CAS 100234-59-1|Picrasidine I

Introduction:Basic information about CAS 100234-59-1|Picrasidine I, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NamePicrasidine I
CAS Number100234-59-1Molecular Weight240.257
Density1.4±0.1 g/cm3Boiling Point528.2±45.0 °C at 760 mmHg
Molecular FormulaC14H12N2O2Melting Point/
MSDS/Flash Point273.3±28.7 °C

Names

Name4-Methoxy-1-vinyl-9H-β-carbolin-8-ol
SynonymMore Synonyms

Picrasidine I BiologicalActivity

DescriptionPicrasidine I is an anti-inflammatory and anti-osteoclastogenic dimeric alkaloid that can be isolated from Picrasma quassioides. Picrasidine I inducs cell cycle arrest, and triggers cell Apoptosis by downregulats ERK and Akt pathways. Picrasidine I inhibits the activation of MAPKs, NF-κB and ROS generation, and suppresses the expression of c-Fos and NFATc1[1][2].
Related CatalogSignaling Pathways >>Apoptosis >>ApoptosisResearch Areas >>Inflammation/Immunology
References

[1]. Ho HY, et al. Picrasidine I Triggers Heme Oxygenase-1-Induced Apoptosis in Nasopharyngeal Carcinoma Cells via ERK and Akt Signaling Pathways. Int J Mol Sci. 2022 May 29;23(11):6103.  

[2]. Kong L, et al. Picrasidine I from Picrasma Quassioides Suppresses Osteoclastogenesis via Inhibition of RANKL Induced Signaling Pathways and Attenuation of ROS Production. Cell Physiol Biochem. 2017;43(4):1425-1435.  

Chemical & Physical Properties

Density1.4±0.1 g/cm3
Boiling Point528.2±45.0 °C at 760 mmHg
Molecular FormulaC14H12N2O2
Molecular Weight240.257
Flash Point273.3±28.7 °C
Exact Mass240.089874
PSA58.14000
LogP3.05
Vapour Pressure0.0±1.4 mmHg at 25°C
Index of Refraction1.772
InChIKeyJOHWQLSNGRWJRK-UHFFFAOYSA-N
SMILESC=Cc1ncc(OC)c2c1[nH]c1c(O)cccc12

Safety Information

Hazard CodesXi

Synonyms

4-Methoxy-1-vinyl-9H-Beta-carbolin-8-ol
Picrasidine I
4-ethyl-quinolin-8-ol
8-Quinolinol,4-ethyl
9H-Pyrido[3,4-b]indol-8-ol, 1-ethenyl-4-methoxy-
8-Hydroxy-4-ethyl-chinolin
4-Methoxy-1-vinyl-9H-β-carbolin-8-ol
8-hydroxydehydrocrenatine
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