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

Details

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Internal ID a9337610-312a-4f6b-9812-b0bbb5d0aa8d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4aS,8S,8aR)-3,8-dimethyl-5-propan-2-ylidene-1,4a,6,7,8,8a-hexahydronaphthalen-2-one
SMILES (Canonical) CC1CCC(=C(C)C)C2C1CC(=O)C(=C2)C
SMILES (Isomeric) C[C@H]1CCC(=C(C)C)[C@H]2[C@@H]1CC(=O)C(=C2)C
InChI InChI=1S/C15H22O/c1-9(2)12-6-5-10(3)13-8-15(16)11(4)7-14(12)13/h7,10,13-14H,5-6,8H2,1-4H3/t10-,13+,14-/m0/s1
InChI Key WCBCKXJLRYPWHZ-GDLCADMTSA-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) 3.90
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 (4aS,8S,8aR)-3,8-dimethyl-5-propan-2-ylidene-1,4a,6,7,8,8a-hexahydronaphthalen-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 + 0.9152 91.52%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5311 53.11%
OATP2B1 inhibitior - 0.8472 84.72%
OATP1B1 inhibitior + 0.9329 93.29%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7867 78.67%
P-glycoprotein inhibitior - 0.9140 91.40%
P-glycoprotein substrate - 0.8855 88.55%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8170 81.70%
CYP2D6 substrate - 0.8598 85.98%
CYP3A4 inhibition - 0.8776 87.76%
CYP2C9 inhibition - 0.8218 82.18%
CYP2C19 inhibition - 0.6410 64.10%
CYP2D6 inhibition - 0.9562 95.62%
CYP1A2 inhibition - 0.6424 64.24%
CYP2C8 inhibition - 0.9013 90.13%
CYP inhibitory promiscuity - 0.7364 73.64%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5390 53.90%
Eye corrosion - 0.9631 96.31%
Eye irritation - 0.5152 51.52%
Skin irritation + 0.6062 60.62%
Skin corrosion - 0.9619 96.19%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4902 49.02%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.7929 79.29%
skin sensitisation + 0.9212 92.12%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.6811 68.11%
Acute Oral Toxicity (c) III 0.4568 45.68%
Estrogen receptor binding - 0.9339 93.39%
Androgen receptor binding - 0.5623 56.23%
Thyroid receptor binding - 0.7002 70.02%
Glucocorticoid receptor binding - 0.7934 79.34%
Aromatase binding - 0.8651 86.51%
PPAR gamma - 0.6457 64.57%
Honey bee toxicity - 0.9050 90.50%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9913 99.13%

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 92.77% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.48% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.42% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.51% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.83% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.96% 99.23%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.43% 93.04%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.11% 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 102575403
LOTUS LTS0139867
wikiData Q105301282