About 8 results found for searched term "DT-3" (0.051 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M7023 | NDT 9513727 | Others |
| NDT 9513727 is a potent, selective human C5a receptor antagonist. | ||
| M9176 | DTP3 | JNK |
| DTP3 is a selective GADD45β/MKK7 inhibitor, which inhibits cancer-selective NF-κB survival pathway. | ||
| M20581 | Desmethylanethol trithione | Apoptosis |
| ADT-OH; 5-(4-Hydroxyphenyl)-3H-1,2-dithiole-3-thione; ACS 1 | ||
| Desmethylanethol trithione (ADT-OH) is a derivative of anethole dithiolethione (ADT) and synthetic hydrogen sulfide (H2S) donor. ADT-OH induces apoptosis and inhibits the development of melanoma in vivo by upregulating FADD. | ||
| M20702 | Alovudine | Reverse Transcriptase |
| CL 184824, FddThd, FLT, MIV-310 | ||
| 3'-Fluoro-3'-deoxythymidine (Alovudine) is a potent inhibitor of polymerase γ and reverse transcriptase that can be used in the treatment of HIV infection. 3'-Fluoro-3'-deoxythymidine (Alovudine) is also a marker of DNA synthesis that can be used as an early response biomarker in the chemotherapy of pancreatic cancer. | ||
| M29154 | FKBP12 PROTAC dTAG-13 | PROTAC |
| dTAG-13 | ||
| FKBP12 PROTAC dTAG-13 (dTAG-13), a PROTAC-based heterobifunctional degrader, is a selective degrader of FKBP12F36V with expression of FKBP12F36V in-frame with a protein of interest. FKBP12 PROTAC dTAG-13 effectively engages FKBP12F36V and CRBN, thereby selectively degrading FKBP12F36V. | ||
| M42097 | BDTX-1535 | EGFR/HER2 |
| EGFR-IN-76 | ||
| BDTX-1535 (EGFR-IN-76) is a potent inhibitor of EGFR. | ||
| M53108 | DT-3 | Guanylate Cyclase |
| DT-3 is a membrane-permeable protein kinase G Iα inhibitory peptide. | ||
| M54506 | DTP3 TFA | DNA/RNA Synthesis |
| DTP3 TFA is a potent and selective GADD45β/MKK7 (growth arrest and DNA-damage-inducible β/mitogen-activated protein kinase kinase 7) inhibitor. | ||
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