(4aR,5S,8S,8aS)-3-(hydroxymethyl)-8-methyl-5-prop-1-en-2-yl-4a,5,6,7,8,8a-hexahydro-1H-naphthalen-2-one

Details

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Internal ID d2cddb0d-3f6e-4b99-b8f4-2acfadc2dfe7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4aR,5S,8S,8aS)-3-(hydroxymethyl)-8-methyl-5-prop-1-en-2-yl-4a,5,6,7,8,8a-hexahydro-1H-naphthalen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O2/c1-9(2)12-5-4-10(3)13-7-15(17)11(8-16)6-14(12)13/h6,10,12-14,16H,1,4-5,7-8H2,2-3H3/t10-,12+,13-,14+/m0/s1
InChI Key YVVIBTNZHLXHRV-AHLTXXRQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O2
Molecular Weight 234.33 g/mol
Exact Mass 234.161979940 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4aR,5S,8S,8aS)-3-(hydroxymethyl)-8-methyl-5-prop-1-en-2-yl-4a,5,6,7,8,8a-hexahydro-1H-naphthalen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.7606 76.06%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6070 60.70%
OATP2B1 inhibitior - 0.8540 85.40%
OATP1B1 inhibitior + 0.8896 88.96%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior + 0.5433 54.33%
BSEP inhibitior - 0.8969 89.69%
P-glycoprotein inhibitior - 0.9234 92.34%
P-glycoprotein substrate - 0.7185 71.85%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8736 87.36%
CYP3A4 inhibition - 0.6990 69.90%
CYP2C9 inhibition - 0.8643 86.43%
CYP2C19 inhibition - 0.6986 69.86%
CYP2D6 inhibition - 0.8955 89.55%
CYP1A2 inhibition + 0.5571 55.71%
CYP2C8 inhibition - 0.8638 86.38%
CYP inhibitory promiscuity - 0.7689 76.89%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6421 64.21%
Eye corrosion - 0.9762 97.62%
Eye irritation - 0.5901 59.01%
Skin irritation - 0.6424 64.24%
Skin corrosion - 0.9647 96.47%
Ames mutagenesis - 0.7678 76.78%
Human Ether-a-go-go-Related Gene inhibition - 0.6484 64.84%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.6553 65.53%
skin sensitisation - 0.6014 60.14%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.5803 58.03%
Acute Oral Toxicity (c) III 0.7518 75.18%
Estrogen receptor binding - 0.9022 90.22%
Androgen receptor binding - 0.6522 65.22%
Thyroid receptor binding - 0.5979 59.79%
Glucocorticoid receptor binding - 0.5614 56.14%
Aromatase binding - 0.7997 79.97%
PPAR gamma - 0.8341 83.41%
Honey bee toxicity - 0.8624 86.24%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9851 98.51%

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
CHEMBL4040 P28482 MAP kinase ERK2 96.94% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.38% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.55% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.00% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.17% 97.25%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 89.29% 94.80%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.06% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.16% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.93% 100.00%

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.
Pteridium esculentum

Cross-Links

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PubChem 163014021
LOTUS LTS0141357
wikiData Q105366034