3,8-dimethyl-5-propan-2-ylidene-2,4a,6,7,8,8a-hexahydro-1H-naphthalen-2-ol

Details

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Internal ID aab7f1a5-e1b8-45e0-9ffc-83572db4df70
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3,8-dimethyl-5-propan-2-ylidene-2,4a,6,7,8,8a-hexahydro-1H-naphthalen-2-ol
SMILES (Canonical) CC1CCC(=C(C)C)C2C1CC(C(=C2)C)O
SMILES (Isomeric) CC1CCC(=C(C)C)C2C1CC(C(=C2)C)O
InChI InChI=1S/C15H24O/c1-9(2)12-6-5-10(3)13-8-15(16)11(4)7-14(12)13/h7,10,13-16H,5-6,8H2,1-4H3
InChI Key DMKWBQROHUFGFK-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 3.30
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 3,8-dimethyl-5-propan-2-ylidene-2,4a,6,7,8,8a-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 + 1.0000 100.00%
Caco-2 + 0.8725 87.25%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.4259 42.59%
OATP2B1 inhibitior - 0.8471 84.71%
OATP1B1 inhibitior + 0.9486 94.86%
OATP1B3 inhibitior + 0.9455 94.55%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9395 93.95%
P-glycoprotein inhibitior - 0.9484 94.84%
P-glycoprotein substrate - 0.8259 82.59%
CYP3A4 substrate - 0.5216 52.16%
CYP2C9 substrate - 0.6107 61.07%
CYP2D6 substrate - 0.6804 68.04%
CYP3A4 inhibition - 0.8177 81.77%
CYP2C9 inhibition - 0.8967 89.67%
CYP2C19 inhibition - 0.8500 85.00%
CYP2D6 inhibition - 0.9393 93.93%
CYP1A2 inhibition - 0.7288 72.88%
CYP2C8 inhibition - 0.8598 85.98%
CYP inhibitory promiscuity - 0.8143 81.43%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6169 61.69%
Eye corrosion - 0.9699 96.99%
Eye irritation - 0.7814 78.14%
Skin irritation + 0.6408 64.08%
Skin corrosion - 0.9255 92.55%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5245 52.45%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation + 0.8220 82.20%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.8163 81.63%
Acute Oral Toxicity (c) III 0.6332 63.32%
Estrogen receptor binding - 0.8707 87.07%
Androgen receptor binding - 0.5586 55.86%
Thyroid receptor binding - 0.5756 57.56%
Glucocorticoid receptor binding - 0.7315 73.15%
Aromatase binding - 0.8757 87.57%
PPAR gamma - 0.7821 78.21%
Honey bee toxicity - 0.9071 90.71%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9816 98.16%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.46% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.73% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.61% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.87% 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 162991925
LOTUS LTS0016286
wikiData Q104985140