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Panobinostat

CAS No.
404950-80-7
Chemical Name:
Panobinostat
Synonyms
CS-422;LBH-589;NVP-LBH589;Palcociclib;panobinosta;PANOBINOSTAT;2-Acrylamide;Palmer than he;Panobinostat D7;Panobinostat, >=98%
CBNumber:
CB61009161
Molecular Formula:
C21H23N3O2
Molecular Weight:
349.43
MDL Number:
MFCD09833242
MOL File:
404950-80-7.mol
Last updated:2023-09-15 16:56:55

Panobinostat Properties

Melting point 114-117?C
Density 1.241±0.06 g/cm3(Predicted)
storage temp. -20°C Freezer, Under Inert Atmosphere
solubility Soluble in DMSO (up to 100 mg/ml) or in Ethanol (up to 5 mg/ml with warming).
form solid
pka 8.71±0.23(Predicted)
color Off-white
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 1 month.
NCI Dictionary of Cancer Terms LBH589; panobinostat
FDA UNII 9647FM7Y3Z
ATC code L01XH03

Pharmacokinetic data

Protein binding 90%
Excreted unchanged in urine <2.5%
Volume of distribution 1000 Litres
Biological half-life 37

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Risk Statements  22-36/37/38-20
Safety Statements  24/25
HS Code  29339900
NFPA 704
0
4 0

Panobinostat price More Price(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 13280 Panobinostat ≥98% 404950-80-7 5mg $29 2024-03-01 Buy
Cayman Chemical 13280 Panobinostat ≥98% 404950-80-7 10mg $55 2024-03-01 Buy
Cayman Chemical 13280 Panobinostat ≥98% 404950-80-7 50mg $99 2024-03-01 Buy
Cayman Chemical 13280 Panobinostat ≥98% 404950-80-7 25mg $147 2021-12-16 Buy
Usbiological 170036 Panobinostat 404950-80-7 1mg $293 2021-12-16 Buy
Product number Packaging Price Buy
13280 5mg $29 Buy
13280 10mg $55 Buy
13280 50mg $99 Buy
13280 25mg $147 Buy
170036 1mg $293 Buy

Panobinostat Chemical Properties,Uses,Production

Description

Panobinostat is a potent inhibitor of all histone deacetylases (HDACs), with Ki values ranging from 0.6 to 31 nM for HDAC1-11. Through this action, it leads to acetylation of a range of cellular proteins, resulting in cell cycle arrest and apoptosis in cancer cells. It has potential applications in several different forms of cancer as well as in spinal muscular atrophy and HIV therapy.

Chemical Properties

Yellow Solid

Uses

The novel histone deacetylase inhibitor, LBH589, induces expression of DNA damage response genes and apoptosis in Ph- acute lymphoblastic leukemia cells.

Uses

The novel labelled histone deacetylase inhibitor, LBH589, induces expression of DNA damage response genes and apoptosis in Ph- acute lymphoblastic leukemia cells.

Definition

ChEBI: A hydroxamic acid obtained by formal condensation of the carboxy group of (2E)-3-[4-({[2-(2-methylindol-3-yl)ethyl]amino}methyl)phenyl]prop-2-enoic acid with the amino group of hydroxylamine. A histone deacetylase inhibitor used (as its la tate salt) in combination with bortezomib and dexamethasone for the treatment of multiple myeloma.

Clinical Use

Histone deacetylase (HDAC) inhibitor:
Treatment of relapsed and/or refractory multiple myeloma

target

HDAC (MOLT-4 cells)

Drug interactions

Potentially hazardous interactions with other drugs
Analgesics: avoid with dextromethorphan possibly increased risk of ventricular arrhythmias with methadone - avoid.
Anti-arrhythmics: increased risk of ventricular arrhythmias with amiodarone and possibly disopyramide - avoid.
Antibacterials: increased risk of ventricular arrhythmias with clarithromycin and moxifloxacin - avoid; avoid with rifampicin.
Antidepressants: avoid with St John’s wort.
Antiepileptics: avoid with carbamazepine, fosphenytoin, phenobarbital, phenytoin and primidone.
Antifungals: concentration increased by ketoconazole and possibly posaconazole and voriconazole - reduce panobinostat dose; concentration possibly increased by itraconazole - avoid.
Antimalarials: possibly increased risk of ventricular arrhythmias with chloroquine - avoid.
Antipsychotics: avoid with pimozide.
Antivirals: concentration possibly increased by ritonavir and saquinavir - reduce dose of panobinostat.
Beta-blockers: possibly increased risk of ventricular arrhythmias with sotalol - avoid.
Grapefruit juice: avoid concomitant use.
5HT3 antagonists: possibly increased risk of ventricular arrhythmias with granisetron and ondansetron - avoid with granisetron.

Metabolism

Panobinostat is extensively metabolised, and a large fraction of the dose is metabolised before reaching the systemic circulation by reduction, hydrolysis, oxidation and glucuronidation. Oxidative metabolism of panobinostat played a less prominent role, with approximately 40% of the dose eliminated by this pathway. Cytochrome P450 3A4 (CYP3A4) is the main oxidation enzyme, with potential minor involvement of CYP2D6 and 2C19.
Panobinostat represented 6-9% of the drug-related exposure in plasma. The parent substance is deemed to be responsible for the overall pharmacological activity of panobinostat.
After a single oral dose of [14C]-panobinostat in patients, 29-51% of administered radioactivity is excreted in the urine and 44-77% in the faeces. Unchanged panobinostat accounted for <2.5% of the dose in urine and <3.5% of the dose in faeces.

storage

Store at -20°C

References

1) Geng et al. (2006), Histone deacetylase (HDAC) inhibitor LBH589 increases duration of gamma H2AX foci and confines HDAC4 to the cytoplasm in irradiated non-small cell lung cancer; Cancer Res., 66 11298 2) George et al. (2005), Combination of the histone deacetylase inhibitor LBH589 and the hsp90 inhibitor 17-AAG is highly active against human CML-BC cells and AML cells with activating mutation of FLT-3; Blood, 105 1768 3) Maiso et al. (2006), The histone deacetylase inhibitor LBH589 is a potent antimyeloma agent that overcomes drug resistance; Cancer Res., 66 5781

441741-66-8
404950-80-7
Synthesis of Panobinostat from Panobinostat Carboxylic Acid Methyl Ester Hydrochloride

Panobinostat Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 238)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Yanxi Chemical Co., Ltd.
+8617531190177 peter@yan-xi.com China 5993 58
Shaanxi Haibo Biotechnology Co., Ltd
+undefined18602966907 qinhe02@xaltbio.com China 1000 58
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21691 55
Nanjing ChemLin Chemical Industry Co., Ltd.
025-83697070 product@chemlin.com.cn CHINA 3012 60
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
SHANDONG ZHI SHANG CHEMICAL CO.LTD
+86 18953170293 sales@sdzschem.com China 2931 58
Biochempartner
0086-13720134139 candy@biochempartner.com CHINA 967 58
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22968 58

View Lastest Price from Panobinostat manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Panobinostat pictures 2024-04-12 Panobinostat
404950-80-7
US $0.00 / kg 1kg 99% 2000ton Shaanxi Haibo Biotechnology Co., Ltd
Panobinostat pictures 2023-09-15 Panobinostat
404950-80-7
US $10.00-1.00 / kg 1kg 0.99 20 tons Hebei Yanxi Chemical Co., Ltd.
Panobinostat pictures 2022-10-18 Panobinostat
404950-80-7
US $50.00 / kg 1kg 99% 1 Hebei Duling International Trade Co. LTD
  • Panobinostat pictures
  • Panobinostat
    404950-80-7
  • US $0.00 / kg
  • 99%
  • Shaanxi Haibo Biotechnology Co., Ltd
  • Panobinostat pictures
  • Panobinostat
    404950-80-7
  • US $10.00-1.00 / kg
  • 0.99
  • Hebei Yanxi Chemical Co., Ltd.
  • Panobinostat pictures
  • Panobinostat
    404950-80-7
  • US $50.00 / kg
  • 99%
  • Hebei Duling International Trade Co. LTD

Panobinostat Spectrum

(E)-N-HYDROXY-3-(4-{[2-(2-METHYL-1H-INDOL-3-YL)-ETHYLAMINO]-METHYL}-PHENYL)-ACRYLAMIDE N-Hydroxy-3-[4-[2-(2-methyl-1H-indol-3-yl)ethylaminomethyl]phenyl]-2(E)-propenamide LBH-589/Panobinostat LBH-589 PANOBINOSTAT 2-Propenamide, N-hydroxy-3-(4-(((2-(2-methyl-1H-indol-3-yl)ethyl)amino)methyl)phenyl)-, (2E)- NVP-LBH589 Panobinostat (LBH589) (2E)-N-Hydroxy-3-[4-[[[2-(2-methyl-1H-indol-3-yl)ethyl]amino]methyl]phenyl]-2-propenamide N-Hydroxy-3-[4-[2-(2-methyl-1H-indol-3-yl)ethylaminomethyl]phenyl]-2(E)-propenamide Panobinostat (LBH589) Panobinostat N-Hydroxy-3-[4-[2-(2-methyl-1H-indol-3-yl)ethylaminomethyl]phenyl]-2(E)-propenamide panobinostat (HDAC inhibitor) Panobinostat (LBH589, NVP-LBH589) Palcociclib Panobinostat, >=98% LBH-589; LBH589; NVP-LBH589 CS-422 LBH 589 - NVP-LBH 589 | Panobinostat 3-[4-[2-(2-Methyl-1H-indol-3-yl)ethylaminomethyl]phenyl]-2(E)-propenohydroxamic acid (2E)-N-hydroxy-3-[4-({[2-(2-methyl-1H-indol-3-yl)ethyl]amino}methyl)phenyl]prop-2-enamide Panobinostat USP/EP/BP 3-[4-[2-(2-Methyl-1H-indol-3-yl)ethylaminomethyl]phenyl]-2(E... Panobinostat D7 3-[4-[2-(2-Methyl-1H-indol-3-yl)ethylaminomethyl]phenyl]-2(E)-propenohydroxamic acid      N-Hydroxy-3-[4-[2-(2-methyl-1H-indol-3-yl)ethylaminomethyl]phenyl]-2(E)-propenamide Palmer than he LBH 589,Human immunodeficiency virus,Histone deacetylases,HIV,HDAC,LBH-589,Autophagy,inhibit,Panobinostat,Inhibitor,Apoptosis panobinosta 2-Acrylamide Papistatin impurity 404950-80-7 C21H19D4N3O2 Inhibitor Intracellular Signaling Aromatics Heterocycles Inhibitors Intermediates & Fine Chemicals Pharmaceuticals Isotope Labelled Compounds API