1. PROTAC
  2. Ligand for E3 Ligase
  3. TD-106

TD-106 

Cat. No.: HY-114406 Purity: 98.98%
Handling Instructions

TD-106 is a cereblon (CRBN) modulator, which can be used for targeted protein degradation. BRD4 PROTACs with TD-106 induce BRD4 degradation.

For research use only. We do not sell to patients.

TD-106 Chemical Structure

TD-106 Chemical Structure

CAS No. : 2250288-69-6

Size Price Stock Quantity
10 mM * 1 mL in DMSO USD 385 In-stock
Estimated Time of Arrival: December 31
5 mg USD 350 In-stock
Estimated Time of Arrival: December 31
10 mg USD 550 In-stock
Estimated Time of Arrival: December 31
50 mg USD 1950 In-stock
Estimated Time of Arrival: December 31
100 mg USD 2950 In-stock
Estimated Time of Arrival: December 31
200 mg   Get quote  
500 mg   Get quote  

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Customer Review

Based on 1 publication(s) in Google Scholar

Top Publications Citing Use of Products
  • Biological Activity

  • Technical Information

  • Purity & Documentation

  • References

Description

TD-106 is a cereblon (CRBN) modulator, which can be used for targeted protein degradation. BRD4 PROTACs with TD-106 induce BRD4 degradation[1].

IC50 & Target

CRBN[1]

In Vitro

TD-106 (0.1 nM, 1 nM, 10 nM, 100 nM, 1000 nM, 10 μM, and 100 μM; 72 hours) inhibits the proliferation of NCI-H929 myeloma cell line with an CC50 of 0.039 μM[1].
TD-106 (1, 10, 100, and 1000 nM) induces the degradation of IKZF1/3 in NCI-H929 cells[1].

Cell Cytotoxicity Assay[1]

Cell Line: NCI-H929 cells
Concentration: 72 hours
Incubation Time: 0.1 nM, 1 nM, 10 nM, 100 nM, 1000 nM, 10 μM, and 100 μM
Result: Inhibited cell proliferation with an CC50 of 0.039 μM.
In Vivo

TD-106 (50 mg/kg; intraperitoneally; q.d. for 14 days) possesses anti-myeloma activity in SCID mice with TMD-8 xenograft model.

Animal Model: Female SCID (CB-17/IcrCri-scid) mice with TMD-8 xenograft model[1]
Dosage: 50 mg/kg
Administration: Intraperitoneally (i.p.); q.d. for 14 days
Result: Treatment inhibited tumor growth during this duration.
Storage
Powder -20°C 3 years
  4°C 2 years
In solvent -80°C 6 months
  -20°C 1 month
Solvent & Solubility
In Vitro: 

DMSO : ≥ 125 mg/mL (457.46 mM)

*"≥" means soluble, but saturation unknown.

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 3.6597 mL 18.2983 mL 36.5965 mL
5 mM 0.7319 mL 3.6597 mL 7.3193 mL
10 mM 0.3660 mL 1.8298 mL 3.6597 mL
*Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

    Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.5 mg/mL (9.15 mM); Clear solution

  • 2.

    Add each solvent one by one:  10% DMSO    40% PEG300    5% Tween-80    45% saline

    Solubility: ≥ 2.5 mg/mL (9.15 mM); Clear solution

*All of the co-solvents are provided by MCE.
References
Molecular Weight

273.25

Formula

C₁₂H₁₁N₅O₃

CAS No.

2250288-69-6

SMILES

NC1=CC=CC(N=NN2C3CCC(NC3=O)=O)=C1C2=O

Shipping

Room temperature in continental US; may vary elsewhere

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The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
× = ×
C1   V1   C2   V2

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Product Name:
TD-106
Cat. No.:
HY-114406
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TD-106

Cat. No.: HY-114406