Verbenone

Details

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Internal ID 6cd8211c-2c7a-425d-b80b-a2212999073e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name 4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one
SMILES (Canonical) CC1=CC(=O)C2CC1C2(C)C
SMILES (Isomeric) CC1=CC(=O)C2CC1C2(C)C
InChI InChI=1S/C10H14O/c1-6-4-9(11)8-5-7(6)10(8,2)3/h4,7-8H,5H2,1-3H3
InChI Key DCSCXTJOXBUFGB-UHFFFAOYSA-N
Popularity 856 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.18
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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4,6,6-Trimethylbicyclo[3.1.1]hept-3-en-2-one
80-57-9
2-Pinen-4-one
d-Verbenone
dl-Verbenone
NSC6832
ST069322
Verbinone
Verbenone, (d)-
Verbenone, (L)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Verbenone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.7290 72.90%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.5296 52.96%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.9309 93.09%
OATP1B3 inhibitior + 0.9494 94.94%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9142 91.42%
P-glycoprotein inhibitior - 0.9727 97.27%
P-glycoprotein substrate - 0.9169 91.69%
CYP3A4 substrate - 0.5462 54.62%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.8721 87.21%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.7575 75.75%
CYP2C19 inhibition + 0.5593 55.93%
CYP2D6 inhibition - 0.8873 88.73%
CYP1A2 inhibition - 0.7658 76.58%
CYP2C8 inhibition - 0.9831 98.31%
CYP inhibitory promiscuity - 0.5888 58.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.4705 47.05%
Eye corrosion - 0.8825 88.25%
Eye irritation + 0.9041 90.41%
Skin irritation + 0.6041 60.41%
Skin corrosion - 0.9286 92.86%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6238 62.38%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.8533 85.33%
skin sensitisation + 0.8755 87.55%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.5430 54.30%
Acute Oral Toxicity (c) III 0.7560 75.60%
Estrogen receptor binding - 0.8767 87.67%
Androgen receptor binding - 0.8512 85.12%
Thyroid receptor binding - 0.8442 84.42%
Glucocorticoid receptor binding - 0.8841 88.41%
Aromatase binding - 0.9381 93.81%
PPAR gamma - 0.8542 85.42%
Honey bee toxicity - 0.8728 87.28%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity + 0.9476 94.76%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.23% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.26% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.03% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.61% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.58% 97.25%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.91% 86.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.87% 97.09%
CHEMBL2581 P07339 Cathepsin D 81.45% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.07% 99.23%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis
Annona squamosa
Artemisia argyi
Artemisia judaica
Artemisia montana
Artemisia princeps
Artemisia salsoloides
Artemisia sericea
Artemisia thuscula
Artemisia verlotiorum
Asarum canadense
Athamanta macedonica
Blepharocalyx salicifolius
Boswellia serrata
Brassica nigra
Chrysanthemum indicum
Citrus × aurantium
Citrus deliciosa
Citrus trifoliata
Cleonia lusitanica
Clinopodium congestum
Corymbia maculata
Cryptomeria japonica
Curcuma kwangsiensis
Curcuma longa
Curcuma phaeocaulis
Curcuma pierreana
Curcuma wenyujin
Curcuma zedoaria
Cyperus rotundus
Daucus carota
Echinophora tenuifolia
Elsholtzia fruticosa
Espeletiopsis guacharaca
Etlingera elatior
Eucalyptus bridgesiana
Eucalyptus globulus
Eucalyptus leucoxylon
Eucalyptus triflora
Foeniculum vulgare
Gossypium hirsutum
Gutierrezia sarothrae
Helianthus annuus
Helichrysum taenari
Hyssopus seravschanicus
Juniperus durangensis
Kunzea salina
Mentha arvensis
Mentha canadensis
Micromeria biflora
Micromeria maderensis
Mikania cordifolia
Myrtus communis
Picea abies
Platycladus orientalis
Polygala senega
Renealmia floribunda
Rhanterium epapposum
Rosmarinus officinalis
Salvia cuspidata subsp. gilliesii
Salvia vermifolia
Santolina chamaecyparissus
Satureja montana
Seriphidium baldshuanicum
Sideritis lyciae
Swertia japonica
Teucrium polium
Thymus camphoratus
Thymus funkii
Thymus zygis
Tithonia diversifolia
Umbellularia californica
Vaccinium vitis-idaea
Vitex negundo
Xylopia aethiopica
Xylopia aromatica
Xylopia sericea
Zingiber officinale

Cross-Links

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PubChem 29025
NPASS NPC30853
LOTUS LTS0264577
wikiData Q421151