(3S)-3beta,8-Dimethyl-5beta-isopropyl-4,4abeta,5,6-tetrahydronaphthalene-2(3H)-one

Details

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Internal ID 6147ec8b-1def-493f-9ec7-50f923538070
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3S,4aR,5R)-3,8-dimethyl-5-propan-2-yl-4,4a,5,6-tetrahydro-3H-naphthalen-2-one
SMILES (Canonical) CC1CC2C(CC=C(C2=CC1=O)C)C(C)C
SMILES (Isomeric) C[C@H]1C[C@@H]2[C@H](CC=C(C2=CC1=O)C)C(C)C
InChI InChI=1S/C15H22O/c1-9(2)12-6-5-10(3)13-8-15(16)11(4)7-14(12)13/h5,8-9,11-12,14H,6-7H2,1-4H3/t11-,12+,14+/m0/s1
InChI Key MTZVTPNRLNIWQL-OUCADQQQSA-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 3.10
Atomic LogP (AlogP) 3.76
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 (3S)-3beta,8-Dimethyl-5beta-isopropyl-4,4abeta,5,6-tetrahydronaphthalene-2(3H)-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 + 0.8896 88.96%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.5168 51.68%
OATP2B1 inhibitior - 0.8528 85.28%
OATP1B1 inhibitior + 0.9183 91.83%
OATP1B3 inhibitior + 0.9623 96.23%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8449 84.49%
P-glycoprotein inhibitior - 0.9541 95.41%
P-glycoprotein substrate - 0.7898 78.98%
CYP3A4 substrate - 0.5143 51.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8579 85.79%
CYP3A4 inhibition - 0.8519 85.19%
CYP2C9 inhibition - 0.7065 70.65%
CYP2C19 inhibition - 0.5421 54.21%
CYP2D6 inhibition - 0.8872 88.72%
CYP1A2 inhibition - 0.5209 52.09%
CYP2C8 inhibition - 0.9533 95.33%
CYP inhibitory promiscuity + 0.5301 53.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.4564 45.64%
Eye corrosion - 0.9659 96.59%
Eye irritation - 0.6526 65.26%
Skin irritation - 0.5527 55.27%
Skin corrosion - 0.9576 95.76%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3845 38.45%
Micronuclear - 0.8767 87.67%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation + 0.8416 84.16%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.7281 72.81%
Acute Oral Toxicity (c) III 0.5561 55.61%
Estrogen receptor binding - 0.8693 86.93%
Androgen receptor binding + 0.6730 67.30%
Thyroid receptor binding - 0.6918 69.18%
Glucocorticoid receptor binding - 0.7145 71.45%
Aromatase binding - 0.8543 85.43%
PPAR gamma - 0.7570 75.70%
Honey bee toxicity - 0.8868 88.68%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9961 99.61%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.75% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.45% 90.71%
CHEMBL2581 P07339 Cathepsin D 89.79% 98.95%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 88.71% 86.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.07% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.56% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.68% 96.09%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.16% 94.80%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.13% 93.56%
CHEMBL1937 Q92769 Histone deacetylase 2 82.12% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.03% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.78% 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.
Helichrysum petiolare
Sinocrassula indica

Cross-Links

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PubChem 10921986
NPASS NPC136897
LOTUS LTS0206357
wikiData Q105172007