(4aR,8S,8aR)-3,8-dimethyl-5-propan-2-ylidene-2,4a,6,7,8,8a-hexahydronaphthalen-1-one

Details

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Internal ID 34a631a1-acfd-466b-aa6d-8e86a392489a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4aR,8S,8aR)-3,8-dimethyl-5-propan-2-ylidene-2,4a,6,7,8,8a-hexahydronaphthalen-1-one
SMILES (Canonical) CC1CCC(=C(C)C)C2C1C(=O)CC(=C2)C
SMILES (Isomeric) C[C@H]1CCC(=C(C)C)[C@H]2[C@@H]1C(=O)CC(=C2)C
InChI InChI=1S/C15H22O/c1-9(2)12-6-5-11(4)15-13(12)7-10(3)8-14(15)16/h7,11,13,15H,5-6,8H2,1-4H3/t11-,13-,15+/m0/s1
InChI Key ABZDLUFXOKZOMD-CORIIIEPSA-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 3.20
Atomic LogP (AlogP) 3.90
H-Bond Acceptor 1
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,8S,8aR)-3,8-dimethyl-5-propan-2-ylidene-2,4a,6,7,8,8a-hexahydronaphthalen-1-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 + 0.9547 95.47%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.4354 43.54%
OATP2B1 inhibitior - 0.8508 85.08%
OATP1B1 inhibitior + 0.9351 93.51%
OATP1B3 inhibitior + 0.9620 96.20%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8645 86.45%
P-glycoprotein inhibitior - 0.9285 92.85%
P-glycoprotein substrate - 0.8811 88.11%
CYP3A4 substrate - 0.5244 52.44%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.7696 76.96%
CYP3A4 inhibition - 0.9120 91.20%
CYP2C9 inhibition - 0.8204 82.04%
CYP2C19 inhibition - 0.6793 67.93%
CYP2D6 inhibition - 0.9305 93.05%
CYP1A2 inhibition - 0.6597 65.97%
CYP2C8 inhibition - 0.9383 93.83%
CYP inhibitory promiscuity - 0.7710 77.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9110 91.10%
Carcinogenicity (trinary) Non-required 0.5270 52.70%
Eye corrosion - 0.9409 94.09%
Eye irritation + 0.6450 64.50%
Skin irritation + 0.6182 61.82%
Skin corrosion - 0.9392 93.92%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4652 46.52%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.8679 86.79%
skin sensitisation + 0.9219 92.19%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.5701 57.01%
Acute Oral Toxicity (c) III 0.7227 72.27%
Estrogen receptor binding - 0.9008 90.08%
Androgen receptor binding - 0.5842 58.42%
Thyroid receptor binding - 0.6613 66.13%
Glucocorticoid receptor binding - 0.7041 70.41%
Aromatase binding - 0.9034 90.34%
PPAR gamma - 0.8409 84.09%
Honey bee toxicity - 0.9309 93.09%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9575 95.75%

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 93.05% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.56% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.82% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.83% 99.23%
CHEMBL2581 P07339 Cathepsin D 87.30% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.38% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.17% 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.
Marsupella aquatica

Cross-Links

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PubChem 163188770
LOTUS LTS0247741
wikiData Q104908956