Elemicin

Details

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Internal ID 55ac1cca-0813-4b58-bbcd-211110e58a21
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name 1,2,3-trimethoxy-5-prop-2-enylbenzene
SMILES (Canonical) COC1=CC(=CC(=C1OC)OC)CC=C
SMILES (Isomeric) COC1=CC(=CC(=C1OC)OC)CC=C
InChI InChI=1S/C12H16O3/c1-5-6-9-7-10(13-2)12(15-4)11(8-9)14-3/h5,7-8H,1,6H2,2-4H3
InChI Key BPLQKQKXWHCZSS-UHFFFAOYSA-N
Popularity 368 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O3
Molecular Weight 208.25 g/mol
Exact Mass 208.109944368 g/mol
Topological Polar Surface Area (TPSA) 27.70 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.44
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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487-11-6
5-Allyl-1,2,3-trimethoxybenzene
Elemicine
3,4,5-Trimethoxyallylbenzene
1,2,3-trimethoxy-5-prop-2-enylbenzene
Benzene, 1,2,3-trimethoxy-5-(2-propenyl)-
1,2,3-Trimethoxy-5-(2-propenyl)benzene
BENZENE, 5-ALLYL-1,2,3-TRIMETHOXY-
CCRIS 6783
3-(3,4,5-Trimethoxyphenyl)-1-propene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Elemicin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.7479 74.79%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.7498 74.98%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8964 89.64%
OATP1B3 inhibitior + 0.9774 97.74%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8020 80.20%
P-glycoprotein inhibitior - 0.9639 96.39%
P-glycoprotein substrate - 0.9368 93.68%
CYP3A4 substrate - 0.6083 60.83%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate + 0.4914 49.14%
CYP3A4 inhibition - 0.5850 58.50%
CYP2C9 inhibition - 0.9659 96.59%
CYP2C19 inhibition - 0.5927 59.27%
CYP2D6 inhibition - 0.9089 90.89%
CYP1A2 inhibition + 0.5958 59.58%
CYP2C8 inhibition + 0.6744 67.44%
CYP inhibitory promiscuity + 0.6823 68.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7521 75.21%
Carcinogenicity (trinary) Non-required 0.5588 55.88%
Eye corrosion + 0.5530 55.30%
Eye irritation + 0.9433 94.33%
Skin irritation - 0.6097 60.97%
Skin corrosion - 0.9179 91.79%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4618 46.18%
Micronuclear - 0.7108 71.08%
Hepatotoxicity + 0.8250 82.50%
skin sensitisation - 0.5933 59.33%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.6617 66.17%
Acute Oral Toxicity (c) III 0.8084 80.84%
Estrogen receptor binding - 0.8278 82.78%
Androgen receptor binding - 0.8773 87.73%
Thyroid receptor binding - 0.7644 76.44%
Glucocorticoid receptor binding - 0.9091 90.91%
Aromatase binding - 0.6560 65.60%
PPAR gamma - 0.8908 89.08%
Honey bee toxicity - 0.7483 74.83%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9592 95.92%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.20% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.25% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.90% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 85.60% 90.20%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.63% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.29% 94.45%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.17% 95.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Aconitum episcopale
Aconitum leucostomum
Acorus calamus
Acorus calamus var. angustatus
Acorus gramineus
Actaea cimicifuga
Actaea dahurica
Actaea simplex
Aiouea montana
Anemopsis californica
Anethum graveolens
Angelica pubescens
Aniba puchury-minor
Anisotome latifolia
Anthriscus sylvestris
Aquilegia ecalcarata
Ardisia humilis
Artemisia annua
Artemisia capillaris
Artemisia dracunculus
Artemisia szowitziana
Asarum asperum
Asarum canadense
Asarum epigynum
Asarum fauriei
Asarum heterotropoides
Asarum hexalobum
Asarum petelotii
Asarum rigescens
Asarum sieboldii
Athamanta vayredana
Atractylodes lancea
Aucklandia costus
Blepharocalyx salicifolius
Blumea axillaris
Boronia pinnata
Bridelia retusa
Bupleurum fruticosum
Bupleurum scorzonerifolium
Castilleja sulphurea
Catalpa bignonioides
Ceanothus velutinus
Chlorophytum borivilianum
Chrysothamnus viscidiflorus
Cinnamomum parthenoxylon
Cirsium arvense var. integrifolium
Cornus officinalis
Croton glandulosus
Croton nepetifolius
Cryptocarya agathophylla
Cymbopogon flexuosus
Cymbopogon nardus
Daphne genkwa
Daucus carota
Daucus carota subsp. carota
Dioscorea villosa
Diplolophium buchananii
Diplotaenia cachrydifolia
Dipterocarpus dyeri
Entada phaseoloides
Eremanthus arboreus
Erymophyllum tenellum
Esenbeckia nesiotica
Eucalyptus brassiana
Ferula communis
Foeniculum vulgare
Forsythia japonica
Fragaria vesca
Gamblea innovans
Garcia parviflora
Garcinia oligantha
Garcinia scortechinii
Gardenia tubifera
Gymnosporia pyria
Huperzia miyoshiana
Hyptis tomentosa
Ipomoea cairica
Ipomoea cristulata
Iris spuria
Isodon lophanthoides
Isodon rubescens
Juniperus gamboana
Kopsia grandifolia
Lasianthus fordii
Laurus nobilis
Ledebouria socialis
Ligusticum porteri
Lindera aggregata
Lindera neesiana
Lycopus europaeus
Melaleuca bracteata
Micranthemum umbrosum
Monocyclanthus vignei
Monopteryx uauca
Musa × paradisiaca
Myristica fragrans
Nepeta tenuifolia
Nothofagus menziesii
Ocimum gratissimum subsp. gratissimum
Paeonia lactiflora
Panax ginseng
Pancratium trianthum
Peperomia circinnata
Perilla frutescens
Perilla frutescens var. crispa
Perilla frutescens var. hirtella
Persea barbujana
Pimenta racemosa
Pinellia ternata
Piper aduncum
Piper auritum
Piper guineense
Piper kadsura
Piper marginatum
Piper pedicellosum
Piper solmsianum
Platostoma africanum
Pogostemon cablin
Polygala sibirica
Polygala tenuifolia
Pseudobrickellia brasiliensis
Pycnocycla spinosa
Rhododendron latoucheae
Rhodotypos scandens
Rubus trifidus
Sassafras albidum
Schisandra chinensis
Scutellaria baicalensis
Scutellaria barbata
Tasmannia lanceolata
Thapsia villosa
Todaroa aurea
Uvariodendron connivens
Vinca major
Virola surinamensis
Xanthostemon oppositifolius
Zieria smithii
Zingiber officinale

Cross-Links

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PubChem 10248
NPASS NPC204120
LOTUS LTS0204673
wikiData Q105252697