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L5139

Sigma-Aldrich

Lycorine hydrochloride

powder, ≥98% (TLC)

Sinônimo(s):

Licorin hydrochloride, Lychorine chloride, Lycorine HCl

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About This Item

Fórmula empírica (Notação de Hill):
C16H17NO4 · HCl
Número CAS:
2188-68-3
Peso molecular:
323.77
Número MDL:
MFCD00243111
Código UNSPSC:
12352202
ID de substância PubChem:
24896395
NACRES:
NA.77

product name

Lycorine hydrochloride, ≥98% (TLC), powder

Nível de qualidade

100

Ensaio

≥98% (TLC)

forma

powder

pf

210-212  °C

solubilidade

ethanol: 10 mg/mL, clear, colorless to very faintly yellow

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

Cl.O[C@H]1C=C2CCN3Cc4cc5OCOc5cc4[C@H]([C@@H]1O)[C@@H]23

InChI

1S/C16H17NO4.ClH/c18-11-3-8-1-2-17-6-9-4-12-13(21-7-20-12)5-10(9)14(15(8)17)16(11)19;/h3-5,11,14-16,18-19H,1-2,6-7H2;1H/t11-,14-,15+,16+;/m0./s1

chave InChI

VUVNTYCHKZBOMV-NVJKKXITSA-N

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Ações bioquímicas/fisiológicas

A selective inhibitor of peptidyl transferase center (PTC). In HL-60 (leukemia) cells, lycorine arrests the cell cycle at G2/M and induces apoptosis by a caspase-mediated pathway.

Atenção

Protect from light.

Pictogramas

Skull and crossbones
GHS06

Palavra indicadora

Danger

Frases de perigo

H301

Declarações de precaução

P264 - P270 - P301 + P310 - P405 - P501

Classificações de perigo

Acute Tox. 3 Oral

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Sascha Kretzing et al.
Archives of toxicology, 85(12), 1565-1573 (2011-06-01)
Lycorine is the main alkaloid of many Amaryllidaceae and known to cause poisoning with still unknown mechanisms. Longer lasting toxicological core symptoms of nausea and emesis may become a burden for human and animal patients and may result in substantial
Raquel Brandt Giordani et al.
Phytochemistry, 72(7), 645-650 (2011-02-18)
In this study, the mechanism of action of the pro-apoptotic alkaloid lycorine on an amitochondriate cell, the parasite Trichomonas vaginalis, was investigated. The cytotoxicity of lycorine against T. vaginalis was studied from 2.5 to 1000μM and several important ultrastructural alterations
Jiangning Liu et al.
Virology journal, 8, 483-483 (2011-10-28)
Human enterovirus 71 (EV71) infection causes hand, foot and mouth disease in children under 6 years old and this infection occasionally induces severe neurological complications. No vaccines or drugs are clinical available to control EV71 epidemics. In present study, we
G Saltan Çitoğlu et al.
Fitoterapia, 83(1), 81-87 (2011-10-05)
The present study reports the potential antinociceptive, anti-inflammatory and hepatoprotective activities of lycorine from Sternbergia fischeriana (Herbert) Rupr. (Amaryllidaceae). Lycorine was evaluated on mice by using acetic-acid induced writhing and tail-flick tests. Lycorine exhibited stronger inhibition than aspirin in acetic-acid
Jerald J Nair et al.
Natural product communications, 7(7), 959-962 (2012-08-23)
The plant family Amaryllidaceae occupies a privileged status within the botanical hierarchy due to its horticultural and ornamental appeal, as well as its widespread usage in the traditional medicinal practices of indigenous peoples across the globe. Of greater significance are
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