3,8-Dimethyl-5-propan-2-yl-1,2,4a,5,6,8a-hexahydronaphthalen-1-ol

Details

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Internal ID e5b8bd8c-ad85-487e-819e-90d0d710b5b7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3,8-dimethyl-5-propan-2-yl-1,2,4a,5,6,8a-hexahydronaphthalen-1-ol
SMILES (Canonical) CC1=CC2C(CC=C(C2C(C1)O)C)C(C)C
SMILES (Isomeric) CC1=CC2C(CC=C(C2C(C1)O)C)C(C)C
InChI InChI=1S/C15H24O/c1-9(2)12-6-5-11(4)15-13(12)7-10(3)8-14(15)16/h5,7,9,12-16H,6,8H2,1-4H3
InChI Key STLBTFMCSOXEAQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.55
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,8-Dimethyl-5-propan-2-yl-1,2,4a,5,6,8a-hexahydronaphthalen-1-ol

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 + 0.8375 83.75%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.5520 55.20%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.9358 93.58%
OATP1B3 inhibitior + 0.9604 96.04%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8855 88.55%
P-glycoprotein inhibitior - 0.9295 92.95%
P-glycoprotein substrate - 0.7339 73.39%
CYP3A4 substrate - 0.5810 58.10%
CYP2C9 substrate - 0.6284 62.84%
CYP2D6 substrate + 0.3479 34.79%
CYP3A4 inhibition - 0.8317 83.17%
CYP2C9 inhibition - 0.8671 86.71%
CYP2C19 inhibition - 0.7171 71.71%
CYP2D6 inhibition - 0.8541 85.41%
CYP1A2 inhibition - 0.6405 64.05%
CYP2C8 inhibition - 0.9753 97.53%
CYP inhibitory promiscuity - 0.7765 77.65%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8118 81.18%
Carcinogenicity (trinary) Non-required 0.5721 57.21%
Eye corrosion - 0.9677 96.77%
Eye irritation - 0.7184 71.84%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9142 91.42%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5258 52.58%
Micronuclear - 0.9141 91.41%
Hepatotoxicity - 0.5601 56.01%
skin sensitisation + 0.8102 81.02%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.5403 54.03%
Acute Oral Toxicity (c) III 0.7913 79.13%
Estrogen receptor binding - 0.8122 81.22%
Androgen receptor binding - 0.6054 60.54%
Thyroid receptor binding - 0.6856 68.56%
Glucocorticoid receptor binding - 0.7927 79.27%
Aromatase binding - 0.8998 89.98%
PPAR gamma - 0.8051 80.51%
Honey bee toxicity - 0.8598 85.98%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9120 91.20%

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 90.64% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.25% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.53% 93.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.20% 86.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.61% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 82.15% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.75% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.11% 95.89%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.77% 97.21%

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.
Jatropha neopauciflora

Cross-Links

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PubChem 13874508
LOTUS LTS0208805
wikiData Q105260346