NSC403140

NSC403140 Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:Haemanthamine
CAS:466-75-1
Purity:98.00% Package:100 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Aladdin Scientific
Tel: +1-+1(833)-552-7181
Email: sales@aladdinsci.com
Products Intro: Product Name:Haemanthamine
CAS:466-75-1
Purity:96% Package:$410.9/1mg;Bulk package Remarks:96%
Company Name: Beijing Jin Ming Biotechnology Co., Ltd.  
Tel: 010-60605840 18892239720
Email: psaitong@jm-bio.com
Products Intro: Product Name:Haemanthamine
CAS:466-75-1
Purity:95% Package:100mg;250mg;500mg
Company Name: Beijing Jin Ming Biotechnology Co., Ltd.  
Tel: 010-60605840
Email: psaitong@jm-bio.com
Products Intro: Product Name:Haemanthamine
CAS:466-75-1
Purity:95% Package:100mg;250mg;500mg
Company Name: Changzhou Xianglong Pharmaceutical Technology Co., LTD  
Tel: 0519-88910898 18661161657
Email: yaoxiangqiu2021@163.com
Products Intro: CAS:466-75-1
Purity:95%+ Package:10mg;25mg;50mg;100mg
NSC403140 Basic information
Product Name:NSC403140
Synonyms:NSC403140;3-Epicrinamine;Haemanthamine;Hemanthamine;Natalensine
CAS:466-75-1
MF:C17H19NO4
MW:301.33706
EINECS:
Product Categories:
Mol File:466-75-1.mol
NSC403140 Structure
NSC403140 Chemical Properties
storage temp. Store at -20°C
solubility DMSO : 100 mg/mL (331.85 mM; Need ultrasonic)
Safety Information
MSDS Information
NSC403140 Usage And Synthesis
DefinitionChEBI: Haemanthamine is an alkaloid.
Biological ActivityHaemanthamine is a rhodophylline-like alkaloid isolated from the Amaryllidaceae plant with potent anticancer activity. It targets the ribosome to inhibit protein biosynthesis during the elongation phase of translation, and has proapoptotic, antioxidant, antiviral, antimalarial and anticonvulsant activities.
in vitro

Haemanthamine (1-100 μM; 24-48 hours; A2780 cells) treatment shows a time- and dose-dependent decrease in cell viability.
Haemanthamine (10 μM; 24-72 hours; A2780 cells) treatment leads to a significant inhibition of A2780 cell proliferation.
Haemanthamine binds at the A-site cleft of the peptidyl transferase center on the large ribosomal subunit, creating unique molecular interactions with the 25S rRNA. Haemanthamine has a highly specific inhibitory effect on pre-rRNA processing, leading to the activation of a p53-dependent antitumoral surveillance pathway known as nucleolar stress.

Cell Viability Assay

< td class="col1"> Cell Line:
A2780 ovarian cancer cells
Concentration: 1 μM, 10 μM, 50 μM, 100 μM
Incubation Time: 24 hours, 48 hours
Result: Showed a time- and dose-dependent decrease in cell viability.

Cell Proliferation Assay

Cell Line: A2780 ovarian cancer cells
Concentration: 10 μM
Incubation Time: 24 hours, 48 hours, 72 hours
Result: Led to a significant inhibition of A2780 cell proliferation.
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in vivo

A pharmacokinetic study of Haemanthamine in rats shows a rapid distribution phase of 30 min, a half-life of 70.4 min, and a major clearance through renal elimination. The high distribution volume of 13.7 L/kg suggests a high intracellular penetration, and its plasmatic concentration remains higher than 1 μM for at least 1 hr after a single 10-mg/kg administration.

NSC403140 Preparation Products And Raw materials
Preparation Products(5α,13β,19α)-1,2-Didehydro-3β-methoxycrinan-11-one
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