5,9-Dimethyl-2-propan-2-ylcyclodeca-5,9-diene-1,4-diol

Details

Top
Internal ID 1ca60c0e-0d6f-4186-a71e-5a7a73744793
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name 5,9-dimethyl-2-propan-2-ylcyclodeca-5,9-diene-1,4-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O2/c1-10(2)13-9-14(16)12(4)7-5-6-11(3)8-15(13)17/h7-8,10,13-17H,5-6,9H2,1-4H3
InChI Key PKOQIYPPSKQSIQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H26O2
Molecular Weight 238.37 g/mol
Exact Mass 238.193280068 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 2.30
Atomic LogP (AlogP) 3.06
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 5,9-Dimethyl-2-propan-2-ylcyclodeca-5,9-diene-1,4-diol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.7407 74.07%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5319 53.19%
OATP2B1 inhibitior - 0.8515 85.15%
OATP1B1 inhibitior + 0.9571 95.71%
OATP1B3 inhibitior + 0.9631 96.31%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8839 88.39%
P-glycoprotein inhibitior - 0.9368 93.68%
P-glycoprotein substrate - 0.8314 83.14%
CYP3A4 substrate - 0.5681 56.81%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.7021 70.21%
CYP3A4 inhibition - 0.8231 82.31%
CYP2C9 inhibition - 0.8726 87.26%
CYP2C19 inhibition - 0.8257 82.57%
CYP2D6 inhibition - 0.9071 90.71%
CYP1A2 inhibition - 0.6800 68.00%
CYP2C8 inhibition - 0.9239 92.39%
CYP inhibitory promiscuity - 0.7867 78.67%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8128 81.28%
Carcinogenicity (trinary) Non-required 0.6437 64.37%
Eye corrosion - 0.9402 94.02%
Eye irritation - 0.9557 95.57%
Skin irritation + 0.5571 55.71%
Skin corrosion - 0.9133 91.33%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5320 53.20%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.7272 72.72%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.5836 58.36%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6025 60.25%
Acute Oral Toxicity (c) III 0.6941 69.41%
Estrogen receptor binding - 0.8788 87.88%
Androgen receptor binding - 0.8209 82.09%
Thyroid receptor binding - 0.6119 61.19%
Glucocorticoid receptor binding - 0.6300 63.00%
Aromatase binding - 0.9094 90.94%
PPAR gamma - 0.7718 77.18%
Honey bee toxicity - 0.8736 87.36%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.8696 86.96%

Targets

Top

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.68% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.89% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.38% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.07% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.41% 97.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.91% 97.21%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.88% 91.11%
CHEMBL4208 P20618 Proteasome component C5 82.40% 90.00%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 82.04% 97.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.33% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.52% 93.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.42% 94.45%

Plants that contains it

Top
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.
Pulicaria glutinosa

Cross-Links

Top
PubChem 163085789
LOTUS LTS0184695
wikiData Q105210527