delta-tocotrienol : A tocotrienol that is chroman-6-ol substituted by methyl groups at positions 2 and 8 and a farnesyl chain at position 2. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]
ID Source | ID |
---|---|
PubMed CID | 5282350 |
CHEMBL ID | 121305 |
CHEBI ID | 33276 |
SCHEMBL ID | 8408117 |
SCHEMBL ID | 16430161 |
MeSH ID | M0218857 |
Synonym |
---|
BIDD:PXR0041 |
delta-tocotrienols |
CHEBI:33276 , |
(2r)-2,8-dimethyl-2-[(3e,7e)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]-3,4-dihydro-2h-chromen-6-ol |
6-chromanol, 2,8-dimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)- (7ci,8ci) |
8-methyltocotrienol |
2h-1-benzopyran-6-ol, 3,4-dihydro-2,8-dimethyl-2-[(3e,7e)-4,8,12-trimethyl-3,7,11-tridecatrienyl]-, (2r)- |
2h-1-benzopyran-6-ol, 3,4-dihydro-2,8-dimethyl-2-[(3e,7e)-4,8,12-trimethyl-3,7,11-tridecatrienyl]-, (2r)- (9ci) |
(r)-delta-tocotrienol |
2h-1-benzopyran-6-ol, 3,4-dihydro-2,8-dimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)-, [r-(e,e)]- |
tocotrienol, delta |
25612-59-3 |
delta-tocotrienol |
CHEMBL121305 |
2r,8-dimethyl-2-[(3e,7e)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]-3,4-dihydro-2h-chromen-6-ol |
LMPR02020056 |
(2r)-2,8-dimethyl-2-[(3e,7e)-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,4-dihydrochromen-6-ol |
unii-1srb74owsi |
2h-1-benzopyran-6-ol, 3,4-dihydro-2,8-dimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)-, (r-(e,e))- |
1srb74owsi , |
2h-1-benzopyran-6-ol, 3,4-dihydro-2,8-dimethyl-2-((3e,7e)-4,8,12-trimethyl-3,7,11-tridecatrienyl)-, (2r)- |
j17.358d , |
2h-1-benzopyran-6-ol, 3,4-dihydro-2,8-dimethyl-2-((3e,7e)-4,8,12-trimethyl-3,7,11-tridecatrien-1-yl)-, (2r)- |
delta tocotrienol [who-dd] |
.delta.-tocotrienol |
d-delta-tocotrienol |
(r)-.delta.-tocotrienol |
6-chromanol, 2,8-dimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)- |
(r)-2,8-dimethyl-2-((3e,7e)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl)chroman-6-ol |
2h-1-benzopyran-6-ol, 3,4-dihydro-2,8-dimethyl-2-[(3e,7e)-4,8,12-trimethyl-3,7,11-tridecatrien-1-yl]-, (2r)- |
SCHEMBL8408117 |
HMS3650C18 |
DTXSID30180288 |
SCHEMBL16430161 |
delta-tocotrienol, analytical standard |
NCGC00253541-03 |
2,8-dimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)-6-chromanol |
3,4-dihydro-2,8-dimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)-2h-1-benzopyran-6-ol, 9ci |
Q27104272 |
SR-01000946270-1 |
sr-01000946270 |
(r-(e,e))-3,4-dihydro-2,8-dimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)-2h-1-benzopyran-6-ol |
delta -tocotrienol |
r-delta-tocotrienol |
HY-122778 |
CS-0089253 |
AS-82630 |
AKOS040760094 |
Excerpt | Reference | Relevance |
---|---|---|
" Neither drug produced detectable toxic effects in any other tissue at the doses tested." | ( Acute toxicity of subcutaneously administered vitamin E isomers delta- and gamma-tocotrienol in mice. Chakraborty, K; Ghosh, SP; Lombardini, E; Pessu, RL; Swift, SN; Villa, V, ) | 0.13 |
" One patient had a drug-related adverse event (diarrhea) at a 3200-mg daily dose level." | ( A Phase I Safety, Pharmacokinetic, and Pharmacodynamic Presurgical Trial of Vitamin E δ-tocotrienol in Patients with Pancreatic Ductal Neoplasia. Centeno, B; Chen, DT; Husain, K; Hutchinson, TZ; Lush, RM; Malafa, MP; Neuger, A; Sebti, S; Springett, GM, 2015) | 0.42 |
"No drug-related adverse events were observed." | ( Pharmacokinetics and safety of vitamin E δ-tocotrienol after single and multiple doses in healthy subjects with measurement of vitamin E metabolites. Chen, DT; Klapman, J; Mahipal, A; Malafa, MP; Neuger, A; Vignesh, S; Yang, CS, 2016) | 0.43 |
Excerpt | Reference | Relevance |
---|---|---|
" Pharmacokinetic data were derived from high-performance liquid chromatography (HPLC) assays." | ( Pharmacokinetics and safety of vitamin E δ-tocotrienol after single and multiple doses in healthy subjects with measurement of vitamin E metabolites. Chen, DT; Klapman, J; Mahipal, A; Malafa, MP; Neuger, A; Vignesh, S; Yang, CS, 2016) | 0.43 |
" Pharmacokinetic parameters for single and multiple doses were, respectively, as follows (shown as range): time to maximum concentration of 4-9." | ( Pharmacokinetics and safety of vitamin E δ-tocotrienol after single and multiple doses in healthy subjects with measurement of vitamin E metabolites. Chen, DT; Klapman, J; Mahipal, A; Malafa, MP; Neuger, A; Vignesh, S; Yang, CS, 2016) | 0.43 |
Excerpt | Reference | Relevance |
---|---|---|
"We have investigated the pharmacokinetics and bioavailability of alpha-, gamma- and delta-tocotrienols under fed and fasted conditions in eight healthy volunteers." | ( Pharmacokinetics and bioavailability of alpha-, gamma- and delta-tocotrienols under different food status. Wong, JW; Yap, SP; Yuen, KH, 2001) | 0.31 |
"A study was conducted to evaluate the bioavailability of alpha-, gamma- and delta-tocotrienols administered via oral, intravenous, intramuscular and intraperitoneal routes in rats." | ( Influence of route of administration on the absorption and disposition of alpha-, gamma- and delta-tocotrienols in rats. Lim, AB; Yap, SP; Yuen, KH, 2003) | 0.32 |
"A single dose comparative bioavailability study was conducted to evaluate the bioavailability of tocotrienols from two self-emulsifying formulations, one of which produced an emulsion that readily lipolysed under in vitro condition (SES-A), while the other produced a finer dispersion with negligible lipolysis (SES-B) in comparison with that of a non-self-emulsifying formulation in soya oil." | ( Influence of lipolysis and droplet size on tocotrienol absorption from self-emulsifying formulations. Yap, SP; Yuen, KH, 2004) | 0.32 |
" This single-dose, randomized, crossover study aimed to compare the safety and bioavailability of a new formulation of Gamma Delta Tocotrienol (GDT) in comparison with the existing Tocotrienol-rich Fraction (TRF) in terms of gamma and delta isomers in healthy volunteers." | ( A new formulation of Gamma Delta Tocotrienol has superior bioavailability compared to existing Tocotrienol-Rich Fraction in healthy human subjects. Bhoo-Pathy, N; Chik, Z; Choudhury, RB; Fuang, HG; Jabir, RS; Meganathan, P; Nesaretnam, K; Taib, NA, 2015) | 0.42 |
" Plasma tocotrienols were significantly increased after VEDT administration, indicating oral bioavailability of VEDT in humans." | ( Pharmacokinetics and safety of vitamin E δ-tocotrienol after single and multiple doses in healthy subjects with measurement of vitamin E metabolites. Chen, DT; Klapman, J; Mahipal, A; Malafa, MP; Neuger, A; Vignesh, S; Yang, CS, 2016) | 0.43 |
" FA significantly increased the intracellular concentration of δ-T3, suggesting that FA improved the bioavailability of δ-T3, thereby increasing the inhibitory potency of δ-T3 on telomerase." | ( A Combination of δ-Tocotrienol and Ferulic Acid Synergistically Inhibits Telomerase Activity in DLD-1 Human Colorectal Adenocarcinoma Cells. Eitsuka, T; Miyazawa, T; Nakagawa, K; Nishida, H; Tatewaki, N, 2016) | 0.43 |
"The ATP-binding cassette transporter P-glycoprotein (P-gp) is known to limit both brain penetration and oral bioavailability of many chemotherapy drugs." | ( A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. Ambudkar, SV; Brimacombe, KR; Chen, L; Gottesman, MM; Guha, R; Hall, MD; Klumpp-Thomas, C; Lee, OW; Lee, TD; Lusvarghi, S; Robey, RW; Shen, M; Tebase, BG, 2019) | 0.51 |
Excerpt | Relevance | Reference |
---|---|---|
" The tocotrienol-rich fraction (TRF) of palm oil inhibited growth of MCF7 cells in both the presence and absence of estradiol with a nonlinear dose-response but such that complete suppression of growth was achieved at 8 microg/mL." | ( Tocotrienols inhibit the growth of human breast cancer cells irrespective of estrogen receptor status. Darbre, P; Dils, R; Nesaretnam, K; Stephen, R, 1998) | 0.3 |
" Tocotrienols were measured in heart, liver and adipose tissue showing that chronic oral dosage delivered tocotrienols to these organs despite low or no detection of tocotrienols in plasma." | ( Anti-inflammatory γ- and δ-tocotrienols improve cardiovascular, liver and metabolic function in diet-induced obese rats. Brown, L; Fong, CW; Ward, LC; Wong, WY; Yap, WN, 2017) | 0.46 |
Product Category | Products |
---|---|
Professional Supplements | 1 |
Vitamins & Supplements | 2 |
Product | Brand | Category | Compounds Matched from Ingredients | Date Retrieved |
---|---|---|---|---|
Dr. Mercola Vitamin E -- 30 Capsules | Dr. Mercola | Professional Supplements | d-Beta Tocopherol, d-Alpha-Tocopherol, d-delta tocopherol, d-Gamma Tocopherol, d-Gamma Tocotrienol, Vitamin E, d-Alpha Tocotrienol, d-Beta Tocotrienol, d-Delta Tocotrienol | 2024-11-29 10:47:42 |
NutriCology Tocomin SupraBio Tocotrienols -- 200 mg - 60 Softgels | NutriCology | Vitamins & Supplements | Vitamin E, d-Gamma Tocotrienol, Vitamin E, glycerin, d-Alpha Tocotrienol, d-Beta Tocotrienol, d-delta tocotrienol | 2024-11-29 10:47:42 |
Olympian Labs Tocomin Vitamin E Complete -- 60 Softgels | Olympian Labs | Vitamins & Supplements | d-Beta Tocopherol, Vitamin E, d-delta tocopherol, d-Gamma Tocopherol, d-Gamma Tocotrienol, Vitamin E, Phytosterols, d-Alpha Tocotrienol, d-Beta Tocotrienol, d-delta tocotrienol | 2024-11-29 10:47:42 |
Role | Description |
---|---|
plant metabolite | Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms. |
NF-kappaB inhibitor | An inhibitor of NF-kappaB (nuclear factor kappa-light-chain-enhancer of activated B cells), a protein complex involved in the transcription of DNA. |
antineoplastic agent | A substance that inhibits or prevents the proliferation of neoplasms. |
apoptosis inducer | Any substance that induces the process of apoptosis (programmed cell death) in multi-celled organisms. |
Saccharomyces cerevisiae metabolite | Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae). |
radiation protective agent | Any compound that is able to protect normal cells from the damage caused by radiation therapy. |
anti-inflammatory agent | Any compound that has anti-inflammatory effects. |
bone density conservation agent | An agent that inhibits bone resorption and/or favor bone mineralization and bone regeneration. Used to heal bone fractures and to treat bone diseases such as osteopenia and osteoporosis. |
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Class | Description |
---|---|
tocotrienol | A tocol in which the hydrocarbon chain at position 2 contains three double bonds. |
vitamin E | Any member of a group of fat-soluble chromanols that exhibit biological activity against vitamin E deficiency. The vitamers in this class consists of a chroman-6-ol core which is substituted at position 2 by a methyl group and (also at position 2) either a saturated or a triply-unsaturated hydrocarbon chain consisting of three isoprenoid units. The major function of vitamin E is to act as a natural antioxidant by scavenging free radicals and molecular oxygen. |
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Pathway | Proteins | Compounds |
---|---|---|
vitamin E biosynthesis (tocotrienols) | 1 | 13 |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID457739 | Antiproliferative activity against human MCF7 cells after 96 hrs by MTT assay | 2010 | Bioorganic & medicinal chemistry, Jan-15, Volume: 18, Issue:2 | Design and preliminary structure-activity relationship of redox-silent semisynthetic tocotrienol analogues as inhibitors for breast cancer proliferation and invasion. |
AID327671 | Antiproliferative activity against mouse +SA mammary epithelial cells after 4 days by MTT assay | 2008 | Journal of natural products, Jan, Volume: 71, Issue:1 | Semisynthetic and biotransformation studies of (1S,2E,4S,6R,7E,11E)-2,7,11-cembratriene-4,6-diol. |
AID1605744 | Agonist activity at LXR-beta (unknown origin) at 10 uM by coactivator recruitment based Alpha-screen assay | 2020 | Journal of medicinal chemistry, 04-09, Volume: 63, Issue:7 | Garcinoic Acid Is a Natural and Selective Agonist of Pregnane X Receptor. |
AID1662279 | Metabolic stability in mouse live microsomes assessed as compound degradation in absence of NADPH | 2020 | Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11 | Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production. |
AID194999 | Compound is evaluated for the inhibition of cholesterol biosynthesis in isolated rat hepatocytes at the concentration 250 (ug/mL) | 1992 | Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20 | Hypocholesterolemic activity of synthetic and natural tocotrienols. |
AID194996 | Inhibitory concentration required to inhibit cholesterol synthesis in isolated rat Hepatocytes | 1992 | Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20 | Hypocholesterolemic activity of synthetic and natural tocotrienols. |
AID1662266 | Tmax in CD2F1 mouse at 200 mg/kg, sc measured up to 24 hrs | 2020 | Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11 | Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production. |
AID1662267 | Cmax in CD2F1 mouse at 200 mg/kg, sc measured up to 24 hrs | 2020 | Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11 | Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production. |
AID366535 | Antiproliferative activity against mouse +SA cells assessed as cell viability after 4 days by MTT assay | 2008 | Journal of natural products, Aug, Volume: 71, Issue:8 | Sinulodurins A and B, antiproliferative and anti-invasive diterpenes from the soft coral Sinularia dura. |
AID195000 | Compound is evaluated for the inhibition of cholesterol biosynthesis in isolated rat hepatocytes at the concentration 500 (ug/mL) | 1992 | Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20 | Hypocholesterolemic activity of synthetic and natural tocotrienols. |
AID1662265 | AUC (0 to last) in CD2F1 mouse at 50 mg/kg, iv measured up to 24 hrs | 2020 | Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11 | Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production. |
AID194998 | Compound is evaluated for the inhibition of cholesterol biosynthesis in isolated rat hepatocytes at the concentration 125 (ug/mL) | 1992 | Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20 | Hypocholesterolemic activity of synthetic and natural tocotrienols. |
AID690597 | Antioxidant activity assessed as ferric ion reducing power by FRAP method | 2011 | Bioorganic & medicinal chemistry, Nov-01, Volume: 19, Issue:21 | Tocotrienamines and tocopheramines: reactions with radicals and metal ions. |
AID1662269 | Intrinsic clearance in mouse liver microsomes | 2020 | Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11 | Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production. |
AID50641 | picomoles of mevalonic acid synthesized per minute per mg of microsomal protein | 1992 | Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20 | Hypocholesterolemic activity of synthetic and natural tocotrienols. |
AID457738 | Antiproliferative activity against human MDA-MB-231 cells after 96 hrs by MTT assay | 2010 | Bioorganic & medicinal chemistry, Jan-15, Volume: 18, Issue:2 | Design and preliminary structure-activity relationship of redox-silent semisynthetic tocotrienol analogues as inhibitors for breast cancer proliferation and invasion. |
AID1612323 | Antiproliferative activity against human A2780 cells assessed as reduction in cell viability incubated for 48 hrs by Alamar blue assay | 2019 | Journal of natural products, 03-22, Volume: 82, Issue:3 | Phloroglucinols from the Roots of Garcinia dauphinensis and Their Antiproliferative and Antiplasmodial Activities. |
AID51430 | Compound is evaluated for the effect on lipid metabolism in 6-week-old male chickens at a concentration of 20 ppm in the diet and measured for total cholesterol | 1992 | Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20 | Hypocholesterolemic activity of synthetic and natural tocotrienols. |
AID1662268 | AUC (0 to last) in CD2F1 mouse at 200 mg/kg, sc measured up to 24 hrs | 2020 | Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11 | Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production. |
AID1662271 | Metabolic stability in mouse liver microsomes assessed as compound degradation at 1 uM preincubated for 30 mins followed by NADPH addition measured up to 30 mins by HPLC-UV analysis | 2020 | Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11 | Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production. |
AID1605741 | Agonist activity at His-tagged PXR-LBD/SRC-1p (unknown origin) expressed in Escherichia coli BL21(DE3) at 10 uM by coactivator recruitment based Alpha-screen assay | 2020 | Journal of medicinal chemistry, 04-09, Volume: 63, Issue:7 | Garcinoic Acid Is a Natural and Selective Agonist of Pregnane X Receptor. |
AID1662273 | Volume of distribution in CD2F1 mouse at 50 mg/kg, iv measured up to 24 hrs | 2020 | Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11 | Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production. |
AID745932 | Antimigratory activity against human MDA-MB-231 cells after 24 hrs by wound-healing assay | 2013 | European journal of medicinal chemistry, Jan, Volume: 59 | Optimization of tocotrienols as antiproliferative and antimigratory leads. |
AID50632 | Compound is evaluated for the effect on lipid metabolism in 6-week-old male chickens at a concentration of 20 ppm in the diet and measured for HDL cholesterol | 1992 | Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20 | Hypocholesterolemic activity of synthetic and natural tocotrienols. |
AID1662274 | Equlibrium constant in CD2F1 mouse at 50 mg/kg, iv measured up to 24 hrs | 2020 | Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11 | Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production. |
AID1662275 | AUC (0 to infinity) in CD2F1 mouse at 50 mg/kg, iv measured up to 24 hrs | 2020 | Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11 | Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production. |
AID537457 | Cytotoxicity against mouse +SA cells after 24 hrs by MTT assay | 2010 | Bioorganic & medicinal chemistry, Nov-15, Volume: 18, Issue:22 | Redox-silent tocotrienol esters as breast cancer proliferation and migration inhibitors. |
AID1662277 | Induction of G-CSF production in CD2F1 mouse at 200 mg/kg, sc by G-CSF ELISA kit method | 2020 | Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11 | Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production. |
AID1662270 | Half life in mouse liver microsomes | 2020 | Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11 | Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production. |
AID86698 | Compound evaluated for Percent inhibition of cholesterol synthesis from HMG-CoA Reductase in HepG2 cell | 1992 | Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20 | Hypocholesterolemic activity of synthetic and natural tocotrienols. |
AID1662272 | Clearance in CD2F1 mouse at 50 mg/kg, iv measured up to 24 hrs | 2020 | Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11 | Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production. |
AID1612324 | Antiplasmodial activity against Plasmodium falciparum Dd2 assessed as reduction in parasite viability incubated for 72 hrs by SYBR Green I dye based assay | 2019 | Journal of natural products, 03-22, Volume: 82, Issue:3 | Phloroglucinols from the Roots of Garcinia dauphinensis and Their Antiproliferative and Antiplasmodial Activities. |
AID1662278 | Induction of G-CSF production in CD2F1 mouse at 200 mg/kg, sc pretreated with ketoconazole after 24 hrs by G-CSF ELISA kit method | 2020 | Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11 | Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production. |
AID422002 | Antiinflammatory activity in human neutrophils assessed as inhibition of fMet-Leu-Phe/Cytochalasin B-induced elastase release treated 5 mins before fMet-Leu-Phe/Cytochalasin B challenge | 2009 | Journal of natural products, Feb-27, Volume: 72, Issue:2 | Benzophenone derivatives from the fruits of Garcinia multiflora and their anti-inflammatory activity. |
AID422001 | Antiinflammatory activity in human neutrophils assessed as inhibition of fMet-Leu-Phe/Cytochalasin B-induced superoxide anion generation treated 5 mins before fMet-Leu-Phe/Cytochalasin B challenge by spectrophotometry | 2009 | Journal of natural products, Feb-27, Volume: 72, Issue:2 | Benzophenone derivatives from the fruits of Garcinia multiflora and their anti-inflammatory activity. |
AID690612 | Antioxidant activity assessed as ABTS+ free radical scavenging activity by TEAC assay | 2011 | Bioorganic & medicinal chemistry, Nov-01, Volume: 19, Issue:21 | Tocotrienamines and tocopheramines: reactions with radicals and metal ions. |
AID1662276 | Plasma concentration in CD2F1 mouse at 200 mg/kg, sc administered as single dose measured after 1 hr by HPLC-fluorescence analysis | 2020 | Bioorganic & medicinal chemistry, 06-01, Volume: 28, Issue:11 | Deuteration of the farnesyl terminal methyl groups of δ-tocotrienol and its effects on the metabolic stability and ability of inducing G-CSF production. |
AID86699 | Compound evaluated for Percent inhibition of cholesterol synthesis from [14C]acetate in HepG2 cell | 1992 | Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20 | Hypocholesterolemic activity of synthetic and natural tocotrienols. |
AID690600 | Antioxidant activity assessed as DPPH free radical scavenging activity | 2011 | Bioorganic & medicinal chemistry, Nov-01, Volume: 19, Issue:21 | Tocotrienamines and tocopheramines: reactions with radicals and metal ions. |
AID50653 | Compound is evaluated for the effect on lipid metabolism in 6-week-old male chickens at a concentration of 20 ppm in the diet and measured for LDL cholesterol | 1992 | Journal of medicinal chemistry, Oct-02, Volume: 35, Issue:20 | Hypocholesterolemic activity of synthetic and natural tocotrienols. |
AID1605748 | Binding affinity to His-tagged PXR-LBD (unknown origin) expressed in Escherichia coli BL21 Gold at 60 uM by ITC analysis | 2020 | Journal of medicinal chemistry, 04-09, Volume: 63, Issue:7 | Garcinoic Acid Is a Natural and Selective Agonist of Pregnane X Receptor. |
AID277824 | Inhibition of alpha-glucosidase in 1.20 mg/200 uL | 2007 | Journal of natural products, Feb, Volume: 70, Issue:2 | Cinnamacrins A-C, cinnafragrin D, and cytostatic metabolites with alpha-glucosidase inhibitory activity from Cinnamosma macrocarpa. |
AID1296008 | Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening | 2020 | SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1 | Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening. |
AID1347160 | Primary screen NINDS Rhodamine qHTS for Zika virus inhibitors | 2020 | Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49 | Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors. |
AID1346986 | P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen | 2019 | Molecular pharmacology, 11, Volume: 96, Issue:5 | A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. |
AID1347159 | Primary screen GU Rhodamine qHTS for Zika virus inhibitors: Unlinked NS2B-NS3 protease assay | 2020 | Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49 | Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors. |
AID1346987 | P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen | 2019 | Molecular pharmacology, 11, Volume: 96, Issue:5 | A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 9 (5.70) | 18.2507 |
2000's | 26 (16.46) | 29.6817 |
2010's | 89 (56.33) | 24.3611 |
2020's | 34 (21.52) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.
| This Compound (28.71) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 12 (7.41%) | 5.53% |
Reviews | 2 (1.23%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 148 (91.36%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |