Umbellulon

Details

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Internal ID 153c530f-9055-4840-84dc-ac8cb6521428
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name 4-methyl-1-propan-2-ylbicyclo[3.1.0]hex-3-en-2-one
SMILES (Canonical) CC1=CC(=O)C2(C1C2)C(C)C
SMILES (Isomeric) CC1=CC(=O)C2(C1C2)C(C)C
InChI InChI=1S/C10H14O/c1-6(2)10-5-8(10)7(3)4-9(10)11/h4,6,8H,5H2,1-3H3
InChI Key LTTVJAQLCIHAFV-UHFFFAOYSA-N
Popularity 23 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 1

Synonyms

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3-Thujen-2-one
THUJEN-2-ONE
24545-81-1
NSC 22046
Bicyclo[3.1.0]hex-3-en-2-one, 4-methyl-1-(1-methylethyl)-
4-Methyl-1-propan-2-ylbicyclo[3.1.0]hex-3-en-2-one
X5YT6KCX2U
BRN 2042730
NSC-22046
4-Methyl-1-(1-methylethyl)-bicyclo(3.1.0)hex-3-en-2-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Umbellulon

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 + 0.5625 56.25%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.4703 47.03%
OATP2B1 inhibitior - 0.8554 85.54%
OATP1B1 inhibitior + 0.9533 95.33%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9092 90.92%
P-glycoprotein inhibitior - 0.9760 97.60%
P-glycoprotein substrate - 0.8909 89.09%
CYP3A4 substrate - 0.5991 59.91%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8766 87.66%
CYP3A4 inhibition - 0.8466 84.66%
CYP2C9 inhibition - 0.8866 88.66%
CYP2C19 inhibition - 0.5652 56.52%
CYP2D6 inhibition - 0.9276 92.76%
CYP1A2 inhibition - 0.6470 64.70%
CYP2C8 inhibition - 0.9961 99.61%
CYP inhibitory promiscuity - 0.6118 61.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7917 79.17%
Carcinogenicity (trinary) Non-required 0.5260 52.60%
Eye corrosion - 0.8655 86.55%
Eye irritation + 0.8636 86.36%
Skin irritation + 0.7652 76.52%
Skin corrosion - 0.8970 89.70%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6622 66.22%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.7926 79.26%
skin sensitisation + 0.9070 90.70%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.5294 52.94%
Acute Oral Toxicity (c) III 0.5236 52.36%
Estrogen receptor binding - 0.9601 96.01%
Androgen receptor binding - 0.6113 61.13%
Thyroid receptor binding - 0.8578 85.78%
Glucocorticoid receptor binding - 0.9178 91.78%
Aromatase binding - 0.8868 88.68%
PPAR gamma - 0.8354 83.54%
Honey bee toxicity - 0.8936 89.36%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9468 94.68%

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
CHEMBL2581 P07339 Cathepsin D 90.77% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.06% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.14% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.97% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.32% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.20% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.79% 94.45%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.64% 90.71%

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.
Artemisia capillaris
Chrysanthemum indicum
Daucus carota
Mentha spicata
Ocimum gratissimum subsp. gratissimum
Pimenta racemosa
Tanacetum vulgare
Umbellularia californica

Cross-Links

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PubChem 91195
NPASS NPC8120
LOTUS LTS0242520
wikiData Q7881242