OTX008 (DC12312) chemical structure
Chemical structureResearch use only
CAT. NO. DC12312Featured

OTX008 (Calixarene 0118; PTX008)

Pack size & price

USD
Ready-made solution
Total$950
We match the best price and quality on market.
Product overview

Description & Application

OTX008 (Calixarene 0118, PTX008) is a galectin-1 inhibitor used in tumor-cell signaling and viability research.

ParameterValue
Chemical NameOTX008 (Calixarene 0118; PTX008)
CAS No.286936-40-1
SynonymsNot available
FormulaC52H72N8O8
M.Wt937.18
SMILESO=C(NCCN(C)C)COC1=C(C2)C=CC=C1CC3=C(OCC(NCCN(C)C)=O)C(CC4=CC=CC(CC5=CC=CC2=C5OCC(NCCN(C)C)=O)=C4OCC(NCCN(C)C)=O)=CC=C3
PurityOn request
Storage2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Galectin-1-associated signaling · Literature evidence

Biological Activity

OTX008 (Calixarene 0118, PTX008) is a galectin-1 inhibitor used in tumor-cell signaling and viability research. OTX008 reduced viability in a dose- and time-dependent manner in both cancer and normal-cell models.

In Vitro

EndpointModel / conditions / sourceReported result
Cell viabilityThree oral squamous-cell carcinoma lines and normal oral keratinocytes; 12.5, 25, 50 or 100 µg/mL. [1]OTX008 reduced viability in a dose- and time-dependent manner in both cancer and normal-cell models.
Transcriptional endpoint25 µg/mL for 48 h; qRT-PCR, n=3. [1]The study assessed FOS-related transcriptional changes after treatment.

In Vivo

No compound-specific animal efficacy result is established by the sources summarized here.

Compound and Evidence Context

EndpointModel / conditions / sourceReported result
Units and selectivityMass-concentration assays. [1]Values are reported in µg/mL rather than being silently converted to µM. Normal-keratinocyte effects limit claims of cancer-specific cytotoxicity.

Interpretation

This study does not demonstrate cancer-cell-exclusive toxicity; normal-cell responses should be considered.

Original studies

References

  1. Greer PFC, et al. Effects of galectin-1 inhibitor OTX008 on oral squamous cell carcinoma cells in vitro and the role of AP-1 and the MAPK/ERK pathway. Archives of oral biology (2022).

Product documentation

Refer to the certificate supplied with your lot for batch-specific release results.

Handling guide

2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

For additional quantities or product documentation, contact info@dcchemicals.com.

Related research products

CD437 chemical structureDC10491

CD437

CD437 is a retinoid-like research compound with direct DNA polymerase α inhibition and antiproliferative activity in cancer-cell models.

View activity & prices
LTX-401 chemical structureDC10988

LTX-401

LTX-401 is an amphipathic amino-acid derivative for cytolytic cell-death and local tumor-immunology research.

View activity & prices

Cart

Request quotation