dTAGV-1 TFA
Based on 6 publication(s) in Google Scholar
dTAGV-1 TFA is a selective FKBP12F36V PORTAC degrader. dTAGV-1 TFA induces rapid degradation of FKBP12F36V-tagged oncogenic fusion proteins, triggering collapse of downstream cellular signaling pathways, reduced proliferative capacity of cancer cells, and decreased levels of target proteins. dTAGV-1 TFA is applicable to functional validation studies of cancer and undegradable oncoproteins.
(Pink: FKBP12 ligand (HY-114420); Blue: VHL ligand (HY-112078); Black: linker (HY-W012001)).
Para uso exclusivo en investigación. No vendemos a pacientes.
- Pureza: 99.92%
- No. CAS: 2624313-15-9
- Fòrmula: C70H91F3N6O16S
- Peso molecular:1361.56
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Almacenamiento:
-20°C, sealed storage, away from moisture and light
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Actividad biológica
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Chemical Information
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Solvente y solubilidad
- Pureza y Documentación
- Referencias
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Help & FAQs
Publications Citing Use of MedChemExpress (MCE) dTAGV-1 TFA
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Customer Validation & Images
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Actividad biológica
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FKBP12 |
VHL |
dTAGV-1 (500 nM; 1-24 h) TFA rapidly degrades FKBP12F36V-KRASG12V and blocks downstream signaling in PATU-8902 FKBP12F36V-KRASG12V; KRAS-/- cells, with its activity dependent on the VHL and proteasome pathways[1].
dTAGV-1 (50-5000 nM; 24 h) TFA potently degrades FKBP12F36V-EWS/FLI and reverses aberrant EWS/FLI-mediated signaling pathways in EWS502 FKBP12F36V-EWS/FLI; EWS/FLI-/- cells, with a hook effect observed at the concentration of 5000 nM[1].
dTAGV-1 (0.1-10 μM; 120 h) TFA reduces the 3D sphere proliferation capacity of PATU-8902 FKBP12F36V-KRASG12V; KRAS-/- cells[1].
dTAGV-1 (1 μM; 0-6 days) TFA inhibits the proliferation of EWS502 FKBP12F36V-EWS/FLI and EWS/FLI-/- cells[1].
Treatment of A549 RPB1dTAG cells with dTAGV-1 (100 nM; 4-12 h) TFA effectively degrades GFP-tagged wild-type RNAPII, enabling acute replacement with Doxycycline (HY-N0565) TFA-induced HA-tagged RNAPII phosphorylation site mutants under conditions where their expression levels match those of wild-type RNAPII[2].
dTAGV-1 (500 nM; 0-48 h) TFA induces rapid degradation of FOCAD protein in MIAPACA2 cells, which in turn causes post-translational depletion of SKIV2L, TTC37 and AVEN proteins without affecting their RNA levels[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:PATU-8902 LACZ-FKBP12F36V
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Concentration:500 nM (in combination with 125-2000 nM THAL-SNS-032 (HY-123937))
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Incubation Time:24 h
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Result:Alone, did not alter CDK9 protein levels.
In combination with THAL-SNS-032, led to pronounced degradation of both LACZ-FKBP12F36V and CDK9 at levels comparable to treatment with each degrader alone, avoiding substrate competition effects.
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Cell Line:PATU-8902 FKBP12F36V-KRASG12V; KRAS-/- (3D-spheroid suspensions)
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Concentration:0.1, 1, 10, 100 nM, 1, 10 μM
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Incubation Time:120 h
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Result:Diminished 3D-spheroid cell proliferation to levels comparable to CRBN-recruiting dTAG molecules.
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Cell Line:A549 cells expressing GFP-FKBP12F36V-tagged wild-type RNAPII (RPB1dTAG) with inducible HA-tagged RNAPII mutants (WT, Y1F, S2A, T4V, S5A, S7A)
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Concentration:100 nM
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Incubation Time:4 h; 12 h
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Result:Rapidly degraded GFP-tagged wild-type RPB1 after 4 hours of treatment.
Confirmed HA-tagged RNAPII mutants were expressed at levels comparable to wild-type RNAPII.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:NOD.Cg-Prkdcscid Il2rgtm1Wjl/SzJ (NSG) (8-week-old female, immunocompromised, leukemia model via tail vein injection of MV4;11 luc-FKBP12F36V cells)[1]
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Dosage:35 mg/kg
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Administration:i.p.; daily; 3 consecutive days
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Result:Induced striking loss of bioluminescent signal 4 hours after the first administration.
Maintained consistent loss of bioluminescent signal 4 hours after each of the three administrations.
Showed evident degradation of bioluminescent signal 28 hours after the final administration.
Chemical Information
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No. CAS 2624313-15-9
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Appearance Solid
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Peso molecular 1361.56
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Fòrmula C70H91F3N6O16S
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Color White to off-white
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SMILES
OC(C(F)(F)F)=O.O=C([C@H]1N(CCCC1)C([C@H](C2=CC(OC)=C(C(OC)=C2)OC)CC)=O)O[C@@H](C3=C(C=CC=C3)OCC(NCCCCCCC(N[C@@H](C(C)(C)C)C(N4[C@@H](C[C@H](C4)O)C(N[C@H](C5=CC=C(C6=C(C)N=CS6)C=C5)C)=O)=O)=O)=O)CCC7=CC(OC)=C(C=C7)OC
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Envío
Room temperature in continental US; may vary elsewhere.
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Almacenamiento
-20°C, sealed storage, away from moisture and light
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
Publications (6)
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Journal Impact Factor
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Most Recent
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Nature
2025 Feb;638(8052):1095-1103. PMID: 39910291
dTAGV-1 TFA purchased from MedChemExpress. Usage Cited in: Nature. 2025 Feb;638(8052):1095-1103. [Abstract]
dTAGV-1 hydrochloride (500 nM; 0-48 h) depleted FOCAD protein levels within four hours. Following FOCAD degradation, levels of SKIV2L, TTC37 and AVEN protein decreased by 8 h, reaching a maximum by 2 days in MIAPACA2 FOCAD-dTAG cells.
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Sci Adv
FeaSion decodes the regulatory landscape and functional diversity of RNA polymerase II CTD phosphorylation. [Abstract]2025 Nov 28;11(48):eadz2345. PMID: 41313762
dTAGV-1 TFA purchased from MedChemExpress. Usage Cited in: Sci Adv. 2025 Nov 28;11(48):eadz2345. [Abstract]
Western blot analysis of total RNAPII, degraded RPB1 (tagged with GFP), and RNAPIImut (tagged with HA; WT, Y1F, S2A, T4V, S5A and S7A) levels before and after Doxycycline (Dox) or dTAGV-1 TFA (100 nM) treatment. α-Tubulin served as the loading control.
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dTAGV-1 TFA purchased from MedChemExpress. Usage Cited in: Mayo Clinic. 2025.
Representative Western blot analysis of KLF5 after 250 nM dTAGV-1 TFA treatment for 0, 1, 4 and 24 h. HSC70 was used as a loading control.
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Solvente y solubilidad
DMSO : ≥ 100 mg/mL (73.45 mM; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
* "≥" means soluble, but saturation unknown.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 3.75 mg/mL (2.75 mM); Clear solution
This protocol yields a clear solution of ≥ 3.75 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (37.5 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Please enter the basic information of animal experiments:
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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
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%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
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%+
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+%Tween-80 + +
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%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL. * In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Pureza y Documentación
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Ficha de datos (282 KB)
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SDS (394 KB)
- English - EN (394 KB)
- Français - FR (394 KB)
- Deutsch - DE (394 KB)
- Norwegian - NO (394 KB)
- Español - ES (394 KB)
- Swedish - SV (394 KB)
- Italian - IT (394 KB)
- Korean - KR (394 KB)
- Portuguese - PT (394 KB)
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Instrucciones de manejo (2659 KB)
Referencias
[1]. Nabet B, et al. Rapid and direct control of target protein levels with VHL-recruiting dTAG molecules. Nature communications. 2020 Sep 18;11(1):4687. [Content Brief]
[2]. Zhu J, et al. FeaSion decodes the regulatory landscape and functional diversity of RNA polymerase II CTD phosphorylation. Science advances. 2025 Nov 28;11(48):eadz2345. [Content Brief]
[3]. Prindle V, et al. Synthetic lethality of mRNA quality control complexes in cancer. Nature. 2025 Feb;638(8052):1095-1103. [Content Brief]
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
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| DMSO | 1 mM | 0.7345 mL | 3.6723 mL | 7.3445 mL | 18.3613 mL |
| 5 mM | 0.1469 mL | 0.7345 mL | 1.4689 mL | 3.6723 mL | |
| 10 mM | 0.0734 mL | 0.3672 mL | 0.7345 mL | 1.8361 mL | |
| 15 mM | 0.0490 mL | 0.2448 mL | 0.4896 mL | 1.2241 mL | |
| 20 mM | 0.0367 mL | 0.1836 mL | 0.3672 mL | 0.9181 mL | |
| 25 mM | 0.0294 mL | 0.1469 mL | 0.2938 mL | 0.7345 mL | |
| 30 mM | 0.0245 mL | 0.1224 mL | 0.2448 mL | 0.6120 mL | |
| 40 mM | 0.0184 mL | 0.0918 mL | 0.1836 mL | 0.4590 mL | |
| 50 mM | 0.0147 mL | 0.0734 mL | 0.1469 mL | 0.3672 mL | |
| 60 mM | 0.0122 mL | 0.0612 mL | 0.1224 mL | 0.3060 mL |
dTAGV-1 TFA Related Classifications
HY-145514 Related Classifications
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