MYRISTICACEAE Myristica fragrans  Houtt.

 Synonym

    none ...
 Thai / English name

  • จันทน์เทศ*

[1-2] of 4 article(s) found

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[1] ENHANCED CELLULAR UPTAKE OF PACLITAXEL IN THE PRESENCE OF MACELIGNAN, A PHYTOESTROGEN AND ITS IMPLICATION IN CANCER CHEMOTHERAPY.
QIANG F,HAN H
PLANTA MED 2010 Vol.76(12),P285  $32009 [Full]

Part Used : ไม่ระบุ
Activity : DRUG INTERACTION
Solvent/Active Compound : macelignan (phytoestrogen)
Type of experiment : in vitro
Type of animal : -
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : -
Dose/Conc.(herb) : 20 micromolar
Duration : -
Type of interaction : Pharmacokinetics
Interaction with drug : Paclitaxel*/Taxol/PTX
Dose/Conc.(drug) : -
Result : Positive
Remark : Type of experiment: NCI/ADR-RES cells Results: Macelignan increased the cellular accumulation of paclitaxel by approximately 1.7 fold in NCI/ADR-RES cells overexpressing P-gp, while it did not alter the cellular accumulation of paclitaxel in OVCAR-8 cells lacking P-gp.
Note : Data incomplete

Part Used : ไม่ระบุ
Activity : DRUG INTERACTION
Solvent/Active Compound : macelignan (phytoestrogen)
Type of experiment : in vitro
Type of animal : -
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : -
Dose/Conc.(herb) : 20 micromolar
Duration : -
Type of interaction : Pharmacokinetics
Interaction with drug : Paclitaxel*/Taxol/PTX
Dose/Conc.(drug) : -
Result : Negative
Remark : Type of experiment: OVCAR-8 cells Results: Macelignan increased the cellular accumulation of paclitaxel by approximately 1.7 fold in NCI/ADR-RES cells overexpressing P-gp, while it did not alter the cellular accumulation of paclitaxel in OVCAR-8 cells lacking P-gp.
Note : Data incomplete

Part Used : ไม่ระบุ
Activity : DRUG INTERACTION
Solvent/Active Compound : macelignan (phytoestrogen)
Type of experiment : in vivo
Type of animal : rat
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : Non-specified
Dose/Conc.(herb) : 20 micromolar
Duration : -
Type of interaction : Pharmacokinetics
Interaction with drug : Paclitaxel*/Taxol/PTX
Dose/Conc.(drug) : -
Result : Positive
Remark : Type of experiment: oral administration of paclitaxel with and without macelignan. Results: The concurrent use of macelignan significantly enhanced the oral exposure of paclitaxel in rats while it did not affect the intravenous pharmacokinetics of paclitaxel, implying that macelignan might be more effective to improve the intestinal absorption rather than reducing hepatic elimination.
Note : Data incomplete

Part Used : ไม่ระบุ
Activity : DRUG INTERACTION
Solvent/Active Compound : macelignan (phytoestrogen)
Type of experiment : in vivo
Type of animal : rat
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : Non-specified
Dose/Conc.(herb) : 20 micromolar
Duration : -
Type of interaction : Pharmacokinetics
Interaction with drug : Paclitaxel*/Taxol/PTX
Dose/Conc.(drug) : -
Result : Negative
Remark : Type of experiment: intrevanous administration of paclitaxel with and without macelignan. Results: The concurrent use of macelignan significantly enhanced the oral exposure of paclitaxel in rats while it did not affect the intravenous pharmacokinetics of paclitaxel, implying that macelignan might be more effective to improve the intestinal absorption rather than reducing hepatic elimination.
Note : Data incomplete

[2] EFFECTS OF MACE AND NUTMEG ON HUMAN CYTOCHROME P450 3A4 AND 2C9 ACTIVITY.
KIMURA Y,ITO H,HATANO T
BIOL PHARM BULL 2010 Vol.33(12),1977-82  $33078 [Full]

Part Used : ไม่ระบุ
Activity : DRUG INTERACTION
Solvent/Active Compound : Mace
Type of experiment : in vitro
Type of animal : -
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : -
Dose/Conc.(herb) : 100 microgram/ml
Duration : -
Type of interaction : Pharmacokinetics
Interaction with drug : -
Dose/Conc.(drug) : -
Result : Positive
Remark : IC50=3.9 microgram/ml

Part Used : ไม่ระบุ
Activity : DRUG INTERACTION
Solvent/Active Compound : Mace
Type of experiment : in vitro
Type of animal : -
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : -
Dose/Conc.(herb) : 100 microgram/ml
Duration : -
Type of interaction : Pharmacokinetics
Interaction with drug : -
Dose/Conc.(drug) : -
Result : Positive
Remark : IC50=1.1 microgram/ml

Part Used : ไม่ระบุ
Activity : DRUG INTERACTION
Solvent/Active Compound : Nutmeg
Type of experiment : in vitro
Type of animal : -
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : -
Dose/Conc.(herb) : 100 microgram/ml
Duration : -
Type of interaction : Pharmacokinetics
Interaction with drug : -
Dose/Conc.(drug) : -
Result : Positive
Remark : IC50=4.2 microgram/ml

Part Used : ไม่ระบุ
Activity : DRUG INTERACTION
Solvent/Active Compound : Nutmeg
Type of experiment : in vitro
Type of animal : -
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : -
Dose/Conc.(herb) : 100 microgram/ml
Duration : -
Type of interaction : Pharmacokinetics
Interaction with drug : -
Dose/Conc.(drug) : -
Result : Positive
Remark : IC50=2.6 microgram/ml

Part Used : รก
Activity : DRUG INTERACTION
Solvent/Active Compound : Total extract
Type of experiment : in vitro
Type of animal : -
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : -
Dose/Conc.(herb) : 5 micromolar/ml
Duration : -
Type of interaction : Pharmacokinetics
Interaction with drug : -
Dose/Conc.(drug) : -
Result : Positive
Remark : Inhibition (%)=77

Part Used : รก
Activity : DRUG INTERACTION
Solvent/Active Compound : Total extract
Type of experiment : in vitro
Type of animal : -
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : -
Dose/Conc.(herb) : 5 micromolar/ml
Duration : -
Type of interaction : Pharmacokinetics
Interaction with drug : -
Dose/Conc.(drug) : -
Result : Positive
Remark : Inhibition (%)=90


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