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SpiD3

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Catalog No. T88296Cas No. 3033533-25-1
Alias SpiD 3

SpiD3 is an antitumor spirocyclic dimer with the advantage of being independent of TME (tumor microenvironment) stimulation. It induces apoptosis in chronic lymphocytic leukemia (CLL) cells, inhibits NF-κB activation, upregulates the UPR (unfolded protein response), and suppresses protein synthesis. It can be used to study BTK-mutated CLL.

SpiD3

SpiD3

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Purity: 99.15%
Catalog No. T88296Alias SpiD 3Cas No. 3033533-25-1
SpiD3 is an antitumor spirocyclic dimer with the advantage of being independent of TME (tumor microenvironment) stimulation. It induces apoptosis in chronic lymphocytic leukemia (CLL) cells, inhibits NF-κB activation, upregulates the UPR (unfolded protein response), and suppresses protein synthesis. It can be used to study BTK-mutated CLL.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$52-In Stock
5 mg$123-In Stock
10 mg$197-In Stock
25 mg$396-In Stock
50 mg$637-In Stock
100 mg$987-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.15%
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Product Introduction

Bioactivity
Description
SpiD3 is an antitumor spirocyclic dimer with the advantage of being independent of TME (tumor microenvironment) stimulation. It induces apoptosis in chronic lymphocytic leukemia (CLL) cells, inhibits NF-κB activation, upregulates the UPR (unfolded protein response), and suppresses protein synthesis. It can be used to study BTK-mutated CLL.
In vitro
SpiD3 (0.01–100 µM; 72 hours) exhibits antiproliferative properties in chronic lymphocytic leukemia (CLL) cell lines [1].
SpiD3 (0.25–1 µM) induced apoptosis in CLL cell lines after 24 hours of treatment and caused CLL cells to accumulate in the G0–G1 phase after 48 hours, with a corresponding decrease in the number of cells in the G2–M phase [1].
SpiD3 (0.5–2 µM; 4 h) induces the unfolded protein response (UPR) and inhibits protein translation in chronic lymphocytic leukemia (CLL) cells [1].
In vivo
Methods: SpiD3_AP (a dimethylamino prodrug of SpiD3) was administered at 10 mg/kg to Eµ-TCL1 transgenic leukemia mice via daily intravenous injection for 3 days.
Results: SpiD3_AP reduced tumor burden in Eµ-TCL1 mice, with significant downregulation of oncogenic MYC protein expression [1].
SynonymsSpiD 3
Chemical Properties
Molecular Weight470.47
FormulaC27H22N2O6
Cas No.3033533-25-1
SmilesO=C1OC2(C(=O)N(C=3C=CC=CC32)CCCN4C(=O)C5(OC(=O)C(=C)C5)C=6C=CC=CC64)CC1=C
ColorYellow
AppearanceSolid
Storage & Solubility Information
Storagekeep away from moisture,store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 20 mg/mL (42.51 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1255 mL10.6277 mL21.2553 mL106.2767 mL
5 mM0.4251 mL2.1255 mL4.2511 mL21.2553 mL
10 mM0.2126 mL1.0628 mL2.1255 mL10.6277 mL
20 mM0.1063 mL0.5314 mL1.0628 mL5.3138 mL

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