Page last updated: 2024-11-05

methylphenyl carbinol

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

Description

1-phenylethanol : An aromatic alcohol that is ethanol substituted by a phenyl group at position 1. [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]

methylbenzyl alcohol : Members of the class of benzyl alcohols substituted by at least one methyl 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]

Cross-References

ID SourceID
PubMed CID7409
CHEMBL ID508917
CHEBI ID669
SCHEMBL ID2164
MeSH IDM0042474

Synonyms (130)

Synonym
.alpha.-methylbenzenemethanol
1-phenylethyl alcohol
methylphenylcarbinol
.alpha.-methylbenzyl alcohol
1-phenethyl alcohol
wln: qy1 & r
.alpha.-phenylethanol
.alpha.-phenylethyl alcohol
styralyl alcohol
ethanol, 1-phenyl-
nsc-25502
1-phenyl-1-hydroxyethane
phenylmethylcarbinol
benzenemethanol, .alpha.-methyl-
.alpha.-phenethyl alcohol
nsc25502
sec-phenethyl alcohol
nci-c55685
benzyl alcohol, .alpha.-methyl-
(1-hydroxyethyl)benzene
methanol, methylphenyl-
fenyl-methylkarbinol [czech]
(1)-alpha-methylbenzyl alcohol
benzyl alcohol, alpha-methyl-
ai3-02936
1-fenylethanol [czech]
einecs 236-361-8
benzenemethanol, alpha-methyl-
methyl phenyl methanol
fema no. 2685
alpha-phenethyl alcohol
hsdb 4164
ccris 2367
1-phenylethan-1-ol
un2937
fema number 2685
alpha-methyl-benzenemethanol
einecs 202-707-1
alpha-methyl-benzmethanol
nsc 25502
CHEBI:669 ,
alpha-phenylethyl alcohol
alpha-phenylethanol
styrallyl alcohol
alpha-methylbenzenemethanol
alpha-methyl-benzyl alcohol
98-85-1
1-phenylethanol
C07112
alpha-methylbenzyl alcohol
methylphenyl carbinol
alpha-methylbenzyl alcohol, >=99%, fcc, fg
1-phenylethanol, 98%
1-phenyl-ethanol
phenyl ethanol
CHEMBL508917
(+/-)-1-phenylethyl alcohol
(+/-)-1-phenylethanol
(+/-)-alpha-methylbenzyl alcohol
M0163
(+/-)-sec-phenethyl alcohol
AKOS000121326
NCGC00248663-01
dtxcid50859
tox21_200505
dtxsid1020859 ,
cas-98-85-1
NCGC00258059-01
ec 202-707-1
fenyl-methylkarbinol
e6o895dq52 ,
1-fenylethanol
unii-e6o895dq52
alpha-methylbenzyl alcohol [un2937] [poison]
FT-0605197
FT-0633624
FT-0647462
FT-0628703
alpha-methylbenzyl alcohol [fcc]
1-phenylethanol, (+/-)-
alpha-methylbenzyl alcohol [hsdb]
(+/-)-.alpha.-methylbenzyl alcohol
methyl phenyl carbinol
styrene alcohol
.alpha.-methylbenzyl alcohol [fhfi]
13323-81-4
AKOS016038258
SCHEMBL2164
(+/-)-a-methylbenzyl alcohol
a-methylbenzyl alcohol
1-phenyl-1-ethanol
1-phenyl ethanol
1-phenyl-1-ethylalcohol
(+) alpha-phenylethanol
racemic 1-phenylethyl alcohol
alpha-methyl benzyl alcohol
1-phenylethane-1-ol
methylbenzyl alcohol
racemic 1-phenylethanol
dl-1-phenylethanol
1-hydroxyethylbenzene
rac.-1-phenylethanol
.alpha.-hydroxyethylbenzene
dl-.alpha.-methylbenzyl alcohol
un 2937
W-100061
methylbenzylalcohol
mfcd00004508
(r)-(+)-1-phenylethanol, 99%, chiraselect(tm)
methylphenyl-methanol
a-hydroxyethylbenzene
a-methylbenzyl alcohol, 8ci
fema 2685
alcohol methyl benzylic
a-methylbenzenemethanol, 9ci
1-(phenylethyl) alcohol
alpha-hydroxyethylbenzene
SY007833
cc(o)c1=cc=cc=c1
BCP24404
Q3740715
5-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-enyl)-3-methylpenta-2,4-dienoicacid
dl-1-phenethylalcohol
AMY3819
1-phenylethan-2,2,2-d3-ol
SB40856
EN300-21267
benzene-d5-methan-d-ol, a-(methyl-d3)-
(s)-(+)-1-phenylethanol
Z104494956

Research Excerpts

Compound-Compound Interactions

ExcerptReferenceRelevance
"The absolute configuration and conformation of 1-phenylethanol (1-PhEtOH) have been determined by matrix-isolation infrared (IR) and vibrational circular dichroism (VCD) spectroscopy combined with quantum chemical calculations."( Absolute configuration and conformation analysis of 1-phenylethanol by matrix-isolation infrared and vibrational circular dichroism spectroscopy combined with density functional theory calculation.
Hamada, Y; Katsumoto, Y; Ohno, K; Shin, S; Shin-ya, K; Sugeta, H, 2007
)
0.34
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
mouse metaboliteAny mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
[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]

Drug Classes (1)

ClassDescription
aromatic alcoholAny alcohol in which the alcoholic hydroxy group is attached to a carbon which is itself bonded to an aromatic ring.
[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]

Protein Targets (1)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency0.19690.003041.611522,387.1992AID1159552
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (7)

Assay IDTitleYearJournalArticle
AID1101947Growth inhibition of intact Triticum aestivum (wheat) seed assessed as appearance of distinct rootlets at 500 ppm after 4 days relative to wheat grains RL4137 germination2002Journal of agricultural and food chemistry, Oct-23, Volume: 50, Issue:22
Germination and growth inhibitors from wheat (Triticum aestivum L.) husks.
AID1101946Growth inhibition of intact Triticum aestivum (wheat) seed assessed as appearance of sprouts at 500 ppm after 4 days relative to wheat grains RL4137 germination2002Journal of agricultural and food chemistry, Oct-23, Volume: 50, Issue:22
Germination and growth inhibitors from wheat (Triticum aestivum L.) husks.
AID1101944Inhibition of intact Triticum aestivum (wheat) seed germination assessed as appearance of sprouts at 500 ppm after 4 days relative to wheat grains RL4137 germination2002Journal of agricultural and food chemistry, Oct-23, Volume: 50, Issue:22
Germination and growth inhibitors from wheat (Triticum aestivum L.) husks.
AID1101945Inhibition of intact Triticum aestivum (wheat) seed germination assessed as appearance of distinct rootlets at 500 ppm after 4 days relative to wheat grains RL4137 germination2002Journal of agricultural and food chemistry, Oct-23, Volume: 50, Issue:22
Germination and growth inhibitors from wheat (Triticum aestivum L.) husks.
AID377984Antifungal activity against Eurotium repens at 50 ug by agar diffusion test1999Journal of natural products, Jan, Volume: 62, Issue:1
Three new metabolites from marine-derived fungi of the genera coniothyrium and microsphaeropsis
AID1080381Nematicidal activity against Bursaphelenchus xylophilus assessed as nematode mortality at 2 mg/mL measured 24 hr post dose by microscopy2008Journal of agricultural and food chemistry, Aug-27, Volume: 56, Issue:16
Nematicidal activity of plant essential oils and components from coriander (Coriandrum sativum), Oriental sweetgum (Liquidambar orientalis), and valerian (Valeriana wallichii) essential oils against pine wood nematode (Bursaphelenchus xylophilus).
AID377985Antifungal activity against Ustilago violacea at 50 ug by agar diffusion test1999Journal of natural products, Jan, Volume: 62, Issue:1
Three new metabolites from marine-derived fungi of the genera coniothyrium and microsphaeropsis
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (84)

TimeframeStudies, This Drug (%)All Drugs %
pre-19905 (5.95)18.7374
1990's10 (11.90)18.2507
2000's26 (30.95)29.6817
2010's40 (47.62)24.3611
2020's3 (3.57)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 29.14

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 Index29.14 (24.57)
Research Supply Index4.47 (2.92)
Research Growth Index4.97 (4.65)
Search Engine Demand Index34.37 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (29.14)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews3 (3.49%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other83 (96.51%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]