1-Methyl-6-methylidene-4-propan-2-ylidene-1,2,3,4a,5,8a-hexahydronaphthalene

Details

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Internal ID 5844fa6a-ce9f-41aa-8b67-bc1a0597b9ff
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1-methyl-6-methylidene-4-propan-2-ylidene-1,2,3,4a,5,8a-hexahydronaphthalene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h5,7,12,14-15H,3,6,8-9H2,1-2,4H3
InChI Key IYQNJZNZDXORJP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22
Molecular Weight 202.33 g/mol
Exact Mass 202.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.50
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Methyl-6-methylidene-4-propan-2-ylidene-1,2,3,4a,5,8a-hexahydronaphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.7802 78.02%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.5920 59.20%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.9057 90.57%
OATP1B3 inhibitior + 0.9000 90.00%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8901 89.01%
P-glycoprotein inhibitior - 0.9678 96.78%
P-glycoprotein substrate - 0.8472 84.72%
CYP3A4 substrate - 0.5313 53.13%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7694 76.94%
CYP3A4 inhibition - 0.8918 89.18%
CYP2C9 inhibition - 0.7328 73.28%
CYP2C19 inhibition - 0.6227 62.27%
CYP2D6 inhibition - 0.9229 92.29%
CYP1A2 inhibition - 0.6706 67.06%
CYP2C8 inhibition - 0.8417 84.17%
CYP inhibitory promiscuity - 0.6044 60.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.4535 45.35%
Eye corrosion - 0.8413 84.13%
Eye irritation - 0.5479 54.79%
Skin irritation - 0.5449 54.49%
Skin corrosion - 0.9405 94.05%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6602 66.02%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.7679 76.79%
skin sensitisation + 0.8644 86.44%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.7923 79.23%
Acute Oral Toxicity (c) III 0.7950 79.50%
Estrogen receptor binding - 0.9406 94.06%
Androgen receptor binding - 0.5377 53.77%
Thyroid receptor binding - 0.6841 68.41%
Glucocorticoid receptor binding - 0.8775 87.75%
Aromatase binding - 0.8159 81.59%
PPAR gamma - 0.7526 75.26%
Honey bee toxicity - 0.9244 92.44%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.26% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.43% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.70% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 83.26% 91.49%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.17% 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.
Carlina diae

Cross-Links

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PubChem 163041460
LOTUS LTS0034627
wikiData Q105122880