Eurycomalactone - ≥93% , CAS No.23062-24-0

CAS: 23062-24-0 Cat. No.: E651728 Fórmula: C19H24O6 Peso molecular: 348.39 PubChem CID: 441793
Disponível para encomenda
GRAU & PUREZA ≥93%
Synonyms
Eurycomalactone | AKOS040760395 | (1S,2R,5S,9S,10S,11R,12R,13R,16R)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.02,11.05,10]hexadec-6-ene-3,8,15-trione | 1H-Phenanthro(10,1-bc)furan-4,6,9(2H,5aH,6aH)-trione, 3,3a,10,10a,10b,10c-hexahydro-
Storage
Store at 2-8°C,Protected from light
Shipped In
Wet ice
★
Tamanho
Alemanha (EU)
USA*
Preço
Qtd
1mg
E651728-1mg
Sob encomenda · 8–12 semanas
365,23€
5mg
E651728-5mg
Sob encomenda · 8–12 semanas
903,23€
Enter a quantity for the sizes you want to add.

Visão geral

Eurycomalactone is an active quassinoid could be isolated from Eurycoma longifolia Jack . Eurycomalactone is a potent NF-κB inhibitor with an IC 50 value of 0.5 μM. Eurycomalactone inhibits protein synthesis and depletes cyclin D1. Eurycomalactone enhances radiosensitivity through arrest cell cycle at G2/M phase and delayed DNA double-strand break repair. Eurycomalactone inhibits the activation of AKT/NF‑κB signaling, induces apoptosis and enhances chemosensitivity to Cisplatin

In Vitro

Eurycomalactone (24, 48 and 72 h) selectively inhibits the viability of A549 and COR-L23 cells Eurycomalactone inhibits the viability of A549 cells with IC 50 values of 20.17, 3.77, and 1.90 μM for 24, 48 and 72 hours, respectively. Eurycomalactone inhibits the viability of COR-L23 cells with IC 50 values of 25.02, 2.74, and 1.80 μM for 24, 48 and 72 hours, respectively. Eurycomalactone (2.29-156.3 μM; 24 h; A549 and Calu-1 cells) promotes Non-small cell lung cancer (NSCLC) cells apoptosis. Eurycomalactone (0-25.05 μM; 24 h; A549 and COR-L23 cells) induces cell cycle arrest at the radiosensitive G2/M phase and induces apoptosis in irradiated Non-small cell lung cancer (NSCLC) cells. Eurycomalactone downregulated the key G2/M regulatory proteins in irradiated Non-small cell lung cancer (NSCLC) cells. Eurycomalactone (2.5-25 μM; 24 h; A549 cells) suppressed the repair of radiation-Induced DNA double-strand breaks. Eurycomalactone (2.29-156.3 μM; 24 h; A549 and Calu-1 cells) suppresses AKT/NF-κB activation in Non-small cell lung cancer (NSCLC) cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Apoptosis AnalysisCell Line: A549 and Calu-1 cells Concentration: 2.29, 10.14, 12.02, 20.81, 80.77, and 156.3 μM Incubation Time: 24 hours Result: Increased the apoptotic rates in a dose-dependent manner. Cell Cycle AnalysisCell Line: A549 and COR-L23 cells Concentration: 1.57, 2.57, 20.17 and 25.05 μM Incubation Time: 24 hours Result: Induced cell cycle arrest at G2/M phase in irradiated cells and increased the sub-G1 population.\nA549 and COR-L23 cells Western Blot AnalysisCell Line: A549 and Calu-1 cells Concentration: 2.29, 10.14, 12.02, 20.81, 80.77, and 156.3 μM Incubation Time: 24 hours Result: Induced the expression levels of active caspase-3 and active PARP (cleaved form), while decreased Bcl-xL and surviving. Western Blot AnalysisCell Line: A549 and COR-L23 cells Concentration: 1.57, 2.57, 20.17 and 25.05 μM Incubation Time: 24 hours Result: Downregulated the expression of both G2/M regulatory proteins in a dose-dependent manner. Western Blot AnalysisCell Line: A549 and COR-L23 cells Concentration: 2.29, 10.14, 12.02, 20.81, 80.77, and 156.3 μM Incubation Time: 24 hours Result: inhibited the expression levels of p (S473) -AKT, total AKT, p (S536) -NF-κB p65 and total NF-κB p65.

Form:Solid

IC50& Target:IC50: 0.5 μM (NF-κB)

Especificações

Sinónimos
Eurycomalactone | AKOS040760395 | (1S,2R,5S,9S,10S,11R,12R,13R,16R)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.02,11.05,10]hexadec-6-ene-3,8,15-trione | 1H-Phenanthro(10,1-bc)furan-4,6,9(2H,5aH,6aH)-trione, 3,3a,10,10a,10b,10c-hexahydro-
Especificações e pureza
≥93%
Mecanismos bioquímicos e fisiológicos
Eurycomalactone is an active quassinoid could be isolated from Eurycoma longifolia Jack . Eurycomalactone is a potent NF-κB inhibitor with an IC 50 value of 0.5 μM. Eurycomalactone inhibits protein synthesis and depletes cyclin D1. Eurycomalactone enhance
Condições de armazenamento de armazenamento
Store at 2-8°C,Protected from light
Enviado em
Wet ice
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Tipo de ação
INHIBITOR
Pureza
≥93%
Nomes e identificadores
Sorrisos canónicos
CC1C2C(C3C4(C(CC(=O)C3(C1C(=O)O2)C)C(=CC(=O)C4O)C)C)O
IUPAC Name
(1S,2R,5S,9S,10S,11R,12R,13R,16R)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.02,11.05,10]hexadec-6-ene-3,8,15-trione
InChIKey
OGHYZHNTIINXEO-MGBQOKOWSA-N
INCHI
1S/C19H24O6/c1-7-5-10(20)16(23)18(3)9(7)6-11(21)19(4)12-8(2)14(25-17(12)24)13(22)15(18)19/h5,8-9,12-16,22-23H,6H2,1-4H3/t8-,9+,12-,13+,14-,15-,16-,18+,19+/m1/s1
SMILES isoméricas
C[C@H]1[C@@H]2[C@@H]([C@@H]3[C@@]4([C@@H](CC(=O)[C@]3([C@H]1C(=O)O2)C)C(=CC(=O)[C@H]4O)C)C)O
CAS alternativo
23062-24-0
PubChem CID
441793
Peso molecular
348.39

Dados avançados

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClasseSteroids and steroid derivatives
SubclassSteroid lactones
Intermediate Tree Nodes Not available
Direct ParentSteroid lactones
Alternative Parents Isocopalane and spongiane diterpenoids  Diterpene lactones  Quassinoids  11-beta-hydroxysteroids  Oxepanes  Cyclohexenones  Gamma butyrolactones  Tetrahydrofurans  Secondary alcohols  Cyclic alcohols and derivatives  Carboxylic acid esters  Oxacyclic compounds  Monocarboxylic acids and derivatives  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteropolycyclic compounds
Substituents Steroid lactone - C-19 quassinoid skeleton - Diterpene lactone - Diterpenoid - Spongiane diterpenoid - Hydroxysteroid - 11-beta-hydroxysteroid - 11-hydroxysteroid - Caprolactone - Cyclohexenone - Oxepane - Gamma butyrolactone - Tetrahydrofuran - Cyclic alcohol - Secondary alcohol - Carboxylic acid ester - Cyclic ketone - Ketone - Lactone - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Alcohol - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Carbonyl group - Organooxygen compound - Aliphatic heteropolycyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton.
External Descriptors Triterpenoids (C30)
Estrutura 3D
Modelo de Estrutura Química Interativa





Alvos associados (humanos)
CHUK Tchem Inhibitor of nuclear factor kappa B kinase alpha subunit (3170 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
IKBKB Tchem Inhibitor of nuclear factor kappa B kinase beta subunit (5554 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NFKBIA Tchem NF-kappaB inhibitor alpha (187 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-1080 (3966 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propriedades químicas e físicas
SolubilidadeDMSO : 100 mg/mL (287.03 mM; Need ultrasonic)
Peso molecular348.400 g/mol
XLogP30.100
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count6
Rotatable Bond Count0
Exact Mass348.157 Da
Monoisotopic Mass348.157 Da
Topological Polar Surface Area101.000 Ų
Heavy Atom Count25
Formal Charge0
Complexity725.000
Isotope Atom Count0
Defined Atom Stereocenter Count9
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluções
Revisões

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