GLPBio

Agarotetrol

Catalog No.: GC30663Purity:>98.00%
Agarotetrol ist ein aus Adlerholz isoliertes Chromonderivat.

Die Produkte sind ausschließlich für Forschungszwecke bestimmt. Nicht zur Anwendung am Menschen. Wir verkaufen nicht an Patienten.


Agarotetrol
Cas No.: 69809-22-9
1mgIn Stock
$27.00
1
5mgIn Stock
$70.00
1
10mgIn Stock
$112.00
1
25mgIn Stock
$238.00
1
50mgIn Stock
$392.00
1

Zitate (Citations)

1 publicationsPublikationen von Forschern, die dieses Produkt verwenden

Beschreibung (Description)

Agarotetrol is the chromone derivative from Agarwood, showing very low phosphodiesterase (PDE) 3A inhibitory activity with IC50 value > 100μM[1]. The aqueous extract of agarwood is characterized by a high concentration of Agarotetrol, a bioactive compound demonstrating significant sedative properties. Upon thermal activation, Agarotetrol compound releases benzylacetone, a characteristic aromatic constituent[2]. Agarotetrol serves as a crucial quality control marker for the standardization of agarwood in herbal medicinal preparations[3].

In vitro, Agarotetrol has potential cell protective activity[4]. After 24 hours of incubation with 20μM Agarotetrol, the 150μM corticosterone-induced damage in PC12 cells was significantly alleviated, with a cell viability of 79.50 ± 1.79% [4]. In silico molecular docking and molecular dynamic simulation showed that Agarotetrol had good binding with humanlegumain protein[5].

In vivo, Agarotetrol can cross the blood-brain barrier in vivo with an estimated blood-brain barrier penetration value of 0.8 in SD rats[5]. The combined administration of agarwood essential oil (24.85mg/kg) and agarotetrol-enriched extract powder (7.28mg/kg) (prepared into a cyclodextrin mixture) demonstrated significant pharmacological effects on sleep parameters in p-Chlorophenylalanine-induced insomnia SD rats. Nasal cavity of administration for 7 days resulted in enhanced sleep onset efficiency, reduced sleep latency, and extended total sleep duration [6]. Following a 30-day oral administration regimen of Agarotetrol at a dosage of 6.0g/kg/day, comprehensive biodistribution analysis demonstrated a tissue-specific accumulation pattern in experimental rats, with the highest concentration detected in renal tissue, followed by hepatic, cardiac, and cerebral tissues in decreasing order of magnitude[7].

References:
[1] Sugiyama T, Narukawa Y, Shibata S, et al. Three new 5, 6, 7, 8-tetrahydroxy-5, 6, 7, 8-tetrahydrochromone derivatives enantiomeric to agarotetrol from agarwood[J]. Journal of natural medicines, 2018, 72: 667-674.
[2] Takamatsu S, Ito M. Agarotetrol: a source compound for low molecular weight aromatic compounds from agarwood heating[J]. Journal of natural medicines, 2018, 72: 537-541.
[3] Takamatsu S, Ito M. Agarotetrol as an index for evaluating agarwood in crude drug products[J]. Journal of Natural Medicines, 2022, 76(4): 857-864.
[4] Zhang L, Yi P, Yan H, et al. Five new 2-(2-phenylethyl) chromone derivatives and three new sesquiterpenoids from the heartwood of Aquilaria sinensis, an aromatic medicine in China[J]. Natural Products and Bioprospecting, 2022, 12(1): 2.
[5] Alugoju P, Bhandare V V, Patil V S, et al. In silico molecular docking and molecular dynamic simulation of agarwood compounds with molecular targets of Alzheimer’s disease[J]. F1000Research, 2024, 12: 230.
[6] Lai Y, Hua L, Yang J, et al. The effect of Chinese agarwood essential oil with cyclodextrin inclusion against PCPA-induced insomnia rats[J]. Molecules, 2023, 28(2): 635.
[7] Hou H, Chen T, Xu Z, et al. Study and exploration of the pharmacokinetics of traditional Tibetan medicine Ruyi Zhenbao tablets after single and long-term administration[J]. Frontiers in Pharmacology, 2022, 13: 948693.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

PC12 cell 

Preparation Method

Undifferentiated PC12 cells were cultured in Dulbecco's Modified Eagle Medium (DMEM) supplemented with 10% heat-inactivated fetal bovine serum, 100U/mL penicillin, and 100μg/mL streptomycin, maintained at 37°C in a humidified 5% CO2 atmosphere. For experimental treatments, cells were divided into three groups: (1) untreated control (blank, 24h), (2) negative control (150μM, 24h), and (3) positive control (150μM corticosterone plus 20μM Agarotetrol, 24h). Cells were plated in 96-well plates at a density of 1 × 104 cells per well and allowed to adhere for 24 hours prior to compound administration. Following 48 hours of treatment, cell viability was assessed using the MTS assay, with absorbance measurements recorded at 492 nm using a microplate reader.

Reaction Conditions

20μM; 24h

Applications

Agarotetrol has significant protective properties against corticosterone-induced PC12 cell injury.
Animal experiment [2]:

Animal models

SD rats

Preparation Method

Sixty-four Sprague-Dawley rats (body weight 180-220g, age 3-4 weeks) were randomly allocated into four experimental groups (n=16 per group) with equal gender distribution (8 males and 8 females): (1) vehicle control, (2) high-dose Agarotetrol (6.0g/kg/day), (3) medium-dose Agarotetrol (3.0g/kg/day), and (4) low-dose Agarotetrol (1.5g/kg/day). Within each group, eight animals were sacrificed at one month post-treatment initiation, and the remaining eight were maintained for an additional two-week withdrawal period prior to sample collection. Serial blood sampling was performed via the retro-orbital plexus at multiple time points: baseline (day 1), mid-treatment (day 15), and treatment completion (day 30). At each sampling day, blood was collected at 0.25, 0.5, 0.75, 1, 2, 4, 8, and 24h post-administration. 

Dosage form

1.5g/kg/day, 3.0g/kg/day and 6.0g/kg/day for 1, 15 and 30 days; p.o.

Applications

Agarotetrol has a wide distribution in the rats, after long-term administration, the distribution order of Agarotetrol in various tissues of rats was kidney > liver > heart > brain.

References:
[1] Zhang L, Yi P, Yan H, et al. Five new 2-(2-phenylethyl) chromone derivatives and three new sesquiterpenoids from the heartwood of Aquilaria sinensis, an aromatic medicine in China[J]. Natural Products and Bioprospecting, 2022, 12(1): 2.
[2] Hou H, Chen T, Xu Z, et al. Study and exploration of the pharmacokinetics of traditional Tibetan medicine Ruyi Zhenbao tablets after single and long-term administration[J]. Frontiers in Pharmacology, 2022, 13: 948693.

Produktdokumente (Product Documents)

Purity:>98.00%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
69809-22-9
SMILES
O=C1C=C(CCC2=CC=CC=C2)OC3=C1[C@H](O)[C@@H](O)[C@@H](O)[C@@H]3O
Summenformel
C17H18O6
Molekulargewicht
318.32
Löslichkeit
DMSO : ≥ 250 mg/mL (785.37 mM)
Lagerung
Store at -20°C
Allgemeine Hinweise
Wählen Sie anhand der Löslichkeitsdaten des Produkts ein geeignetes Lösungsmittel. Aliquotieren Sie die Stammlösung nach der Herstellung, um wiederholte Gefrier-Auftau-Zyklen zu vermeiden.
Verwenden Sie Stammlösungen bei Lagerung bei -80°C innerhalb von 6 Monaten bzw. bei -20°C innerhalb von 1 Monat.
Zur Verbesserung der Löslichkeit das Röhrchen auf 37°C erwärmen und für eine angemessene Dauer beschallen.
Versandbedingungen
Evaluierungsmuster werden mit Kühlakkus versandt. Andere verfügbare Größen werden bei Raumtemperatur oder auf Anfrage mit Kühlakkus versandt.

Rechner (Calculators)Molarität / Verdünnung / Molekulargewicht / Einheitenumrechnung / In-vivo-Formulierung / Löslichkeit

g/mol

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