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Chemical Structure| 254964-60-8 Chemical Structure| 254964-60-8

Structure of Tasquinimod
CAS No.: 254964-60-8

Chemical Structure| 254964-60-8

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Tasquinimod allosterically inhibits HDAC4 signalling with antiangiogenic and antineoplastic activities. It is a quinoline-3-carboxamide linomide analogue.

Synonyms: ABR-215050

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Product Details of Tasquinimod

CAS No. :254964-60-8
Formula : C20H17F3N2O4
M.W : 406.36
SMILES Code : O=C(C1=C(O)C2=C(N(C)C1=O)C=CC=C2OC)N(C)C3=CC=C(C(F)(F)F)C=C3
Synonyms :
ABR-215050
MDL No. :MFCD18251454
InChI Key :ONDYALNGTUAJDX-UHFFFAOYSA-N
Pubchem ID :54682876

Safety of Tasquinimod

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Related Pathways of Tasquinimod

epigenetics

Isoform Comparison

Biological Activity

Target
  • HDAC4

In Vitro:

Cell Line
Concentration Treated Time Description References
LNCaP cells 50 µM 24 hours To investigate the effect of Tasquinimod on gene expression, results showed significant up-regulation of TSP1 gene. Mol Cancer. 2010 May 17;9:107.
LP-1 10 µM and 25 µM 24 hours, 48 hours, 72 hours and 120 hours Tasquinimod significantly decreased myeloma cell proliferation and colony formation in vitro, associated with an inhibition of c- MYC and increased p27 expression. J Immunother Cancer. 2023 Jan;11(1):e005319.
OPM-2 10 µM and 25 µM 24 hours, 48 hours, 72 hours and 120 hours Tasquinimod significantly decreased myeloma cell proliferation and colony formation in vitro, associated with an inhibition of c- MYC and increased p27 expression. J Immunother Cancer. 2023 Jan;11(1):e005319.
RPMI-8226 10 µM and 25 µM 24 hours, 48 hours, 72 hours and 120 hours Tasquinimod significantly decreased myeloma cell proliferation and colony formation in vitro, associated with an inhibition of c- MYC and increased p27 expression. J Immunother Cancer. 2023 Jan;11(1):e005319.
5TGM1 10 µM and 25 µM 24 hours, 48 hours, 72 hours and 120 hours Tasquinimod significantly decreased myeloma cell proliferation and colony formation in vitro, associated with an inhibition of c- MYC and increased p27 expression. J Immunother Cancer. 2023 Jan;11(1):e005319.
KG-1a cells 10, 25 µM 24, 48 hours To evaluate the effect of tasquinimod on AML cell survival and proliferation, results showed that tasquinimod significantly reduced AML cell viability and proliferation, and increased apoptosis. Blood Cancer J. 2023 Dec 18;13(1):188.
MOLM-13 cells 10, 25 µM 24, 48 hours To evaluate the effect of tasquinimod on AML cell survival and proliferation, results showed that tasquinimod significantly reduced AML cell viability and proliferation, and increased apoptosis. Blood Cancer J. 2023 Dec 18;13(1):188.
MCF-10A/ErbB2* cells 10 µM 48 hours To study the effect of Tasquinimod on S100A8/9 expression, results showed that Tasquinimod significantly inhibited the expression of S100A8/9. Genes Dev. 2015 Aug 1;29(15):1631-48.
Nasopharyngeal carcinoma cells 5 µM 48 hours Tasquinimod significantly impaired cell proliferation and colony formation in HDAC4-overexpressing cells, indicating that Tasquinimod suppresses nasopharyngeal carcinoma cell proliferation by inhibiting HDAC4 activity. Cell Death Dis. 2021 Feb 1;12(2):137.
LNCaP cells 10 µM 72 hours To investigate the effect of Tasquinimod on TSP1 mRNA expression, results showed significant up-regulation of TSP1 mRNA after 72 hours. Mol Cancer. 2010 May 17;9:107.
LNCaP19 cells 10 µM 72 hours To investigate the effect of Tasquinimod on TSP1 mRNA expression, results showed up-regulation of TSP1 mRNA in LNCaP19 cells. Mol Cancer. 2010 May 17;9:107.
MC38-C215 cells 1 –10 µM 72 hours To evaluate the effect of Tasquinimod on the proliferation of MC38-C215 cells, results showed that Tasquinimod did not significantly inhibit cell proliferation under normoxic or hypoxic conditions. J Immunother Cancer. 2015 Dec 15;3:53.
HUVECs 1 µM one week Tasquinimod inhibits the growth of HUVECs under stressful conditions Cancer Res. 2013 Feb 15;73(4):1386-99.
LNCaP cells 1 µM one week Tasquinimod induces cell death in LNCaP cells under stressful conditions Cancer Res. 2013 Feb 15;73(4):1386-99.

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Mice MBT-2 mouse model Oral gavage 0.1, 1, 10, and 30 mg/kg Twice daily for 21 days Tasquinimod was effective in preventing early stage tumor growth but did not achieve a clear antitumor effect in advanced tumors. The combination of tasquinimod with an Anti-PD-L1 antibody enhanced the antitumor immune response in bladder tumors. Oncoimmunology. 2016 Feb 18;5(6):e1145333
Mice NOD scid mice Oral 10 mg/kg Once daily for 4 days To study the effect of Tasquinimod on the growth of HR?/HER2+ breast cancer tumors, results showed that Tasquinimod significantly reduced tumor growth. Genes Dev. 2015 Aug 1;29(15):1631-48.
Nude mice Nasopharyngeal carcinoma subcutaneous xenograft model Intragastric administration 10 mg/kg Every 3 days for 5 weeks Tasquinimod significantly inhibited tumor growth in HDAC4-overexpressing cells, indicating that Tasquinimod suppresses nasopharyngeal carcinoma tumor growth by inhibiting HDAC4 activity. Cell Death Dis. 2021 Feb 1;12(2):137.
Mice Tuberculosis infection model Oral 10 mg/kg Once daily, 7 days/week Tasquinimod monotherapy enhances bacterial clearance in a mouse model of tuberculosis infection, reduces bacterial burden in lungs and spleens, and significantly decreases the frequency of regulatory T cells (Tregs) and myeloid-derived suppressor cells (MDSCs). Am J Respir Crit Care Med. 2019 Feb 1;199(3):386-389
BABL/C mice DSS-induced ulcerative colitis model Oral 10 mg/kg Administered on days 1, 3, and 5, lasting for 7 days To evaluate the therapeutic effect of MM-PLGA-TAS on DSS-induced ulcerative colitis, the results showed that MM-PLGA-TAS significantly improved weight loss and disease activity index (DAI) scores in mice, and reduced colonic inflammation. J Innate Immun. 2022;14(4):380-392
Nude mice LNCaP prostate tumor model Oral 10 mg/kg/day Once daily for 3 weeks To investigate the effect of Tasquinimod on tumor growth, results showed significant inhibition of tumor growth and up-regulation of TSP1 mRNA and protein levels. Mol Cancer. 2010 May 17;9:107.
Nude mice CWR22-RH human prostate cancer xenograft model Oral 10 mg/kg/day Daily administration until tumor growth reaches 0.250cc Tasquinimod inhibits tumor growth under tumor microenvironment stress Cancer Res. 2013 Feb 15;73(4):1386-99.
FVB mice Castration-resistant prostate cancer model Drinking water 10 mg/kg/day Daily, for 3-4 weeks Tasquinimod significantly enhanced the antitumor effects of two different immunotherapeutics and inhibited distinct MDSC populations and M2-polarized TAMs. Cancer Immunol Res. 2015 Feb;3(2):136-48
Rats AY-27 rat model Oral gavage 2 mg/kg 28 days Tasquinimod was effective in preventing early stage tumor growth but did not achieve a clear antitumor effect in advanced tumors. The combination of tasquinimod with an Anti-PD-L1 antibody enhanced the antitumor immune response in bladder tumors. Oncoimmunology. 2016 Feb 18;5(6):e1145333
C57Bl/6 mice MC38-C215 colon carcinoma model Oral 30 mg/kg Daily, for 14 days To evaluate the effect of Tasquinimod on the growth of MC38-C215 tumors, results showed that Tasquinimod significantly inhibited tumor growth, reduced the number of M2 macrophages in the tumor, and increased the number of M1 macrophages. J Immunother Cancer. 2015 Dec 15;3:53.
C57BL/KaLwRij mice 5TGM1 and 5T33MM models Oral 30 mg/kg Daily until the end of the experiment Tasquinimod significantly reduced the tumor load and increased the trabecular bone volume, which resulted in prolonged overall survival of MM- bearing mice in vivo. J Immunother Cancer. 2023 Jan;11(1):e005319.
C57BL/6 mice MC38 colon cancer model Oral gavage 30 mg/kg Once daily for 15 days To evaluate the antitumor efficacy of Tasquinimod in combination with anti-PD-1 antibody in the MC38 colon cancer model. The results showed that the combination treatment significantly delayed tumor growth and exhibited higher tumor inhibition efficacy compared to anti-PD-1 or Tasquinimod alone. Cell Rep Med. 2023 Apr 18;4(4):100987

Clinical Trial:

NCT Number Conditions Phases Recruitment Completion Date Locations
NCT01048203 Healthy PHASE1 COMPLETED 2025-03-09 JJ Berzelius Clinical Research... More >> Center AB, Berzelius Science Park, Link?ping, 582 25, Sweden Less <<
NCT06605586 Myelofibrosis PHASE1|PHASE2 NOT_YET_RECRUITING 2025-03-30 DE-Aachen-UKAACHEN, Aachen, Ge... More >>rmany|NL-Amsterdam-AmsterdamUMC, Amsterdam, Netherlands|NL-Groningen-UMCG, Groningen, Netherlands|NL-Nijmegen-RADBOUDUMC, Nijmegen, Netherlands|NL-Rotterdam-ERASMUSMC, Rotterdam, Netherlands|NL-Utrecht-UMCUTRECHT, Utrecht-, Netherlands Less <<

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.46mL

0.49mL

0.25mL

12.30mL

2.46mL

1.23mL

24.61mL

4.92mL

2.46mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

 

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