1,9-Eremophiladien-11-ol

Details

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Internal ID 43593423-4f0d-4c34-8719-9fe74a916a1f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
IUPAC Name 2-(8,8a-dimethyl-2,3,7,8-tetrahydro-1H-naphthalen-2-yl)propan-2-ol
SMILES (Canonical) CC1CC=CC2=CCC(CC12C)C(C)(C)O
SMILES (Isomeric) CC1CC=CC2=CCC(CC12C)C(C)(C)O
InChI InChI=1S/C15H24O/c1-11-6-5-7-12-8-9-13(14(2,3)16)10-15(11,12)4/h5,7-8,11,13,16H,6,9-10H2,1-4H3
InChI Key WINATCPPCIWJCQ-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 3.40
Atomic LogP (AlogP) 3.70
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 1,9-Eremophiladien-11-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 + 0.9382 93.82%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.4178 41.78%
OATP2B1 inhibitior - 0.8560 85.60%
OATP1B1 inhibitior + 0.9417 94.17%
OATP1B3 inhibitior + 0.8837 88.37%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8800 88.00%
P-glycoprotein inhibitior - 0.9696 96.96%
P-glycoprotein substrate - 0.7767 77.67%
CYP3A4 substrate + 0.5289 52.89%
CYP2C9 substrate - 0.5886 58.86%
CYP2D6 substrate - 0.8006 80.06%
CYP3A4 inhibition - 0.7817 78.17%
CYP2C9 inhibition - 0.5967 59.67%
CYP2C19 inhibition - 0.5591 55.91%
CYP2D6 inhibition - 0.9249 92.49%
CYP1A2 inhibition - 0.8426 84.26%
CYP2C8 inhibition - 0.7704 77.04%
CYP inhibitory promiscuity - 0.5406 54.06%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.5924 59.24%
Eye corrosion - 0.9791 97.91%
Eye irritation - 0.8931 89.31%
Skin irritation - 0.6031 60.31%
Skin corrosion - 0.9631 96.31%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4306 43.06%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation + 0.7106 71.06%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6405 64.05%
Acute Oral Toxicity (c) III 0.6111 61.11%
Estrogen receptor binding - 0.8968 89.68%
Androgen receptor binding - 0.7867 78.67%
Thyroid receptor binding - 0.5560 55.60%
Glucocorticoid receptor binding - 0.6882 68.82%
Aromatase binding - 0.6656 66.56%
PPAR gamma - 0.8643 86.43%
Honey bee toxicity - 0.9077 90.77%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 1.0000 100.00%

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 94.72% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.41% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.52% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.90% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.38% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.34% 97.09%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.58% 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.
Aquilaria malaccensis

Cross-Links

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PubChem 5316454
NPASS NPC112619