8,11-Dihydro-15-hydroxylaurene

Details

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Internal ID b3f19b27-57cd-4368-adc3-08f59d725562
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name [4-[(1R,2S)-1,2-dimethyl-3-methylidenecyclopentyl]cyclohexa-1,4-dien-1-yl]methanol
SMILES (Canonical) CC1C(=C)CCC1(C)C2=CCC(=CC2)CO
SMILES (Isomeric) C[C@H]1C(=C)CC[C@@]1(C)C2=CCC(=CC2)CO
InChI InChI=1S/C15H22O/c1-11-8-9-15(3,12(11)2)14-6-4-13(10-16)5-7-14/h4,7,12,16H,1,5-6,8-10H2,2-3H3/t12-,15+/m0/s1
InChI Key FFSGCOHFSZTTRC-SWLSCSKDSA-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) 20.20 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.62
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8,11-Dihydro-15-hydroxylaurene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9890 98.90%
Caco-2 + 0.9073 90.73%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.6610 66.10%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.8868 88.68%
OATP1B3 inhibitior + 0.8732 87.32%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8617 86.17%
P-glycoprotein inhibitior - 0.9658 96.58%
P-glycoprotein substrate - 0.8663 86.63%
CYP3A4 substrate + 0.5580 55.80%
CYP2C9 substrate - 0.7919 79.19%
CYP2D6 substrate - 0.7754 77.54%
CYP3A4 inhibition - 0.8319 83.19%
CYP2C9 inhibition - 0.7970 79.70%
CYP2C19 inhibition - 0.8317 83.17%
CYP2D6 inhibition - 0.9036 90.36%
CYP1A2 inhibition - 0.8223 82.23%
CYP2C8 inhibition - 0.7205 72.05%
CYP inhibitory promiscuity - 0.6239 62.39%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8528 85.28%
Carcinogenicity (trinary) Non-required 0.6077 60.77%
Eye corrosion - 0.9261 92.61%
Eye irritation - 0.8607 86.07%
Skin irritation - 0.7772 77.72%
Skin corrosion - 0.9790 97.90%
Ames mutagenesis - 0.6574 65.74%
Human Ether-a-go-go-Related Gene inhibition + 0.6490 64.90%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5526 55.26%
skin sensitisation + 0.6214 62.14%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.7804 78.04%
Acute Oral Toxicity (c) III 0.8038 80.38%
Estrogen receptor binding - 0.8000 80.00%
Androgen receptor binding - 0.5973 59.73%
Thyroid receptor binding + 0.5252 52.52%
Glucocorticoid receptor binding - 0.5401 54.01%
Aromatase binding - 0.5067 50.67%
PPAR gamma - 0.5359 53.59%
Honey bee toxicity - 0.9423 94.23%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9962 99.62%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.65% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.20% 97.25%
CHEMBL226 P30542 Adenosine A1 receptor 91.21% 95.93%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.97% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.29% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.19% 97.09%
CHEMBL2581 P07339 Cathepsin D 85.73% 98.95%
CHEMBL1871 P10275 Androgen Receptor 81.96% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.81% 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.
Eleutherococcus giraldii
Lespedeza davidii
Solanum aethiopicum
Tectona grandis

Cross-Links

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PubChem 23426953
NPASS NPC227750
LOTUS LTS0153504
wikiData Q104994652