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P7262

Sigma-Aldrich

Plumbagin from Plumbago indica

Sinonimo/i:

5-Hydroxy-2-methyl-1,4-naphthoquinone

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About This Item

Formula empirica (notazione di Hill):
C11H8O3
Numero CAS:
Peso molecolare:
188.18
Numero CE:
Numero MDL:
Codice UNSPSC:
12352205
ID PubChem:
NACRES:
NA.79
Prezzi e disponibilità al momento non sono disponibili

Origine biologica

Plumbago indica

Stato

powder

Colore

faint orange to dark orange

Punto di fusione

76-78 °C (lit.)

Temperatura di conservazione

−20°C

Stringa SMILE

CC1=CC(C2=C(C1=O)C=CC=C2O)=O

InChI

1S/C11H8O3/c1-6-5-9(13)10-7(11(6)14)3-2-4-8(10)12/h2-5,12H,1H3
VCMMXZQDRFWYSE-UHFFFAOYSA-N

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Descrizione generale

Plumbagin is a bioactive naphthoquinone present majorly in Plumbago indica L.[1] It is a quinoid and is also derived from the roots of Plumbago zeylanica roots.[2]

Applicazioni

Plumbagin from Plumbago indica has been used:
  • as a reactive oxygen species agent (ROS) to induce cytotoxicity in mouse embryonic fibroblasts[3]
  • as an oxidative stress inducer to generate superoxide anion in Saccharomyces cerevisiae[4]
  • as a reference standard in thin layer chromatography and in spectrophotometric analysis for quantification of plumbagin in Plumbago auriculate samples[5]

Azioni biochim/fisiol

Exhibits cytotoxicity in rodent models of carcinogenesis and carcinoma; has antifungal, antiviral, and antibacterial action.
Plumbagin exhibits various pharmacological activities including antimicrobial, anticancer,[1] anti-atherosclerotic, antidiabetic, anti-inflammatory, hypolipidemic, and neuroprotective activities.[6] It inhibits the signal transducer and activator of transcription 3 (STAT3) signaling and halts the proliferation of esophageal squamous cell carcinoma (ESCC).[2] Plumbagin elicits protective antioxidative functionality in 4-nitroquinoline-N-oxide (NQNO) induced stress in lymphoma.[7] Plumbagin in a nanoemulsion formulation has antiproliferative effect towards prostate cancer.[6]

Pittogrammi

Skull and crossbones

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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In vitro callus induction and estimation of plumbagin content from Plumbago auriculata Lam.
Deshpande J, et al.
Indian Journal of Experimental Biology, 52(11), 122-1127 (2014)
Plumbagin inhibits the proliferation and survival of esophageal cancer cells by blocking STAT3-PLK1-AKT signaling
Cao YY, et al.
Cell Death & Disease, 9(2), 17-17 (2018)
Plumbagin-Loaded Nanoemulsion Drug Delivery Formulation and Evaluation of Antiproliferative Effect on Prostate Cancer Cells
Chrastina A, et al.
BioMed Research International, 2018 (2018)
María Marcén et al.
International journal of food microbiology, 241, 198-205 (2016-10-30)
Heat treatments are widely used by the food industry to inactivate microorganisms, however their mode of action on microbial cells is not fully known. In the last years, it has been proposed that the generation of oxidative species could be
Gloria Brusotti et al.
Scientific reports, 7(1), 5777-5777 (2017-07-20)
PPAR antagonists are ligands that bind their receptor with high affinity without transactivation activity. Recently, they have been demonstrated to maintain insulin-sensitizing and antidiabetic properties, and they serve as an alternative treatment for metabolic diseases. In this work, an affinity-based

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