4a,5-dimethyl-3-prop-1-en-2-yl-3,4,5,6,7,8-hexahydro-2H-naphthalen-2-ol

Details

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Internal ID b9da2c85-6be9-4bff-a103-6bcc67504325
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
IUPAC Name 4a,5-dimethyl-3-prop-1-en-2-yl-3,4,5,6,7,8-hexahydro-2H-naphthalen-2-ol
SMILES (Canonical) CC1CCCC2=CC(C(CC12C)C(=C)C)O
SMILES (Isomeric) CC1CCCC2=CC(C(CC12C)C(=C)C)O
InChI InChI=1S/C15H24O/c1-10(2)13-9-15(4)11(3)6-5-7-12(15)8-14(13)16/h8,11,13-14,16H,1,5-7,9H2,2-4H3
InChI Key SYNWLDWKTARJOJ-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 3.90
Atomic LogP (AlogP) 3.70
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 4a,5-dimethyl-3-prop-1-en-2-yl-3,4,5,6,7,8-hexahydro-2H-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 + 0.9959 99.59%
Caco-2 + 0.8194 81.94%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Lysosomes 0.4769 47.69%
OATP2B1 inhibitior - 0.8520 85.20%
OATP1B1 inhibitior + 0.8986 89.86%
OATP1B3 inhibitior + 0.8468 84.68%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.8958 89.58%
P-glycoprotein inhibitior - 0.9413 94.13%
P-glycoprotein substrate - 0.8124 81.24%
CYP3A4 substrate + 0.5125 51.25%
CYP2C9 substrate - 0.6499 64.99%
CYP2D6 substrate - 0.6843 68.43%
CYP3A4 inhibition - 0.7321 73.21%
CYP2C9 inhibition - 0.5483 54.83%
CYP2C19 inhibition - 0.5092 50.92%
CYP2D6 inhibition - 0.9252 92.52%
CYP1A2 inhibition - 0.6549 65.49%
CYP2C8 inhibition - 0.7347 73.47%
CYP inhibitory promiscuity - 0.7291 72.91%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5519 55.19%
Eye corrosion - 0.9774 97.74%
Eye irritation - 0.6475 64.75%
Skin irritation + 0.5553 55.53%
Skin corrosion - 0.9336 93.36%
Ames mutagenesis - 0.8254 82.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5372 53.72%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5157 51.57%
skin sensitisation + 0.6054 60.54%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.6786 67.86%
Acute Oral Toxicity (c) III 0.7425 74.25%
Estrogen receptor binding - 0.9047 90.47%
Androgen receptor binding - 0.8176 81.76%
Thyroid receptor binding - 0.7088 70.88%
Glucocorticoid receptor binding - 0.6677 66.77%
Aromatase binding - 0.4883 48.83%
PPAR gamma - 0.8625 86.25%
Honey bee toxicity - 0.8999 89.99%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 1.0000 100.00%

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 96.54% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 92.45% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.10% 91.11%
CHEMBL2581 P07339 Cathepsin D 90.94% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.17% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.61% 97.25%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.47% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.76% 97.09%
CHEMBL1871 P10275 Androgen Receptor 82.68% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.55% 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.
Marsupella aquatica
Marsupella emarginata

Cross-Links

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PubChem 101417525
LOTUS LTS0190125
wikiData Q105263683