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Type HazMat fee for 500 gram (Estimated)
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Limited Quantity USD 15-60
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Inaccessible (Haz class 6.1), International USD 150+
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Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 960055-56-5 Chemical Structure| 960055-56-5

Structure of Panobinostat lactate
CAS No.: 960055-56-5

Chemical Structure| 960055-56-5

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Panobinostat lactate is a potent, orally active non-selective HDAC inhibitor with antineoplastic activities. It disrupts HIV latency, induces cell apoptosis and autophagy, and is used in the study of refractory or relapsed multiple myeloma.

Synonyms: LBH589 lactate; NVP-LBH589 lactate

4.5 *For Research Use Only !

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Product Details of Panobinostat lactate

CAS No. :960055-56-5
Formula : C24H29N3O5
M.W : 439.50
SMILES Code : O=C(NO)/C=C/C1=CC=C(CNCCC2=C(C)NC3=C2C=CC=C3)C=C1.CC(O)C(O)=O
Synonyms :
LBH589 lactate; NVP-LBH589 lactate
MDL No. :N/A

Safety of Panobinostat lactate

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301+H331-H315-H318-H360-H373
Precautionary Statements:P201-P202-P260-P264-P270-P271-P280-P301+P310+P330-P302+P352-P304+P340+P311-P305+P351+P338+P310-P308+P313-P332+P313-P403+P233-P405-P501
Class:6.1
UN#:2811
Packing Group:

Related Pathways of Panobinostat lactate

epigenetics

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
J89GFP lymphocyte 40 nM 24 h To evaluate the anti-latency activity of Panobinostat in J89GFP cell line PMC6529996
THP89GFP monocyte 40 nM 24 h To evaluate the anti-latency activity of Panobinostat in THP89GFP cell line PMC6529996
CT26 cells 0.2 μMol/L 24 hours To investigate the synergistic anti-proliferative effect of Panobinostat and JQ1 on CT26 cells, the results showed that the combination of Panobinostat and JQ1 significantly inhibited the proliferation of CT26 cells. PMC9279642
BMDM cells 0.2 μMol/L 24 hours To investigate the inhibitory effect of Panobinostat and JQ1 on M2 polarization of BMDM cells, the results showed that the combination of Panobinostat and JQ1 significantly inhibited M2 polarization. PMC9279642
HCC-LM3 50 nM, 100 nM 24, 48, 72 hours LBH589 significantly inhibited HCC cell growth, induced histone acetylation and apoptosis PMC3853770
HepG2 50 nM, 100 nM 24, 48, 72 hours LBH589 significantly inhibited HCC cell growth, induced histone acetylation and apoptosis PMC3853770
SμMC-7721 50 nM, 100 nM 24, 48, 72 hours LBH589 significantly inhibited HCC cell growth, induced histone acetylation and apoptosis PMC3853770

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
BALB/c mice CT26 subcutaneous tumor model Tail vein injection 5 and 10 mg/kg Every two days To investigate the anti-tumor effect of Panobinostat and JQ1 in the CT26 subcutaneous tumor model, the results showed that the LF-Lipo group exhibited the highest tumor growth inhibition rate. PMC9279642
Mice t(8;21) AML mouse model Intraperitoneal injection 5 mg/kg Every two days, continued treatment To evaluate the therapeutic effect of panobinostat in the t(8;21) AML mouse model, results showed that panobinostat significantly reduced tumor burden and prolonged the survival of the mice. PMC9355625
Nude mice Orthotopic liver tumor model Intraperitoneal injection 25 mg/kg 5 days per week for 4 weeks LBH589 significantly inhibited tumor growth and metastasis without discernable adverse effects PMC3853770

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.28mL

0.46mL

0.23mL

11.38mL

2.28mL

1.14mL

22.75mL

4.55mL

2.28mL

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