(1S,5R,8E)-10,10-dimethyl-2,6-dimethylidenecycloundec-8-ene-1,5-diol

Details

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Internal ID 2a0644e6-b2f1-4baf-8cd5-5446ef4d52a8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,5R,8E)-10,10-dimethyl-2,6-dimethylidenecycloundec-8-ene-1,5-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O2/c1-11-6-5-9-15(3,4)10-14(17)12(2)7-8-13(11)16/h5,9,13-14,16-17H,1-2,6-8,10H2,3-4H3/b9-5+/t13-,14+/m1/s1
InChI Key LWOKOFIEKUJQMC-JEELVDDXSA-N
Popularity 2 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 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,5R,8E)-10,10-dimethyl-2,6-dimethylidenecycloundec-8-ene-1,5-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9920 99.20%
Caco-2 + 0.7537 75.37%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.6287 62.87%
OATP2B1 inhibitior - 0.8506 85.06%
OATP1B1 inhibitior + 0.9380 93.80%
OATP1B3 inhibitior + 0.9526 95.26%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8600 86.00%
P-glycoprotein inhibitior - 0.9393 93.93%
P-glycoprotein substrate - 0.8374 83.74%
CYP3A4 substrate + 0.5329 53.29%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.7543 75.43%
CYP3A4 inhibition - 0.8430 84.30%
CYP2C9 inhibition - 0.8693 86.93%
CYP2C19 inhibition - 0.7659 76.59%
CYP2D6 inhibition - 0.9278 92.78%
CYP1A2 inhibition - 0.7687 76.87%
CYP2C8 inhibition - 0.8714 87.14%
CYP inhibitory promiscuity - 0.8330 83.30%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8028 80.28%
Carcinogenicity (trinary) Non-required 0.5639 56.39%
Eye corrosion - 0.9452 94.52%
Eye irritation + 0.6132 61.32%
Skin irritation - 0.5647 56.47%
Skin corrosion - 0.9446 94.46%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6973 69.73%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation + 0.7264 72.64%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5974 59.74%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.5067 50.67%
Acute Oral Toxicity (c) III 0.7760 77.60%
Estrogen receptor binding - 0.6896 68.96%
Androgen receptor binding - 0.7742 77.42%
Thyroid receptor binding - 0.6074 60.74%
Glucocorticoid receptor binding + 0.7049 70.49%
Aromatase binding - 0.5934 59.34%
PPAR gamma - 0.6090 60.90%
Honey bee toxicity - 0.9372 93.72%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9416 94.16%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.94% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.60% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.92% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.55% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.88% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.34% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 83.33% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.36% 95.89%

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.
Torilis japonica

Cross-Links

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PubChem 15624790
LOTUS LTS0146865
wikiData Q105158444