Neriifolin

Modify Date: 2026-07-12 08:30:38

Neriifolin Structure
Neriifolin structure
Common Name Neriifolin
CAS Number 466-07-9 Molecular Weight 534.68100
Density 1.274g/cm3 Boiling Point 700.079ºC at 760 mmHg
Molecular Formula C30H46O8 Melting Point 218-225ºC
MSDS N/A Flash Point 224.862ºC

 Use of Neriifolin


Neriifolin, a CNS-penetrating cardiac glycoside, is an inhibitor of the Na+, K+-ATPase. Neriifolin can target beclin 1, inhibits the formation of LC3-associated phagosomes and ameliorates experimental autoimmune encephalomyelitis (EAE) development. Neriifolin induces cell cycle arrest and apoptosis in human hepatocellular carcinoma HepG2 cells[1][2.

 Names

Name neriifolin
Synonym More Synonyms

 Neriifolin Biological Activity

Description Neriifolin, a CNS-penetrating cardiac glycoside, is an inhibitor of the Na+, K+-ATPase. Neriifolin can target beclin 1, inhibits the formation of LC3-associated phagosomes and ameliorates experimental autoimmune encephalomyelitis (EAE) development. Neriifolin induces cell cycle arrest and apoptosis in human hepatocellular carcinoma HepG2 cells[1][2.
Related Catalog
In Vitro Neriifolin (0.1μg/mL; 48 hours) induces apoptosis in HepG2 cells. Neriifolin (0-8 μg/mL; 72 hours) reduces viability of HepG2 cells. Neriifolin also induces S and G2/M phase arrests of the cell cycle and stimulates apoptosis of HepG2 cells. Stimulation of HepG2 cells with Neriifolin induced activation of caspase-3, -8, and -9, and up-regulated expression of Fas and FasL proteins[1].
References

[1]. Keller CW, et al. ATG-dependent phagocytosis in dendritic cells drives myelin-specific CD4+ T cell pathogenicity during CNS inflammation. Proc Natl Acad Sci U S A. 2017;114(52):E11228-E11237.

[2]. Zhao Q, et al. Neriifolin from seeds of Cerbera manghas L. induces cell cycle arrest and apoptosis in human hepatocellular carcinoma HepG2 cells. Fitoterapia. 2011;82(5):735-741.

 Chemical & Physical Properties

Density 1.274g/cm3
Boiling Point 700.079ºC at 760 mmHg
Melting Point 218-225ºC
Molecular Formula C30H46O8
Molecular Weight 534.68100
Flash Point 224.862ºC
Exact Mass 534.31900
PSA 114.68000
LogP 3.11020
Vapour Pressure 0mmHg at 25°C
Index of Refraction 1.581
InChIKey VPUNMTHWNSJUOG-BAOINKAISA-N
SMILES COC1C(O)C(C)OC(OC2CCC3(C)C(CCC4C3CCC3(C)C(C5=CC(=O)OC5)CCC43O)C2)C1O

 Safety Information

Hazard Codes T+
Risk Phrases 26/27/28
Safety Phrases 22-36/37/39-45
RIDADR UN 2811 6.1/PG 1
WGK Germany 3
RTECS FH4906100

 NeriifolinBioassay

View more

Name: DNA damaging activity against DNA repair-deficient Saccharomyces cerevisiae W303-1A R...
Source: ChEMBL
Target: Saccharomyces cerevisiae
External Id: CHEMBL966059
Name: Insecticidal activity against Ostrinia nubilalis
Source: ChEMBL
Target: Ostrinia nubilalis
External Id: CHEMBL1057807
Name: Cytotoxicity against human TRAIL-resistant AGS cells at 29.2 nM after 24 hrs by FMCA ...
Source: ChEMBL
Target: AGS
External Id: CHEMBL1100558
Name: Cytotoxicity against human TRAIL-resistant AGS cells at 29.2 nM after 24 hrs by FMCA ...
Source: ChEMBL
Target: AGS
External Id: CHEMBL1100556
Name: Inhibition of sodium fluorescein uptake in OATP1B3-transfected CHO cells at an equimo...
Source: ChEMBL
Target: Solute carrier organic anion transporter family member 1B3
External Id: CHEMBL3039491
Name: Cytotoxicity against human SW1990 cells after 48 hrs by MTT assay
Source: ChEMBL
Target: SW1990
External Id: CHEMBL3796675
Name: Antiviral activity against Vaccinia virus infected in African green monkey CV-1 cells...
Source: ChEMBL
Target: Vaccinia virus
External Id: CHEMBL5349973
Name: Cytotoxicity against human MGC803 cells after 48 hrs by MTT assay
Source: ChEMBL
Target: NON-PROTEIN TARGET
External Id: CHEMBL3796674
Name: Inhibition of sodium fluorescein uptake in OATP1B1-transfected CHO cells at an equimo...
Source: ChEMBL
Target: Solute carrier organic anion transporter family member 1B1
External Id: CHEMBL3039488
Name: Cytotoxicity against human HT-29 cells assessed as survival index at 10 uM after 72 h...
Source: ChEMBL
Target: HT-29
External Id: CHEMBL1100180
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 Synonyms

NERIIFOLIN
17Beta-Neriifolin
xy)-14-hydroxy
digitoxigenin+thevetose
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