1,6-dimethyl-4-propan-2-ylidene-2,3,4a,7,8,8a-hexahydro-1H-naphthalen-2-ol

Details

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Internal ID 8270514e-140b-4ab1-96eb-e84c2956ffab
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,6-dimethyl-4-propan-2-ylidene-2,3,4a,7,8,8a-hexahydro-1H-naphthalen-2-ol
SMILES (Canonical) CC1C2CCC(=CC2C(=C(C)C)CC1O)C
SMILES (Isomeric) CC1C2CCC(=CC2C(=C(C)C)CC1O)C
InChI InChI=1S/C15H24O/c1-9(2)13-8-15(16)11(4)12-6-5-10(3)7-14(12)13/h7,11-12,14-16H,5-6,8H2,1-4H3
InChI Key VYRPEQZTLXTRND-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 3.40
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,6-dimethyl-4-propan-2-ylidene-2,3,4a,7,8,8a-hexahydro-1H-naphthalen-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.8964 89.64%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.5002 50.02%
OATP2B1 inhibitior - 0.8462 84.62%
OATP1B1 inhibitior + 0.9418 94.18%
OATP1B3 inhibitior + 0.9501 95.01%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9229 92.29%
P-glycoprotein inhibitior - 0.9336 93.36%
P-glycoprotein substrate - 0.7633 76.33%
CYP3A4 substrate - 0.5280 52.80%
CYP2C9 substrate - 0.6107 61.07%
CYP2D6 substrate - 0.6804 68.04%
CYP3A4 inhibition - 0.8802 88.02%
CYP2C9 inhibition - 0.8552 85.52%
CYP2C19 inhibition - 0.7791 77.91%
CYP2D6 inhibition - 0.9160 91.60%
CYP1A2 inhibition - 0.6950 69.50%
CYP2C8 inhibition - 0.8792 87.92%
CYP inhibitory promiscuity - 0.7411 74.11%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6149 61.49%
Eye corrosion - 0.9753 97.53%
Eye irritation - 0.8679 86.79%
Skin irritation + 0.6708 67.08%
Skin corrosion - 0.8862 88.62%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3916 39.16%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6876 68.76%
skin sensitisation + 0.7774 77.74%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.7584 75.84%
Acute Oral Toxicity (c) III 0.7520 75.20%
Estrogen receptor binding - 0.9267 92.67%
Androgen receptor binding + 0.5888 58.88%
Thyroid receptor binding - 0.5845 58.45%
Glucocorticoid receptor binding - 0.7687 76.87%
Aromatase binding - 0.8528 85.28%
PPAR gamma - 0.7542 75.42%
Honey bee toxicity - 0.9177 91.77%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9603 96.03%

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 93.28% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.45% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.04% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.63% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.98% 100.00%
CHEMBL1951 P21397 Monoamine oxidase A 84.08% 91.49%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.92% 92.94%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 82.58% 97.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.65% 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.
Marsupella aquatica

Cross-Links

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PubChem 163033575
LOTUS LTS0058724
wikiData Q105299281