5-Methyl-2-methylidene-8-propan-2-yl-1,3,4,4a,6,7,8,8a-octahydronaphthalene-1,5-diol

Details

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Internal ID 5b0f110c-c118-439d-884e-018b8b24576c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 5-methyl-2-methylidene-8-propan-2-yl-1,3,4,4a,6,7,8,8a-octahydronaphthalene-1,5-diol
SMILES (Canonical) CC(C)C1CCC(C2C1C(C(=C)CC2)O)(C)O
SMILES (Isomeric) CC(C)C1CCC(C2C1C(C(=C)CC2)O)(C)O
InChI InChI=1S/C15H26O2/c1-9(2)11-7-8-15(4,17)12-6-5-10(3)14(16)13(11)12/h9,11-14,16-17H,3,5-8H2,1-2,4H3
InChI Key UDOYEVPXAOVCET-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O2
Molecular Weight 238.37 g/mol
Exact Mass 238.193280068 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.75
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Methyl-2-methylidene-8-propan-2-yl-1,3,4,4a,6,7,8,8a-octahydronaphthalene-1,5-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.6128 61.28%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5452 54.52%
OATP2B1 inhibitior - 0.8476 84.76%
OATP1B1 inhibitior + 0.8991 89.91%
OATP1B3 inhibitior + 0.8850 88.50%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9028 90.28%
P-glycoprotein inhibitior - 0.9358 93.58%
P-glycoprotein substrate - 0.8620 86.20%
CYP3A4 substrate + 0.5663 56.63%
CYP2C9 substrate - 0.7574 75.74%
CYP2D6 substrate - 0.7094 70.94%
CYP3A4 inhibition - 0.7473 74.73%
CYP2C9 inhibition - 0.8889 88.89%
CYP2C19 inhibition - 0.6823 68.23%
CYP2D6 inhibition - 0.9411 94.11%
CYP1A2 inhibition - 0.8202 82.02%
CYP2C8 inhibition - 0.8465 84.65%
CYP inhibitory promiscuity - 0.7637 76.37%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6132 61.32%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.5608 56.08%
Skin irritation + 0.5231 52.31%
Skin corrosion - 0.9580 95.80%
Ames mutagenesis - 0.7053 70.53%
Human Ether-a-go-go-Related Gene inhibition - 0.5798 57.98%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6527 65.27%
skin sensitisation + 0.6438 64.38%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.7273 72.73%
Acute Oral Toxicity (c) III 0.8057 80.57%
Estrogen receptor binding - 0.6259 62.59%
Androgen receptor binding - 0.5147 51.47%
Thyroid receptor binding - 0.5055 50.55%
Glucocorticoid receptor binding - 0.5523 55.23%
Aromatase binding - 0.7493 74.93%
PPAR gamma - 0.8036 80.36%
Honey bee toxicity - 0.8675 86.75%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9920 99.20%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.71% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.47% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.51% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.39% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 89.16% 90.17%
CHEMBL226 P30542 Adenosine A1 receptor 87.70% 95.93%
CHEMBL1871 P10275 Androgen Receptor 86.97% 96.43%
CHEMBL1937 Q92769 Histone deacetylase 2 86.11% 94.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.83% 95.89%
CHEMBL2996 Q05655 Protein kinase C delta 83.27% 97.79%
CHEMBL2581 P07339 Cathepsin D 82.93% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.19% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.00% 97.09%

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.
Jacobaea erucifolia subsp. argunensis

Cross-Links

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PubChem 85288293
LOTUS LTS0202855
wikiData Q105270470