All ProductsDisplaying Products by Catalog Number (7100 - 7199)
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| Cat. No. | Product Name / Activity |
|---|---|
| 7104 | VH 032 amide-PEG1-acid New |
| VHL ligand with PEG linker and terminal acid for onward chemistry | |
| 7105 | VH 032 amide-PEG5-acid New |
| VHL ligand with PEG linker and terminal acid for onward chemistry | |
| 7106 | VH 032 amide-alkylC2-acid New |
| VHL ligand with alkyl linker and terminal acid for onward chemistry | |
| 7107 | VH 032 amide-alkylC6-acid |
| VHL ligand with alkyl linker and terminal acid for onward chemistry | |
| 7108 | VH 032 amide-alkylC8-acid |
| VHL ligand with alkyl linker and terminal acid for onward chemistry | |
| 7116 | Chemerin-9, Human |
| Potent CMKLR1 agonist; c-terminal peptide of full length human chemerin | |
| 7117 | Chemerin-9, Mouse |
| Potent CMKLR1 agonist; c-terminal peptide of full length mouse chemerin | |
| 7119 | Sorbic acid |
| Activator of hFFA2-DREADDs | |
| 7121 | 7-Aminoactinomycin D |
| Fluorescent DNA stain | |
| 7131 | TM 38837 New |
| Highly potent CB1 inverse agonist; peripherally restricted | |
| 7143 | VX 765 New |
| High affinity and selective caspase-4 and caspase 1/ICE inhibitor; orally bioavailable | |
| 7150 | Tocriscreen 2.0 Max |
| Bioactive compound library for high-throughput screening, high-content screening and chemical biology applications; comprised of 1280 biologically active compounds (250 μL 10 mM DMSO solutions) | |
| 7151 | Tocriscreen 2.0 Mini |
| Bioactive compound library for high-throughput screening, high-content screening and chemical biology applications; comprised of 1280 compounds (50 μL 10 mM DMSO solutions) | |
| 7152 | Tocriscreen 2.0 Micro |
| Bioactive compound library for high-throughput screening, high-content screening and chemical biology applications; comprised of 1280 biologically active compounds (15 μL 10 mM DMSO solutions) | |
| 7156 | WQ 1 New |
| Potent and selective σ1 receptor antagonist; active in vivo | |
| 7158 | FMF-04-159-2 New |
| Potent covalent CDK14 and CDK16 inhibitor; also inhibits other TAIRE kinase family members | |
| 7159 | FMF-04-159-R New |
| Potent CDK14 and CDK16 inhibitor; displays reversible inhibition of CDK14 | |
| 7160 | DD 03-171 |
| Potent and selective BTK Degrader | |
| 7162 | iFSP1 |
| Ferroptosis suppressor protein 1 (FSP1) inhibitor; ferroptosis inducer | |
| 7163 | Chroman 1 |
| Highly potent and selective ROCK 2 inhibitor; improves cell survival after cryogeneisis | |
| 7170 | D-GsMTx4 New |
| TRPC1/6 and Piezo2 inhibitor; resistant to proteolytic digestion | |
| 7175 | DOPE New |
| Liposome/lipoplex transfection reagent | |
| 7177 | NR 7h |
| Potent and selective p38α and p38β degrader; active in vivo | |
| 7178 | LCL 161, phenol New |
| Functionalized IAP ligand for PROTACs | |
| 7182 | SGC 6870 New |
| Potent and selective PRMT6 inhibitor | |
| 7184 | SGC 6870N New |
| Negative control for SGC 6870 (Cat. No. 7182) | |
| 7187 | Zanamivir New |
| Potent influenza virus neuraminidase inhibitor | |
| 7188 | Carfilzomib New |
| Potent irreversible proteasome inhibitor; active in vivo | |
| 7189 | Saracatinib New |
| Potent and selective Src tyrosine kinase family inhibitor; anticancer; antiviral; orally bioavailable | |
| 7191 | Santacruzamate A New |
| Highly potent and selective HDAC2 inhibitor | |
| 7192 | SMIP 004 New |
| SKP2 (S-phase kinase-associated protein 2) inhibitor; upregulates p27 and arrests cell cycle in G1 phase | |
| 7193 | Deschloroclozapine New |
| High affinity and highly potent activator of hM3Dq and hM4Di DREADDs; rapidly blood brain barrier penetrant | |
| 7197 | JHU 37152 New |
| High affinity and highly potent hM3Dq and hM4Di DREADD agonist; blood brain barrier penetrant | |
| 7198 | JHU 37160 New |
| High affinity and highly potent hM3Dq and hM4Di DREADD agonist; blood brain barrier penetrant | |
| 7199 | (±)-Eriodictyol New |
| Potent TRPV1 antagonist; also antioxidant; activates Nrf2/ARE signaling |