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TD034 is a selective, reversible, non-covalent inhibitor of HDAC11, with an IC50 of 5.1 nM and a Ki of 1.5 nM. It does not inhibit other HDACs or sirtuins. TD034 inhibits the desuccinylation of SHMT2 (a substrate of HDAC11) and lowers YAP1 levels by inhibiting HDAC11. TD034 is applicable for lung cancer research.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | TD034 is a selective, reversible, non-covalent inhibitor of HDAC11, with an IC50 of 5.1 nM and a Ki of 1.5 nM. It does not inhibit other HDACs or sirtuins. TD034 inhibits the desuccinylation of SHMT2 (a substrate of HDAC11) and lowers YAP1 levels by inhibiting HDAC11. TD034 is applicable for lung cancer research. |
| Targets&IC50 | HDAC11:5.1 nM |
| In vitro | TD034 at a concentration of 2 μM significantly enhances the acylation level of SHMT2 in HEK293T cells. At concentrations ranging from 5 to 10 μM, TD034 notably reduces the protein levels of YAP1 in A549 cells and decreases the mRNA levels of the two YAP1 target genes, CTGF and CYR61. |
| Molecular Weight | 757.01 |
| Formula | C45H64N4O6 |
| Cas No. | 3030718-42-1 |
| Smiles | C(CCCCCCCCCC)[C@@H]1[C@@H](C(CCCCC[C@@H]2NC(=O)[C@@]3(N(C(=O)[C@H](CC4=CC=CC=C4)NC(=O)[C@H](CC5=CC=CC=C5)NC2=O)CCCC3)[H])=O)O1 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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