Description
A synthetic peptide that is potent, cell permeable, nontoxic and irreversibly inhibits caspase activity to blocks apoptosis. The new generation of caspase inhibitor is more stable in aqueous environment and exhibits several folds higher activity than the corresponding FMK caspase inhibitors. Q-VD-OPH is the inhibitor of choice for both in vitro and in vivo studies.
Q-VD-Oph is a potent, cell-permeable, non-toxic, next generation pan-caspase inhibitor useful for in vivo studies.
Alternate Name/Synonyms: Q-Val-Asp-Oph, Q-VD-Oph
Appearance: Lyophilized solid
Formulation: N/A
CAS Number: 1135695-98-5
Structure Available?: Yes
Peptide sequence: Quinolyl-Val-Asp-OPh
Salt Form: No
Molecular Formula: C₂₆H₂₅F₂N₃O₆
Molecular Weight: 513.49
Cell-Permeable?: Yes
Purity: >95% by HPLC
Solubilities: DMSO
Handling: Protect from light and moisture
Country of Origin: USA
Tag Line: A pan-caspase inhibitor
MDL Number: MFCD20527311
PubChem CID: 11237609
SMILES: CC(C)C(C(=O)NC(CC(=O)O)C(=O)COC1=C(C=CC=C1F)F)NC(=O)C2=NC3=CC=CC=C3C=C2
InChi: InChI=1S/C26H25F2N3O6/c1-14(2)23(31-25(35)19-11-10-15-6-3-4-9-18(15)29-19)26(36)30-20(12-22(33)34)21(32)13-37-24-16(27)7-5-8-17(24)28/h3-11,14,20,23H,12-13H2,1-2H3,(H,30,36)(H,31,35)(H,33,34)
InChi Key: OOBJCYKITXPCNS-UHFFFAOYSA-N
Additional Information
Storage Condition: |
-20°C |
Shipping Condition: |
Gel Pack |
Shelf Life: |
12 months |