3,9-Dimethyl-6-prop-1-en-2-ylcyclodeca-3,9-diene-1,2-diol

Details

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Internal ID 946d374b-628e-45ea-80e2-c13b8f28f713
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name 3,9-dimethyl-6-prop-1-en-2-ylcyclodeca-3,9-diene-1,2-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O2/c1-10(2)13-7-5-11(3)9-14(16)15(17)12(4)6-8-13/h6,9,13-17H,1,5,7-8H2,2-4H3
InChI Key CNJFKLRIMOBKBS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O2
Molecular Weight 236.35 g/mol
Exact Mass 236.177630004 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.98
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,9-Dimethyl-6-prop-1-en-2-ylcyclodeca-3,9-diene-1,2-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9793 97.93%
Caco-2 + 0.8035 80.35%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4299 42.99%
OATP2B1 inhibitior - 0.8539 85.39%
OATP1B1 inhibitior + 0.9509 95.09%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8832 88.32%
P-glycoprotein inhibitior - 0.9268 92.68%
P-glycoprotein substrate - 0.8440 84.40%
CYP3A4 substrate - 0.5349 53.49%
CYP2C9 substrate - 0.8066 80.66%
CYP2D6 substrate - 0.7282 72.82%
CYP3A4 inhibition - 0.7052 70.52%
CYP2C9 inhibition - 0.7594 75.94%
CYP2C19 inhibition - 0.6917 69.17%
CYP2D6 inhibition - 0.8447 84.47%
CYP1A2 inhibition - 0.5201 52.01%
CYP2C8 inhibition - 0.8653 86.53%
CYP inhibitory promiscuity - 0.7619 76.19%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.5694 56.94%
Eye corrosion - 0.9066 90.66%
Eye irritation - 0.7920 79.20%
Skin irritation + 0.5634 56.34%
Skin corrosion - 0.8607 86.07%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4058 40.58%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.6239 62.39%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.5917 59.17%
Acute Oral Toxicity (c) III 0.7358 73.58%
Estrogen receptor binding - 0.7683 76.83%
Androgen receptor binding - 0.7543 75.43%
Thyroid receptor binding - 0.6512 65.12%
Glucocorticoid receptor binding - 0.7149 71.49%
Aromatase binding - 0.7075 70.75%
PPAR gamma - 0.6993 69.93%
Honey bee toxicity - 0.8899 88.99%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9682 96.82%

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
CHEMBL4040 P28482 MAP kinase ERK2 96.73% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.26% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.54% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.96% 100.00%
CHEMBL2581 P07339 Cathepsin D 85.93% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.34% 97.21%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.55% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.50% 95.56%

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.
Datura stramonium

Cross-Links

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PubChem 162974641
LOTUS LTS0273974
wikiData Q104965909