1-Methyl-6-methylidene-4-prop-1-en-2-yl-1,3,4,4a,5,7,8,8a-octahydronaphthalen-2-one

Details

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Internal ID e03978f3-ee67-492c-b87d-b90377f5a159
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1-methyl-6-methylidene-4-prop-1-en-2-yl-1,3,4,4a,5,7,8,8a-octahydronaphthalen-2-one
SMILES (Canonical) CC1C2CCC(=C)CC2C(CC1=O)C(=C)C
SMILES (Isomeric) CC1C2CCC(=C)CC2C(CC1=O)C(=C)C
InChI InChI=1S/C15H22O/c1-9(2)13-8-15(16)11(4)12-6-5-10(3)7-14(12)13/h11-14H,1,3,5-8H2,2,4H3
InChI Key VBTALUUAPIOMQJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.76
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Methyl-6-methylidene-4-prop-1-en-2-yl-1,3,4,4a,5,7,8,8a-octahydronaphthalen-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 + 1.0000 100.00%
Caco-2 + 0.7521 75.21%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.4996 49.96%
OATP2B1 inhibitior - 0.8510 85.10%
OATP1B1 inhibitior + 0.9459 94.59%
OATP1B3 inhibitior + 0.9169 91.69%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8487 84.87%
P-glycoprotein inhibitior - 0.9076 90.76%
P-glycoprotein substrate - 0.7731 77.31%
CYP3A4 substrate - 0.5404 54.04%
CYP2C9 substrate - 0.8058 80.58%
CYP2D6 substrate - 0.7529 75.29%
CYP3A4 inhibition - 0.7600 76.00%
CYP2C9 inhibition - 0.8984 89.84%
CYP2C19 inhibition - 0.6944 69.44%
CYP2D6 inhibition - 0.9293 92.93%
CYP1A2 inhibition - 0.6270 62.70%
CYP2C8 inhibition - 0.9575 95.75%
CYP inhibitory promiscuity - 0.7079 70.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5504 55.04%
Eye corrosion - 0.9329 93.29%
Eye irritation + 0.8315 83.15%
Skin irritation - 0.5148 51.48%
Skin corrosion - 0.9606 96.06%
Ames mutagenesis - 0.8298 82.98%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.7533 75.33%
skin sensitisation + 0.8943 89.43%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.6410 64.10%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.4586 45.86%
Acute Oral Toxicity (c) III 0.7341 73.41%
Estrogen receptor binding - 0.8020 80.20%
Androgen receptor binding + 0.5718 57.18%
Thyroid receptor binding - 0.6592 65.92%
Glucocorticoid receptor binding - 0.7476 74.76%
Aromatase binding - 0.7870 78.70%
PPAR gamma - 0.7604 76.04%
Honey bee toxicity - 0.8706 87.06%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9885 98.85%

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 96.01% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.19% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.28% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.59% 100.00%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 84.75% 97.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.34% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.17% 85.14%
CHEMBL1902 P62942 FK506-binding protein 1A 82.49% 97.05%
CHEMBL1871 P10275 Androgen Receptor 80.28% 96.43%

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.
Artemisia annua

Cross-Links

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PubChem 101417153
LOTUS LTS0087578
wikiData Q105283475