1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (1E,4E,8E)-

Details

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Internal ID 71604cbe-9872-44ea-8a2a-15e14fe0a26b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2,6,6,9-tetramethylcycloundeca-1,4,8-triene
SMILES (Canonical) CC1=CCC(C=CCC(=CCC1)C)(C)C
SMILES (Isomeric) CC1=CCC(C=CCC(=CCC1)C)(C)C
InChI InChI=1S/C15H24/c1-13-7-5-8-14(2)10-12-15(3,4)11-6-9-13/h6-7,10-11H,5,8-9,12H2,1-4H3
InChI Key FAMPSKZZVDUYOS-UHFFFAOYSA-N
Popularity 323 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 4.50
Atomic LogP (AlogP) 5.04
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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6753-98-6
HUMULENE (alpha)
Humulene; alpha-Caryophyllene
1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (1E,4E,8E)-
?-Humulene
Spectrum_000133
SpecPlus_000469
Spectrum2_001995
Spectrum3_001125
Spectrum4_001969
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (1E,4E,8E)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9907 99.07%
Caco-2 + 0.9671 96.71%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.5788 57.88%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.9636 96.36%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.7719 77.19%
P-glycoprotein inhibitior - 0.9665 96.65%
P-glycoprotein substrate - 0.9444 94.44%
CYP3A4 substrate - 0.5518 55.18%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.7848 78.48%
CYP3A4 inhibition - 0.9106 91.06%
CYP2C9 inhibition - 0.7994 79.94%
CYP2C19 inhibition - 0.7952 79.52%
CYP2D6 inhibition - 0.9406 94.06%
CYP1A2 inhibition - 0.8014 80.14%
CYP2C8 inhibition - 0.8842 88.42%
CYP inhibitory promiscuity - 0.7646 76.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Warning 0.5028 50.28%
Eye corrosion - 0.6888 68.88%
Eye irritation + 0.9628 96.28%
Skin irritation + 0.6995 69.95%
Skin corrosion - 0.9762 97.62%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3698 36.98%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation + 0.9074 90.74%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.6272 62.72%
Acute Oral Toxicity (c) III 0.6889 68.89%
Estrogen receptor binding - 0.9296 92.96%
Androgen receptor binding - 0.9198 91.98%
Thyroid receptor binding - 0.7942 79.42%
Glucocorticoid receptor binding - 0.8339 83.39%
Aromatase binding - 0.6964 69.64%
PPAR gamma - 0.7562 75.62%
Honey bee toxicity - 0.9286 92.86%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9940 99.40%

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 90.62% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.17% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.76% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.03% 97.25%

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 gramineus
Acritopappus confertus
Acritopappus prunifolius
Actinobole uliginosum
Ageratina tristis
Ageratum fastigiatum
Araucaria cunninghamii
Artabotrys hexapetalus
Artemisia annua
Artemisia dracunculus
Artemisia gmelinii
Artemisia vulgaris
Athrixia elata
Aucklandia costus
Ayapana amygdalina
Baccharis darwinii
Baccharis tricuneata
Berkheya bergiana
Betula pendula
Calea pilosa
Calea rotundifolia
Calea sickii
Callicarpa japonica
Callilepis salicifolia
Cannabis sativa
Chamaecyparis formosensis
Chamaecyparis obtusa
Chromolaena tunariensis
Comptonia peregrina
Cyrtocymura scorpioides
Dacrydium cupressinum
Dimerostemma asperatum
Dimerostemma brasilianum
Dimerostemma lippioides
Disynaphia multicrenulata
Eremanthus crotonoides
Eremanthus glomerulatus
Eupatorium serotinum
Fleischmannia pratensis
Frullania tamarisci
Geigeria burkei
Grangea maderaspatana
Grindelia hirsutula
Gymnanthemum myrianthum
Helichrysum chionosphaerum
Helichrysum cymosum
Helichrysum nanum
Helichrysum zeyheri
Humulus lupulus
Hymenoxys integrifolia
Juniperus communis
Juniperus oxycedrus
Juniperus rigida
Lantana camara
Lasiolaena morii
Lepidaploa cotoneaster
Lessingianthus linearis
Liabum eggersii
Libocedrus bidwillii
Lindera aggregata
Lippia alba
Mikania goyazensis
Mikania grazielae
Morithamnus crassus
Nidorella hottentotica
Ophryosporus charua
Perilla frutescens
Petasites albus
Pinus brutia var. pityusa
Pinus heldreichii
Pinus koraiensis
Pinus pinaster
Pinus sibirica
Piper aduncum
Piptolepis leptospermoides
Planaltoa lychnophoroides
Pseudoconyza viscosa
Rhododendron groenlandicum
Rugelia nudicaulis
Schistostephium crataegifolium
Senecio pleistocephalus
Senecio richii
Senecio rosmarinifolius
Seriphidium herba-alba
Silphium asteriscus
Sphaeromorphaea australis
Stilpnopappus glomeratus
Symphyopappus reticulatus
Tamaulipa azurea
Torilis japonica
Trichogonia villosa
Valeriana officinalis
Vitex agnus-castus
Zingiber ottensii
Zingiber zerumbet

Cross-Links

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PubChem 23204
LOTUS LTS0076944
wikiData Q27121615