisplaying Products by Catalog Number (7900 - 7999)
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| Cat. No. | Product Name / Activity |
|---|---|
| 7900 | SCOTfluor 510 Fmoc-Dapa-OH |
| Fmoc protected fluorescent amino acid for use in solid-phase peptide synthesis to prepare PAINT imaging probes | |
| 7901 | tri-GalNAc-C5-AF647 |
| Fluorescent ASGPR ligand. Application: flow cytometry, fluorescence microscopy | |
| 7902 | PIK 90 |
| Potent PI3K inhibitor, also used in hPSCs mesendoderm differentiation | |
| 7903 | VL 285 |
| VHL inhibitor | |
| 7904 | RU.521 |
| Potent and selective inhibitor of cyclic GMP-AMP synthase (cGAS) | |
| 7909 | ARN 11391 |
| Potentiator of the IP3-gated calcium channel ITPR1 | |
| 7913 | Pomalidomide 5'-piperidine-acid |
| Cereblon ligand with piperidine linker and terminal acid for onward chemistry | |
| 7916 | Risdiplam |
| Selective SMN2 gene splicing modifier | |
| 7917 | TM2 TEAD inhibitor |
| Potent and reversible inhibitor of TEAD mediated Hippo/Yap signalling | |
| 7920 | CoraFluor™ 1, amine reactive |
| Terbium cryptate FRET donor for TR-FRET assay development; amine reactive for conjugation | |
| 7921 | DBCO-NHS |
| Amine reactive and azide reactive building block | |
| 7923 | Pomalidomide 4'-alkylC6-amine |
| Cereblon ligand with alkyl linker and terminal amine for onward chemistry | |
| 7924 | Pomalidomide 4'-PEG5-amine |
| Cereblon ligand with PEG linker and terminal amine for onward chemistry | |
| 7925 | VH 032 amide-alkylC7-acid |
| VHL ligand with alkyl linker and terminal acid for onward chemistry | |
| 7926 | MOMBA |
| Selective orthostatic agonist of hFFA2-DREADDs | |
| 7927 | MSC 1186 |
| Potent and selective SRPK family inhibitor | |
| 7932 | Ac4GalN6yne |
| Alkyne containing monosaccharide building block; used in BOCTAG | |
| 7936 | Ac-Cys-NHMe |
| Building block for the lysine acylation using conjugating enzymes (LACE) technique | |
| 7937 | Trofinetide |
| IGF-1 synthetic analogue | |
| 7940 | HEMTAC 26 New |
| CDK6 and CDK4 HSP90-mediated targeting chimera (HEMTAC) Degrader | |
| 7941 | FSEN 1 |
| Induces ferroptosis; inhibits FSP1 | |
| 7942 | Lac-Phe New |
| Metabolite generated by cytosol nonspecific dipeptidase (CNDP2) during intense exercise | |
| 7943 | DSPC |
| Neutral phospholipid; component of lipid nanoparticles (LNPs) | |
| 7944 | DMG-PEG 2000 |
| PEGylated myristoyl diglyceride; commonly used in the formation of lipid nanoparticles (LNPs) | |
| 7945 | Cholesterol |
| Component of lipid nanoparticles (LNPs); modulator of lipid bilayer fluidity | |
| 7946 | DLin-MC3-DMA |
| Component of lipid nanoparticles (LNPs); ionizable cationic lipid | |
| 7947 | DSPE-PEG 2000 Maleimide |
| PEGylated DSPE with a maleimide reactive group | |
| 7950 | CoraFluor™ 2, amine reactive |
| Terbium cryptate FRET donor for TR-FRET assay development; amine reactive for conjugation | |
| 7952 | CELT-133 |
| Selective hα1A adrenergic receptor fluorescent antagonist | |
| 7953 | CELT-211 |
| Fluorescent serotonin 5HT2B receptor ligand for HTS | |
| 7954 | CELT-327 |
| Potent and selective hA2B/A3 adenosine receptor fluorescent antagonist | |
| 7955 | CELT-426 |
| Potent and partially selective hD2 dopamine receptor fluorescent antagonist | |
| 7956 | VU 0546110 |
| Selective SLO3 potassium channel inhibitor | |
| 7958 | QM-FN-SO3 |
| Blood-brain barrier penetrant, NIR aggregation-induced emission active probe of amyloid β plaques. Used for: in vitro, in situ and in vivo imaging of amyloid β plaques. Application: confocal microscopy and in vivo imaging | |
| 7959 | LSN 3318839 |
| Glucagon-like peptide-1 receptor (GLP1-R) positive allosteric modulator | |
| 7960 | PFI 7 New |
| Selective GID4 antagonist | |
| 7962 | TAT-SAMβA Peptide |
| Selective antagonist of Mfn1-βIIPKC association | |
| 7963 | PFI 653 |
| Potent and selective vanin 1 inhibitor | |
| 7964 | hCAII Degrader 11 New |
| Potent human carbonic anhydrase II Degrader (PROTAC®) | |
| 7969 | SIS17 |
| Selective HDAC11 inhibitor | |
| 7970 | SAHA-FITC |
| Fluorescent HDAC1/2 probe; suitable for use in TR-FRET and FP assays | |
| 7973 | 5-InoAz |
| Metabolic probe for labeling mycobacterium cell envelope | |
| 7974 | P3S |
| Reagent for modifying RNA at 2'-OH position, for SHAPE-MAP experiments | |
| 7978 | BAY 390 |
| Potent and selective TRPA1 antagonist. Brain penetrant and orally bioavailable | |
| 7979 | MU 1742 |
| Potent and selective CK1α, CK1δ and CK1ε inhibitor | |
| 7980 | MTK 458 |
| PINK1 activator | |
| 7981 | Belinostat |
| Potent pan-HDAC inhibitor | |
| 7982 | CS 640 |
| Potent CaM kinase I inhibitor | |
| 7983 | IRAK3 Degrader 23 |
| IRAK3 Degrader (PROTAC® | |
| 7984 | BAY 805 New |
| Potent and selective inhibitor of USP21; also NF-κB activator | |
| 7985 | BDY FL Staurosporine |
| Fluorescent probe targeting kinases; kinase tracer for TR-FRET assays | |
| 7988 | Thalidomide 5'-amine-alkylC6-amine |
| Cereblon ligand with alkyl linker and terminal amine for onward chemistry | |
| 7990 | NRX 252114 |
| Molecular glue Degrader of mutant β-catenin | |
| 7991 | CEPT Cocktail Kit |
| Cell culture supplement for improving stem cell survival | |
| 7994 | PAG 3'-fluoro-4'-piperazine |
| Functionalized cereblon ligand for PROTAC development | |
| 7996 | PAG 3'-piperazine |
| Functionalized cereblon ligand for PROTAC development | |
| 7997 | PAG 3'-piperazine-4-methylpiperidine |
| Cereblon ligand with terminal piperidine for onward chemistry | |
| 7998 | PAG 4'-piperazine |
| Functionalized cereblon ligand for PROTAC development | |
| 7999 | PAG 4'-piperazine-4-methylpiperidine |
| Cereblon ligand with terminal piperidine for onward chemistry |