(4aS,5Z,8S,8aR)-5-(1-hydroxypropan-2-ylidene)-3,8-dimethyl-4a,7,8,8a-tetrahydro-1H-naphthalene-2,6-dione

Details

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Internal ID 340bbd8f-f0cd-4718-a7f7-f9023d7fcdc8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4aS,5Z,8S,8aR)-5-(1-hydroxypropan-2-ylidene)-3,8-dimethyl-4a,7,8,8a-tetrahydro-1H-naphthalene-2,6-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H20O3/c1-8-5-14(18)15(10(3)7-16)12-4-9(2)13(17)6-11(8)12/h4,8,11-12,16H,5-7H2,1-3H3/b15-10-/t8-,11+,12+/m0/s1
InChI Key TYBMHGBQRJQXQU-KZKSEWEJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O3
Molecular Weight 248.32 g/mol
Exact Mass 248.14124450 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 1.40
Atomic LogP (AlogP) 2.06
H-Bond Acceptor 3
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 (4aS,5Z,8S,8aR)-5-(1-hydroxypropan-2-ylidene)-3,8-dimethyl-4a,7,8,8a-tetrahydro-1H-naphthalene-2,6-dione

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 + 0.9162 91.62%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8026 80.26%
OATP2B1 inhibitior - 0.8540 85.40%
OATP1B1 inhibitior + 0.9322 93.22%
OATP1B3 inhibitior + 0.9528 95.28%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8708 87.08%
P-glycoprotein inhibitior - 0.9451 94.51%
P-glycoprotein substrate - 0.7255 72.55%
CYP3A4 substrate - 0.5081 50.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8736 87.36%
CYP3A4 inhibition + 0.5443 54.43%
CYP2C9 inhibition - 0.7776 77.76%
CYP2C19 inhibition - 0.7255 72.55%
CYP2D6 inhibition - 0.8569 85.69%
CYP1A2 inhibition - 0.5683 56.83%
CYP2C8 inhibition - 0.9162 91.62%
CYP inhibitory promiscuity - 0.7946 79.46%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8513 85.13%
Carcinogenicity (trinary) Non-required 0.6582 65.82%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.8270 82.70%
Skin irritation - 0.7075 70.75%
Skin corrosion - 0.9723 97.23%
Ames mutagenesis - 0.7578 75.78%
Human Ether-a-go-go-Related Gene inhibition - 0.7059 70.59%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.6051 60.51%
skin sensitisation - 0.6314 63.14%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6389 63.89%
Acute Oral Toxicity (c) III 0.6659 66.59%
Estrogen receptor binding - 0.9152 91.52%
Androgen receptor binding - 0.6379 63.79%
Thyroid receptor binding - 0.6661 66.61%
Glucocorticoid receptor binding - 0.7483 74.83%
Aromatase binding - 0.8467 84.67%
PPAR gamma - 0.7661 76.61%
Honey bee toxicity - 0.9033 90.33%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9903 99.03%

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
CHEMBL2581 P07339 Cathepsin D 95.02% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.76% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.19% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.17% 85.14%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.60% 94.80%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.45% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.40% 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.
Ageratina adenophora

Cross-Links

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PubChem 162852925
LOTUS LTS0252545
wikiData Q105267221