(E)-beta-farnesene

Details

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Internal ID 3bde311d-9faf-4056-85c3-33dd8fd9fed0
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 7,11-dimethyl-3-methylidenedodeca-1,6,10-triene
SMILES (Canonical) CC(=CCCC(=CCCC(=C)C=C)C)C
SMILES (Isomeric) CC(=CCCC(=CCCC(=C)C=C)C)C
InChI InChI=1S/C15H24/c1-6-14(4)10-8-12-15(5)11-7-9-13(2)3/h6,9,12H,1,4,7-8,10-11H2,2-3,5H3
InChI Key JSNRRGGBADWTMC-UHFFFAOYSA-N
Popularity 168 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.20
Atomic LogP (AlogP) 5.20
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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7,11-dimethyl-3-methylidenedodeca-1,6,10-triene
BETA-FARNESENE
DTXSID30860230
FT-0604950
FT-0637749
FT-0700008
Q27119784

2D Structure

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2D Structure of (E)-beta-farnesene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 + 0.8952 89.52%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Nucleus 0.6326 63.26%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.9330 93.30%
OATP1B3 inhibitior + 0.9322 93.22%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6943 69.43%
P-glycoprotein inhibitior - 0.9495 94.95%
P-glycoprotein substrate - 0.9484 94.84%
CYP3A4 substrate - 0.6041 60.41%
CYP2C9 substrate - 0.8209 82.09%
CYP2D6 substrate - 0.7550 75.50%
CYP3A4 inhibition - 0.9627 96.27%
CYP2C9 inhibition - 0.8903 89.03%
CYP2C19 inhibition - 0.8891 88.91%
CYP2D6 inhibition - 0.9474 94.74%
CYP1A2 inhibition - 0.7161 71.61%
CYP2C8 inhibition - 0.9426 94.26%
CYP inhibitory promiscuity - 0.7252 72.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Warning 0.4862 48.62%
Eye corrosion + 0.7167 71.67%
Eye irritation + 0.9581 95.81%
Skin irritation + 0.8426 84.26%
Skin corrosion - 0.9833 98.33%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4581 45.81%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation + 0.9235 92.35%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.8004 80.04%
Acute Oral Toxicity (c) III 0.9077 90.77%
Estrogen receptor binding - 0.9438 94.38%
Androgen receptor binding - 0.8594 85.94%
Thyroid receptor binding - 0.8512 85.12%
Glucocorticoid receptor binding - 0.5706 57.06%
Aromatase binding - 0.6809 68.09%
PPAR gamma + 0.5948 59.48%
Honey bee toxicity - 0.8406 84.06%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9962 99.62%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.83% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.16% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.49% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.99% 94.45%
CHEMBL2581 P07339 Cathepsin D 81.30% 98.95%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 80.32% 82.05%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.01% 99.17%

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.
Acorus calamus
Agrimonia pilosa
Angelica acutiloba
Angelica gigas
Angelica sinensis
Anthriscus sylvestris
Artemisia annua
Artemisia argyi
Artemisia capillaris
Artemisia carvifolia
Artemisia montana
Artemisia pontica
Artemisia princeps
Artemisia vulgaris
Bedfordia arborescens
Capsicum annuum
Caucasalia pontica
Chromolaena arnottiana
Chrysanthemum indicum
Citrus × aurantium
Citrus medica
Citrus trifoliata
Conioselinum anthriscoides
Croton sonderianus
Cupressus nootkatensis
Curcuma kwangsiensis
Curcuma longa
Curcuma phaeocaulis
Curcuma wenyujin
Curcuma zedoaria
Daucus carota
Dipteryx lacunifera
Duhaldea cuspidata
Eclipta prostrata
Elsholtzia ciliata
Erigeron philadelphicus
Ferula fukanensis
Foeniculum vulgare
Glehnia littoralis
Grindelia hirsutula
Helichrysum cephaloideum
Helichrysum chrysargyrum
Helichrysum cymosum
Heptapleurum arboricola
Houttuynia cordata
Humulus lupulus
Hydrocotyle sibthorpioides
Hypericum perforatum
Isocoma tenuisecta
Larix gmelinii var. gmelinii
Ligusticum officinale
Litsea cubeba
Lobelia chinensis
Lonicera japonica
Mentha arvensis
Mentha canadensis
Mentha suaveolens
Mosla chinensis
Panax ginseng
Panax notoginseng
Panax quinquefolius
Perilla frutescens
Picradeniopsis multiflora
Pimpinella anisum
Pinellia ternata
Pinus koraiensis
Pinus pinaster
Piper cubeba
Piper nigrum
Psiadia ceylanica
Rhododendron groenlandicum
Roldana aschenborniana
Rugelia nudicaulis
Schisandra chinensis
Senecio erosus
Senecio inaequidens
Senecio lydenburgensis
Senecio pseudoorientalis
Senecio squalidus
Senecio variabilis
Senna alexandrina
Seriphidium herba-alba
Sideritis tragoriganum
Smallanthus uvedalia
Solidago odora
Sphaeromorphaea australis
Symphyopappus reticulatus
Tanacetum annuum
Zanthoxylum bungeanum
Zanthoxylum schinifolium
Zingiber officinale

Cross-Links

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PubChem 10407
NPASS NPC248726
LOTUS LTS0091648
wikiData Q27119784