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

Details

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Internal ID 0ccd16a6-8bfe-49e1-b7a0-8d0597510925
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,6-dimethyl-4-prop-1-en-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol
SMILES (Canonical) CC1=CC2C(CCC(C2CC1)(C)O)C(=C)C
SMILES (Isomeric) CC1=CC2C(CCC(C2CC1)(C)O)C(=C)C
InChI InChI=1S/C15H24O/c1-10(2)12-7-8-15(4,16)14-6-5-11(3)9-13(12)14/h9,12-14,16H,1,5-8H2,2-4H3
InChI Key NRNOOMCOYPENIN-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 1

Synonyms

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There are no found synonyms.

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.7991 79.91%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.6062 60.62%
OATP2B1 inhibitior - 0.8473 84.73%
OATP1B1 inhibitior + 0.9362 93.62%
OATP1B3 inhibitior + 0.8782 87.82%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.9245 92.45%
P-glycoprotein inhibitior - 0.9451 94.51%
P-glycoprotein substrate - 0.8264 82.64%
CYP3A4 substrate + 0.5616 56.16%
CYP2C9 substrate - 0.5471 54.71%
CYP2D6 substrate - 0.7267 72.67%
CYP3A4 inhibition - 0.7073 70.73%
CYP2C9 inhibition - 0.6388 63.88%
CYP2C19 inhibition - 0.5712 57.12%
CYP2D6 inhibition - 0.9372 93.72%
CYP1A2 inhibition - 0.7697 76.97%
CYP2C8 inhibition - 0.7393 73.93%
CYP inhibitory promiscuity - 0.8746 87.46%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5655 56.55%
Eye corrosion - 0.9777 97.77%
Eye irritation + 0.5611 56.11%
Skin irritation + 0.6266 62.66%
Skin corrosion - 0.9389 93.89%
Ames mutagenesis - 0.7470 74.70%
Human Ether-a-go-go-Related Gene inhibition - 0.3660 36.60%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6307 63.07%
skin sensitisation + 0.6473 64.73%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.6604 66.04%
Acute Oral Toxicity (c) III 0.8681 86.81%
Estrogen receptor binding - 0.6934 69.34%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.5938 59.38%
Glucocorticoid receptor binding - 0.6694 66.94%
Aromatase binding - 0.7364 73.64%
PPAR gamma - 0.7572 75.72%
Honey bee toxicity - 0.9058 90.58%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9831 98.31%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.31% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.43% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.19% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.98% 100.00%
CHEMBL1871 P10275 Androgen Receptor 84.32% 96.43%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.21% 92.94%
CHEMBL2996 Q05655 Protein kinase C delta 83.85% 97.79%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.32% 95.56%
CHEMBL259 P32245 Melanocortin receptor 4 80.37% 95.38%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.29% 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.
Swartzia polyphylla

Cross-Links

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PubChem 163063170
LOTUS LTS0093626
wikiData Q105184663