(4aS,7R)-4a-methyl-7-prop-1-en-2-yl-5,6,7,8-tetrahydronaphthalen-2-one

Details

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Internal ID 2cc60be8-093f-47fd-a20c-e8d280cc9c0e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name (4aS,7R)-4a-methyl-7-prop-1-en-2-yl-5,6,7,8-tetrahydronaphthalen-2-one
SMILES (Canonical) CC(=C)C1CCC2(C=CC(=O)C=C2C1)C
SMILES (Isomeric) CC(=C)[C@@H]1CC[C@]2(C=CC(=O)C=C2C1)C
InChI InChI=1S/C14H18O/c1-10(2)11-4-6-14(3)7-5-13(15)9-12(14)8-11/h5,7,9,11H,1,4,6,8H2,2-3H3/t11-,14+/m1/s1
InChI Key HCGLSNXCQRJVMY-RISCZKNCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O
Molecular Weight 202.29 g/mol
Exact Mass 202.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.43
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 (4aS,7R)-4a-methyl-7-prop-1-en-2-yl-5,6,7,8-tetrahydronaphthalen-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 + 0.9974 99.74%
Caco-2 + 0.8124 81.24%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.4309 43.09%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.9149 91.49%
OATP1B3 inhibitior + 0.9445 94.45%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.6705 67.05%
P-glycoprotein inhibitior - 0.9749 97.49%
P-glycoprotein substrate - 0.7986 79.86%
CYP3A4 substrate + 0.5806 58.06%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8854 88.54%
CYP3A4 inhibition - 0.8445 84.45%
CYP2C9 inhibition - 0.7341 73.41%
CYP2C19 inhibition - 0.6196 61.96%
CYP2D6 inhibition - 0.9181 91.81%
CYP1A2 inhibition - 0.7330 73.30%
CYP2C8 inhibition - 0.8498 84.98%
CYP inhibitory promiscuity - 0.7764 77.64%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.4669 46.69%
Eye corrosion - 0.9562 95.62%
Eye irritation + 0.6307 63.07%
Skin irritation - 0.5640 56.40%
Skin corrosion - 0.9664 96.64%
Ames mutagenesis - 0.7924 79.24%
Human Ether-a-go-go-Related Gene inhibition - 0.5297 52.97%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.6120 61.20%
skin sensitisation + 0.7938 79.38%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.5465 54.65%
Acute Oral Toxicity (c) III 0.7727 77.27%
Estrogen receptor binding - 0.8601 86.01%
Androgen receptor binding - 0.5498 54.98%
Thyroid receptor binding - 0.7323 73.23%
Glucocorticoid receptor binding - 0.5938 59.38%
Aromatase binding - 0.6895 68.95%
PPAR gamma - 0.7149 71.49%
Honey bee toxicity - 0.9234 92.34%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9959 99.59%

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 95.49% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.85% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.89% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.05% 85.14%
CHEMBL2581 P07339 Cathepsin D 88.37% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.39% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.45% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.09% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.05% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.78% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.84% 97.09%
CHEMBL1871 P10275 Androgen Receptor 82.64% 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.
Lycium barbarum

Cross-Links

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PubChem 15726782
NPASS NPC203142