Page last updated: 2024-12-06

1-triacontanol

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

1-Triacontanol is a long-chain aliphatic alcohol found in plants, with the molecular formula CH3(CH2)28CH2OH. It has been studied for its potential effects on plant growth and development. Research has suggested that 1-triacontanol can promote seed germination, root elongation, and overall plant growth. Its effects are thought to be mediated through its interaction with plant hormones and its influence on cellular metabolism. 1-triacontanol is a natural compound, and its potential as a plant growth regulator has made it an area of interest for agricultural research.'

1-triacontanol: constituent of Apocynum venetum leaf & Cirsium segetum [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

triacontan-1-ol : An ultra-long-chain primary fatty alcohol that is triacontane in which one of the terminal methyl hydrogens is replaced by a hydroxy group. [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]

FloraRankFlora DefinitionFamilyFamily Definition
CirsiumgenusA plant genus of the family ASTERACEAE. Members contain pectolinarin (a flavonoid glycoside).[MeSH]AsteraceaeA large plant family of the order Asterales, subclass Asteridae, class Magnoliopsida. The family is also known as Compositae. Flower petals are joined near the base and stamens alternate with the corolla lobes. The common name of daisy refers to several genera of this family including Aster; CHRYSANTHEMUM; RUDBECKIA; TANACETUM.[MeSH]
ApocynumgenusA plant genus of the family APOCYNACEAE. On rare occasions it is called Milkweed, but should not be confused with true Milkweed (ASCLEPIAS).[MeSH]ApocynaceaeThe dogbane family of the order Gentianales. Members of the family have milky, often poisonous juice, smooth-margined leaves, and flowers in clusters.[MeSH]
Apocynum venetumspecies[no description available]ApocynaceaeThe dogbane family of the order Gentianales. Members of the family have milky, often poisonous juice, smooth-margined leaves, and flowers in clusters.[MeSH]

Cross-References

ID SourceID
PubMed CID68972
CHEMBL ID1079147
CHEBI ID28409
SCHEMBL ID16858
MeSH IDM0137348

Synonyms (58)

Synonym
CHEBI:28409 ,
nsc402492
nsc-405588
triacontyl alcohol
NSC405588 ,
n-triacontanol
melissyl alcohol
triacontanol-1
nsc-402492
1-triacontanol
593-50-0
C08392
triacontan-1-ol
myricyl alcohol
1-triacontanol, >=98% (capillary gc)
LMFA05000006
1-triacontanol, 96%
ai3-20480
nsc 402492
myricyl alcohol (van)
einecs 209-794-5
nsc 405588
triacontanyl alcohol
T1049
CHEMBL1079147
A832277
miraculan
triacontanol
28351-05-5
767rd0e90b ,
unii-767rd0e90b
1-hydroxytriacontane
FT-0608318
tricontanol
ultria
myricyl alcohol [inci]
tricontanol (constituent of saw palmetto) [dsc]
1-triacontanol [mi]
well-bloom
AKOS015902949
S5172
SCHEMBL16858
W-105327
HMS3649O04
DTXSID5029188 ,
mfcd00002963
1-triacontanol 100 microg/ml in methyl-tert-butyl ether
Q4860821
1-triacontanol,(s)
AS-14880
sr-01000946625
SR-01000946625-1
CS-W011606
P50010
HY-N6933
1-?triacontanol
tricontanol (constituent of saw palmetto)
dtxcid709188

Research Excerpts

Toxicity

ExcerptReferenceRelevance
"Arsenic (As), recognized as a toxic metalloid globally, has posed a serious threat to soil, plants and aquatic resources."( Exogenous triacontanol provides tolerance against arsenic-induced toxicity by scavenging ROS and improving morphology and physiological activities of Mentha arvensis L.
Aftab, T; Khan, A; Masroor, M; Nabi, A; Naeem, M, 2022
)
0.72

Pharmacokinetics

ExcerptReferenceRelevance
"9% reduction in Cmax (120 and 180 mg kg(-1), respectively) compared with the control."( Effect of triacontanol on the pharmacokinetics of docetaxel in rats associated with induction of cytochrome P450 3A1/2.
Chen, X; Deng, S; Fan, A; Gao, W; Li, C; Li, N; Liu, Q; Wang, C; Wen, X; Zhang, Q; Zhang, W; Zhang, Y; Zhao, D; Zhao, J, 2014
)
0.4
" The present study was aimed to develop a sensitive gas chromatography-tandem mass spectrometry method to explore the pharmacokinetic profiles, distribution and excretion of TA in Sprague-Dawley rats after oral administration of TA."( Investigation on pharmacokinetics, tissue distribution and excretion of 1-triacontanol in rats by gas chromatography-tandem mass spectrometry (GC-MS/MS).
Chen, X; Deng, S; Fan, A; Gao, W; Lu, Y; Wang, C; Yang, W; Zhang, W; Zhu, X, 2015
)
0.65
" The validated method was successfully applied to a pharmacokinetic study of TA in beagles."( Trace quantification of 1-triacontanol in beagle plasma by GC-MS/MS and its application to a pharmacokinetic study.
Chen, X; Deng, S; Fan, A; Gao, W; Liu, Q; Lu, Y; Wang, C; Zhang, W; Zhu, X, 2015
)
0.72

Dosage Studied

ExcerptRelevanceReference
" Hepatic clearance of docetaxel was enhanced in vitro and in vivo at dosage of 120 and 180 mg kg(-1), and CYP3A activity was up-regulated by measuring the formation rate of 1-hydroxymidazolam."( Effect of triacontanol on the pharmacokinetics of docetaxel in rats associated with induction of cytochrome P450 3A1/2.
Chen, X; Deng, S; Fan, A; Gao, W; Li, C; Li, N; Liu, Q; Wang, C; Wen, X; Zhang, Q; Zhang, W; Zhang, Y; Zhao, D; Zhao, J, 2014
)
0.4
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (2)

ClassDescription
fatty alcohol 30:0Any fatty alcohol containing 30 carbons.
ultra-long-chain primary fatty alcoholAny primary fatty alcohol with a chain length greater than C27.
[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]

Bioassays (3)

Assay IDTitleYearJournalArticle
AID471325Antiviral activity against HIV-1 NL4-3 expressing VSV-G envelope infected in human 293T cells assessed as inhibition of viral replication after 48 hrs by Luciferase reporter gene assay2009Journal of natural products, Sep, Volume: 72, Issue:9
Chemical Constituents of the Roots of Euphorbia micractina.
AID471323Cytotoxicity against human A2780 cells after 4 days by MTT assay2009Journal of natural products, Sep, Volume: 72, Issue:9
Chemical Constituents of the Roots of Euphorbia micractina.
AID471324Inhibition of GST-tagged human PTP1B2009Journal of natural products, Sep, Volume: 72, Issue:9
Chemical Constituents of the Roots of Euphorbia micractina.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (66)

TimeframeStudies, This Drug (%)All Drugs %
pre-19906 (9.09)18.7374
1990's8 (12.12)18.2507
2000's20 (30.30)29.6817
2010's19 (28.79)24.3611
2020's13 (19.70)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 26.23

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.

MetricThis Compound (vs All)
Research Demand Index26.23 (24.57)
Research Supply Index4.22 (2.92)
Research Growth Index4.90 (4.65)
Search Engine Demand Index36.91 (26.88)
Search Engine Supply Index2.78 (0.95)

This Compound (26.23)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other67 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]