beta-Humulene

Details

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Internal ID 3cc3f7e5-e5ec-4fb3-90d7-c5963aab4f17
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1E,5E)-1,4,4-trimethyl-8-methylidenecycloundeca-1,5-diene
SMILES (Canonical) CC1=CCC(C=CCC(=C)CCC1)(C)C
SMILES (Isomeric) C/C/1=C\CC(/C=C/CC(=C)CCC1)(C)C
InChI InChI=1S/C15H24/c1-13-7-5-8-14(2)10-12-15(3,4)11-6-9-13/h6,10-11H,1,5,7-9,12H2,2-4H3/b11-6+,14-10+
InChI Key HAVYZKHVTLAPDZ-PPGMXFKZSA-N
Popularity 34 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 4.80
Atomic LogP (AlogP) 5.04
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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.beta.-Humulene
(E,E)-1,4,4-Trimethyl-8-methylene-1,5-cycloundecadiene
(4E,8E)-beta-humulene
UNII-KK0W1K5Z3S
KK0W1K5Z3S
116-04-1
(1E,5E)-1,4,4-trimethyl-8-methylidenecycloundeca-1,5-diene
1,5-Cycloundecadiene, 1,4,4-trimethyl-8-methylene-, (1E,5E)-
(1E,5E)-1,4,4-trimethyl-8-methylenecycloundeca-1,5-diene
1,5-Cycloundecadiene, 1,4,4-trimethyl-8-methylene-, (E,E)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of beta-Humulene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.9542 95.42%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.6135 61.35%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior + 0.9220 92.20%
OATP1B3 inhibitior + 0.9265 92.65%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9016 90.16%
P-glycoprotein inhibitior - 0.9485 94.85%
P-glycoprotein substrate - 0.9230 92.30%
CYP3A4 substrate - 0.5115 51.15%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.7848 78.48%
CYP3A4 inhibition - 0.8953 89.53%
CYP2C9 inhibition - 0.7430 74.30%
CYP2C19 inhibition - 0.7356 73.56%
CYP2D6 inhibition - 0.9386 93.86%
CYP1A2 inhibition - 0.7590 75.90%
CYP2C8 inhibition - 0.8482 84.82%
CYP inhibitory promiscuity - 0.7893 78.93%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Warning 0.5069 50.69%
Eye corrosion - 0.6668 66.68%
Eye irritation + 0.9343 93.43%
Skin irritation + 0.6623 66.23%
Skin corrosion - 0.9847 98.47%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7247 72.47%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation + 0.8828 88.28%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.4553 45.53%
Acute Oral Toxicity (c) III 0.7989 79.89%
Estrogen receptor binding - 0.9085 90.85%
Androgen receptor binding - 0.9095 90.95%
Thyroid receptor binding - 0.7536 75.36%
Glucocorticoid receptor binding - 0.7578 75.78%
Aromatase binding - 0.6206 62.06%
PPAR gamma - 0.6636 66.36%
Honey bee toxicity - 0.9151 91.51%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9972 99.72%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.82% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.77% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.27% 86.00%
CHEMBL1871 P10275 Androgen Receptor 83.75% 96.43%
CHEMBL2581 P07339 Cathepsin D 80.44% 98.95%

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.
Abies sibirica
Achillea ageratum
Aconitum sajanense
Aconitum violaceum
Alkanna cappadocica
Alstonia muelleriana
Artemisia jacutica
Artemisia rupestris subsp. rupestris
Astilbe rubra
Atalantia racemosa
Barbarea vulgaris
Bersama abyssinica
Buddleja cordata
Cannabis sativa
Chuquiraga spinosa
Codonopsis pilosula
Copaifera langsdorffii
Coreopsis nodosa
Crambe tatarica
Cryptocarya triplinervis
Dacrydium cupressinum
Damnacanthus major
Delphinium shawurense
Diospyros eriantha
Fagraea gracilipes
Fritillaria monantha
Garcinia xipshuanbannaensis
Glycine tomentella
Gutierrezia microcephala
Helichrysum graveolens
Helichrysum odoratissimum
Heracleum dissectum
Hoffmannia strigillosa
Humulus lupulus
Hydnocarpus venenata
Illicium verum
Iryanthera paraensis
Larix sibirica
Lathyrus nissolia
Leonurus persicus
Lycopodium casuarinoides
Macleaya cordata
Magnolia sieboldii
Millettia erythrocalyx
Murraya exotica
Murraya paniculata
Myrsine lancifolia
Nicotiana undulata
Ononis vaginalis
Panax ginseng
Passiflora incarnata
Peltogyne floribunda
Piper attenuatum
Pteris semipinnata
Ratibida mexicana
Ribes nigrum
Rubus sanctus
Salvia hispanica
Sambucus nigra
Scorzonera pseudodivaricata
Senecio paludaffinis
Senegalia tenuifolia
Senna santanderensis
Seriphidium cinum
Stauntonia hexaphylla
Stenocereus griseus
Strychnos trinervis
Syncarpia hillii
Syzygium aromaticum
Trigonella grandiflora
Tripolium pannonicum
Uvaria calamistrata
Uvaria chamae

Cross-Links

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PubChem 5318102
NPASS NPC247266
LOTUS LTS0193661
wikiData Q27121617