4,7-Dimethyl-1-propan-2-ylidene-2,3,4,5,6,8a-hexahydronaphthalen-4a-ol

Details

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Internal ID 47b559e9-b481-460b-988f-46b42a837859
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 4,7-dimethyl-1-propan-2-ylidene-2,3,4,5,6,8a-hexahydronaphthalen-4a-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-10(2)13-6-5-12(4)15(16)8-7-11(3)9-14(13)15/h9,12,14,16H,5-8H2,1-4H3
InChI Key RLQQLZPOMNLHJN-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 3.10
Atomic LogP (AlogP) 3.84
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,7-Dimethyl-1-propan-2-ylidene-2,3,4,5,6,8a-hexahydronaphthalen-4a-ol

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 + 0.8860 88.60%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.4847 48.47%
OATP2B1 inhibitior - 0.8406 84.06%
OATP1B1 inhibitior + 0.9488 94.88%
OATP1B3 inhibitior + 0.9335 93.35%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8972 89.72%
P-glycoprotein inhibitior - 0.9389 93.89%
P-glycoprotein substrate - 0.8688 86.88%
CYP3A4 substrate + 0.5121 51.21%
CYP2C9 substrate - 0.7433 74.33%
CYP2D6 substrate - 0.7450 74.50%
CYP3A4 inhibition - 0.8040 80.40%
CYP2C9 inhibition - 0.8039 80.39%
CYP2C19 inhibition - 0.6920 69.20%
CYP2D6 inhibition - 0.9487 94.87%
CYP1A2 inhibition - 0.8479 84.79%
CYP2C8 inhibition - 0.8468 84.68%
CYP inhibitory promiscuity - 0.7935 79.35%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5859 58.59%
Eye corrosion - 0.9859 98.59%
Eye irritation + 0.7680 76.80%
Skin irritation + 0.6931 69.31%
Skin corrosion - 0.9484 94.84%
Ames mutagenesis - 0.7370 73.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4536 45.36%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6450 64.50%
skin sensitisation + 0.7035 70.35%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7063 70.63%
Acute Oral Toxicity (c) III 0.8508 85.08%
Estrogen receptor binding - 0.9130 91.30%
Androgen receptor binding - 0.4837 48.37%
Thyroid receptor binding - 0.5859 58.59%
Glucocorticoid receptor binding - 0.7297 72.97%
Aromatase binding - 0.8025 80.25%
PPAR gamma - 0.6424 64.24%
Honey bee toxicity - 0.8972 89.72%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9860 98.60%

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 94.38% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.86% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.82% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.67% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.89% 92.94%

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.
Croton hieronymi

Cross-Links

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PubChem 162998101
LOTUS LTS0269390
wikiData Q105240448