(4aR,8aR)-4-methylidene-6-propan-2-ylidene-1,2,3,4a,5,7,8,8a-octahydronaphthalene

Details

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Internal ID cb899099-39ec-441d-9097-2340ef7e3acf
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name (4aR,8aR)-4-methylidene-6-propan-2-ylidene-1,2,3,4a,5,7,8,8a-octahydronaphthalene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H22/c1-10(2)13-8-7-12-6-4-5-11(3)14(12)9-13/h12,14H,3-9H2,1-2H3/t12-,14+/m1/s1
InChI Key VHFYCADQVMYJEI-OCCSQVGLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H22
Molecular Weight 190.32 g/mol
Exact Mass 190.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.48
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 (4aR,8aR)-4-methylidene-6-propan-2-ylidene-1,2,3,4a,5,7,8,8a-octahydronaphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.8257 82.57%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Lysosomes 0.7167 71.67%
OATP2B1 inhibitior - 0.8506 85.06%
OATP1B1 inhibitior + 0.8920 89.20%
OATP1B3 inhibitior + 0.9235 92.35%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9164 91.64%
P-glycoprotein inhibitior - 0.9280 92.80%
P-glycoprotein substrate - 0.8957 89.57%
CYP3A4 substrate - 0.5652 56.52%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7217 72.17%
CYP3A4 inhibition - 0.9067 90.67%
CYP2C9 inhibition - 0.8079 80.79%
CYP2C19 inhibition - 0.7035 70.35%
CYP2D6 inhibition - 0.9075 90.75%
CYP1A2 inhibition - 0.6554 65.54%
CYP2C8 inhibition - 0.8653 86.53%
CYP inhibitory promiscuity - 0.5419 54.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.4826 48.26%
Eye corrosion - 0.6999 69.99%
Eye irritation + 0.9468 94.68%
Skin irritation - 0.5689 56.89%
Skin corrosion - 0.9355 93.55%
Ames mutagenesis - 0.9154 91.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4335 43.35%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.7210 72.10%
skin sensitisation + 0.8947 89.47%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.5718 57.18%
Acute Oral Toxicity (c) III 0.6707 67.07%
Estrogen receptor binding - 0.9199 91.99%
Androgen receptor binding - 0.5463 54.63%
Thyroid receptor binding - 0.7015 70.15%
Glucocorticoid receptor binding - 0.8251 82.51%
Aromatase binding - 0.8427 84.27%
PPAR gamma - 0.8242 82.42%
Honey bee toxicity - 0.9559 95.59%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5500 55.00%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.87% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.13% 91.11%
CHEMBL217 P14416 Dopamine D2 receptor 83.90% 95.62%
CHEMBL2581 P07339 Cathepsin D 83.41% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.05% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.10% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.87% 97.25%

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.
Trichogonia salviifolia

Cross-Links

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PubChem 162845205
LOTUS LTS0172840
wikiData Q105286406