LDC-4297 HCl (1453834-21-3(free base))

SKU: orb1302877

Description

LDC4297 is a highly potent and selective inhibitor of CDK7, exhibiting an IC50 value of 0.13 nM. This compound is a valuable chemical probe for researching transcription and cell cycle regulation in vitro and has shown antitumor activity in preclinical cancer models.

Research Area

Cell Biology

Key Properties

• MW: 469.02
• Purity: 99.81% (May vary between batches)
• Formula: C₂₃H₂₉ClN₈O
• SMILES: Cl.CC(C)c1cnn2c(NCc3ccccc3-n3cccn3)nc(OC3CCCNC3)nc12
• Target: CDK
• Solubility: DMSO:60 mg/mL (127.93 mM)

Bioactivity

• Target IC50:
  CDK7:0.13 nM
• In Vivo:
  An analysis of the PK parameters in CD1 mice reveals positive characteristics after oral administration, as demonstrated for a single-dose treatment (100 mg/kg of LDC4297). The half-life (t1/2z) is determined to be 1.6 h, and a time (Tmax) to a mean peak plasma concentration of 1,297.6 ng/mL is reached 0.5 h after administration, with a continued presence of LDC4297 plasma levels for at least 8 h and a bioavailability of 97.7%
• In Vitro:
  The affinity of LDC4297 for CDK7 proves to be extremely high. Kinase assays performed for CDK1, CDK2, CDK4, CDK6, CDK7, and CDK9 confirms the selective inhibitory activity of LDC4297 for CDK7 in the nano-picomolar range (IC50, 0.13±0.06 nM for CDK7 versus IC50s between 10 nM and 10,000 nM for all other analyzed CDKs). LDC4297 exerts anticytomegaloviral activity. Human cytomegalovirus (HCMV) replication is inhibited by LDC4297 in a concentration-dependent manner with an EC50 value of 24.5±1.3 nM. Inhibition is statistically significant and morphological signs of cytotoxicity only occurrs at concentrations of 3.3 μM or higher. Anti-HCMV activity of LDC4297 is exerted through a multifaceted mode of action that involves an interference with virus-induced Rb phosphorylation. Virus replication is broadly blocked by LDC4297, whereby the antiviral efficacies varied between the viruses used, i.e., strong efficacy for HSV-1 and VZV (EC50s = 0.02 and 0.06 μM, respectively) and intermediate to low efficacy for HSV-2 and EBV (EC50s = 0.27 and 1.21 μM, respectively
• Cell Research:
  A trypan blue exclusion assay is performed with cultured cells seeded in 24-well plates and incubated with increasing concentrations of antiviral compound LDC4297 (range, 0.1 to 50 μM) for the durations indicated. Cell staining is achieved with 0.1% trypan blue for 10 min at room temperature before the percentage of viable cells is determined by microscopic counting

Storage & Handling

• Storage: -20°C
• Expiration Date: 12 months from date of receipt.
• Disclaimer: For research use only

Alternative Names

CDK7, LDC4297 HCl (1453834213(free base)), LDC-4297 HCl (1453834-21-3(free base)), LDC 4297 HCl (1453834 21 3(free base))

Compound Identifiers

PubChem CID

137958370