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Displaying Products by Catalog Number (7100 - 7199)

Cat. No. Product Name / Activity
7104 VH 032 amide-PEG1-acid
VHL ligand with PEG linker and terminal acid for onward chemistry
7105 VH 032 amide-PEG5-acid
VHL ligand with PEG linker and terminal acid for onward chemistry
7106 VH 032 amide-alkylC2-acid
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
Highly potent CB1 inverse agonist; peripherally restricted
7143 VX 765
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
Potent and selective σ1 receptor antagonist; active in vivo
7158 FMF-04-159-2
Potent covalent CDK14 and CDK16 inhibitor; also inhibits other TAIRE kinase family members
7159 FMF-04-159-R
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
TRPC1/6 and Piezo2 inhibitor; resistant to proteolytic digestion
7175 DOPE
Liposome/lipoplex transfection reagent
7177 NR 7h
Potent and selective p38α and p38β degrader; active in vivo
7178 LCL 161, phenol
Functionalized IAP ligand for PROTACs
7182 SGC 6870
Potent and selective PRMT6 inhibitor
7184 SGC 6870N
Negative control for SGC 6870 (Cat. No. 7182)
7187 Zanamivir
Potent influenza virus neuraminidase inhibitor
7188 Carfilzomib
Potent irreversible proteasome inhibitor; active in vivo
7189 Saracatinib
Potent and selective Src tyrosine kinase family inhibitor; anticancer; antiviral; orally bioavailable
7191 Santacruzamate A
Highly potent and selective HDAC2 inhibitor
7192 SMIP 004
SKP2 (S-phase kinase-associated protein 2) inhibitor; upregulates p27 and arrests cell cycle in G1 phase
7193 Deschloroclozapine
High affinity and highly potent activator of hM3Dq and hM4Di DREADDs; rapidly blood brain barrier penetrant
7197 JHU 37152
High affinity and highly potent hM3Dq and hM4Di DREADD agonist; blood brain barrier penetrant
7198 JHU 37160
High affinity and highly potent hM3Dq and hM4Di DREADD agonist; blood brain barrier penetrant
7199 (±)-Eriodictyol
Potent TRPV1 antagonist; also antioxidant; activates Nrf2/ARE signaling

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