DIOSCOREACEAE Dioscorea spp.  

 Synonym

    none ...
 Thai / English name

  • Dioscorea spp.

[1-2] of 2 article(s) found

 หน้า  1  

[1] CHARACTERIZATION OF IN VITRO ADME PROPERTIES OF DIOSGENIN AND DIOSCIN FROM DIOSCOREA VILLOSA.
VAMSHI K. MANDA,BHARATHI AVULA,ZULFIQAR ALI,ET AL.
PLANTA MED 2013 Vol.79(),1421-8  $47890 [Full]

Part Used : ไม่ระบุ
Activity : CYP2D6 INHIBITION
Solvent/Active Compound : Diosgenin and dioscin
Type of experiment : in vitro
Type of animal : -
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : Non-specified
Dose/Conc.(herb) : *
Duration : *
Type of interaction : Pharmacokinetics
Interaction with drug : -
Dose/Conc.(drug) : -
Result : Negative
Remark :
Note : *Dose/Duration: The assay was performed in a total volume of 200 micro liters using 96-well microtiter plates. Test compounds (50-0.2 micro molar) or postive control (5.0.02 micro molar), cofactors mix, and G-6-PDH were added to the wells and pre incubated for 10 min at 37 degrees celsius, and the plates were read to account for any fluorescence caused by the test compounds (0-min readouts, both diosgenin and dioscin had no measurable auto fluorescence). Reaction was initiated by adding the enzyme substrate mixtre and incubated for 30 min. Reaction was stopped by adding ice cold acetonitrile/0.5M Trisbase (80:20).

[2] INHIBITORY ACTIVITIES OF THAI MEDICINAL PLANTS WITH PROMISING ACTIVITIES AGAINST MALARIA AND CHOLANGIOCARCINOMA ON HUMAN CYTOCHROME P450.
WIRIYAPORN SUMSAKUL,WIRATCHANEE MAHAVORASIRIKUL,KESARA NA-BANGCHANG
PHYTOTHER RES 2015 Vol.29(),1926-33  $60695 [Full]

Part Used : เหง้า
Activity : CYP2D6 INHIBITION
Solvent/Active Compound : ethanol
Type of experiment : in vitro
Type of animal : -
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : -
Dose/Conc.(herb) : -
Duration : -
Type of interaction : Pharmacokinetics
Interaction with drug : -
Dose/Conc.(drug) : -
Result : Positive
Remark : The selective inhibitor quinidine showed the most potent inhibitory activity on CYP2D6 activity with mean IC50 of 0.97 microgram/mL. DM, DL and PI showed the highest inhibitory activities (mean IC50 2.93-9.57 microgram/mL). The potency of inhibitory activity of DM was comparable to that of quinidine (p > 0.05). PC, GM and ZO exhibited moderate potencies (mean IC50 23.40-31.32 microgram/mL), and MF and AL exhibited relatively low potencies (mean IC50 195.83 and 313.51 microgram/mL, respectively). (substrate: dextromethorphan)
Note : Piper chaba (PC), Dioscroea membranacea (DI), Dracaenal oureiri (DG), Atractylodes lancea (AL), Plumbago indica (PI), Zingiber officinale (ZO), Myristica fragrans (MF), Garcinia mangostana (GM).


 หน้า  1