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

Details

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Internal ID 73c97399-1152-4557-a45f-4e8282a08662
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 4,7-dimethyl-1-prop-1-en-2-yl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-4a-ol
SMILES (Canonical) CC1CCC(C2C1(CCC(=C2)C)O)C(=C)C
SMILES (Isomeric) CC1CCC(C2C1(CCC(=C2)C)O)C(=C)C
InChI InChI=1S/C15H24O/c1-10(2)13-6-5-12(4)15(16)8-7-11(3)9-14(13)15/h9,12-14,16H,1,5-8H2,2-4H3
InChI Key PWEFVGUEHRMHKN-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) 3.70
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 4,7-dimethyl-1-prop-1-en-2-yl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-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 + 0.7803 78.03%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.5767 57.67%
OATP2B1 inhibitior - 0.8482 84.82%
OATP1B1 inhibitior + 0.9277 92.77%
OATP1B3 inhibitior + 0.8378 83.78%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.9321 93.21%
P-glycoprotein inhibitior - 0.9405 94.05%
P-glycoprotein substrate - 0.7701 77.01%
CYP3A4 substrate + 0.5348 53.48%
CYP2C9 substrate - 0.5471 54.71%
CYP2D6 substrate - 0.7267 72.67%
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 - 0.8154 81.54%
CYP inhibitory promiscuity - 0.8519 85.19%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5630 56.30%
Eye corrosion - 0.9843 98.43%
Eye irritation + 0.6164 61.64%
Skin irritation + 0.6580 65.80%
Skin corrosion - 0.9387 93.87%
Ames mutagenesis - 0.8293 82.93%
Human Ether-a-go-go-Related Gene inhibition - 0.4837 48.37%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5004 50.04%
skin sensitisation + 0.6147 61.47%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.8018 80.18%
Acute Oral Toxicity (c) III 0.8654 86.54%
Estrogen receptor binding - 0.7968 79.68%
Androgen receptor binding - 0.6182 61.82%
Thyroid receptor binding - 0.6511 65.11%
Glucocorticoid receptor binding - 0.6244 62.44%
Aromatase binding - 0.6605 66.05%
PPAR gamma - 0.7611 76.11%
Honey bee toxicity - 0.8200 82.00%
Biodegradation + 0.5250 52.50%
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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.72% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.11% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.23% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.41% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.84% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.70% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 83.08% 97.79%
CHEMBL259 P32245 Melanocortin receptor 4 81.87% 95.38%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.77% 86.00%

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 162873668
LOTUS LTS0233484
wikiData Q105215790