Guaia-1(10),11-dien-9-one

Details

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Internal ID fcd3fe65-7243-44ef-a144-0e924ac003ec
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Guaianes
IUPAC Name 3-methyl-8-methylidene-5-propan-2-yl-1,2,5,6,7,8a-hexahydroazulen-4-one
SMILES (Canonical) CC1=C2C(CC1)C(=C)CCC(C2=O)C(C)C
SMILES (Isomeric) CC1=C2C(CC1)C(=C)CCC(C2=O)C(C)C
InChI InChI=1S/C15H22O/c1-9(2)12-7-5-10(3)13-8-6-11(4)14(13)15(12)16/h9,12-13H,3,5-8H2,1-2,4H3
InChI Key UYGROYIOOPLGAS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.90
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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UYGROYIOOPLGAS-UHFFFAOYSA-N

2D Structure

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2D Structure of Guaia-1(10),11-dien-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.8910 89.10%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.4212 42.12%
OATP2B1 inhibitior - 0.8480 84.80%
OATP1B1 inhibitior + 0.9380 93.80%
OATP1B3 inhibitior + 0.8792 87.92%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7772 77.72%
P-glycoprotein inhibitior - 0.8323 83.23%
P-glycoprotein substrate - 0.8853 88.53%
CYP3A4 substrate - 0.5373 53.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8579 85.79%
CYP3A4 inhibition - 0.9537 95.37%
CYP2C9 inhibition - 0.7448 74.48%
CYP2C19 inhibition - 0.7041 70.41%
CYP2D6 inhibition - 0.9254 92.54%
CYP1A2 inhibition + 0.5113 51.13%
CYP2C8 inhibition - 0.9729 97.29%
CYP inhibitory promiscuity - 0.8050 80.50%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5437 54.37%
Eye corrosion - 0.9300 93.00%
Eye irritation + 0.8384 83.84%
Skin irritation + 0.5862 58.62%
Skin corrosion - 0.9537 95.37%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4711 47.11%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.9125 91.25%
skin sensitisation + 0.8014 80.14%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.5609 56.09%
Acute Oral Toxicity (c) III 0.6497 64.97%
Estrogen receptor binding - 0.8996 89.96%
Androgen receptor binding + 0.6039 60.39%
Thyroid receptor binding - 0.6006 60.06%
Glucocorticoid receptor binding - 0.5793 57.93%
Aromatase binding - 0.8460 84.60%
PPAR gamma - 0.8066 80.66%
Honey bee toxicity - 0.9111 91.11%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9952 99.52%

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 92.37% 98.95%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 88.52% 96.47%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.48% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.18% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.49% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.62% 90.71%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.50% 93.03%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.48% 97.25%
CHEMBL1937 Q92769 Histone deacetylase 2 83.00% 94.75%
CHEMBL1871 P10275 Androgen Receptor 82.97% 96.43%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.41% 99.23%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.16% 90.08%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.15% 100.00%

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.
Aquilaria malaccensis
Aquilaria sinensis

Cross-Links

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PubChem 529455
NPASS NPC243047