5,8a-Dimethyl-3-prop-1-en-2-yl-1,2,3,4,7,8-hexahydronaphthalen-4a-ol

Details

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Internal ID a00db7fc-0adf-4c5f-a140-13369c621453
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name 5,8a-dimethyl-3-prop-1-en-2-yl-1,2,3,4,7,8-hexahydronaphthalen-4a-ol
SMILES (Canonical) CC1=CCCC2(C1(CC(CC2)C(=C)C)O)C
SMILES (Isomeric) CC1=CCCC2(C1(CC(CC2)C(=C)C)O)C
InChI InChI=1S/C15H24O/c1-11(2)13-7-9-14(4)8-5-6-12(3)15(14,16)10-13/h6,13,16H,1,5,7-10H2,2-4H3
InChI Key PWKUFWSNBDVOCV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.84
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,8a-Dimethyl-3-prop-1-en-2-yl-1,2,3,4,7,8-hexahydronaphthalen-4a-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.8281 82.81%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Lysosomes 0.5767 57.67%
OATP2B1 inhibitior - 0.8494 84.94%
OATP1B1 inhibitior + 0.9568 95.68%
OATP1B3 inhibitior + 0.8378 83.78%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.7093 70.93%
P-glycoprotein inhibitior - 0.9684 96.84%
P-glycoprotein substrate - 0.7850 78.50%
CYP3A4 substrate + 0.5323 53.23%
CYP2C9 substrate + 0.5024 50.24%
CYP2D6 substrate - 0.7533 75.33%
CYP3A4 inhibition - 0.6920 69.20%
CYP2C9 inhibition - 0.7452 74.52%
CYP2C19 inhibition - 0.6314 63.14%
CYP2D6 inhibition - 0.9473 94.73%
CYP1A2 inhibition - 0.7889 78.89%
CYP2C8 inhibition - 0.7839 78.39%
CYP inhibitory promiscuity - 0.8519 85.19%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5630 56.30%
Eye corrosion - 0.9843 98.43%
Eye irritation + 0.7208 72.08%
Skin irritation + 0.6580 65.80%
Skin corrosion - 0.9387 93.87%
Ames mutagenesis - 0.8137 81.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5290 52.90%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5051 50.51%
skin sensitisation + 0.6147 61.47%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.5851 58.51%
Acute Oral Toxicity (c) III 0.8654 86.54%
Estrogen receptor binding - 0.8045 80.45%
Androgen receptor binding - 0.6390 63.90%
Thyroid receptor binding - 0.7714 77.14%
Glucocorticoid receptor binding - 0.5996 59.96%
Aromatase binding - 0.5704 57.04%
PPAR gamma - 0.7759 77.59%
Honey bee toxicity - 0.9206 92.06%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9907 99.07%

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 96.37% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.33% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.22% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 86.87% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.33% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.13% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.12% 100.00%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.15% 86.00%
CHEMBL1871 P10275 Androgen Receptor 80.77% 96.43%

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.
Cyperus alopecuroides

Cross-Links

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PubChem 162965390
LOTUS LTS0062057
wikiData Q105215882